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	<description>Indonesia Nanobiology Institute</description>
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		<title>Atomic Mineral Characteristics of Indonesian Osteoporosis by High-Resolution Inductively Coupled Plasma Mass Spectrometry</title>
		<link>http://smartbio.org/publications/atomic-mineral-characteristics-of-indonesian-osteoporosis-by-high-resolution-inductively-coupled-plasma-mass-spectrometry/</link>
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		<pubDate>Thu, 03 May 2012 04:05:50 +0000</pubDate>
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		<description><![CDATA[Zairin Noor (1), Sutiman Bambang Sumitro (2),Mohammad Hidayat (3), Agus Hadian Rahim (4), Akhmad Sabarudin (5,6), and Tomonari Umemura (6) Department of Orthopaedics, Ulin General Hospital, Faculty of Medicine, Lambung   Mangkurat University, Banjarmasin 70232, Indonesia Department of Biology, Faculty &#8230; <a href="http://smartbio.org/publications/atomic-mineral-characteristics-of-indonesian-osteoporosis-by-high-resolution-inductively-coupled-plasma-mass-spectrometry/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>Z<strong>airin Noor (1), Sutiman Bambang Sumitro (2),Mohammad Hidayat (3), Agus Hadian Rahim (4), Akhmad Sabarudin (5,6), and Tomonari Umemura (6)</strong></p>
<ol>
<li>Department of Orthopaedics, Ulin General Hospital, Faculty of Medicine, Lambung   Mangkurat University, Banjarmasin 70232, Indonesia</li>
<li>Department of Biology, Faculty of Science, Brawijaya University, Malang 65145, Indonesia</li>
<li>Department of Orthopaedics, Syaiful Anwar General Hospital, Faculty of Medicine, Brawijaya University, Malang 65122, Indonesia</li>
<li>Department of Orthopaedics, Hasan Sadikin Hospital, Faculty of Medicine, Padjadjaran University, Bandung 40161, Indonesia</li>
<li>Department of Chemistry, Faculty of Science, Brawijaya University, Malang 65145, Indonesia</li>
<li>Division of Nanomaterial Sciences, EcoTopia Science Institute, Nagoya University, Nagoya 464-8603, Japan</li>
</ol>
<p>Received 31 October 2011; Accepted 25 December 2011</p>
<p>Academic Editor: Jameela Banu</p>
<p>Copyright © 2012 Zairin Noor et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
<p>Abstract</p>
<p>Clinical research indicates that negative calcium balance is associated with low bone mass, rapid bone loss, and high fracture rates. However, some studies revealed that not only calcium is involved in bone strengthening as risk factor of fracture osteoporosis. Thus, in this report, the difference of metallic and nonmetallic elements in osteoporosis and normal bones was studied by high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS). The influence of these elements on bone metabolic processes is also discussed. Inclusion criteria of bone samples consist of postmenopausal woman, trabecular bone fracture, normal and osteoporosis BMD value, and no history of previous disease. The results showed that the concentration of B, Al, S, V, Co, Mo, Te, Ba, La, Ni, As, and Ca/P ratio is higher in osteoporosis than normal. These atomic minerals have negative role to imbalance between bone resorption and bone formation activity. Conversely, concentrations of Na, Mg, P, K, Ca, Cr, Pd, Ag, Mn, Fe, Cu, Zn, Rb, Sr, Pb, and Se are lower in osteoporosis than in normal bones. Among these atoms, known to have important roles in bone structure, we found involvement of atomic mineral and calcium which are considerable to contribute to osteoporotic phenomena.</p>
<p>Full publication text : <a href="http://www.tswj.com/2012/372972/">The Scientific World Journal</a></p>
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		<title>Can tobacco be used to cure cancer?</title>
		<link>http://smartbio.org/articles/can-tobacco-be-used-to-cure-cancer/</link>
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		<pubDate>Thu, 03 May 2012 04:01:34 +0000</pubDate>
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		<description><![CDATA[LISA PRIEST From Wednesday&#8217;s Globe and Mail Published Tuesday, Jan. 31, 2012 8:04PM EST In a Toronto laboratory, an experiment on mice is seeking to answer a question that could turn conventional wisdom on its head: Can tobacco cure cancer? &#8230; <a href="http://smartbio.org/articles/can-tobacco-be-used-to-cure-cancer/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>LISA PRIEST<br />
From Wednesday&#8217;s Globe and Mail<br />
Published Tuesday, Jan. 31, 2012 8:04PM EST</p>
<p>In a Toronto laboratory, an experiment on mice is seeking to answer a question that could turn conventional wisdom on its head: Can tobacco cure cancer?</p>
<p>The plant best known for its negative health effects has been genetically engineered to create a drug comparable to Herceptin that could one day be used to treat highly aggressive breast cancers at a lower cost.That development is part of a plant-based trend in pharmaceuticals. It is based on the belief that proteins can be made faster, cheaper and easier, allowing patients in remote parts of the world to gain access to medicines once unaffordable. And it’s not just tobacco. Plants being tested as biological drugs sound like they belong not in the laboratory but in the vegetable section at the health-food store: carrots for Gaucher’s disease, duckweed – those green flecks on top of ponds – to treat hepatitis C, and safflower to make insulin.</p>
<p>“One day we’re going to be able to grow these antibodies in plants like tobacco,” said Leigh Revers, the associate director of the master of biotechnology program at the University of Toronto. “…The question is can you make this drug identically the same as the other guy and prove it’s safe?”</p>
<p>Don Stewart, president and chief executive officer of PlantForm Corp. based in Guelph, Ont., whose company is running animal studies on tobacco, thinks so. The key, he said, is to remove sugars from the protein molecule, which can cause adverse side effects in humans, adding that using plants is a way of thinking “that’s enjoying a resurgence at the moment.”</p>
<p>In this case, the process takes place in Kentucky, where the tobacco is engineered, then cut and pounded with a giant screw, similar to those used in food manufacturing. From there, a pulp resembling crème de menthe is made; out of that extract, the drug is purified. It’s this act of purification that transforms it into a potentially cancer-curing drug.</p>
<p>A hearty plant with leaves the size of elephants ears, tobacco can be grown close together, inside a greenhouse or out. And it is not part of the food chain like corn, so there is no danger of viruses getting into the food supply.</p>
<p>“The beauty is being able to produce a very sophisticated protein-based drug in a bioreactor in a plant that basically requires fertilizer, water and sunlight,” said Michael McLean, director of research at PlantForm. “It’s as simple as possible for a manufacturing process.”</p>
<p>The developers have a long way to go – animal studies just began Jan. 26. Human studies with as many as 50 people aren’t slated to take place until late 2013, followed by a larger trial of up to 400 subjects in 2014. Still, Mr. Stewart believes the lower projected cost of the drug – $20,000 to $28,000 – will be attractive globally, something he will have to prove against four other competitors vying for that part of the cancer-treatment market.</p>
<p>Herceptin (the trade name for trastuzumab) is used to treat people with HER-2 positive breast cancer – about 20 to 25 per cent of breast-cancer patients. It has turned one of the most aggressive forms of the disease into one of the most treatable, though at a high cost: about $40,000 for a course of treatment, which consists of intravenous medication provided every three weeks for one year.</p>
<p>The drug comes off patent in Europe in 2014 and in North America in 2017.</p>
<p>Making a bio-similar drug is like making a generic – but not exactly: It isn’t a perfect copy like a chemically made compound, but it should come close and perform comparably well. While these types of drugs are intended to reach patients faster – it takes five to six years instead of 15 years to make a brand-name drug – their makers still must show that their product is safe and efficacious.</p>
<p>Typically, government regulators, which license and approve drugs, don’t look at how innovative the process is but merely whether the generic version looks the same under a microscope as the brand-name version. Herceptin is made in a bio-reactor from mammalian cells that have been originally derived from a Chinese hamster, not a plant.</p>
<p>“They have managed to engineer it so that it’s more human-like,” said Dr. Turner, who holds a PhD in chemistry. “It [tobacco] could be a great vehicle for producing all sorts of biological medicines, but I think it still could be 10 years away.”</p>
<p>link: <a href="http://www.theglobeandmail.com/life/health/new-health/health-news/can-tobacco-be-used-to-cure-cancer/article2321906/">The Globe and Mail</a></p>
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		<title>The Toxic Effects of  The Mercury in Dental Amalgam Fillings on The Environment and Human Health</title>
		<link>http://smartbio.org/articles/the-toxic-effects-of-the-mercury-in-dental-amalgam-fillings-on-the-environment-and-human-health/</link>
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		<pubDate>Sat, 17 Dec 2011 04:32:56 +0000</pubDate>
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		<description><![CDATA[A FACT SHEET PREPARED BY The International Academy of Oral Medicine and Toxicology www.iaomt.org “For medical reasons, amalgam should be eliminated in dental care as soon as possible. As a result, one of our largest sources of mercury in the environment &#8230; <a href="http://smartbio.org/articles/the-toxic-effects-of-the-mercury-in-dental-amalgam-fillings-on-the-environment-and-human-health/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<div>
<h1 style="text-align: left;"><strong><em>A FACT SHEET PREPARED BY</em></strong></h1>
<h1 style="text-align: left;"><strong><em><em></em></em></strong>The International Academy of Oral Medicine and Toxicology <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a></h1>
<div style="text-align: left;"><em>“For medical reasons, amalgam should be eliminated in dental care as soon as possible. As a result, one of our largest sources of mercury in the environment can be eliminated.’’</em><em>1</em></div>
<div style="text-align: left;"><em>&#8211;Dr. Maths Berlin, the Dental Material Commission of Sweden, 2003</em></div>
<p></p>
<div style="text-align: left;"><strong>About IAOMT</strong></div>
<p></p>
<div style="text-align: left;">Representing a network of dental, medical, and research professionals with members in North America and affiliated chapters in over fourteen other countries, the International Academy of Oral Medicine and Toxicology (IAOMT) has been researching the damage dental mercury inflicts on the environment and humans since the non-profit organization was created in 1984.</div>
<p></p>
<div style="text-align: left;"><strong>Brief Overview of Mercury Used in Dentistry</strong></p>
<div>Millions of dentists around the world routinely use dental amalgam as a filling material to repair decayed teeth. Often referred to as “silver” fillings, amalgam fillings actually consist of 45-55% metallic mercury.2</div>
<div>According to the United States Environmental Protection Agency (EPA), there are currently over 1,000 tons of mercury in the mouths of Americans, which is more than half of all the mercury being used in the U.S. today.3 Also according to the EPA, dentistry accounts for 14% of the U.S. domestic usage of mercury annually.4</div>
<div>Controversy has surrounded the use of mercury in dentistry since the 1800’s, when the neurotoxin was first widely introduced as a filling material. The American Society of Dental Surgeons, the predecessor to the American Dental Association, made its members pledge not to use mercury because of its known toxicity,5 and in more recent years, government officials, scientists, dentists, consumers, and many others have raised serious concerns about the threats dental mercury poses to humans and to the environment at large.</div>
<div>Today, authorities including the United Nations Environmental Programme (UNEP), the United States Food and Drug Administration (FDA), and the European Commission (EC) are actively assessing health risks associated with dental amalgam. 6 7 8</div>
<div>However, the governments of Norway, Sweden, and Denmark have already banned the use of mercury fillings in dentistry,9 Germany and Canada have limited their use for pregnant women,10 11 and France, Finland, and Austria have recommended that alternative dental materials be used for pregnant women.12</div>
<div>Meanwhile, scientific studies continue to demonstrate the harm that mercury in dentistry inflicts upon each one of us and our environment.</div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a>2</div>
<p></p>
<div><strong>Dental Amalgam Pollutes the Environment in a Variety of Ways:</strong></p>
<div><em>A 2002 report from the New York Academy of Sciences found that 40-60% of the mercury in New York/New Jersey harbor is a result of discharges from dental offices.</em><em>13</em></div>
<div><strong>1) Wastewater from Dental Offices</strong></div>
<div>According to the EPA, dental offices were found to have been the source of 50% of all mercury pollution entering publically-owned treatment works in 2003.14</div>
<div>Studies in the United States, Canada, and other countries have also shown that dental offices play a significant role in causing mercury to enter the environment.15 In the United States, the dental industry is the third largest user of mercury, accounting for over 45 tons of mercury per year,16 and the discharge per dentist ranges from 270 to 484 milligrams per day.17 18</div>
<div>Because wastewater treatment facilities are designed to process human waste, not heavy metals, the mercury from dental discharges is separated out into sludge, or biosolids.19 These biosolids are usually incinerated or used as fertilizer, with the mercury content again being directly emitted into the environment.20</div>
<div><em>“If the average fecal excretion was applied to the entire Swedish population, a total emission of 150 kg/yr (330 lb/year) can be estimated. This is roughly comparable to the yearly mercury leakage from a modern chloralkali plant.”</em><em>21 </em><em>&#8211;Skare and Enqvist, 1992</em></div>
<div><strong>2) Human Waste</strong></div>
<div>Research has shown that the average person with amalgam excretes approximately .1 mg of mercury per day in his/her feces.22 In the United States, this amounts to over eight tons of mercury per year eventually being flushed out to sewers, streams, and lakes.23</div>
<div><em>“In Sweden, scientists have estimated that as much as 620 pounds of dental amalgam mercury are released into the atmosphere each year from cremation.”</em><em>24 </em><em>&#8211;The Institute of Environmental Medicine, Sweden, 1992</em></div>
<div><strong>3) Cremation</strong></div>
<div>Cremation of bodies with amalgam fillings adds to air emissions and deposition onto land and waterways. A Swiss study confirmed that cremation released over 65 kilograms of mercury per year as emissions, often exceeding site air mercury standards.25 In 1991, cremation of 320,372 bodies added an estimated 2,800 pounds of mercury into the atmosphere in the United States.26</div>
<div><em>“Hg vapor release to the atmosphere from dental vacuums can be substantial and can exceed human exposure levels.”</em><em>27 </em><em>&#8211;Stone, Cohen, and Debban, Naval Institute for Dental and Biomedical Research, 2007</em></div>
<div><strong>4) Mercury Vapor</strong></div>
<div>In offices with air/water separator tanks as part of the central vacuum system, mercury vapor has been found in air vented to the outside of the dental office.28 29 Dr. Paul G. Rubin of IAOMT explains, “[M]ercury-containing material is discharged into waste streams via the dental office vacuum-pump system. This system also discharges large quantities of air, either into the atmosphere exterior to the office building or into the sewer system, depending on the type of equipment used.”30</div>
<div>Furthermore, mercury vapor is continuously emitted from amalgam fillings,31 which means that people are directly exposed to the mercury in their mouths. The output of mercury vapor can be intensified by the number of fillings present and other activities associated with the human mouth, such as</div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>3</div>
<div>chewing, teeth-grinding, and the consumption of hot liquids.32 33</div>
<p></p>
<div><strong>Dental Amalgam Harms Humans in a Variety of Ways:</strong></div>
<p></p>
<div><em>“There is really no place for mercury in children.”</em><em>34 </em><em>&#8211;Dr. Suresh Kotagal, FDA Dental Products Panel, December 2010</em></div>
<div><strong>1) Pregnant Women and Children</strong></div>
<div>International legislation has already warned of the clear and present danger that the mercury in dental amalgam fillings poses to pregnant women and children: as stated earlier in this document, the governments of Norway, Sweden, and Denmark have banned the use of mercury fillings in dentistry,35 while Germany and Canada have limited their use for pregnant women,36 37 and France, Finland, and Austria have recommended that alternative dental materials be used for pregnant women.38</div>
<div>Additionally, 19 members of the United States Congress wrote a letter to the FDA in 2009 to express their concern about mercury used in amalgam fillings, with a focus on potential dangers to pregnant women and children,39 and when Representative Diane Watson of California introduced the <em>Mercury Filling Disclosure and Prohibition Act </em>(H.R. 2101), she explained, “It is, in fact, children who are at greatest risk from these fillings.”40</div>
<div>Scientific studies proving the devastating impact of mercury on pregnant woman and children are abundant, which is why pregnant women and children are advised not to eat certain types of seafood that might contain methylmercury.41 42 43</div>
<div>The dangers of fetal and infant exposure to mercury via maternal dental amalgam have likewise been scientifically established.44 45 46 47 48 49 50 51 52 53 54 55</div>
<div>Although two studies (commonly referred to as the “New England Children‘s Amalgam Trial”56 and the “Casa Pia Children’s Amalgam Trial”57) have repeatedly been referenced to defend the use of amalgam in children, researchers and commentators have demonstrated that these studies failed to take essential factors such as long-term effects, genetic predisposition, detection of smaller effects, and measurement errors into account.58 59 60 61 62 63 64</div>
<div>Furthermore, the most up-to-date science continues to expose the havoc that the mercury in dental amalgam fillings wreaks upon pregnant women and children. A study published in the April 2011 edition of<em>Environmental Monitoring and Assessment </em>notes, “As we showed, the number of amalgam filled teeth in breast-feeding mothers strongly influences the mercury level in their milk. Take it into consideration that maternal milk is the only source of nutrition during the first few months after birth.”65 Another recent study published in <em>Science of the Total Environment </em>cautions, “Changes in dental practices involving amalgam, especially for children, are highly recommended in order to avoid unnecessary exposure to Hg.”66</div>
<div>Meanwhile, mercury has been found to be a factor in autism,67 68 69 70 71 72 73 74 75 76 and as such dental amalgam fillings (maternal) have been directly linked to autism as well.77 78 79 80 81</div>
<div><em>“Dental amalgam fillings are the primary source of mercury exposure for the general population (Skare,1995; Health Canada, 1997).”</em><em>82 </em><em>&#8211;Cited in paper published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organization, and the World Health Organization</em></div>
<div><strong>2) The General Population</strong></div>
<div>An extensive number of international research studies thoroughly document the human health risks</div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>4</div>
<div>associated with the use of dental amalgam. Scientific data from reputable scientists all over the world has investigated how the mercury in amalgam fillings can relate to dysfunction of the immune system,83 84 85 86 87 88 89 90 multiple sclerosis,91 92 93 94 95 96 kidney ailments,97 98 99 100 101 chronic fatigue syndrome,102 103 104 105 allergies,106 107 108 109 reproductive issues,110 111 112 cardiovascular problems,113 114 absorption of heavy metals in the brain,115 116 Lou Gehrig’s disease,117 118 Alzheimer’s disease,119 120 antibiotic resistance,121 122 hearing loss,123 and a myriad of other health problems.124</div>
<div>125 126 127 128 129 130 131 132 133 134 135 136 137 138 139</div>
<div><em>“Provide pre-placement and periodic medical exams for those regularly exposed to mercury with emphasis directed to CNS-central nervous system, skin, lungs, liver, kidneys, and G.I. tract.”</em><em>140 </em><em>&#8211;Material Safety Data Sheet (MSDS), Safe Handling and Use Section, provided with dental amalgam product by Original D Wykle</em></div>
<div><strong>3) Dentists and Dental Personnel</strong></div>
<div>Dentists and their staffs are occupationally exposed to constant levels of mercury released from</div>
<div>dental amalgam on a routine basis, and thus, researchers have also raised concerns about the safety of dental personnel who work with amalgam.141 142 143 144 145 146 147 148 149 150 151 152 153 154 155</div>
<div><em>“&#8230;we urge you to consider the many ill effects of mercury amalgam&#8230; Even though dental amalgam is the predominant source of human exposure to mercury, it is not regulated by the FDA.”</em><em>156 </em><em>&#8211;Letter to the FDA from 19 Members of Congress, 2009</em></div>
<div><strong>4) Additional Considerations about Dental Amalgam and Human Health</strong></div>
<div>Reference Exposure Levels</div>
<div>After Health Canada was sued by a group of consumer activists over safety of medical devices, they</div>
<div>hired Dr. G. Mark Richardson to make recommendations about dental amalgam. Dr. Richardson presented a chart summarizing seventeen separate estimates of mercury exposure due to amalgam in adults. If the US Agency for Toxic Substances and Disease Registry (ATSDR) minimal risk level</div>
<div>(MRL) for non–occupational exposure of .014 μg Hg0/m3 in air standard is used, even one amalgam filling would expose the individual to more mercury than would be allowed by Dr. Richardson’s proposed tolerable daily intake.157</div>
<div>In new research published this year, Dr. Richardson reports that more than 67 million Americans aged 2 years and older exceed the intake of mercury vapor considered “safe” by the U.S. EPA due to the presence of dental amalgam fillings, whereas over 122 million Americans exceed the intake of mercury vapor considered “safe” by the California EPA due to their amalgam fillings.158</div>
<div>Methylization of Mercury in the Human Body Research has also already begun to explore how the mercury in amalgam and its vapor can be altered into methylmercury (commonly accepted to be the most toxic form of mercury) within the human body. Bacteria in soil and water can convert mercury into methylmercury, a form of the element sometimes consumed by fish and shellfish,159 and as noted above, pregnant women and children are advised not to eat seafood that might contain methylmercury.160 161 162</div>
<div>Several studies have documented the ability of metallic mercury rooted in the human system (such as that from amalgam fillings) to be transformed into methylmercury in the mouth163 164 165 and by specific strains of yeast and bacteria that dwell in the gut,166 167 168 thus revealing that the problem already addressed in maritime environments is one which even more intimately impacts human health.</div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>5</div>
<div>Genetic Predisposition</div>
<div>The issue of genetic predisposition to mercury poisoning has also been noted in several studies.169 170 171 172 173 174 175 One study specifies that roughly 25% of the U.S. population is polymorphic for a specific genotype associated with sensitivity to mercury toxicity,176 which amounts to 78 million Americans today.</div>
<div>Mercury allergies In 1972, the North American Contact Dermatitis Group determined that 5 &#8211; 8% of the U.S. population demonstrates allergy to mercury by skin patch testing,177 which would amount to approximately 21 million Americans today. Since dentists do not test their patients for mercury allergies prior to using amalgam, this would mean that millions of Americans are unknowingly allergic to the fillings in their mouths.</div>
<div>Other scientific research offers even more startling results. In one study, 180 subjects with amalgam fillings were patch tested, and 16.1% of those without allergic disease and 22.5% of those with allergic disease tested positive for mercury allergy. Of sixty subjects without amalgam fillings, none tested positive for mercury allergy.178 In another study of 29 patients with oral lichen planus, 62% were positive for mercury allergy.179 And at Baylor College of Dentistry, of 171 dental students patch tested, 32% were positive for mercury allergy. The percentage of positive tests correlated with the students’ own amalgam scores and with the length of time they had been in dental school.180</div>
<div>Co-existing Factors Finally, it should be noted that mercury influences each individual differently based on a wide-range of co-existing factors. Thoughtful research has explored how the number of amalgam fillings in the mouth,181 182 183 184 185 186 187 188 189 various routes of exposure from mercury fillings,190 191 192 gender,193 194 plaque,195 consumption of selenium,196 milk,197 198 199 or alcohol,200 201 202 and other circumstances203 204 205 206 can play a role in each person’s unique reaction to mercury.</div>
<div><em>“Dental treatment without mercury is becoming the norm.”</em><em>207 </em><em>&#8211;Carsten Lassen and Jakob Maag, Nordic Council of Ministers, INC1, June 2010</em></div>
<p></p>
<div><strong>Suggested Solutions to Mercury Risks Caused by Dental Amalgam</strong></div>
<p></p>
<div>Since some countries have successfully eliminated dental mercury, banning mercury from dentistry has already proven to be both feasible and economical.208</div>
<div>Various considerations should be part of any effort to end the use of mercury in dental amalgam:</div>
<div><strong>1) Amalgam Separators</strong></div>
<div>Amalgam separators can successfully reduce the amount of mercury discharge in wastewater from dental offices209 210 and are essential in stopping mercury from entering the environment. However, it would be helpful to enforce maintenance requirements for amalgam separators, as the Royal College of Dental Surgeons has done in Ontario, Canada.211 It should also be remembered that amalgam separators only contribute to solving the problem of dental mercury in wastewater and not the additional burdens placed by amalgam fillings on the environment and human health.</div>
<div><strong>2) Alternatives to Amalgam as a Filling Material</strong></div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>6</div>
<div>Many consumers choose composite fillings because the coloring matches the tooth better, and the American Dental Association (ADA) explains that the cost for a composite filling is moderate.212 The ADA also offers ionomers, indirect restorative dental materials, all porcelain (ceramic) dental materials, gold alloys, and indirect composites, among other alternatives to amalgam.213</div>
<div>Although a poll showed that just less than half of dentists are using amalgam in the U.S. today,214 a recent survey published in the <em>Journal of the American Dental Association </em>offers statistics demonstrating that mercury fillings are still being used routinely on ethnic minority groups, including 53.4% of Black/African Americans and 72.9% of American Indians/Alaska Natives/Asians/Pacific Islanders.215</div>
<div>Additionally, a study about new recruits to the U.S. Navy and Marines, also published in the <em>Journal of the American Dental Association, </em>notes that while the use of resin composite among dentists is increasing, “Our data show that dental amalgam remains the predominant material in use, accounting for more than 75 percent of all posterior restorations among new recruits.”216</div>
<div><strong>3) Safe Removal of Existing Amalgam Fillings</strong></div>
<div>Unsafe removal of amalgam fillings can cause more mercury-related health problems to patients because mercury vapor is released in greater quantities as a result of drilling. IAOMT funds and studies international research about the safety of dental materials and has created a safe protocol for taking mercury fillings out of patients’ mouths.217</div>
<div><strong>4) Educating Dentists</strong></div>
<div>While some dentists have already stopped using amalgam, others will require training in mercury-free dentistry. Since Norway, Sweden, and Denmark have banned dental mercury, their dental schools shed light upon how to make a transition away from amalgam.</div>
<div><strong>5) Economic Perspective</strong></div>
<div>In a report entitled “The Economics of Dental Amalgam Regulation,” the authors note that amalgam use is already declining and that restrictions on mercury are inevitable.218 The authors conclude, “We can then make the case that the overall health care expenditures necessary to deal with diseases and conditions, known or unknown, arising from the continued installation of amalgam could far exceed the relatively manageable cost increases to the consumer for the alternatives&#8230;This is not to mention the cost to the U.S. economy of lost work time owing to concomitant illness and disability.”219</div>
<div><strong>&#8230;</strong></div>
<div>An international timeline to ban dental mercury would save people and the environment, while also fostering a cooperative global effort.</div>
<div><em>&#8220;Mercury is among the most dangerous environmental toxins. Satisfactory alternatives to mercury in products are available, and it is therefore fitting to introduce a ban.&#8221;</em><em>220 </em><em>&#8211;Erik Solheim, Norway’s Minister of Environment and Development, 2007</em></div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>1 Dr. Maths Berlin. “Mercury in Dental Materials—an updated risk analysis in environmental medical terms.” <em>An Overview of Scientific Literature published in 1997 to 2002. </em>(The Dental Material Commission, Sweden).</div>
<div>2 World Health Organization. <em>Mercury in Health Care</em>. (Geneva, Switzerland: policy paper, August 2005), 1. http:// <a href="http://www.who.int/water_sanitation_health/medicalwaste/mercurypolpaper.pdf" rel="nofollow" target="_blank">www.who.int/water_sanitation_health/medicalwaste/mercurypolpaper.pdf</a></div>
<div>3 United States Environmental Protection Agency. <em>International Mercury Market Study and the Role and Impact of US Environmental Policy. </em>2004.</div>
<div>4 <em>Ibid</em>. 5 Health Canada. <em>The Safety of Dental Amalgam. </em>1996. <a href="http://www.hc-sc.gc.ca/dhp-mps/alt_formats/hpfb-dgpsa/pdf/md-" rel="nofollow" target="_blank">http://www.hc-sc.gc.ca/dhp-mps/alt_formats/hpfb-dgpsa/pdf/md-</a></div>
<div>im/dent_amalgam-eng.pdf</div>
<div>6 United Nations Environmental Programme. <em>Reducing the Risk from Mercury. </em><a href="http://www.unep.org/" rel="nofollow" target="_blank">http://www.unep.org/</a> hazardoussubstances/Mercury/tabid/434/language/en-US/Default.aspx</div>
<div>7 United States Food and Drug Administration. <em>2010 Meeting of the Dental Products Panel. </em>December 14-15, 2010.</div>
<div>8 European Commission. <em>Dental Amalgams 9: What further information is needed on the environmental risks of dental amalgam? </em>Europa DG Health and Consumer Protection. <a href="http://ec.europa.eu/health/opinions/en/dental-amalgam/l-2/9-" rel="nofollow" target="_blank">http://ec.europa.eu/health/opinions/en/dental-amalgam/l-2/9-</a>research-needed.htm#0</div>
<div>9 “Dental Mercury Use Banned in Norway, Sweden and Denmark because Composites are Adequate Replacements,” <em>Reuters/PRNewswire-USNewswire Online</em>. January 3, 2008. <a href="http://www.reuters.com/article/idUS108558+03-" rel="nofollow" target="_blank">http://www.reuters.com/article/idUS108558+03-</a> Jan-2008+PRN20080103</div>
<div>10 Working Group on Dental Amalgam for the United States Department of Health and Human Services. <em>Dental Amalgam and Restorative Materials: An Update Report to the Environmental Health Policy Committee. </em>(Washington, D.C.: update report, October 1997), 4-6. <a href="http://web.health.gov/environment/amalgam2/contents.html" rel="nofollow" target="_blank">http://web.health.gov/environment/amalgam2/contents.html</a></div>
<div>11 Health Canada. <em>The Safety of Dental Amalgam. </em>1996. <a href="http://www.hc-sc.gc.ca/dhp-mps/alt_formats/hpfb-dgpsa/pdf/" rel="nofollow" target="_blank">http://www.hc-sc.gc.ca/dhp-mps/alt_formats/hpfb-dgpsa/pdf/</a> md-im/dent_amalgam-eng.pdf</div>
<div>12 Health and Environment Alliance. <em>Mercury and Dental Amalgams. </em>(Brussels, Belgium: fact sheet, May 2007): 3. http:// <a href="http://www.env-health.org/IMG/pdf/HEA_009-07.pdf" rel="nofollow" target="_blank">www.env-health.org/IMG/pdf/HEA_009-07.pdf</a></div>
<div>13 New York Academy of Sciences. <em>Pollution Prevention and Management Strategies for Mercury in the NY/NJ Harbor</em>. June 2002. <a href="http://www.nyas.org/Publications/Annals/Detail.aspx?cid=8454dd76-8998-4ee7-b7a2-5a97f68c790c" rel="nofollow" target="_blank">http://www.nyas.org/Publications/Annals/Detail.aspx?cid=8454dd76-8998-4ee7-b7a2-5a97f68c790c</a></div>
<div>14 United States Environmental Protection Agency. <em>Mercury in Dental Amalgam. </em>August 5, 2011. <a href="http://www.epa.gov/" rel="nofollow" target="_blank">http://www.epa.gov/</a> mercury/dentalamalgam.html</div>
<div>15 Arenholt-Bindslev, D., <em>et al.</em>, <em>Mercury Levels and Discharge in Waste Water from Dental Clinics</em>, Water Air Soil Pollution, 86(1-4):93-9 (1996); AMSA, <em>Evaluation of Domestic Sources of Mercury </em>(Aug 2000); Metropolitan Council Environmental Services (MCES), <em>Controlling Dental Facility Discharges in Wastewater</em>, Twin Cities, Minnesota (1999); <a href="http://www.pca.state.mn.us/publications/mercury-va-mces.pdf" rel="nofollow" target="_blank">www.pca.state.mn.us/publications/mercury-va-mces.pdf</a> ; Stone ME, et al., “Determination of methylmercury in dental-unit wastewater,” <em>Dent Mater</em>.,2003, 19(7):675-679; AMSA/U.S. EPA, <em>Mercury Source Control Program Evaluation</em>, Larry Walker Associates, Final Report (March 2002); <em>Dentist the Menace: The Uncontrolled Release of Dental Mercury in the Environment</em>, Mercury Policy Project and Healthcare Without Harm (June 2002). <a href="http://www.mercurypolicy.org/new/documents/" rel="nofollow" target="_blank">www.mercurypolicy.org/new/documents/</a> DentistTheMenace.pdf; Sustainable Hospitals Program, S.M. Jasindki, U.S. Bureau of Mines, <em>The Materials Flow of Mercury in the U.S.</em>, Information Circular; 9412 (1994); United Nations Environment Program, <em>Global Mercury Assessment-Appendix: Overview of Existing and Future National Actions</em>, April 25 2002 Draft; al-Shraideh, M., al- Wahadni, A., <em>The mercury burden in waste water released from dental clinics in Jordan</em>; SADJ, 57(6):213-5 (June 2002).</div>
<div>16 <em>Ibid. </em>17 Arenholdt-Bindslev,D., Larsen,AH. “Mercury Levels and Discharge in Waste Water from Dental Clinics.” <em>Water, Air, Soil,</em></div>
<div><em>Pollution</em>, 86(1-4):93-9, 1996. Abstract available at <a href="http://www.springerlink.com/content/pp65v404t276p450/" rel="nofollow" target="_blank">http://www.springerlink.com/content/pp65v404t276p450/</a></div>
<div>18 Naleway,C et al. “Characteristics of Amalgam in Dental Wastewater” (abstract). <em>JDentRes. </em>73:105, 1994. The Toxic Effects of Dental Amalgam; August 2011</div>
<div>Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>19 Larose, Pierre. <em>Position Paper</em>. IAOMT Environmental Committee, 2011. 20 Balogh S; Liang L. “Mercury Pathways in Municipal Wastewater Treatment Plants.” <em>Water, Air, Soil Pollution.</em></div>
<div>80:1181-90, 1995. 21 Skare, I., Enqvist, A. “Amalgam Restorations: an important source of human exposure of mercury and silver.”</div>
<div><em>Lakartidningen. </em>15:1299-1301, 1992). <a href="http://www.tandfonline.com/doi/abs/10.1080/00039896.1994.9954991" rel="nofollow" target="_blank">http://www.tandfonline.com/doi/abs/10.1080/00039896.1994.9954991</a> 22 Bjorkman et al. “Mercury in Saliva and Feces after Removal of Amalgam Fillings.” <em>Tox. Appl Pharm. </em>144(1): 156-162.</div>
<div>1997. <a href="http://www.sciencedirect.com/science/article/pii/S0041008X9798128X" rel="nofollow" target="_blank">http://www.sciencedirect.com/science/article/pii/S0041008X9798128X</a></div>
<div>23 Larose, Pierre. <em>Position Paper</em>. IAOMT Environmental Committee, 2011.</div>
<div>24 Institute of Environmental Medicine (Sweden). <em>Karolinska Institute Report. </em>IMM 1/92.</div>
<div>25 Rivola J; Krejci I; Imfeld T; Lutz F. “Cremation and the Environmental Mercury Burden.” <em>Schweiz Monatsschr Zahnmed </em>100(11):1299-303, 1990.</div>
<div>26 Fdn for Toxic Free Dentistry, <em>Dental and Health Facts Newsletter</em>, 5(3), Sept 1992.</div>
<div>28 <em>Ibid. </em>29 Rubin PG, Yu M-H, “Mercury vapor in amalgam waste discharged from the dental office vacuum units.” <em>Arch Environ</em></div>
<div><em>Health </em>51(4):335-7, 1996 Jul-Aug. <a href="http://www.tandfonline.com/doi/abs/10.1080/00039896.1996.9936036" rel="nofollow" target="_blank">http://www.tandfonline.com/doi/abs/10.1080/00039896.1996.9936036</a> 30 <em>Ibid.</em></div>
<div>31 Health Canada. <em>The Safety of Dental Amalgam. </em>(Ottawa, Ontario: report, 1996), 4. <a href="http://www.hc-sc.gc.ca/dhp-mps/" rel="nofollow" target="_blank">http://www.hc-sc.gc.ca/dhp-mps/</a> alt_formats/hpfb-dgpsa/pdf/md-im/dent_amalgam-eng.pdf</div>
<div>32 Advisory Committee on Mercury Pollution. <em>Dental Amalgam Fillings: Environmental and Health Facts for Dental Patients</em>. (Waterbury, VT: online dental fact sheet, accessed October 27, 2010), 1. <a href="http://www.mercvt.org/PDF/" rel="nofollow" target="_blank">http://www.mercvt.org/PDF/</a>DentalAmalgamFactSheet.pdf</div>
<div>33 State of Connecticut Department of Environmental Protection. <em>Fillings: The Choices You Have: Mercury Amalgam and Other Filling Materials</em>. (Hartford, CT, USA: Brochure, Revised January 2006), 3. <a href="http://www.ct.gov/dep/lib/dep/mercury/" rel="nofollow" target="_blank">http://www.ct.gov/dep/lib/dep/mercury/</a>gen_info/fillings_brochure.pdf</div>
<div>34 United States Food and Drug Administration. <em>2010 Meeting of the Dental Products Panel. </em>December 14-15, 2010.available.</div>
<div>35 “Dental Mercury Use Banned in Norway, Sweden and Denmark because Composites are Adequate Replacements,” <em>Reuters/PRNewswire-USNewswire Online</em>. January 3, 2008. <a href="http://www.reuters.com/article/idUS108558+03-" rel="nofollow" target="_blank">http://www.reuters.com/article/idUS108558+03-</a> Jan-2008+PRN20080103</div>
<div>36 Working Group on Dental Amalgam for the United States Department of Health and Human Services. <em>Dental Amalgam and Restorative Materials: An Update Report to the Environmental Health Policy Committee. </em>(Washington, D.C.: update report, October 1997), 4-6. <a href="http://web.health.gov/environment/amalgam2/contents.html" rel="nofollow" target="_blank">http://web.health.gov/environment/amalgam2/contents.html</a></div>
<div>37 Health Canada. <em>The Safety of Dental Amalgam. </em>1996. <a href="http://www.hc-sc.gc.ca/dhp-mps/alt_formats/hpfb-dgpsa/pdf/" rel="nofollow" target="_blank">http://www.hc-sc.gc.ca/dhp-mps/alt_formats/hpfb-dgpsa/pdf/</a> md-im/dent_amalgam-eng.pdf</div>
<div>38 Health and Environment Alliance. <em>Mercury and Dental Amalgams. </em>(Brussels, Belgium: fact sheet, May 2007): 3. http:// <a href="http://www.env-health.org/IMG/pdf/HEA_009-07.pdf" rel="nofollow" target="_blank">www.env-health.org/IMG/pdf/HEA_009-07.pdf</a></div>
<div>39 Watson, Diane and 18 other members of Congress. “Dear Acting Commissioner Dr. Joshua Sharfstein&#8230;” (Washington, D.C.: Congressional letter, May 14, 2009). Copy of letter available upon request to <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=john.donnelly@mail.house.gov" rel="nofollow" target="_blank">john.donnelly@mail.house.gov</a></div>
<div><a href="http://amalgamillness.com/Text_DCAct.html" rel="nofollow" target="_blank">amalgamillness.com/Text_DCAct.html</a>.</div>
<div>27 Stone, ME, Cohen, ME, Debban, BA, “Mercury vapor levels in exhaust air from dental vacuum systems,” <em>Dental Materials, </em>23 (5): 527-532, May 2007. Abstract available at <a href="http://www.sciencedirect.com/science/article/pii/" rel="nofollow" target="_blank">http://www.sciencedirect.com/science/article/pii/</a>S0109564106000881</div>
<div>40 Watson, Diane, Congresswoman, Mercury in Dental Filling Disclosure and Prohibition Act, November 5, 2001, http://</div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>41 United States Environmental Protection Agency. <em>Mercury: Human Exposure, </em>October 2010, 1. <a href="http://www.epa.gov/hg/" rel="nofollow" target="_blank">http://www.epa.gov/hg/</a> exposure.htm</div>
<div>42 State of Connecticut Department of Public Health. <em>A Woman’s Guide to Eating Fish Safely: Special Advice for Pregnant Women &amp; Young Children</em>, 2010, <a href="http://www.ct.gov/dph/lib/dph/environmental_health/eoha/pdf/womans_guide_-" rel="nofollow" target="_blank">http://www.ct.gov/dph/lib/dph/environmental_health/eoha/pdf/womans_guide_-</a>english_2010.pdf</div>
<div>43 United States Food and Drug Administration. <em>What You Need to Know about Mercury in Fish and Shellfish</em>, 2009. http:// <a href="http://www.fda.gov/Food/ResourcesForYou/Consumers/ucm110591.htm" rel="nofollow" target="_blank">www.fda.gov/Food/ResourcesForYou/Consumers/ucm110591.htm</a></div>
<div>44 Geier, David A, Kern, Janet K., Geier, Mark R. “A prospective study of prenatal mercury exposure from dental amalgams and autism severity,” <em>Neurobiolgiae Experimentals Polish Neuroscience Society </em>69 (2009): 1, 4, 6 &amp; 7. http://<a href="http://www.iaomt.org/news/files/files302/Amalgam_Autism_Geier_2009.pdf" rel="nofollow" target="_blank">www.iaomt.org/news/files/files302/Amalgam_Autism_Geier_2009.pdf</a></div>
<div>45 London, Susan. “Amalgam fillings during pregnancy linked to infant cleft palate.” <em>Elsevier Global Medical News. </em>July 21, 2010. <a href="http://www.medconnect.com.sg/tabid/92/s4/Obstetrics-Gynecology/p21/Pregnancy-Lactation/ct1/c37751/" rel="nofollow" target="_blank">http://www.medconnect.com.sg/tabid/92/s4/Obstetrics-Gynecology/p21/Pregnancy-Lactation/ct1/c37751/</a>Amalgam-Fillings-During-Pregnancy-Linked-to-Infant-Cleft-Palate/Default.aspx</div>
<div>46 Laks, Dan R. “Environmental Mercury Exposure and the Risk of Autism.” <em>White Paper for Safe Minds. </em>August 27, 2008.</div>
<div>47 K. Ask, A. Akesson, M. Berglund, M. Vahter,. “Inorganic mercury and methylmercury in placentas of Swedish women,” <em>Environ Health Perspect 110 </em>(2002) 523-6. <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1240842/pdf/" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1240842/pdf/</a> ehp0110-000523.pdf</div>
<div>48 Richardson, G. Mark et al., “Mercury vapour (Hg(0)): Continuing toxicological uncertainties, and establishing a Canadian reference exposure level,” <em>Regul Toxicol Pharmicol</em>, 2009 Feb;53(1):32-8. 35. Abstract available at http://<a href="http://www.ncbi.nlm.nih.gov/pubmed/18992295" rel="nofollow" target="_blank">www.ncbi.nlm.nih.gov/pubmed/18992295</a></div>
<div>49 Mutter, J. et al., “Amalgam risk assessment with coverage of references up to 2005,” <em>Gesundheitswesen</em>. 2005 Mar; 67(3):204 16, 204-216. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/15789284" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/15789284</a></div>
<div>50 M. Vahter, A. Akesson, B. Lind, U. Bjors, A. Schutz, M. Berglund. “Longitudinal study of methylmercury and inorganic mercury in blood and urine of pregnant and lactating women, as well as in umbilical cord blood” <em>Environ Res </em>84 (2000) 186-94. Abstract available at <a href="http://www.sciencedirect.com/science/article/pii/S0013935100940982" rel="nofollow" target="_blank">http://www.sciencedirect.com/science/article/pii/S0013935100940982</a></div>
<div>51 Windham, Bernard, “New studies into effect of dental amalgam,” <em>The Natural Recovery Plan</em>. <a href="http://www.thenaturalrecoveryplan.com/" rel="nofollow" target="_blank">www.thenaturalrecoveryplan.com</a></div>
<div>52 Nourouzi E et al. “Effect of teeth amalgam on mercury levels in the colostrums human milk in Lenjan.” <em>Environ Monit Access. </em>15 April 2011. Abstract available at <a href="http://www.springerlink.com/content/c374t8m515323xq7/" rel="nofollow" target="_blank">http://www.springerlink.com/content/c374t8m515323xq7/</a></div>
<div>53 Al-Saleh I, Al-Sedairi A. “Mercury (Hg) burden in children: The impact of dental amalgam,” <em>Sci Total Environ </em>(2011), doi:10.1016/j.scitotenv.2011.04.047. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/21601239" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/21601239</a></div>
<div>54 Vimy, MJ; et al. “Mercury from Maternal Silver Fillings in Sheep and Human Breast Milk: A Source of Neonatal Exposure.” <em>Biolog Trace Element Res</em>., 56:143-52, 1997. Abstract available at <a href="http://www.springerlink.com/content/" rel="nofollow" target="_blank">http://www.springerlink.com/content/</a>j77w36j606738240/</div>
<div>55 Drasch, G; et al. “Mercury in Human Colostrum and Early Breast Milk. Its Dependence on Dental Amalgam and Other Factors<em>.” J Trace Elem Med Biol.</em>, 12(1):23-7, Mar (1998). Abstract available at <a href="http://cat.inist.fr/?" rel="nofollow" target="_blank">http://cat.inist.fr/?</a>aModele=afficheN&amp;cpsidt=2252430</div>
<div>56 Bellinger, DC; Trachtenberg, F; Barregard, L, et al. “Neuropyschological and renal effects of dental amalgam in children: a randomized clinical trial.” <em>JAMA. </em>2006; 295: 1775-1783. Abstract available at <a href="http://jama.ama-assn.org/content/" rel="nofollow" target="_blank">http://jama.ama-assn.org/content/</a>295/15/1775.short</div>
<div>57 DeRouen, TA; Martin, MD;; Leroux, BG et al. “Neurobehavioral effects of dental amalgam in children: a randomized clinical trial.” <em>JAMA. </em>2006; 295:1784-1792. Abstract available at <a href="http://jama.ama-assn.org/content/295/15/1784.short" rel="nofollow" target="_blank">http://jama.ama-assn.org/content/295/15/1784.short</a></div>
<div>58 Needleman, Herbert. “Mercury in Dental Amalgam—A Neurotoxic Risk?” <em>JAMA </em>2006 295:1835-1836. Beginning of text available at <a href="http://jama.ama-assn.org/content/295/15/1835.short" rel="nofollow" target="_blank">http://jama.ama-assn.org/content/295/15/1835.short</a></div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>59 Geier, DA et al., “A dose-dependent relationship between mercury exposure from dental amalgams and urinary mercury levels: a further assessment of the Casa Pia Children&#8217;s Dental Amalgam Trial,” <em>Hum Exp Toxicol, </em>published online 29 July 2011, DOI: 10.1177/0960327111417264. Available online on at <a href="http://het.sagepub.com/content/early/" rel="nofollow" target="_blank">http://het.sagepub.com/content/early/</a> 2011/07/27/0960327111417264</div>
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<div>61 Haley, Boyd. <em>Response to the NIDCR Funded Children’s Amalgam Testing publications in the JAMA 2006</em>. IAOMT document. <a href="http://www.iaomt.org/articles/category_view.asp?intReleaseID=280&amp;month=9&amp;year=2006&amp;catid=30" rel="nofollow" target="_blank">http://www.iaomt.org/articles/category_view.asp?intReleaseID=280&amp;month=9&amp;year=2006&amp;catid=30</a></div>
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<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
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<div>113 Mutter, J. et al. “Amalgam risk assessment with coverage of references up to 2005,” <em>Gesundheitswesen </em>67:3 (Review in German, March 2005): 204-216. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/15789284" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/15789284</a></div>
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<div>179 Finne, K; et al. “Oral Lichen Planus and Contact Allergy to Mercury.” <em>Int J Oral Surg</em>., 11:236-9, 1982. Abstract available at <a href="http://www.sciencedirect.com/science/article/pii/S0300978582800732" rel="nofollow" target="_blank">http://www.sciencedirect.com/science/article/pii/S0300978582800732</a></div>
<div>180 Miller, EG, et. al. “Prevalence of mercury hypersensitivity in dental students.” <em>J Dent Res</em>. 64: Special Issue, p. 338, Abstact #1472, (1985). Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/2957496" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/2957496</a></div>
<div>181 Rothwell, Janet A; Boyd, Paul J. “Amalgam fillings and hearing loss,” <em>International Journal of Audiology </em>47: 12 (December 1, 2008): 771. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/19085401" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/19085401</a></div>
<div>182 Geier, David A, Kern, Janet K., Geier, Mark R. “A prospective study of prenatal mercury exposure from dental amalgams and autism severity,” <em>Neurobiolgiae Experimentals Polish Neuroscience Society </em>69 (2009): 1, 4, 6 &amp; 7. http://<a href="http://www.iaomt.org/news/files/files302/Amalgam_Autism_Geier_2009.pdf" rel="nofollow" target="_blank">www.iaomt.org/news/files/files302/Amalgam_Autism_Geier_2009.pdf</a></div>
<div>183 Barregard, L. et al. “Cadmium, mercury, and lead in kidney cortex of living kidney donors: impact of different exposure sources,” <em>Environ, Res. </em>110 (Sweden, 2009): 47-54. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/19931045" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/19931045</a></div>
<div>184 Richardson, G. Mark et al., “Mercury vapour (Hg(0)): Continuing toxicological uncertainties, and establishing a Canadian reference exposure level,” <em>Regul Toxicol Pharmicol</em>, 2009 Feb;53(1):32-8. 36. Abstract available at http://<a href="http://www.ncbi.nlm.nih.gov/pubmed/18992295" rel="nofollow" target="_blank">www.ncbi.nlm.nih.gov/pubmed/18992295</a></div>
<div>185 Eggleston, DW, Nylander, M. “Correlation of dental amalgam with mercury in brain tissue,” <em>J Prosthet Dent </em>58:6</div>
<div>(December 1987): 704-707. <a href="http://www.nvbt.nl/hot-metalen4.html" rel="nofollow" target="_blank">http://www.nvbt.nl/hot-metalen4.html</a></div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>186 Nylander, M., Friberg, L, Lind, B. “Mercury concentrations in the human brain and kidneys in relation to exposure from dental amalgam fillings,” <em>Swed Dent J </em>11:5 (1987): 179-187. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/</a>3481133</div>
<div>187 Kraub, P. and Deyhle, M. “Field study on the mercury content of saliva,” <em>Universitat Tubingen-Institut for Organische Chemie </em>(1997). <a href="http://www.xs4all.nl/~stgvisie/AMALGAM/EN/SCIENCE/tubingen.html" rel="nofollow" target="_blank">http://www.xs4all.nl/~stgvisie/AMALGAM/EN/SCIENCE/tubingen.html</a></div>
<div>188 Godrey, ME, Wojcik, DP, Krone, CA. “Apolipoprotein E genotyping as a potential biomarker for mercury toxicity,” <em>Journal of Alzheimer’s Disease </em>5 (2003): 189-195. Abstract available at <a href="http://iospress.metapress.com/content/" rel="nofollow" target="_blank">http://iospress.metapress.com/content/</a>2bpp5fdar3r06e11/</div>
<div>189 Craelius, W., “Comparative epidemiology of multiple sclerosis and dental caries,” <em>Journal of Epidemiology and Community Health </em>35 (1978): 155-165. Abstract available at <a href="http://jech.bmj.com/content/32/3/155.abstract" rel="nofollow" target="_blank">http://jech.bmj.com/content/32/3/155.abstract</a></div>
<div>190 Mercola, Joseph and Klinghardt, Dietrich. “Mercury toxicity and systemic elimination agents,” <em>Journal of Nutritional and Environmental Medicine </em>11 (2001) 53-62. <a href="http://www.scribd.com/doc/32403160/Mercury-Toxicity-and-Systemic-" rel="nofollow" target="_blank">http://www.scribd.com/doc/32403160/Mercury-Toxicity-and-Systemic-</a>Elimination-Agents</div>
<div>191 Bjorkman, L., Sanborgh-Englund, G., Ekstrand, J. “Mercury in saliva and feces after removal of mercury fillings,” <em>Toxicology and Applied Pharmacology </em>144:1 (May 1997): 156-162. Abstract available at <a href="http://www.ingentaconnect.com/" rel="nofollow" target="_blank">http://www.ingentaconnect.com/</a>content/ap/to/1997/00000144/00000001/art08128</div>
<div>192 Bergerow, J. et al. “Long-term mercury excretion in urine,” <em>International Archives of Occupational and Environmental Health </em>66:3 (1994): 209-212. Abstract available at <a href="http://www.springerlink.com/content/w5274366726q6020/" rel="nofollow" target="_blank">http://www.springerlink.com/content/w5274366726q6020/</a></div>
<div>193 Rothwell, Janet A; Boyd, Paul J. “Amalgam fillings and hearing loss,” <em>International Journal of Audiology </em>47: 12 (December 1, 2008): 771. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/19085401" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/19085401</a></div>
<div>194 Richardson, G. Mark et al. “Mercury vapour: Continuing toxicological uncertainties, and establishing a Canadian reference exposure level,” <em>Regulatory Toxicology and Pharmacology </em>53. (January 2008): 32. Abstract available at http://<a href="http://www.ncbi.nlm.nih.gov/pubmed/18992295" rel="nofollow" target="_blank">www.ncbi.nlm.nih.gov/pubmed/18992295</a></div>
<div>195 Lyttle, H.A. and Bowden, G.H. “The level of mercury in human dental plaque and interaction in vitro between biofilms of streptococcus mutans and dental amalgam,” <em>Journal of Dental Research </em>72:9 (September 1993): 1320-1324. http://<a href="http://jdr.sagepub.com/content/72/9/1320" rel="nofollow" target="_blank">jdr.sagepub.com/content/72/9/1320</a></div>
<div>196 Raymond, Laura J., Ralston, Nicholas VC. “Mercury: selenium interactions and health complications,” <em>Seychelles Medical and Dental Journal </em>7:1 (November 2004): 72-77. <a href="http://www.wfoa-tuna.org/health/ralstonraymond.pdf" rel="nofollow" target="_blank">http://www.wfoa-tuna.org/health/ralstonraymond.pdf</a></div>
<div>197 Haley, Boyd. Affidavit: An Evaluation of Dental Amalgam and Its Ability to Injure Human Health, 5. 198 Mata, l., Sanchez, L. and Calvo, M. “Interaction of mercury with human and bovine milk proteins<em>,” Biosci Biotechnol</em></div>
<div><em>Biochem </em>61:10 (October 1997): 1641-4. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/9362112" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/9362112</a></div>
<div>199 Kostial, Krista. “Effect of milk on mercury absorption and gut retention in rats.” <em>Bulletin of Environmental Contamination and Toxicology </em>23:1 (New York: Springer-Verlag, 1979): 566-571. Abstract available at http://<a href="http://www.springerlink.com/content/1080867702348071/" rel="nofollow" target="_blank">www.springerlink.com/content/1080867702348071/</a></div>
<div>200 State of Massachusetts Department of Environmental Protection. <em>Appendix D-Mercury Toxicity: Technical Overview. </em>(Boston, MA: website appendix, accessed on October 27, 2010), 3. <a href="http://www.mass.gov/dep/toxics/stypes/appd.htm" rel="nofollow" target="_blank">http://www.mass.gov/dep/toxics/stypes/appd.htm</a></div>
<div>201 Grandjean, Philippe, et al. “Neurobehavioral Epidemiology: Application in Risk Assessment,” <em>Environmental Health Perspectives </em>104:2 (April 1996): 398. <a href="http://www.ehp.niehs.nih.gov/realfiles/members/1996/Suppl-2/grandjean.html" rel="nofollow" target="_blank">http://www.ehp.niehs.nih.gov/realfiles/members/1996/Suppl-2/grandjean.html</a></div>
<div>202 Nylander, M., Friberg, L, Lind, B. “Mercury concentrations in the human brain and kidneys in relation to exposure from dental amalgam fillings,” <em>Swed Dent J </em>11:5 (1987): 179-187. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pubmed/" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pubmed/</a>3481133</div>
<div>203 Chang, Louis W., Hartmann, Henrik. “Blood-drain barrier dysfunction in experimental mercury intoxication,” <em>Acta Neuropathologica </em>21:2 (April 4, 1972): 179-184. Abstract available at <a href="http://www.springerlink.com/content/" rel="nofollow" target="_blank">http://www.springerlink.com/content/</a>m631756162455150/</div>
<div>204 Chang, Louis, Hartmann, Henrik. “Electron microscopic histochemical study of the localization and distribution of mercury in the nervous system after mercury intoxification,” <em>Experimental Neurology </em>35:1 (April 1972): 122-137. Abstract available at <a href="http://www.sciencedirect.com/science/article/pii/0014488672900" rel="nofollow" target="_blank">http://www.sciencedirect.com/science/article/pii/0014488672900</a>T6h4e7Toxic Effects of Dental Amalgam; August 2011</div>
<div>Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
<div>205 Skare, I. “Mass balance and systemic uptake of mercury released from dental fillings,” <em>Water, Air and Soil Pollution </em>80:1-4 (1995): 59-67. Abstract available at <a href="http://www.springerlink.com/content/h5gr2031316857vt/" rel="nofollow" target="_blank">http://www.springerlink.com/content/h5gr2031316857vt/</a></div>
<div>206 Barregard, L., Sallsten, G., and Jarvholm, B. “People with high mercury uptake from their own dental fillings,” <em>Occup Envir Med </em>52 (1995): 124-128. Abstract available at <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1128166/" rel="nofollow" target="_blank">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1128166/</a></div>
<div>207 Lassen, Carsten, Maag, Jakob for the Nordic Council of Ministers. <em>Mercury Reductions are Feasible: Reducing Mercury Releases with Known Technologies and Management Solutions. </em>(INC1, Stockholm). 8 June 2010. <a href="http://www.norden.org/" rel="nofollow" target="_blank">www.norden.org</a></div>
<div>208 <em>Ibid. </em>209 Hylander, Lars D. et al. “Mercury recovery in situ of four different amalgam separators.” <em>Science of the Total</em></div>
<div><em>Environment. </em>2006. <a href="http://www.sciencedirect.com/science/article/pii/S0048969705004961" rel="nofollow" target="_blank">http://www.sciencedirect.com/science/article/pii/S0048969705004961</a> 210 Arenholt-Bindslev, D., <em>et al.</em>, <em>Mercury Levels and Discharge in Waste Water from Dental Clinics</em>, Water Air Soil</div>
<div>Pollution, 86(1-4):93-9 (1996). Abstract available at <a href="http://www.springerlink.com/content/pp65v404t276p450/" rel="nofollow" target="_blank">http://www.springerlink.com/content/pp65v404t276p450/</a> 211 Royal College of Dental Surgeons in Ontario. “Amalgam Waste Disposal.” <em>Standard of Practice. </em>November 2003.</div>
<div><a href="http://www.rcdso.org/" rel="nofollow" target="_blank">www.rcdso.org</a></div>
<div>212 American Dental Association. <em>Restoring Your Smile: Dental Filling Choices. </em>Available online at <a href="http://www.ada.org/" rel="nofollow" target="_blank">http://www.ada.org/</a> 3094.aspx#comfillings</div>
<div>213 <em>Ibid.</em></div>
<div>214 Poll available online at <a href="http://thewealthydentist.com/survey/surveyresults/16_MercuryAmalgam_Results.htm" rel="nofollow" target="_blank">http://thewealthydentist.com/survey/surveyresults/16_MercuryAmalgam_Results.htm</a> . Poll cited in Fleming, M and Janosky, J. <em>The Economics of Dental Amalgam Regulation</em>. Report Submitted for Review and Publication to “Public Health Reports.” Available online at <a href="http://www.iaomt.org/articles/files/files303/The%20Economics" rel="nofollow" target="_blank">http://www.iaomt.org/articles/files/files303/The%20Economics</a> %20of%20Dental%20Amalgam%20Regulation.pdf</div>
<div>215 Makhija, SK et al. “Dental Practice-Based Research Network restorative material: Findings from the characteristics associated with type of Practitioner, patient and carious lesion,” <em>J Am Dent Assoc </em>2011; 142: 622-632. Available online at<a href="http://jada.ada.org/content/142/6/622" rel="nofollow" target="_blank">http://jada.ada.org/content/142/6/622</a></div>
<div>216 Simececk, JW, Diefenderfer, KE, Cohen, ME. “An Evaluation of Replacement Rates for Posterior Resin-Based Composite and Amalgam Restorations in U.S. Navy and Marine Recruits,” <em>J Am Dent Assoc </em>2009; 140 (2): 200-209. Available online at <a href="http://www.jada.info/content/140/2/200.full" rel="nofollow" target="_blank">http://www.jada.info/content/140/2/200.full</a></div>
<div>217 IAOMT. <em>Safe Removal of Amalgam Fillings. </em>Available online at <a href="http://www.iaomt.com/articles/files/files288/Safe" rel="nofollow" target="_blank">http://www.iaomt.com/articles/files/files288/Safe</a> %20Removal%20of%20Amalgam%20Fillings.pdf</div>
<div>218 Fleming, M and Janosky, J. <em>The Economics of Dental Amalgam Regulation</em>. Report Submitted for Review and Publication to “Public Health Reports.” Available online at <a href="http://www.iaomt.org/articles/files/files303/The%20Economics" rel="nofollow" target="_blank">http://www.iaomt.org/articles/files/files303/The%20Economics</a>%20of%20Dental%20Amalgam%20Regulation.pdf</div>
<div>219 <em>Ibid.</em></div>
<div>220 Norway Ministry of the Environment. <em>Minister of the Environment and International Development Erik Solheim Bans Mercury in Products</em>. Press Release. 12/21/2007. <a href="http://www.regjeringen.no/en/dep/md/press-centre/Press-releases/" rel="nofollow" target="_blank">http://www.regjeringen.no/en/dep/md/press-centre/Press-releases/</a>2007/Bans-mercury-in-products.html?id=495138</div>
<div>The Toxic Effects of Dental Amalgam; August 2011 Website: <a href="http://www.iaomt.org/" rel="nofollow" target="_blank">www.iaomt.org</a> ; Contact: <a href="http://us.mc1207.mail.yahoo.com/mc/compose?to=info@iaomt.org" rel="nofollow" target="_blank">info@iaomt.org</a></div>
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		<title>Heavy Metals, Mercury and Cancer</title>
		<link>http://smartbio.org/articles/heavy-metals-mercury-and-cancer/</link>
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		<pubDate>Sun, 11 Dec 2011 11:07:06 +0000</pubDate>
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		<description><![CDATA[March 23, 2010 by Mark Sircus &#8211; Director Dr. Rashid Buttar testified before congress that “the association of mercury to chronic diseases is well documented in the didactic scientific literature. The search for the association between mercury and cardiovascular disease reveals 358 &#8230; <a href="http://smartbio.org/articles/heavy-metals-mercury-and-cancer/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>March 23, 2010 by <a title="Posts by Mark Sircus - Director" href="http://winningcancer.com/index.php/author/winningcancer/" rel="author">Mark Sircus &#8211; Director</a></p>
<p><img src="http://imva.info/wp-content/uploads/2010/04/clip_image001.jpg" alt="image" /></p>
<p>Dr. Rashid Buttar testified before congress that “the association of mercury to chronic diseases is well documented in the didactic scientific literature. The search for the association between mercury and cardiovascular disease reveals 358 scientific papers exemplifying the relationship<strong>; between mercury and cancer we find 643 scientific papers</strong>. The association of mercury with neurodegenerative diseases is the most significant, with the references numbering 1,445.” The official position currently is that there is “some” evidence that methylmercury can cause cancer in humans.  The International Agency for Research on Cancer (IARC) has classified methylmercury as “possibly carcinogenic to humans”.</p>
<p>Lead and aluminum are other common heavy metals that have been shown to dramatically increase the toxicity of mercury. Interestingly, lead is the final end product of the step by step radioactive decay of uranium, no wonder it’s so toxic. Medical researchers are still trying to understand the numerous processes by which various heavy metals (lead, mercury, cadmium, arsenic, chromium, etc.) contribute to carcinogenesis but everywhere in officialdom we find ridiculous doubts about their effects especially when it comes to mercury and its high state of toxicity.</p>
<p>It has been shown that mercury rapidly depletes the immune system. Mercury has also been shown to induce auto-immune diseases. <strong>Anything that depletes and disturbs the immune system will increase one’s chances of contracting cancer.</strong> Mercury binds with hemoglobin, which is responsible for oxygen transport to the tissues. This results in less oxygen reaching the tissues when the body is polluted with mercury. We don’t have to look far in understanding how a heavy metal like mercury can eventually lead one to cancer’s door.</p>
<p>“There is no safe level of mercury, and no one has actually shown that there is a safe level,” said Dr. Lars Friberg, Chief Adviser to the WHO on mercury safety. <a href="http://publications.imva.info/index.php/survival-medicine.html">Survival Medicine for the 21st Century</a> (2,200 page compendium) has a two hundred page section called The Rising Tide of Mercury because mercury toxicity needs to be factored into all notions of health and disease today. According to the observations made by the internationally recognized medical researcher, Yoshiaki Omura, MD, <strong>all cancer cells have mercury in them</strong>.</p>
<p>Dr. Hans Nolte wrote, “The wave spectrum of mercury contains more than thirteen wavelengths, whereas only one or two frequencies or wavelengths are usually observed for the other heavy or noble metals.”<a id="_ednref1" name="_ednref1" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn1"></a>[1] It is Dr. Nolte’s belief that the many harmful effects of mercury could be explained to some degree on the basis of this great variety of wavelengths. Dr. Omura’s clinical observation concludes that one of the primary reasons cancer returns is because residual mercury reignites a pathological environment even after surgery, chemotherapy, radiation, and alternative therapies report a positive effect.</p>
<p><em>Heavy metals clog up receptor sites, break and bend sulfur bonds in<br />
important enzymes like insulin, damage the DNA and in general<br />
muck up everything and anything to do with healthy biological life.</em></p>
<p>There is a growing body of scientific research that suggests heavy metals contribute to carcinogenesis by inducing/increasing oxidative stress.<a id="_ednref2" name="_ednref2" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn2"></a>[2] Oxidative stress damages DNA and can lead to mutations which promote cancer.<a id="_ednref3" name="_ednref3" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn3"></a>[3],<a id="_ednref4" name="_ednref4" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn4"></a>[4],<a id="_ednref5" name="_ednref5" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn5"></a>[5] Heavy metals also disrupt the process of Apoptosis (programmed cell death).<a id="_ednref6" name="_ednref6" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn6"></a>[6] Apoptosis is vital for safe removal of sick/unhealthy cells, including cells that may become cancerous.</p>
<p>Heavy metals create contaminated environments both inside and outside the cells. These environments attract all kinds of pathogens – viruses, bacteria and fungi. Some say many cancers are caused by infections others say cancer is an infection and others will insist until they reach their graves that cancer is strictly human cells running amuck with their DNA gone crazy. That many doctors believe this it does not make it true.</p>
<p>Our definition of cancer is a little more broad minded than blaming malfunctioning human DNA as the sole cause of cancer. Cancer is a prime example of how heavy metal toxicity, free radical damage, pathogen infection, mineral and vitamin deficiencies, inflammation, mitochondria dysfunction, immune system depression, genetic mutation, cell wall damage and oxidative stress all come together into an end stage life threatening condition. Cancer treatment can be approached in many ways but the best way would be to address all these problems simultaneously.</p>
<p><strong>Cancer and Mercury Laden Dental Amalgam</strong></p>
<p><em>Most of our cancer patients have</em><br />
<em>a lot of amalgam dental fillings.</em><br />
<em>Professor W Kostler</em></p>
<p>Mercury vapors in the mouth which spreads mercury to all points in the body, increased use of antibiotics, periodontal disease, inappropriate oral care, yeast and fungal overgrowth, and decreasing immune strength are all colliding and reinforcing each other in a downward spiral that leads to chronic diseases and cancer. <strong>Each year in the U.S. an estimated 40 tons of mercury are used to prepare mercury-amalgam dental restorations</strong>. Scientific studies have concluded that the amalgam is the source for more than two thirds of the mercury in our human population. On a daily basis each amalgam releases on the order of 10 micrograms of mercury into the body. This mercury either accumulates in the body or is excreted via urine and feces into our wastewater systems.</p>
<p><em>Mercury from amalgam fillings has been shown to be neurotoxic,<br />
embryotoxic, mutagenic, teratogenic, immunotoxic and clastogenic.<br />
It is capable of causing immune dysfunction and auto-immune diseases.</em><br />
<em>Dr. Robert Gammal</em></p>
<p>Dentists and their parent dental associations are loath to inform patients that the mercury they place in the mouth is a deadly poison that negatively influences not only their oral environments but total body physiology as well. This is a shame that the majority of dentists will take to their grave. “Mercury is one of the most potent chemical inhibitors of thiol-sensitive enzymes and mercury vapour easily penetrates into the central nervous system,” writes Dr. Boyd Haley who goes on to say, “Amalgams leak mercury, this is a fact that any chemistry department can confirm. We have made amalgam fillings outside of the mouth, placed these fillings in sterile water for 15 minutes to several hours. We then tested this water for toxicity to tubulin and creatine kinase. The result was that the solutions in which amalgams were soaked (even for fifteen minutes) were extremely toxic. This work is supported by reports doing similar experiments at the University of Michigan Dental School where they described solutions in which amalgams were soaked as being ‘extremely cytotoxic.’</p>
<p><em>It is estimated that an amalgam filling will release up to half of</em><br />
<em>its mercury content over a ten year period (50% corrosion rate).</em><br />
<em>Dr. Robert Gammal</em></p>
<p><a name="arrive"></a>Dr. Hal A. Huggins stated that amalgam fillings can devastate human health. The most common form of exposure to mercury is by inhalation of vapor and there is widespread general agreement that this leads to a slowly developing and insidious poisoning, which at first yields psychic and other general effects that are vague and difficult to diagnose. Yet dentists have continued to expose children to the toxic effects of mercury.</p>
<p><strong>Periodontitis, Mercury and Candida</strong></p>
<p>According to an article recently published in the Archives of Otolaryngology—Head and Neck Surgery, <strong>chronic periodontitis is associated with an increased risk of developing cancer of the tongue</strong> among men. Researchers at the University at Buffalo and Roswell Park Cancer Institute have found the same thing. Another recent study published in the Journal of the <strong>National Cancer Institute linked periodontal disease to pancreatic cancer</strong> as well. “Our study provides the first strong evidence that periodontal disease may increase the risk of pancreatic cancer,” said Dr Dominique Michaud of the Harvard School of Public Health in Boston, who led the research. Men with a history of periodontal disease had a 64 per cent increased risk of pancreatic cancer than men with no such history.</p>
<p>And increased severity of periodontitis, for example with recent tooth loss, had the greatest risk. People with periodontal disease have an increased level of inflammatory markers such as C reactive protein (CRP) in their blood. These markers are part of an early immune system response to persistent inflammation and have been linked to the development of pancreatic cancer. It is the high levels of carcinogenic compounds (especially mercury) that are present in the mouths of people with periodontal disease that increases risk of pancreatic cancer.</p>
<p>Mercury is invisible in vapor form. The FDA says it’s everywhere. People with mercury fillings suffer VAPORS FROM HELL in their mouths, fumes from their mercury dental fillings that rise up from their teeth 24/7 with more powerful bursts when chewing or drinking hot fluids. <strong>Mercury vapors play havoc on the body through a host of means the least of which is to feed the bacteria, fungi and yeasts that thrive on mercury.</strong> Mercury will promote the growth of Candida, though as it adsorbs the mercury it thereby protects the system to a certain extent from its toxicity until they are saturated then they begin to re-release the mercury in organic form.</p>
<p><em>The list of organisms that have the highest affinity for toxic metals</em><br />
<em>reads like a “who’s who” of our typical human infectious diseases:</em><br />
<em>fungi of the Candida species, streptococci, staphylococci, amoebas, etc.</em><br />
<em>Dr. Dietrich Klinghardt</em></p>
<p>Candida (yeast) overgrowth, which is very difficult to get rid of, is also associated with mercury in the mouth. Dr. Tullio Simoncini insists cancer is intimately linked to Candida overgrowth and that life threatening tumors are actually fungi colonies sucking up all available nutrients. The general line of thought though is the body produces yeast as a defense against excess metals. The yeast cell binds and absorbs its own weight in mercury and prevents it from entering the blood stream. Dr. J. Trowbridge has written in his book “The Yeast Syndrome,” that some doctors specializing in Candida treatment have reported to him that they have discovered clinically that 98% of their patients with chronic Candida also had mercury toxicity.</p>
<p>When we look at the fungal and yeast infections that are an integral aspect of cancer we should begin to understand the desperate need to include chelation of mercury in each and every cancer treatment. Mercury fed Candida become more and more virulent and eventually penetrates and roots into the intestinal walls and invades the cells. These fungal microorganisms become quite at home in the cell, and can easily be considered a principle characteristic of cancer. <strong>Sodium bicarbonate, which is proving to be effective against cancer, is lethal to yeasts and fungi growths because it increases the flow of Oxygen to all cells including the cancer cells that thrive on Oxygen’s absence.</strong></p>
<p><strong>Bone Cancer</strong></p>
<p><img src="http://imva.info/wp-content/uploads/2010/04/clip_image003_0000.jpg" alt="image" width="156" height="101" border="0" /></p>
<p><strong>Some 65% to 75% of advanced breast and prostate cancer patients eventually suffer bone metastases</strong> so there is an immense need for a medicinal that will reach into the bones. The resulting swelling and fractures can cause excruciating pain and may require radiation, chemotherapy, or amputation. To ease the agony and strengthen the bones, doctors prescribed $1.4 billion worth of a bone-boosting drug called Zometa, from Novartis in 2008. The only treatment that will reach down to the bones is sodium bicarbonate. Intravenous application is ineffective but one can throw oneself into bathtubs full of several pounds of baking soda and magnesium salts and take the bicarbonate also orally to radically change the pH in all the tissues including the bones. Sodium bicarbonate increases CO2 levels which also will have the effect of increasing Oxygen to the tissues.</p>
<p><strong>Antibiotics as a Cause of Cancer?</strong></p>
<p>When we consider mercury as one of the basic causes of cancer we can begin to review our estimates on iatrogenic death and disease. Mercury weakens the immune system and leaves people vulnerable to acute infection. Mercury is often at the heart of periodontitis and many other diseases yet the vast majority of dentists, the American Dental Association and the FDA are still in denial. It is bad enough that they plant the mercury in the mouth but then<strong> they add insult and injury by prescribing, as they do, antibiotics that make the entire situation worse with the yeasts and fungus</strong>. Fungal overgrowth occurs because its natural competitors have been removed, which easily becomes the case with antibiotic usage.</p>
<p>Iatrogenic dentistry is a new concept that has yet to be explored but already a great part of the civilized world understands the incredible stupidity and cruelty of fluoridated water, toothpaste and fluoride treatments at the dental clinic and the continued widespread use of mercury containing dental amalgam. Harvard University Medical Center is just one of many universities that recognize fluoride as a cause of cancer. If one wants to study the basic elements of terrorism one need look no further than the people and organizations that support the fluoridation of public water supplies and those who insist on putting mercury in peoples’ and children’s mouths. It is very difficult to accept the devastating reality about what dentists have done to humanity.</p>
<p>It’s impossible for the government to be honest about mercury pollution because they themselves sponsor injecting mercury directly into the blood stream with their flu vaccines and the government still supports its use in dentistry no matter how dangerous it is. Doctors and dentists have a hard time coming clean about their public betrayal. “I don’t feel comfortable using a substance designated by the Environmental Protection Agency to be a waste disposal hazard. I can’t throw it in the trash, bury it in the ground, or put it in a landfill, but they say it is OK to put it in people’s mouths. That doesn’t make sense.”—Richard. Fischer, D.D.S</p>
<p><strong>Mercury Rising</strong></p>
<p><em>A primary route for the toxicity of mercury, cadmium and nickel<br />
is depletion of glutathione and bonding to sulfhydryl groups<br />
of proteins. Arsenic (As) is thought to bind directly to critical thiols.</em></p>
<p>It is through mercury’s attack on these sulfide bonds (SH) that mercury is able to transform the biological properties of proteins and change important physiological functions. <strong>Mercury is attracted to ‘active sites’ on genetic code molecules called deoxyribonucleic acid (DNA).</strong> The inter-relationships between cancer and mercury deserve much more attention as mercury is bioaccumulating in the environment becoming more prevalent globally.</p>
<p>“Thiol poisons, especially mercury and its compounds, reacting with SH groups of proteins lead to the lowered activity of various enzymes containing sulfhydryl groups. This produces a series of disruptions in the functional activity of many organs and tissues of the organism,” writes Professor I.M. Trakhtenberg from Russia.</p>
<p>“Mercury is like the 200 pound bully attacking a 7 pound baby; the small baby doesn’t have much of a chance. 200 and 7 are the molecular weights of mercury (the bully) and lithium (the baby) respectively,” says <a href="http://www.evenbetternow.com/heavy-metal-poisoning-mercury.asp">Dr. Thomas Nissen.</a> Mercury is the most toxic non radioactive element but it does share toxic properties of uranium and thus lead.</p>
<p>Every physician knows that radiation can lead to cancer. What they don’t know is how heavy metals and radiation share similar toxic pathways on a chemical level. For example,<strong> </strong>“Depleted (DU) uranium is highly toxic to humans, both chemically as a heavy metal and radiological as an alpha particle emitter, is very dangerous when taken internally,” writes Dr. Rosalie Bertell, Canadian Epidemiologist.<a id="_ednref7" name="_ednref7" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn7"></a>[7] A new study, conducted by biochemist Dr. Diane Stearns at Northern Arizona University confirms that, separate from any radiation risks, cells exposed to uranium will bond with the metal chemically.<a id="_ednref8" name="_ednref8" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn8"></a>[8] Uranium and phosphate have a strong chemical affinity for each other and the DNA and Mitochondria are loaded with phosphate so <strong>uranium is a DNA and Mitochondria deep penetration bomb.</strong> The uranium is attacking on fundamental cellular levels while mercury offers a knock out punch by attacking the sulfur bonds besides being highly toxic to nerve cells.</p>
<p><em>Both mercury and uranium oxide are floating in the<br />
environment like invisible clouds that have spread out everywhere.<br />
They are raining down on us, damaging and damning our future.</em></p>
<p>Simultaneous exposure to mercury and uranium shows markedly increased damage to the kidneys than when exposure is to each metal singly. Insulin has three sulfur-containing cross-linkages and the insulin receptor has a <em>tyrosine kinase-</em>containing sulfur bond, which are the preferred targets for binding by both mercury and lead. Should mercury attach to one of these three sulfur bonds it will interfere with the normal biological function of the insulin molecule. Nephrotoxicity of the kidneys with necrosis of proximal tubules has been seen to increase significantly with dual exposure to both uranium and mercury.<a id="_ednref9" name="_ednref9" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn9"></a>[9] In February, 2007 The Canadian Institute for Health Information (CIHI) reported that the number of new cases of kidney failure jumped 114 per cent. Chronic kidney disease (CKD) is a worldwide public health problem.<a id="_ednref10" name="_ednref10" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_edn10"></a>[10]</p>
<p>At Los Alamos National Laboratory in New Mexico, researcher Don York has used baking soda to clean soil contaminated with uranium. <strong>Sodium bicarbonate binds with uranium, separating it from the dirt; so far, York has removed as much as 92 percent of the uranium from contaminated soil samples</strong>.</p>
<p>Dr. Paul R. Epstein of Harvard Medical School released a report about the severe health impacts of coal on Kentuckians. Because of Kentucky’s 22 coal-burning power plants, every mile of Kentucky waterways flow with unsafe levels of mercury, the leading cause of birth defects in this country. <strong>The risk of death for people living within 30 miles of a power plant is three to four times greater than for those living further away</strong>. In Kentucky, 811,993 children live within that 30-mile radius. Of the chemicals known to be used while processing coal, 19 are cancer-causing and 24 are linked to lung and heart disease.</p>
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<div>
<div id="edn1">
<p><a id="_edn1" name="_edn1" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref1"></a>[1] The Pathogenic Multi-potency of Mercury, by Hans Nolte, MD (Biological Therapy, Journal of Natural Medicine, Vol. VI, No. 3, June 1988).</p>
</div>
<div id="edn2">
<p><a id="_edn2" name="_edn2" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref2"></a>[2] Mitochondria as an important target in heavy metal toxicity in rat hepatoma AS-30D cells;<a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Belyaeva%20EA%22%5BAuthor%5D">Belyaeva EA</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Dymkowska%20D%22%5BAuthor%5D">Dymkowska D</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Wieckowski%20MR%22%5BAuthor%5D">Wieckowski MR</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Wojtczak%20L%22%5BAuthor%5D">Wojtczak L</a>.j; <a title="Toxicology and applied pharmacology." href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/">Toxicol Appl Pharmacol.</a>2008 Aug 15;231(1):34-42. Epub 2008 Apr 7.  <a href="http://www.ncbi.nlm.nih.gov/pubmed/18501399?ordinalpos=7&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum">PubMed</a></p>
</div>
<div id="edn3">
<p><a id="_edn3" name="_edn3" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref3"></a>[3] Effect of mercury vapor exposure on metallothionein and glutathione s-transferase gene expression in the kidney of nonpregnant, pregnant, and neonatal rats;.<a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Brambila%20E%22%5BAuthor%5D">Brambila E</a>,<a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Liu%20J%22%5BAuthor%5D">Liu J</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Morgan%20DL%22%5BAuthor%5D">Morgan DL</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Beliles%20RP%22%5BAuthor%5D">Beliles RP</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Waalkes%20MP%22%5BAuthor%5D">Waalkes MP</a>; <a title="Journal of toxicology and environmental health. Part A." href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/">J Toxicol Environ Health A.</a> 2002 Sep 13;65(17):1273-88.  <a href="http://www.ncbi.nlm.nih.gov/pubmed/12167210?ordinalpos=11&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum">PubMed</a></p>
</div>
<div id="edn4">
<p><a id="_edn4" name="_edn4" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref4"></a>[4] Metal-mediated formation of free radicals causes various modifications to DNA bases, enhanced lipid peroxidation, and altered calcium and sulfhydryl homeostasis; <a href="http://www.ncbi.nlm.nih.gov/pubmed/15892631?ordinalpos=1&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DiscoveryPanel.Pubmed_Discovery_RA&amp;linkpos=2&amp;log$=relatedreviews&amp;logdbfrom=pubmed">PubMed</a></p>
</div>
<div id="edn5">
<p><a id="_edn5" name="_edn5" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref5"></a>[5]Free radicals, metals and antioxidants in oxidative stress-induced cancer. <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Valko%20M%22%5BAuthor%5D">Valko M</a>,<a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Rhodes%20CJ%22%5BAuthor%5D">Rhodes CJ</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Moncol%20J%22%5BAuthor%5D">Moncol J</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Izakovic%20M%22%5BAuthor%5D">Izakovic M</a>, <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Mazur%20M%22%5BAuthor%5D">Mazur M</a>.; <a title="Chemico-biological interactions." href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/">Chem Biol Interact.</a> 2006 Mar 10;160(1):1-40. Epub 2006 Jan 23.;<a href="http://winningcancer.com/index.php/2010/03/AppData/Roaming/Skype/My%20Skype%20Received%20Files/Chem%20Biol%20Interact.%202006%20Mar%2010;160(1):1-40.%20Epub%202006%20Jan%2023.">PubMed</a></p>
</div>
<div id="edn6">
<p><a id="_edn6" name="_edn6" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref6"></a>[6] Disorders of apoptosis may play a critical role in some of the most debilitating metal-induced afflictions including hepatotoxicity, renal toxicity, neurotoxicity, autoimmunity and carcinogenesis.  Metals and apoptosis: recent developments.<a href="http://www.ncbi.nlm.nih.gov/pubmed?term=%22Rana%20SV%22%5BAuthor%5D">Rana SV</a>.  <a title="Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)." href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/">J Trace Elem Med Biol.</a> 2008;22(4):262-84. Epub 2008 Oct 10; <a href="http://www.ncbi.nlm.nih.gov/pubmed/19013355?ordinalpos=1&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum">PubMed</a></p>
</div>
<div id="edn7">
<p><a id="_edn7" name="_edn7" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref7"></a>[7] <a href="http://cndyorks.gn.apc.org/news/articles/du/drrb.htm">http://cndyorks.gn.apc.org/news/articles/du/drrb.htm</a></p>
</div>
<div id="edn8">
<p><a id="_edn8" name="_edn8" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref8"></a>[8] A radioisotope of an element will bind best to the same substrates which a non-radioactive isotope of the same element will bind. Dr. Stearns has established that when cells are exposed to uranium, the uranium binds to DNA and the cells acquire mutations, triggering a whole slew of protein replication errors, some of which can lead to various cancers. Stearns’ research, published in the journals Mutagenesis and Molecular Carcinogenesis, confirms what many have suspected for some time – that uranium can damage DNA as a heavy metal, independent of its radioactive properties. The biochemical reaction of heavy metals can cause genetic mutations, which in turn can curtail cell growth and cause cancer. Heavy metals that are also radioactive amplify this effect and can cause distortions in shape and thus function even of red blood cells.</p>
</div>
<div id="edn9">
<p><a id="_edn9" name="_edn9" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref9"></a>[9] Biol Trace Elem Res. 2001 Winter;84(1-3):139-54.<br />
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=PubMed&amp;list_uids=11817685&amp;dopt=Abstract">http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=PubMed&amp;list_uids=11817685&amp;dopt=Abstract</a></p>
</div>
<div id="edn10">
<p><a id="_edn10" name="_edn10" href="http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#_ednref10"></a>[10] In February, 2007 The Canadian Institute for Health Information (CIHI) reported that the number of new cases of kidney failure jumped 114 per cent, from just fewer than 1,100 in the first year to more than 2,100 cases in 2004, adding that the incidence of Type 2 diabetes jumped during the same period. In the United States (US), there is a rising incidence and prevalence of kidney failure. The number of patients enrolled in the end-stage renal disease (ESRD) Medicare-funded program has increased from approximately 10,000 beneficiaries in 1973 to 86,354 in 1983, and to 452,957 as of December 31, 2003. In 2003 alone 100,499 patients entered the US ESRD program.</p>
<p>source: winningcancer.com</p>
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		<title>Smoking Teeth = Poison Gas</title>
		<link>http://smartbio.org/others/smoking-teeth-poison-gas-2/</link>
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		<pubDate>Sat, 26 Nov 2011 05:09:47 +0000</pubDate>
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		<description><![CDATA[How mercury has so dramatically impacted your life, exposed from the teeth contains amalgam]]></description>
			<content:encoded><![CDATA[<p> How mercury has so dramatically impacted your life, exposed from the teeth contains amalgam</p>
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		<title>Nicotine study surprises scientists / Substance promotes blood vessel growth, tumors, artery plaque</title>
		<link>http://smartbio.org/articles/nicotine-study-surprises-scientists-substance-promotes-blood-vessel-growth-tumors-artery-plaque/</link>
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		<pubDate>Tue, 22 Nov 2011 02:53:44 +0000</pubDate>
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		<description><![CDATA[July 03, 2001&#124;David Perlman, Chronicle Science Editor In an unexpected finding, Stanford University researchers have discovered for the first time that nicotine can promote the dangerous growth of new blood vessels, increase the growth of tumors and stimulate formation of the artery- &#8230; <a href="http://smartbio.org/articles/nicotine-study-surprises-scientists-substance-promotes-blood-vessel-growth-tumors-artery-plaque/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>July 03, 2001|David Perlman, Chronicle Science Editor</p>
<div id="mod-a-body-first-para">
<p>In an unexpected finding, Stanford <a href="http://www.sfgate.com/education-guide/">University</a> researchers have discovered for the first time that nicotine can promote the dangerous growth of new blood vessels, increase the growth of tumors and stimulate formation of the artery- clogging substance called plaque.</p>
<p>At the same time, the researchers said, nicotine may ultimately prove useful in treating disorders where blood flow is impaired or new blood vessels are needed.</p>
<p>The drug is now being evaluated by other researchers as a possible treatment for Alzheimer&#8217;s and Parkinson&#8217;s diseases as well as for pain and sleep disorders.</p>
</div>
<div id="mod-a-body-after-first-para">
<p>The newest findings on nicotine&#8217;s harmful effects are reported this month in the journal Nature Medicine by a Stanford research team headed by Dr. John P. Cooke, a heart specialist and chief of vascular medicine there.</p>
<p>The drug &#8220;is much like fire &#8212; it can be very harmful, and yet it can be useful if you know how to control it,&#8221; Cooke said in an interview.</p>
<p>Earlier research on smoking had indicated that nicotine prevented or at least limited the formation of new blood vessels, a process known as angiogenesis. Cooke and his team were experimenting with mice to prove that theory when they found the drug had exactly the opposite effect.</p>
<p>&#8220;We didn&#8217;t expect it,&#8221; Cooke said, &#8220;but it was a great finding.&#8221;</p>
<p>Dr. Rakesh Jain, a Harvard Medical School biomedical engineer who studies the formation of blood vessels, agreed. In a commentary also published in Nature Medicine, Jain called the Cooke team&#8217;s results &#8220;significant and timely.&#8221;</p>
<p>In experiments, the researchers looked at the effects of nicotine in several groups of mice. They implanted tiny plastic disks impregnated with nicotine into one group. They injected the drug into the hind legs of mice whose legs were deprived of normal blood supplies. They implanted lung cancer tumors in a group of mice who then drank nicotine-laced water. And they administered nicotine to a colony of mice who were specially bred to accumulate plaque in their arteries.</p>
<p>When the researchers compared the results of the treated and untreated mice,</p>
<p>they found that:</p>
<p>&#8211; New blood vessels formed within the implanted plastic disks.</p>
<p>&#8211; The hind legs of mice whose normal blood supply had been cut off developed networks of new blood vessels.</p>
<p>&#8211; The tumors in the mice developed fresh blood vessels, and the cancers grew rapidly.</p>
<p>&#8211; And finally, plaque grew faster and more thickly in the mouse arteries that were already blocked by the fatty material.</p>
<div id="mod-a-body-first-para">
<p>To Cooke the implications of the research are clear: Many people now using nicotine patches or nicotine gum in an effort to curb their smoking may be courting danger from cancer and heart disease if they use their nicotine devices for too long, he said.</p>
<p>There is also a danger that the nicotine they use will promote the growth of tumors if they already have cancer, or that they will develop more plaque in their arteries if they already show signs that plaque formation has begun, he said.</p>
<p>On the other hand, Cooke said, future research may show potential benefits from nicotine where tissues are starved of oxygen and need more blood:</p>
</div>
<div id="mod-a-body-after-first-para">
<p>If the brain&#8217;s blood supply is impaired, and strokes become possible, for example, the drug might prove useful in improving blood flow there. And where clogged arteries limit blood flow in the legs, nicotine might possibly help to increase the flow. The drug might even prove useful in wound healing, Cooke said.</p>
<p>As a result of the group&#8217;s research, Stanford has already patented the use of nicotine to promote the formation of new blood vessels, the university said.</p>
<p>Endovasc Inc., a pharmaceutical research company in Montgomery, Texas, has been granted a license to the patent. Cooke and his colleagues were &#8220;inventors of this patent, and might receive royalties from the license,&#8221; says a statement accompanying the report in the journal.</p>
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		<title>The Balur and Divine Kretek Therapy (The philosophy and basic ideas)</title>
		<link>http://smartbio.org/research/the-balur-and-divine-kretek-therapy-the-philosophy-and-basic-ideas/</link>
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		<pubDate>Sun, 06 Nov 2011 13:32:54 +0000</pubDate>
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		<description><![CDATA[By Gretha Zahar In principal we are trying to understand the living system using the modern physic theory. We do understand that many people are in doubts curiosity since the logical manner for the discussion is at the subatomic level. &#8230; <a href="http://smartbio.org/research/the-balur-and-divine-kretek-therapy-the-philosophy-and-basic-ideas/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p style="text-align: center;"><strong>By Gretha Zahar</strong></p>
<p>In principal we are trying to understand the living system using the modern physic theory. We do understand that many people are in doubts curiosity since the logical manner for the discussion is at the subatomic level. In fact, we are really inspired by the Dr. Fritjof Capra’s thought presented at First Biennial International Seminar on the Philosophical of Complexity Theory in Havana (January 2002). The full paper of his thought is written in a book entitled “<em>Reframing complexity, Perspective from the North to South</em>”. We can also find further inquiries of the ideas in his other book entitled “The Tao of Physics”. We are interested in a complexity science approach which may help our understanding of the unity of dynamics of non-living and living phenomena. A complexity theory together with relativity theory and quantum mechanics, phenomenology and cognitivism has led further to recognize the inseparability of subject and object of cognition.</p>
<p>We consider this complexity concepts cover self-organization and edge-of-chaos phenomena in the living systems. As may we know that in the basic process of life (called metabolism), there is ceaseless flow of energy and matter through a network of chemical reactions, which enables a living organism to continually generate, repair and perpetuate itself. Thermodynamically, the ordered structure of the living system is maintained by continually exert entropy to the outside of the system. The characteristic of living system is that they are self-generating. Our experience in introducing tubulin proteins isolated from bovine brain, which can be polymerized into microtubule of both <em>in vitro </em>as well as in sea urchin cells, then also autonomously disassembled at the end of the biological events (namely anaphase stage of the mitosis), indicated that the tubulin has the idea of where, when and to whom it may contact with to proceed role in a living system.</p>
<p>In case of <em>Balur </em>treatment, our technique aimed to leach free radicals overwhelmingly produced in unhealthy body, we realized a Mandelbrot set of crystals of <em>Balur </em>liquid after rubbed over the human body. The Balur waste proceeds self- producing structures when it is either freeze or dried. Since the chemicals used in <em>Balur </em>can only proceeds self-producing structures after it was rubbed over the human skin, we consider that they may interact with components coming out from the human bodies. The chemical analytic procedures done indicate some heavy metals such as Mercury enabled to be pulled out from the body and persist in the waste. We also realized that the electrical current from the copper plate move into the ground shows more and more patterned order as much as the repeating number of <em>balur </em>treatments. The electrical current pattern indicates the improving metabolicorder of the patients. We also observe and analyze the existing metal radicals as well as possible existing biradicals in the waste using Electron Spin Resonance (ESR) Apparatus. The data indicates some characteristic of the ESR pattern of the waste can be concluding to be relating with the kind of diseases. We are now use ESR patterns to diagnose of improving conditions of the patients.</p>
<p>In case of cigarette smoke, our opinion is in regard with nano-particulates of the smokes. Please note that we used cigarette commonly formulated as <em>Kretek </em>cigarette, a special Indonesian cigarette. The, cigarette is not only containing tobacco leaves but also clove and some other plant materials used for traditional medicine. We add some chemical scavenger to formulate the cigarette which is mostly aromatic compounds enables to develop biradicals complex structures with the smoke components when it is burned. The aromatic compounds used in the formulation designed to involve in these complex structures without involving the chemical bonding capacities, but they use their magnetic and paramagnetic as well as diamagnetic capacities. As it may seen in the web-site, we hypothesized complex particulates of the smoke which is drawn below, are rich with electron dense. The smoke of these cigarettes can also develop Mandelbrot set of crystals when introduced to some amino acids indicating a self-producing structures capacity. In the term of metabolic logic this complex particulate are having high energetic potential to transfer electron.</p>
<p><img class="alignnone size-full wp-image-680" title="nanostructure" src="http://smartbio.org/wp-content/uploads/2011/11/nanostructure.jpg" alt="" width="348" height="358" /></p>
<p>This is mostly similar character with some other biological complex structures having role on transferring and carrying electron such as Chlorophyll, Cytochrome as well as Hemoglobin.</p>
<p><img class="alignnone size-full wp-image-681" title="chloropyl-cytochrome" src="http://smartbio.org/wp-content/uploads/2011/11/chloropyl-cytochrome.jpg" alt="" width="417" height="166" /></p>
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		<title>Pengembangan Teknologi Kretek Sehat Tanpa Kehilangkan Cita-rasa</title>
		<link>http://smartbio.org/research/pengembangan-teknologi-kretek-sehat-tanpa-kehilangkan-cita-rasa/</link>
		<comments>http://smartbio.org/research/pengembangan-teknologi-kretek-sehat-tanpa-kehilangkan-cita-rasa/#comments</comments>
		<pubDate>Fri, 04 Nov 2011 02:13:50 +0000</pubDate>
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				<category><![CDATA[Research]]></category>

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		<description><![CDATA[Oleh: Pusat Studi Nano Biologi, Universitas Brawijaya   A. Latar Belakang dan Dasar Inovasi Mengingat kretek merupakan bagian dari budaya dan merupakan bagian dari masalah nasional yang pelik menyangkut aspek isu kesehatan, maka Kelompok Studi UB bekerjasama dengan Lembaga Penelitian &#8230; <a href="http://smartbio.org/research/pengembangan-teknologi-kretek-sehat-tanpa-kehilangkan-cita-rasa/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p align="center">Oleh:</p>
<p align="center">Pusat Studi Nano Biologi, Universitas Brawijaya</p>
<p><strong> </strong></p>
<p><strong>A. Latar Belakang dan Dasar Inovasi </strong></p>
<p>Mengingat kretek merupakan bagian dari budaya dan merupakan bagian dari masalah nasional yang pelik menyangkut aspek isu kesehatan, maka Kelompok Studi UB bekerjasama dengan Lembaga Penelitian Peluruhan Radikal Bebas berusaha ikut memecahkan permasalahan. Dari kompetensi yang kami miliki, dan dari hasil telaah penelitian tentang asap rokok selama ini, kita berkesimpulan untuk tidak semata-mata menggunakan kajian berbasis Kimia Analitik dan kajian Biologi yang reduksionistik, seperti yang selama ini dipakai untuk mendiskusikan dampak asap rokok terhadap kesehatan. Kita berusaha mengembangkan cara berfikir berbeda dengan membangun konsep Kretek Sehat menggunakan titik pandang baru yang basisnya adalah pemikiran yang lebih holistik dan fundamental dengan memanfaatkan pengetahuan di bidang Fisika Modern dikombinasikan dengan Biologi Sel dan Molekuler. Asap selanjutnya dikaji dengan memandangnya sebagai kumpulan partikel organik dan mendiskusikannya dengan memperhatikan sifat magnetik dari setiap konfigurasi atomik dan molekulernya, agar dapat mengarah pada perolehan kesimpulan untuk dasar inovasi teknologi pengurangan dampak negatif merokok.</p>
<p>Asap rokok sering dinilai sebagai penyebab berbagai masalah kesehatan karena dapat menimbulkan berbagai penyakit fisiologis maupun genetik. Kesimpulan ini sudah dipublikasikan di banyak sekali hasil penelitian. Namun demikian ada beberapa hal yang perlu dicermati dari hasil-hasil penelitian yang sudah sangat banyak tersebut, dan ternyata ada beberapa kelemahan yang perlu kita pertimbangkan sebelum kita memakainya  untuk membuat keputusan, kebijakan maupun fatwa. Catatan kami menunjukkan hal-hal sebagai berikut yang perlu diperhatikan dan dipertimbangkan:</p>
<p><strong> </strong></p>
<p>Pertama:</p>
<p>Asap rokok termasuk Kretek mengandung komponen kimiawi yang jenisnya dapat mencapai puluhan ribu komponen. Komponen-komponen kimia yang terdapat dalam asap rokok terbukti membentuk partikulasi antara 1 sampai 10.000 nanometer (nm) (Lidia et al, 1996, Ning et al., 2006, Wayne et al., 2005, Wardoyo (disertasi), 2008). Partkel-partikel ini terbentuk dari gabungan senyawa-senyawa organik dalam asap. Senyawa-senyawa tersebut memiliki potensi gaya magnetik dan elektromagnetik, dengan demikian  komponen-komponen kimia khususnya yang bersifat aromatik di ujung batang rokok yang  bersuhu 400-600<sup>o</sup>C dapat membentuk partikel (polimer). Secara sendiri-sendiri komponen-komponen kimia asap itu bisa jadi berbahaya, namun dalam bentuk partikulasi yang merupakan gabungan komponen-komponen belum tentu berbahaya. Pembentukan polimer gabungan secara teoritis akan membentuk sifat gabungan yang berbeda dengan sifat masing-masing komponen (Albert et al., 1996). Dengan memakai pandangan ini, sesungguhnya terlalu dini bila hasil analisis kimia tentang kandungan asap kretek langsung dihubungkan dan disimpulkan sebagai dampak negatip asap kretek terhadap kesehatan atau sistem biologis pada umumnya. <strong></strong></p>
<p>Pada dasarnya senyawa-senyawa yang ada pada asap rokok adalah senyawa aromatis, beberapa diantaranya dianggap mempunyai gugus radikal yang dapat bereaksi dengan senyawa-senyawa penyusun tubuh. Berbagai kandungan  kimia dalam asap rokok seperti benzapyren, nikotin karbon monooksida dan lain-lain merupakan senyawa kimia yang dianggap memiliki kemampuan bereaksi dan mengganggu dalam tubuh manusia (Novello, S, and  E. Baldin, 2006, Sumitro, 1996). Pandangan inilah yang kemudian dipakai sebagai dasar penjelasan mengapa muncul penyakit pada perokok yang dikonfirmasi dari hasil eksperimen laboratorium dengan hewan coba yang diasapi dengan asap rokok. Pada hal di sisi lain, senyawa-senyawa yang terkandung dalam asap rokok tersebut juga merupakan bagian yang memunculkan cita rasa kenikmatan merokok.</p>
<p>&nbsp;</p>
<p>Kedua:</p>
<p>Banyaknya orang di Indonesia merokok yang tetap sehat dan beberapa studi yang sering dianggap kontroversial seperti studi yang dilakukan oleh James E. Enstrom, Ph.D., M.P.H dari UCLA, sesungguhnya cukup memberikan signal kemungkinan adanya sifat positip asap rokok yang perlu kita kenali. Sementara itu kita tidak punya data primer yang dibangun dari hasil survei dengan pendekatan pengambilan data berbasis populasi (<em>population based sampling method</em>). Artinya kita belum memiliki penelitian tentang dampak merokok ini dengan menggunakan sampel perokok (dapat difokuskan di Kretek), dan bukannya sampel dari orang sakit yang datang di rumah sakit (<em>hospital base sampling method</em>). Mengingat besaran dampak masalahnya, maka sangat perlu untuk melakukan penelitian bersifat <em>population based survei</em> secara mandiri berskala nasional yang dilakukan oleh pemerintah untuk tujuan menakar dampak Kretek secara komprehensif dan cermat serta tepat.</p>
<p>&nbsp;</p>
<p>Ketiga:</p>
<p>Rokok Kretek adalah rokok khas Indonesia yang berbeda dengan rokok dan cerutu yang sudah banyak diteliti di Barat. Belum pernah ada penelitian yang komprehensif secara khusus ditujukan untuk menakar dampak rokok kretek ini. Penelitian yang ada umumnya bersifat parsial, sektorial dan belum memberikan nuansa secara holistik. Dampak rokok ini perlu diukur dan ditakar dengan memperhatikan aspek secara keseluruhan baik dari aspek kesehatan, ekonomi, sosial, budaya sampai dengan dampaknya di aspek psikologi sosial maupun individual. Benarkah Kretek menyebabkan ketagihan (adiksi?), ataukah sebaliknya, Kretek memang diperlukan oleh orang-orang yang sedang dalam kondisi Psikologis tidak baik (stres, tertekan)? Hal ini perlu diteliti lebih jauh</p>
<p>&nbsp;</p>
<p><strong>B. Penyebab Masalah Adalah Radikal Bebas Khususnya Merkuri</strong></p>
<p>Kami memiliki logika pemikiran berbeda tentang efek asap rokok ini hubungannya dengan kesehatan. Kami menaruh kecurigaan terhadap radikal bebas akibat pembakaran tidak sempurna (Richard R. Baker, 2006), dan keberadaan merkuri dalam tembakau dan lingkungan (Zahar, G. 2006). Publikasi-publikasi tentang kemungkinan peran merkuri dalam menimbulkan bahaya dalam merokok beberapa kali muncul (Michael J. Et al., 2002, Qun Hu, et al., 2003), namun kurang memperoleh perhatian. Pada hal melihat sifat merkuri yang luar biasa mustinya harus dicurigai. Sifat merkuri cenderung membentuk senyawa biradikal dan memiliki wilayah medan gaya sangat besar dan terus-menerus secara otomatis dapat membesar dalam bentuk gas dengan perilakukanya yang bagaikan siluman (relativistik) (Hess, B, 1990, Sumitro, S.B., and G. Zahar, 2010, Sumitro, SB., 2011). Dengan demikian, fakta sebarannya yang sangat luas di Biosfir maupun penggunaannya yang sangat luas dalam kehidupan manusia (seperti kosmetik, pertambangan, pewarna, dan tambalan gigi), peran merkuri sebagai penyebab utama gangguan kesehatan dari asap rokok sangat perlu dipertimbangkan. Apalagi saat ini intensitas sinar UV matahari jenis C yang semakin intensif sampai ke permukaan bumi akibat dari adanya kerusakan lapisan ozon di lapisan atas atmosfir, kami menduga kuat merkuri menjadi sangat mudah mengalami transisi elektron dan teraktifkan untuk membentuk berbagai inisiatif gangguan terhadap sistem kehidupan di bumi. Atas dasar inilah, kami cenderung berpendapat bahwa penyebab utama gangguan kesehatan (sebagai biangnya masalah) adalah radikal bebas khususnya atom-atom logam berat seperti merkuri dan bukannya senyawa-senyawa organik dalam asap rokok.</p>
<p>&nbsp;</p>
<p><strong>C. Beberapa  Temuan Awal yang Sudah Kami Miliki</strong></p>
<p>Menghilangkan radikal bebas terutama unsur merkuri dan logam berat dalam Kretek, adalah strategi kami dalam membuat asap Kretek jauh lebih aman. Lebih dari itu, setelah radikal bebas dapat dijinakkan dalam asap, keberadaan partikel yang merupakan polimer gabungan komponen organik diperkirakan justru cenderung menyehatkan. Dari hasil simulasi dengan <em>computer software</em> <em>crystal makers</em> yang kami lakukan, partikel-partikel tersebut dapat berpeluang memberdayakan energi unsur merkuri yang terperangkap di dalamnya untuk didonasikan ke dalam system fisiologis tubuh dalam bentuk transport elektron skala <em>milli Volt</em>. Dari dasar berfikir seperti inilah kita membuat inovasi Kretek Sehat (divine Kretek) dan tidak menghilangkan unsur nikmatnya.</p>
<p>Merkuri adalah radikal bebas yang berada dalam fase gas dan memiliki sifat relatifistik. Sifat-sifatnya ini ditambah lagi sifatnya sebagai logam berat yang khas dan kemungkinan peluangnya yang besar untuk membentuk Plumbum atau Aurum artificial, jauh lebih reaktif dibandingkan senyawa-senyawa tersebut di atas (Hess B., 1990).  Kami memiliki teknik merubah sifat merkuri dari keberadaannya di dalam senyawa-senyawa aromatis yang terkandung dalam rokok, serta mengikatnya agar lebih tenang. Hasilnya adalah asap rokok yang lebih tenang dengan partikel yang lebih kecil, tidak berbau dan dapat menjernihkan ruangan berasap. Berbagai hasil eksperimen kami dengan hewan coba tidak membahayakan. Selain itu, uji coba pada perokok yang secara suka-rela menjadi <em>probandus</em> percobaan membuktikan bahwa Asap Kretek memperbaiki keluhan-keluhan mereka sementara  tidak mengurangi kualitas cita rasa kenikmatan merokok khususnya bagi mereka yang merokok kretek jenis <em>mild</em>.</p>
<p>Untuk selanjutnya kami ingin melangkah lebih jauh.  Kami ingin tahu bagaimana persisnya mekanisme “penjinakan” asap rokok ini, dan bagaimana mekanisme terjadinya polimerisasi struktur komplek untuk menjadi partikel agar diperoleh formulasi yang lebih mudah dan efektif untuk pengembangan Kretek Sehat.</p>
<p>&nbsp;</p>
<p><strong>Daftar Pustaka</strong></p>
<ol start="1">
<li>Albert, B., D. Bray, J. Lewis, M. Raff, K. Roberts, J.D. Watson, 1994. Molecular Biology of the Cell, 3rd ed.  Garland Publish., Inc. New York.</li>
<li>Bernd Hess (ed.), 1990. Relativistic Effects in Heavy-Element Chemistry and Physics. Book of Theoretical Chemistry , University of Erlangen –Nuremberg 91058 Erlangen, Germany <a href="mailto:bernd.hess@chemie.uni-erlangen.de">bernd.hess@chemie.uni-erlangen.de</a></li>
<li><strong>James Enstrom</strong><strong>, 2007. </strong><strong>Defending Legitimate Epidemiologic Research; Combating Lysenko Pseudoscience</strong>. <strong><a href="http://rs6.net/tn.jsp?t=n5tbnhcab.0.untfnhcab.rc5nt5bab.0&amp;ts=S0300&amp;p=http%3A%2F%2Fjunkscience.com%2Fdec07%2FEnstrom_Second-hand_tobacco_smoke_2007pdf.pdf" target="_blank">Epidemiologic Perspectives &amp; Innovations, 4:11 doi:10.1186/1742-5573-4-11</a></strong></li>
<li>Lidia Morawska, Milan Jamriska, and Neville D. Bofingerb, 1997. Size characteristics and ageing of the environmental tobacco smoke. The Science of the Total Environment 196 (1997) 43—55.</li>
<li>Michael J. Chang, Reta L. McDaniel, John D. Naworal and David A. Self, 2002. A rapid method for the determination of mercury in mainstream cigarette smoke by two-stage amalgamation cold vapor atomic absorption spectrometry. J. Anal. At. Spectrom, 2002, 17, 710–715</li>
<li>Paul R Nelson, Fred W. Conrad, Susan P. Kelly, Katherine C Maiolo, Joel D. Richardson, and Michael W. Ogden, 1997. Composition of Environtmental Tobacco Smoke (ETS)from International Cigarettes Part II. Environtal International, 24 (3): 251-257.</li>
<li>Ning Z., C.S. Cheung, J. Fu, M.A. Liu, M.A. Schnell, 2006. Experimental study of environmental tobacco smoke particles under actual indoor environment. Science of the Total Environment 367 (2006) 822–830.</li>
<li>Qun Hu, Guangyu Yang, Jing Ma,  and Jikai Liu, 2003. Simultaneous Determination of Tin, Nickel, Lead, Cadmium and Mercury in Cigarette Material by Solid Phase Extraction and HPLC. Bull. Korean Chem Soc. 24 (10): 1433-1436.</li>
<li>Richard R. Baker, 2006. Smoke generation inside a burning cigarette:  Modifying combustion to develop cigarettes that may be less hazardous to health. Progress in Energy and Combustion Science 32: 373–385</li>
<li>Sutiman B. Sumitro, Sri Widyarti, and Fatchiyah Fatah, 1996-1999. Benzapyren on Heat Shock Ptotein expresion in proliferative bronchioli cells of mice and rats. Program Riset Unggulan Nasional III.</li>
<li>Sutiman B. Sumitro and Gretha Zahar, 2010. The relativistic character of mercury is important factor in deteriorating the living system. ICEME,  <strong>April 6<sup>th</sup> &#8211; 9<sup>th</sup>, 2010 – Orlando, Florida, USA</strong><strong></strong></li>
<li><strong>Sutiman B. Sumitro, 2011. </strong>Study on biradical base complex structure: A possible way to find out natural nanoparticles from the human body. <a href="http://www.iiis-2011.org/iceme" target="_blank">www.iiis-2011.org/iceme</a></li>
<li>Wayne R. Ott, and Hans C. Siegmann, 2005. Using multiple continuous fine particle monitors to characterize tobacco, incense, candle, cooking, wood burning, and vehicular sources in indoor, outdoor, and in-transit settings. Atmospheric Environment 40 (2006) 821–84.</li>
<li>Novello, S, and  E. Baldin. 2006. Women and lung cancer. Annals of Oncology 17 (Supplement 2): ii79–ii82,</li>
<li>Zahar G, 2006. Divine cigarette.com dan Balur.com</li>
</ol>
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		<title>Overcoming Cigarette for Health without altering the Flavor (Brief illustration of scientific background and evidences)</title>
		<link>http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/</link>
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		<pubDate>Thu, 27 Oct 2011 04:01:52 +0000</pubDate>
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		<description><![CDATA[SB. Sumitro* and G. Zahar** *Nanobiology and Molecular Biology Laboratory, Faculty of Science and Mathematics, Brawijaya University, Malang 65145 **Free Radicals Institute, Jl. Surakarta 5, Malang 65143 A. The Basic Philosophy and Concept This is about technology to eliminate free-radicals and &#8230; <a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p style="text-align: center;"><strong>SB. Sumitro* and G. Zahar**</strong></p>
<p style="text-align: center;">*Nanobiology and Molecular Biology Laboratory, Faculty of Science and Mathematics, Brawijaya University, Malang 65145 **Free Radicals Institute, Jl. Surakarta 5, Malang 65143</p>
<p><strong>A. </strong><strong>The Basic Philosophy and Concept</strong></p>
<p>This is about technology to eliminate free-radicals and to transform particulates contained in the smoke having characteristic to develop order. The idea is based on the assumption that in the biological system, life is an ordered system with internal driven activities. We consider a complexity concepts cover self-organization and edge-of-chaos phenomena in the living systems. As may we know that in the basic process of life (called metabolism), there is ceaseless flow of energy and matter through a network of chemical reactions, which enables a living organism to continually generate, repair and perpetuate itself. Thermodynamically, the ordered structure of the living system is maintained by continually exert entropy to the outside of the system. The living system is self-generating while having interacting with the environments. The ordered system is a dynamic process with homeostatic character of complex process in which simple molecules behave autonomously construct complex structure. The simple molecule, using their potentials, interact within their local relationships enable to develop higher order complex structure, and finally to emerge complex system with adaptive behavior (individual organism). On the other way round, within the process of life there is also decay as part of homeostatic character of living system (figure 1).</p>
<div id="attachment_591" class="wp-caption alignnone" style="width: 314px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-7/" rel="attachment wp-att-591"><img class="size-full wp-image-591" title="image-7" src="http://smartbio.org/wp-content/uploads/2011/10/image-7.jpg" alt="" width="304" height="243" /></a><p class="wp-caption-text">Figure 1: A diagram depicting complexity in living system which should be considered in every idea in developing understanding of life and medical technologies</p></div>
<p>The innovation is dealing with constructing huge molecule block (nano structure) which has sensitizer character in which thermodynamically potential to develop biological order. Molecular bio-nanostructures of tobaccos having advantages as compared to other’s smart material structures that is <em>the intra spin-spin interaction of the conjugated di- HO•-Phenanthrenedienyl </em>were very mobile electron. The polymers are also having high density of electron beneficial for normal biological process</p>
<p>When the cigarette smoke either passes through the <strong><em>divine filter</em></strong>, or the tobacco are formulated with sets of scavengers and freeze, the free radicals are filtered off, and the particulates, complex structures of non-chemically bonding interacting exited components, become smaller in their size. The smaller sized particulates are having higher electron dense, and due to its radical free-situation, they will have capacity to donate electron in which thermodynamically may enable to contribute on the development of biological order.</p>
<p>During the process of burning, all aromatic compounds which have sensitizer capacity tend to form ligands with metals. These aromatic compounds such as, Benzenepyrene*, exitedantracene*, and chrycene* are unstable and exited. Along with this, all heavy metals such as Cd, Pb, As and Mercuro* (Hg*) produce amalgamate*. As illustrated on the figure 1, both of sensitizer components and amalgamated metals can be induce to be exited, and they will form a stable complex structure by means of hydroxycyclohexadienyl (HCHD). The size of this complex structure can be reduced by freezing and when the free-radicals are filtered off.</p>
<div id="attachment_592" class="wp-caption alignnone" style="width: 490px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-8/" rel="attachment wp-att-592"><img class="size-full wp-image-592" title="image-8" src="http://smartbio.org/wp-content/uploads/2011/10/image-8.jpg" alt="" width="480" height="255" /></a><p class="wp-caption-text">Figure 2: The diagrammatic illustrating the excited amalgamated heavy metals induce interaction of aromatic compounds to form nanostructure (particulates)</p></div>
<p>Hg* or metal-Hg* always being exited, they are absorbing energy to form variety of pattern. It was reported that they have 13 kinds of electromagnetic waves. This is the basic Principe of our hypothesis about their role in inducing complex nanostructures.</p>
<p><strong>Scavengers and freezing treatments</strong></p>
<p>Thus, the exiting mercury is a crucial event in generating the complex structure. Since they are also known to behave as gaseous radicals, in case of cigarette smoke, it should be taken into consideration to control its negative impacts.</p>
<p><a href="http://smartbio.org/wp-content/uploads/2011/10/image-9.jpg"><img class="alignnone size-full wp-image-593" title="image-9" src="http://smartbio.org/wp-content/uploads/2011/10/image-9.jpg" alt="" width="313" height="100" /></a></p>
<p>The stable complex nanostructures (figure 2) can be formed by aromatic compounds which have biradical capacity as proposed by Kosower (1968) (figure 3), and confirmed by our ESR profile (Figure 4). We hypothesized that it should put the heavy metals and nicotine in side by pushing electron aside quite long way from the centre. The complex structure resulted are nanometer size particulates with high electron dense. Each component of these complex structures are interacting each other by means of their para- and diamagnetic power. The existing free radicals contained such as NO, NO2, HCN, CO, CO2, and unsaturated Hydrocarbon, are eliminated by capturing them with scavengers applied, and leaving the non-sensitizer compounds such as naphtalenes, and quinones which have also form ligand with Ca, Ni, Fe, and Cr becoming energy ashes. The successful application of scavengers in tobacco as well as filters is indicated by fumeless ashes, odorless smoke and smaller size particles.</p>
<div id="attachment_602" class="wp-caption alignnone" style="width: 459px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-10/" rel="attachment wp-att-602"><img class="size-full wp-image-602" title="image-10" src="http://smartbio.org/wp-content/uploads/2011/10/image-10.jpg" alt="" width="449" height="159" /></a><p class="wp-caption-text">Figure 3: The biradical phenomena of “Aromatic + ̇OH”, a concept proposed by Dr. Kosower (1968): Hydroxyclohexadienyl (HCHD Sensitizer)</p></div>
<p>The smaller smoke particulates can be convincingly seen when observed using P- TRAK Ultrafine Particle Counter combined with Kanomax-Anemomaster Model AO31. The smoke volume calculated based on continued formulation of Bernoulli. The result was as the following figure:</p>
<div id="attachment_594" class="wp-caption alignnone" style="width: 434px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-18/" rel="attachment wp-att-594"><img class="size-full wp-image-594  " title="image-18" src="http://smartbio.org/wp-content/uploads/2011/10/image-18.jpg" alt="" width="424" height="285" /></a><p class="wp-caption-text">Figure 4: The number smokes particles higher when scavenger sensitizers were put on the tobacco as well as laminated on the surface of the filter. This indicates the treatment enable induc smaller size of particulates as compared to the commercial Kretek</p></div>
<div id="attachment_601" class="wp-caption alignnone" style="width: 510px"><a href="http://smartbio.org/wp-content/uploads/2011/10/image-111.jpg"><img class="size-full wp-image-601 " title="image-11" src="http://smartbio.org/wp-content/uploads/2011/10/image-111.jpg" alt="" width="500" height="279" /></a><p class="wp-caption-text">Figure 5: The biradical spectrum of Hydroxyclohexadienyl as showed by Electron Spin Resonance (ESR) apparatus. The peak of triplet association are indicated by arrow</p></div>
<p>The observation of their electromagnetic resonances using Electron Spain Resonance Apparatus as seen on figure 5, indicates that the particles are excites similar to any biological complex structures such as Chlorophyll and Cytochrome.</p>
<p><strong>B. The Experiments</strong></p>
<p><strong>a. Experiment 1:</strong></p>
<p>Experiments are done in order to observe the capacity of smoke particulates in contributing action to develop order by observing their capability to induce complex crystals formation. The result showed many different unique architecture types of crystal structures can be developed after application of the smoke into different kind of amino acids solution (Figure 6). These crystals are easily formed when they were dried, and unique frozen structure also can be observed when they were freeze. Microscopic observation showed that the crystals are tube-like structure and having green fluorescence (Figure 7). The capacity of the smoke to induce amino acid solution forming unique complex structure when it was either dried or frozen, are interpreted as their capacity to develop order. The structure is repeatable to form consistence typical structure when it was either resolute and defreeze.</p>
<div id="attachment_600" class="wp-caption alignnone" style="width: 309px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-12-2/" rel="attachment wp-att-600"><img class="size-full wp-image-600" title="image-12" src="http://smartbio.org/wp-content/uploads/2011/10/image-12.jpg" alt="" width="299" height="292" /></a><p class="wp-caption-text">Figure 6: Crystals of threonine (A) and Manitol (B) after treated with define smoke, and spine like structure of frozen phenyl-alanin solution (C) after being smoked and freeze at -30 ̊C</p></div>
<div id="attachment_599" class="wp-caption alignnone" style="width: 311px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-13/" rel="attachment wp-att-599"><img class="size-full wp-image-599" title="image-13" src="http://smartbio.org/wp-content/uploads/2011/10/image-13.jpg" alt="" width="301" height="137" /></a><p class="wp-caption-text">Figure 7 : Crystal observed with Fluorescence microscope (A), and it’s cross sectional image of digital imaging Confocal Laser Microscopy. This figure showed tube-like structure of the crystal</p></div>
<p><strong>b. </strong><strong>Experiments 2</strong></p>
<p>This experiment is aimed to know the effect of divine smoke on Mammalian physiology using groups of mice and rats. The result indicated that the smoke had any significant effect on animal’s vital signs such as feeding activities and their other physiological signs. Indeed the graphic shows that the body weight of treated mice are more fluctuation, but it was considered due to the effect of technique (fogging) rather than due to the toxicity of smoke. The interesting result is dealing with the effect of smoke on their body weight are the facts that when treated juvenile animals showed slower rate of increasing body weight, but the adults shows that within their mature age, the animals had shown more stabile in their body weight as compared to the control (untreated) groups (Figure 8). The experiments were done using “Kretek” cigarettes, an Indonesian specific cigarette. These cigarettes do not only contain tobacco but also mixing herbal components including clove.</p>
<p>Some other experiments (data not shown) are dealing with Western Cigarettes commercially available in Indonesia, showed similar results. Histological observations also done for liver, kidneys and lungs of treated mice (data not shown). It was confirmed that all tissues are normal and having any suspected different histological figure as compared to the control (untreated) groups. These histological observations were done on control and experimental animals which are daily fogged with divine smoke within the period of 6 months.</p>
<div id="attachment_598" class="wp-caption alignnone" style="width: 491px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-14/" rel="attachment wp-att-598"><img class="size-full wp-image-598" title="image-14" src="http://smartbio.org/wp-content/uploads/2011/10/image-14.jpg" alt="" width="481" height="400" /></a><p class="wp-caption-text">Figure 8: The effect of cigarette smoke on the body weight of mice</p></div>
<p><strong>C. Clinical trials</strong></p>
<p>The clinical trials of the divine smokes had been done involving 50 respondents in every trial. Respondents are consisting of smokers and non-smokers. Most respondents said that the use of divine filter to replace the original filter of commercial cigarettes make the smoke taste is milder and odorless as compared to its original. Some respondents had medical symptoms such as migraine, cough, fever, hardly breathings indicated better improvement (Figure 10). The data below indicate their opinion:</p>
<p><strong>Smokers, male </strong><strong>Non-Smokers, male </strong><strong>Smokers, female </strong><strong>Non-smokers, female</strong></p>
<div id="attachment_597" class="wp-caption alignnone" style="width: 472px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-15/" rel="attachment wp-att-597"><img class="size-full wp-image-597" title="image-15" src="http://smartbio.org/wp-content/uploads/2011/10/image-15.jpg" alt="" width="462" height="87" /></a><p class="wp-caption-text">Figure 9: The number of respondents out of 50 who indicate that divine cigarette smoke is odorless</p></div>
<div id="attachment_596" class="wp-caption alignnone" style="width: 402px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-16/" rel="attachment wp-att-596"><img class="size-full wp-image-596" title="image-16" src="http://smartbio.org/wp-content/uploads/2011/10/image-16.jpg" alt="" width="392" height="84" /></a><p class="wp-caption-text">Figure 10: Number of respondents out of 50 who indicated that the filter gives milder smokes and better taste</p></div>
<p><strong>Expectorant Heavy Breath Vertigo Fever unexpected heartburn mouth odor</strong></p>
<div id="attachment_595" class="wp-caption alignnone" style="width: 432px"><a href="http://smartbio.org/publications/overcoming-cigarette-for-health-without-altering-the-flavor-brief-illustration-of-scientific-background-and-evidences/attachment/image-17/" rel="attachment wp-att-595"><img class="size-full wp-image-595" title="image-17" src="http://smartbio.org/wp-content/uploads/2011/10/image-17.jpg" alt="" width="422" height="101" /></a><p class="wp-caption-text">Figure 11: Number of respondents stating that the divine cigarette overcoming their chronic problem</p></div>
<p>&nbsp;</p>
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		<title>Tsutimanco could be GOOD for you: Modified cigarette plant used to create HIV drug in landmark trial</title>
		<link>http://smartbio.org/articles/tsutimanco-could-be-good-for-you-modified-cigarette-plant-used-to-create-hiv-drug-in-landmark-trial/</link>
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		<pubDate>Sat, 15 Oct 2011 16:41:09 +0000</pubDate>
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		<description><![CDATA[By Daily Mail Reporter Aspirin, Ginseng and Caffeine are just some of the useful medications produced by plants. Now scientists have adapted the much maligned tobacco plant to create a drug they hope will combat HIV. UK regulators have approved the first clinical &#8230; <a href="http://smartbio.org/articles/tsutimanco-could-be-good-for-you-modified-cigarette-plant-used-to-create-hiv-drug-in-landmark-trial/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<p>By <a href="http://www.dailymail.co.uk/home/search.html?s=&amp;authornamef=Daily+Mail+Reporter" rel="nofollow" target="_blank">Daily Mail Reporter</a></p>
<p>Aspirin, Ginseng and Caffeine are just some of the useful medications produced by plants. Now scientists have adapted the much maligned tobacco plant to create a drug they hope will combat HIV. UK regulators have approved the first clinical trial of specially designed antibodies that stop the virus passing from person to person.</p>
<div id="attachment_559" class="wp-caption alignnone" style="width: 305px"><img class="size-medium wp-image-559" title="article-2017195-016FAB01000004B0-716_468x475" src="http://smartbio.org/wp-content/uploads/2011/10/article-2017195-016FAB01000004B0-716_468x475-295x300.jpg" alt="" width="295" height="300" /><p class="wp-caption-text">Tobacco plants are being used to create a potentially life-saving HIV treatment</p></div>
<p>Eleven women will be treated with the topical treatment, which has been createdfrom genetically modified tobacco plants. Should it prove safe at different doses, larger trials will follow to test its effectiveness. It is hoped that the antibodies will reduce the risk of treated women from catching the disease.</p>
<p>The landmark trial marks the culmination of a controversial E.U funded project to develop a drug from an engineered plant and take it through all the manufacturing stages. Most drugs are currently made at great expense in fermentation vats containing bacteria or mammalian cells, but the mass production of medicines in genetically modified plants could reduce costs by as many as 100 times, making it far cheaper to produce life-saving drugs.</p>
<div id="attachment_561" class="wp-caption alignnone" style="width: 243px"><img class="size-full wp-image-561" title="article-2017195-067DAD6D000005DC-136_233x296" src="http://smartbio.org/wp-content/uploads/2011/10/article-2017195-067DAD6D000005DC-136_233x296.jpg" alt="" width="233" height="296" /><p class="wp-caption-text">The HIV virus, seen here under a microscope, develops into deadly AIDs over time</p></div>
<p>Project researcher Professor Julian Ma, at St George’s, University of London, said: ‘This is a red letter day for the field. ‘The approval from the MHRA (Medicines and Healthcare products Regulatory Agency) for us to proceed with human trials is an acknowledgement that monoclonal antibodies can be made in plants to the same quality as those made using existing conventional production systems.</p>
<p>‘That is something many people did not believe could be achieved.’ The clinical trial is being carried out at the University of Surrey Clinical Research Centre. HIV is exchanged via bodily fluids and is most commonly spread during sex. At the end of 2008, an estimated 83,000 adults aged over 15 were living with HIV in the UK. Of these, just over a quarter did not know they were infected.</p>
<p>The last stage of the virus is Aids, when the patient’s immune system stops working and they develop life-threatening illnesses. Patients in western countries can live with HIV for many years thanks to antiretroviral drugs, but these are often not available in the developing world.</p>
<p>The active ingredient in the vaginal cream is an antibody called P2G12. If successful, the investigators will try combining it with other HIV-neutralising antibodies. The genetically modified tobacco plants producing P2G12 were grown in containment greenhouses at the Fraunhofer Institute in Aachen, Germany.</p>
<p id="yui_3_2_0_1_131622148965756">The antibody was isolated and purified in a custom-designed processing plant on the same site. It is the first time a license has been granted to manufacture engineered pharmaceutical products from plants in Europe. Professor Rainer Fischer, Pharma-Planta coordinator and Fraunhofer Director, said: ‘We now have a facility in Europe for producing modern medicines in transgenic plants that is unique in the world, although this has taken many years and much investment to establish. ‘This approval is a springboard for European plant biotechnology and will enable many important medical products to be realised.’</p>
<p>The researchers claim there is next to no risk of such GM plants spreading or contaminating other crops because they are contained and would not be grown on an agricultural scale.</p>
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