Details

Endocrine Disruptors in the Environment


Endocrine Disruptors in the Environment


1. Aufl.

von: Sushil K. Khetan

90,99 €

Verlag: Wiley
Format: EPUB
Veröffentl.: 23.05.2014
ISBN/EAN: 9781118891155
Sprache: englisch
Anzahl Seiten: 408

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Beschreibungen

<b>Endocrine Disruptors in the Environment</b> <p><b>A concise and engaging overview of endocrine disruption phenomena that brings complex concepts within the reach of non-specialists </b> <p>For most of the last decade, the science of endocrine disruption has evolved with more definitive evidence of its damaging potential to health and environment. This book lists the major environmental chemicals of concern and their mechanism of endocrine disruption including remedial measures for them. <p>Divided into three parts, <i>Endocrine Disruptors in the Environment</i> begins with an overview of the endocrine system and endocrine disruptors, discussing their salient features and presenting a historical perspective of endocrine disruption phenomena. It then goes on to cover hormone- signaling mechanisms, followed by various broad classes of putative endocrine disruptors, before introducing readers to environmental epigenetic modifications. Part two of the book focuses on removal processes of various EDCs by biotic and abiotic transformation/degradation. The last section consists of four chapters embracing themes on finding solutions to environmental EDCs—including their detection, regulation, replacement, and remediation. <p><i>Endocrine Disruptors in the Environment</i> is the first book to detail the endocrine effects of several known environmental contaminants and their mechanism of endocrine disruption. Additionally, it: <ul><li>Covers both the chemistry and biology of endocrine disruption and compiles almost all the known endocrine disrupting environmental chemicals and their mechanisms of toxicity</li> <li>Addresses policy and regulatory issues relevant to EDCs including scientific uncertainty and precautionary policy </li> <li>Brings forth the use of Green Chemistry principles in avoiding endocrine disruption in the designing and screening for safer chemicals and remediation of the EDCs in aquatic environment</li> <li>Includes a useful glossary of technical terms, a list of acronyms, topical references, and a subject index</li></ul> <p><i>Endocrine Disruptors in the Environment</i> is an ideal book for environmental chemists and endocrine toxicologists, developmental biologists, endocrinologists, epidemiologists, environmental health scientists and advocates, and regulatory officials tasked with risk assessment in environment and health areas.
<p>Foreword xiv</p> <p>Preface xviii</p> <p>Acronyms xxi</p> <p>Glossary xxvi</p> <p><b>1 Environmental Endocrine Disruptors 1</b></p> <p>1.1 Introduction 1</p> <p>1.1.1 The Endocrine System 1</p> <p>1.1.2 Endocrine Disrupting Chemicals (EDCs) 3</p> <p>1.1.3 Sources of EDCs in the Environment 4</p> <p>1.1.4 Deleterious Effects of EDCs on Wildlife and on Humans 6</p> <p>1.1.5 Endocrine Disruption Endpoints 6</p> <p>1.2 Salient Aspects about Endocrine Disruption 7</p> <p>1.2.1 Low-Dose Effects and Nonmonotonic Dose Responses 7</p> <p>1.2.2 Exposures during Periods of Heightened Susceptibility in Critical Life Stages 9</p> <p>1.2.3 Delayed Dysfunction 11</p> <p>1.2.4 Importance of Mixtures 11</p> <p>1.2.5 Transgenerational Epigenetic Effects 12</p> <p>1.3 Historical Perspective of Endocrine Disruption 12</p> <p>1.4 Scope and Layout of this Book 19</p> <p>1.5 Conclusion 20</p> <p>References 21</p> <p><b>Part I Mechanisms Of Hormonal Action And Putative Endocrine Disruptors 27</b></p> <p><b>2 Mechanisms of Endocrine System Function 29</b></p> <p>2.1 Introduction 29</p> <p>2.2 Hormonal Axes 29</p> <p>2.2.1 Hypothalamus–Pituitary–Gonad (HPG) Axis 31</p> <p>2.2.2 The Hypothalamic–Pituitary–Thyroid (HPT) Axis 33</p> <p>2.2.3 The Hypothalamic–Pituitary–Adrenal (HPA) Axis 34</p> <p>2.3 Hormonal Cell Signaling 35</p> <p>2.3.1 Receptors and Hormone Action 35</p> <p>2.3.2 Genomic Signaling Pathway 36</p> <p>2.3.3 Rapid-Response Pathway (Nongenomic Signaling) 38</p> <p>2.3.4 Receptor Agonists Partial Agonists and Antagonists 40</p> <p>2.4 Sex Steroids 41</p> <p>2.4.1 Physiologic Estrogens 41</p> <p>2.4.2 Androgens 43</p> <p>2.5 Thyroid Hormones 45</p> <p>2.6 Conclusions and Future Prospects 46</p> <p>References 47</p> <p><b>3 Environmental Chemicals Targeting Estrogen Signaling Pathways 51</b></p> <p>3.1 Introduction 51</p> <p>3.1.1 Gonadal Estrogen Function Disruptors 52</p> <p>3.2 Steroidal Estrogens 54</p> <p>3.2.1 Physiologic Estrogens 55</p> <p>3.2.2 17α-Ethinylestradiol (EE2) 55</p> <p>3.2.3 Phytoestrogens 57</p> <p>3.2.4 Mycoestrogen – Zearalenone (ZEN) 59</p> <p>3.3 Nonsteroidal Estrogenic Chemicals 60</p> <p>3.3.1 Diethylstilbestrol (DES) 60</p> <p>3.3.2 Organochlorine Insecticides 62</p> <p>3.3.3 Polychlorinated Biphenyls (PCBs) 65</p> <p>3.3.4 Alkyphenols 65</p> <p>3.3.5 Parabens (Hydroxy Benzoates) 73</p> <p>3.3.6 Sun Screens (Chemical UV Filters) 74</p> <p>3.4 Metalloestrogens 75</p> <p>3.4.1 Cadmium (Cd) 76</p> <p>3.4.2 Lead (Pb) 76</p> <p>3.4.3 Mercury (Hg) 77</p> <p>3.4.4 Arsenic (As) 77</p> <p>3.5 Conclusion and Future Prospects 78</p> <p>References 78</p> <p><b>4 Anti-Androgenic Chemicals 91</b></p> <p>4.1 Introduction 91</p> <p>4.2 Testosterone Synthesis Inhibitors 92</p> <p>4.2.1 Phthalates 92</p> <p>4.3 Androgen Receptor (AR) Antagonists 96</p> <p>4.3.1 Organochlorine (OC) Pesticides 96</p> <p>4.3.2 Organophosphorus (OP) Insecticides 98</p> <p>4.3.3 Bisphenol A (BPA) 99</p> <p>4.3.4 Polybrominated Diphenyl Ethers (PBDEs) 99</p> <p>4.3.5 Vinclozolin (VZ) 100</p> <p>4.3.6 Procymidone 101</p> <p>4.4 AR Antagonists and Fetal Testosterone Synthesis Inhibitors 102</p> <p>4.4.1 Prochloraz 102</p> <p>4.4.2 Linuron 103</p> <p>4.5 Comparative Anti-Androgenic Effects of Pesticides to Androgen Agonist DHT 103</p> <p>4.6 Conclusions and Future Prospects 103</p> <p>References 104</p> <p><b>5 Thyroid-Disrupting Chemicals 111</b></p> <p>5.1 Introduction 111</p> <p>5.2 Thyroid Synthesis Inhibition by Interference in Iodide Uptake 113</p> <p>5.2.1 Perchlorate 113</p> <p>5.3 TH Transport Disruptors and Estrogen Sulfotransferases Inhibitors 114</p> <p>5.3.1 Polychlorinated Biphenyls (PCBs) 114</p> <p>5.3.2 Triclosan 116</p> <p>5.4 Thyroid Hormone Level Disruptors 117</p> <p>5.4.1 Polybrominated Diphenyl Ethers (PBDEs) 117</p> <p>5.5 Selective Thyroid Hormone Antagonists 119</p> <p>5.5.1 Bisphenols 119</p> <p>5.5.2 Perfluoroalkyl Acids (PFAAs) 120</p> <p>5.5.3 Phthalates 120</p> <p>5.6 Conclusions and Future Prospects 121</p> <p>References 121</p> <p><b>6 Activators of PPAR RXR AhR and Steroidogenic Factor 1 126</b></p> <p>6.1 Introduction 126</p> <p>6.2 Peroxisome Proliferator-Activated Receptor (PPAR) Agonists 127</p> <p>6.2.1 Organotin Antifoulant Biocides 128</p> <p>6.2.2 Perfluoroalkyl Compounds (PFCs) 130</p> <p>6.2.3 Phthalates 132</p> <p>6.3 Aryl Hydrocarbon Receptor (AhR) Agonists 133</p> <p>6.3.1 Polychlorinated-Dibenzodioxins (PCDDs) and -Dibenzofurans (PCDFs) 133</p> <p>6.3.2 Coplanar Polychlorinated Biphenyls 135</p> <p>6.3.3 Substituted Urea and Anilide Herbicides 135</p> <p>6.4 Steroidogenesis Modulator (Aromatase Expression Inducer) 136</p> <p>6.4.1 Atrazine 136</p> <p>6.5 Conclusions and Future Prospects 138</p> <p>References 139</p> <p><b>7 Effects of EDC Mixtures 146</b></p> <p>7.1 Introduction 146</p> <p>7.2 Combined Effect of Exposure to Multiple Chemicals 146</p> <p>7.3 Mixture Effects of Estrogenic Chemicals 148</p> <p>7.4 Mixture Effects of Estrogens and Anti-Estrogens 151</p> <p>7.5 Mixture Effects of Anti-Androgens 152</p> <p>7.5.1 Anti-Androgens with Common Mechanism of Action 152</p> <p>7.5.2 Anti-Androgens with Different Modes of Action 154</p> <p>7.5.3 Chronic Exposure of Low Dose Mixture of Anti-Androgens Versus Acute Exposure to High Dose Individual Compounds 156</p> <p>7.6 Mixture Effects of Thyroid Disrupting Chemicals 157</p> <p>7.7 Mixture Effects of Chemicals Acting via AhR 158</p> <p>7.8 Conclusions and Future Prospects 158</p> <p>References 161</p> <p><b>8 Environmentally Induced Epigenetic Modifications and Transgenerational Effects 166</b></p> <p>8.1 Introduction 166</p> <p>8.2 Regulatory Epigenetic Modifications 168</p> <p>8.2.1 Methylation of Cytosine Residues in the DNA and Impact on Gene Expression (Transcriptional Silencing) 168</p> <p>8.2.2 Remodeling of Chromatin Structure through Post-Translational Modifications of Histone Tails (Determinants of Accessibility) 170</p> <p>8.2.3 Regulation of Gene Expression by Noncoding RNAs 173</p> <p>8.2.4 DNA Demethylation 174</p> <p>8.2.5 Assays for Epigenetic Modification 175</p> <p>8.3 Epigenetic Dysregulation Effects of Endocrine Disruption 176</p> <p>8.3.1 Bisphenol A (BPA): A Case Study 177</p> <p>8.3.2 DEHP 179</p> <p>8.4 Environmental Epigenetic Effects of Heavy Metals Exposure 179</p> <p>8.4.1 Cadmium 180</p> <p>8.4.2 Arsenic 180</p> <p>8.4.3 Nickel 180</p> <p>8.4.4 Lead 181</p> <p>8.5 Transgenerational Inheritance of Environmentally Induced Epigenetic Alterations 181</p> <p>8.5.1 DES 182</p> <p>8.5.2 Vinclozolin 183</p> <p>8.5.3 Methoxychlor 185</p> <p>8.5.4 BPA 185</p> <p>8.5.5 2,3,7,8-Tetrachlorodibenzo-<i>p</i>-dioxin (TCDD) 185</p> <p>8.6 Transgenerational Actions of EDCs Mixture on Reproductive Disease 186</p> <p>8.7 Conclusions and Future Prospects 187</p> <p>References 188</p> <p><b>Part II Removal Mechanisms Of Edcs Through Biotic And Abiotic Processes 195</b></p> <p><b>9 Biodegradations and Biotransformations of Selected Examples of EDCs 197</b></p> <p>9.1 Introduction 197</p> <p>9.2 Natural and Synthetic Steroidal Estrogens 199</p> <p>9.2.1 17β-Estradiol and Estrone 199</p> <p>9.2.2 17α-Ethynylestradiol 202</p> <p>9.3 Alkylphenols 205</p> <p>9.3.1 4-<i>n</i>-Nonylphenol (4-NP<sub>1</sub>) 205</p> <p>9.3.2 4-<i>tert</i>-Nonylphenol Isomer 4-(1-Ethyl-1,4-Eimethylpentyl) Phenol (NP<sub>112</sub>) 208</p> <p>9.3.3 4-<i>tert</i>-Nonylphenol Isomer 4-[1-Ethyl-1,3-Dimethylpentyl] Phenol (4-NP<sub>111</sub>) 210</p> <p>9.3.4 4-<i>n</i>- and 4-<i>tert</i>-Octylphenols 212</p> <p>9.3.5 Bisphenol A 214</p> <p>9.4 Phthalates 220</p> <p>9.4.1 Di-<i>n</i>-butyl Phthalate (DBP) 221</p> <p>9.4.2 <i>n</i>-Butyl Benzyl Phthalate (BBP) 222</p> <p>9.4.3 Di-(2-ethylhexyl) Phthalate (DEHP) 223</p> <p>9.4.4 Di-<i>n</i>-octyl Phthalate (DOP) 226</p> <p>9.5 Insecticides 226</p> <p>9.5.1 Methoxychlor 226</p> <p>9.6 Fungicides 228</p> <p>9.6.1 Vinclozolin 228</p> <p>9.6.2 Procymidone 231</p> <p>9.6.3 Prochloraz 232</p> <p>9.7 Herbicides 232</p> <p>9.7.1 Linuron 232</p> <p>9.7.2 Atrazine 233</p> <p>9.8 Polychlorinated Biphenyls (PCBs) 236</p> <p>9.9 Polybrominated Diphenyl Ethers (PBDEs) 238</p> <p>9.9.1 2,2’,4,4’ -Tetrabromodiphenyl Ether (BDE-47) 238</p> <p>9.9.2 2,2’,4,4’,5-Penta-bromodiphenyl Ether (BDE-99) 243</p> <p>9.9.3 3,3’,4,4’,5,5’,6,6’-Decabromodiphenyl Ether (BDE-209) 243</p> <p>9.10 Triclosan 245</p> <p>9.11 Conclusions and Future Prospects 245</p> <p>References 246</p> <p><b>10 Abiotic Degradations/Transformations of EDCs Through Oxidation Processes 254</b></p> <p>10.1 Introduction 254</p> <p>10.2 Natural and Synthetic Estrogens 256</p> <p>10.2.1 17β-Estradiol (E2) and Estrone (E1) 256</p> <p>10.2.2 17α-Ethinylestradiol (EE2) 260</p> <p>10.3 Bisphenol A 260</p> <p>10.3.1 Chlorination with HOCl 263</p> <p>10.3.2 Catalytic Oxidation with H<sub>2</sub>O<sub>2</sub> 263</p> <p>10.3.3 Oxidation with KMnO<sub>4</sub> 266</p> <p>10.3.4 Oxidation with MnO<sub>2</sub> 267</p> <p>10.3.5 Treatment with Zero-Valent Aluminum 267</p> <p>10.3.6 Ozonation 267</p> <p>10.3.7 Fenton Reaction 270</p> <p>10.3.8 Photolytic and Photocatalytic Degradation 272</p> <p>10.4 4-Octylphenol and 4-Nonylphenol 272</p> <p>10.4.1 Chlorination 272</p> <p>10.4.2 Ozonation 274</p> <p>10.4.3 Photocatalytic Degradation 274</p> <p>10.5 Parabens 274</p> <p>10.5.1 Ozonation 276</p> <p>10.5.2 Photocatalytic Degradation 276</p> <p>10.6 Phthalates – Photocatalytic Degradation 276</p> <p>10.6.1 Dibutyl Phthalate (DBP) 277</p> <p>10.6.2 <i>n</i>-Butyl Benzylphthalate 277</p> <p>10.6.3 Di(2-Ethylhexyl)phthalate (DEHP) 279</p> <p>10.7 Linuron 279</p> <p>10.7.1 Treatment with O<sub>3</sub> UV and UV/O<sub>3</sub> 279</p> <p>10.8 Atrazine 281</p> <p>10.8.1 Fenton Reaction 281</p> <p>10.8.2 Reaction with Ozone Ozone/H<sub>2</sub>O<sub>2</sub> and Ozone/OH Radicals 282</p> <p>10.8.3 Treatment with δ-MnO2 282</p> <p>10.8.4 Reductive Dechlorination 282</p> <p>10.8.5 Photocatalytic Degradation 282</p> <p>10.9 Polybrominated Diphenyl Ether (PBDE) Flame Retardants 282</p> <p>10.9.1 Photochemical Degradation 282</p> <p>10.9.2 TiO2-Mediated Photocatalytic Debromination 284</p> <p>10.9.3 Zero-Valent Iron Reductive Debromination 285</p> <p>10.10 Triclosan 285</p> <p>10.10.1 Clorination with HOCl 285</p> <p>10.10.2 Oxidation with KMnO<sub>4</sub>/MnO<sub>2</sub> 286</p> <p>10.10.3 Ozonation 286</p> <p>10.10.4 Photochemical Transformation 286</p> <p>10.11 PFOA and PFOS 289</p> <p>10.11.1 Modified Fenton Reaction 289</p> <p>10.11.2 Sonochemical Degradation 289</p> <p>10.11.3 Photocatalytic Reaction 289</p> <p>10.12 Conclusions 289</p> <p>References 290</p> <p><b>Part III Screening And Testing For Potential Edcs Implications For Water Quality Sustainability Policy And Regulatory Issues And Green Chemistry Principles In The Design Of Safe Chemicals And Remediation Of Edcs 297</b></p> <p><b>11 Screening and Testing Programs for EDCs 299</b></p> <p>11.1 Introduction 299</p> <p>11.2 Endocrine Disruptor Screening Program (EDSP) 300</p> <p>11.2.1 EDSP Tier 1 301</p> <p>11.2.2 EDSP Tier 2 302</p> <p>11.3 Assays for the Detection of Chemicals that Alter the Estrogen Signaling Pathway 304</p> <p>11.3.1 The ER Binding Assay (USEPA OPPTS 890.1250) 304</p> <p>11.3.2 ERα Transcriptional Activation Assay (USEPA OPPTS 890.1300; OECD 455) 304</p> <p>11.3.3 Aromatase Assay (USEPA OPPTS 890.1200) 306</p> <p>11.3.4 In vivo Uterotrophic Bioassay in Rodents (USEPA OPPTS 890.1600; OECD 440) 307</p> <p>11.3.5 Pubertal Female Rat Assay (USEPA OPPTS 890.1450) 308</p> <p>11.3.6 Twenty-One-Day Fish Reproduction Assay (USEPA OPPTS 890.1350; OECD 229) 308</p> <p>11.4 Assays for the Detection of Chemicals that Alter the Androgenic Signaling Pathway 308</p> <p>11.4.1 AR Binding Assay (Rat Prostate Cytosol) (USEPA OPPTS 890.1150) 309</p> <p>11.4.2 H295R Steroidogenesis Assay (USEPA OPPTS 890.1550) 309</p> <p>11.4.3 Hershberger Bioassay in Rats for Androgenicity (USEPA OCSPP 890.1400; OECD 441) 309</p> <p>11.4.4 Pubertal Male Rat Assay (USEPA OPPTS 890.1500) 310</p> <p>11.4.5 Strengths and Limitations of Assays for Interference with Androgen Action 310</p> <p>11.5 Assays for the Detection of Chemicals that Alter the HPT Axis 311</p> <p>11.5.1 Amphibian Metamorphosis Assay (OPPTS 890.1100) 311</p> <p>11.5.2 Strengths and Limitations of Thyroid Disrupting Chemical Assays 311</p> <p>11.6 The USEPA’s EDSP21 Work Plan 312</p> <p>11.6.1 The USEPA ToxCast Program 313</p> <p>11.6.2 Tox21 HTS Programs 314</p> <p>11.7 Conclusions and Future Prospects 316</p> <p>References 317</p> <p><b>12 Trace Contaminants: Implications for Water Quality Sustainability 320</b></p> <p>12.1 Introduction 320</p> <p>12.2 Trace Contaminants Sources in Water 321</p> <p>12.3 Wastewater Reclamation Processes 323</p> <p>12.3.1 Primary Treatment: Sedimentation/Coagulation 323</p> <p>12.3.2 Secondary Treatment: Removal by Physical Methods or Biological Process 324</p> <p>12.3.3 Tertiary Treatment: Redox Processes 325</p> <p>12.4 Indirect Water Reuse Systems 326</p> <p>12.4.1 Removal of Trace Contaminants for Potable Water Reuse Applications 326</p> <p>12.5 Leaching of Contaminants in Water – the Case of Bottled Water 327</p> <p>12.6 Water Quality Sustainability and Health Effects 328</p> <p>12.7 Toxicological Implications 329</p> <p>12.8 Regulatory Structures to Maintain Water Quality 330</p> <p>12.9 Conclusions and Future Prospects 331</p> <p>References 333</p> <p><b>13 Policy and Regulatory Considerations for EDCs 339</b></p> <p>13.1 Introduction 339</p> <p>13.2 Regulating Paradigm Shift in Conventional Toxicology 340</p> <p>13.2.1 Downward Movement of Safe Thresholds 341</p> <p>13.2.2 Nonmonotonic Low-Dose Effects (Nonthreshold substances) 341</p> <p>13.2.3 Sensitivity of Development Periods 342</p> <p>13.2.4 Cumulative Exposures to Multiple EDCs (Exposures can be Additive) 342</p> <p>13.2.5 Long Latency Between Exposure and Effect (Delayed Effects) 343</p> <p>13.3 Policy Options for EDC Regulation 344</p> <p>13.3.1 Scientific Uncertainty and Precautionary Policy 344</p> <p>13.3.2 Shifting the Burden of Proving Safe Products 345</p> <p>13.3.3 Need to Broaden the Risk Assessment 346</p> <p>13.3.4 Cutting-Edge Bioassays Showing Developmental Endpoints 346</p> <p>13.4 Controversy on Regulatory Framework for EDCs 348</p> <p>13.4.1 Diversity of Viewpoints of the Risk Assessors and the Endocrine Scientists 348</p> <p>13.4.2 A Debate on EU Regulatory Framework for EDCs 350</p> <p>13.5 Conclusions and Future Prospects 351</p> <p>References 353</p> <p><b>14 Green Chemistry Principles in the Designing and Screening for Safe Chemicals and Remediation of EDCs 357</b></p> <p>14.1 Introduction 357</p> <p>14.2 Benign by Design Chemicals 358</p> <p>14.3 Chemical Endocrine Disruption Screening Protocol 361</p> <p>14.3.1 Tiered Protocol for Endocrine Disruption 361</p> <p>14.4 Green Oxidative Remediation of EDCs 363</p> <p>14.4.1 Catalytic Oxidation Processes 364</p> <p>14.5 Conclusions and Future Prospects 366</p> <p>References 368</p> <p>Index 371</p>
<p>“This book is a great resource for those wanting an overview of this grand collaborative enterprise, or for those preparing the next generation for investigating, problem-solving, and managing our bio-chemical future, giving us a chance to balance modern living with safety.”  (<i>Endocrine Disruptors</i>, 1 October 2014)</p>
<p><b>SUSHIL K. KHETAN, PhD,</b> a research chemist at the Institute for Green Science in Carnegie Mellon University, has been working at the confluence of environmental and green chemistry. Earlier he worked in the agrochemicals industry and published two books on environmentally-friendly pest control technologies. He has consulted globally for several international organizations.</p>
<p><b>A concise and engaging overview of endocrine disruption phenomena that brings complex concepts within the reach of non-specialists </b></p> <p>For most of the last decade, the science of endocrine disruption has evolved with more definitive evidence of its damaging potential to health and environment. This book lists the major environmental chemicals of concern and their mechanism of endocrine disruption including remedial measures for them. <p>Divided into three parts, <i>Endocrine Disruptors in the Environment</i> begins with an overview of the endocrine system and endocrine disruptors, discussing their salient features and presenting a historical perspective of endocrine disruption phenomena. It then goes on to cover hormone- signaling mechanisms, followed by various broad classes of putative endocrine disruptors, before introducing readers to environmental epigenetic modifications. Part two of the book focuses on removal processes of various EDCs by biotic and abiotic transformation/degradation. The last section consists of four chapters embracing themes on finding solutions to environmental EDCs—including their detection, regulation, replacement, and remediation. <p><i>Endocrine Disruptors in the Environment</i> is the first book to detail the endocrine effects of several known environmental contaminants and their mechanism of endocrine disruption. Additionally, it: <ul><li>Covers both the chemistry and biology of endocrine disruption and compiles almost all the known endocrine disrupting environmental chemicals and their mechanisms of toxicity</li> <li>Addresses policy and regulatory issues relevant to EDCs including scientific uncertainty and precautionary policy </li> <li>Brings forth the use of Green Chemistry principles in avoiding endocrine disruption in the designing and screening for safer chemicals and remediation of the EDCs in aquatic environment</li> <li>Includes a useful glossary of technical terms, a list of acronyms, topical references, and a subject index</li></ul> <p><i>Endocrine Disruptors in the Environment</i> is an ideal book for environmental chemists and endocrine toxicologists, developmental biologists, endocrinologists, epidemiologists, environmental health scientists and advocates, and regulatory officials tasked with risk assessment in environment and health areas.

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