{"id":1367,"date":"2011-05-12T11:11:07","date_gmt":"2011-05-12T16:11:07","guid":{"rendered":"http:\/\/blogs.edf.org\/nanotechnology\/?p=1367"},"modified":"2026-04-02T11:16:13","modified_gmt":"2026-04-02T16:16:13","slug":"chemical-safety-evaluation-potential-benefits-of-emerging-test-methods","status":"publish","type":"post","link":"https:\/\/blogs.edf.org\/health\/2011\/05\/12\/chemical-safety-evaluation-potential-benefits-of-emerging-test-methods\/","title":{"rendered":"Chemical safety evaluation: Potential benefits of emerging test methods"},"content":{"rendered":"<p><a href=\"http:\/\/environmentaldefense.org\/page.cfm?tagID=62101\"><em>Jennifer McPartland, Ph.D.<\/em><\/a><em>, is a Health Scientist.<\/em><\/p>\n<p><strong>Parts in this series:\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong><a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2011\/03\/02\/epa-is-doing-the-%e2%80%9crobot%e2%80%9d-21st-century-style\/\"><strong>Part 1<\/strong><\/a><strong>\u00a0\u00a0\u00a0\u00a0 <\/strong><a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2011\/03\/17\/chemical-safety-evaluation-packing-tox-tests-into-single-drops-of-liquid\/\"><strong>Part 2<\/strong><\/a><strong>\u00a0\u00a0\u00a0\u00a0 <\/strong><a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2011\/05\/12\/chemical-safety-evaluation-potential-benefits-of-emerging-test-methods\/\"><strong>Part 3<\/strong><\/a><strong>\u00a0\u00a0\u00a0\u00a0 <\/strong><a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2011\/06\/14\/chemical-safety-evaluation-limitations-of-emerging-test-methods\/\"><strong>Part 4<\/strong><\/a><\/p>\n<p>This is the third in a series of blog posts on new approaches that federal agencies are exploring to improve how chemicals are evaluated for safety.\u00a0 Previous posts primarily focused on the scientific principles underlying these efforts.\u00a0 This post will take a pause from scientific fundamentals to discuss some of the opportunities presented by these more novel methods, while subsequent posts will address some of their limitations and remaining challenges.\u00a0 (Not to worry, though, I\u2019ll soon get back to computer-simulated organs as promised.)\u00a0 <!--more--><\/p>\n<p>A cornerstone of the new approaches is high-throughput (HT) chemical testing tools, housed within projects like EPA\u2019s <a href=\"http:\/\/www.epa.gov\/ncct\/download_files\/factsheets\/Tox_Cast_Fact_Sheet.pdf\">ToxCast<\/a> (see <a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2011\/03\/17\/chemical-safety-evaluation-packing-tox-tests-into-single-drops-of-liquid\/\">earlier post<\/a>).\u00a0 Below are some of the potential advantages that HT tools offer over the conventional chemical assessment paradigm:<\/p>\n<ul>\n<li><span style=\"text-decoration: underline;\">Speed<\/span>.\u00a0 Conventional toxicology testing methods generally involve dosing an animal with a chemical of interest and after some period of time\u2014days to months to years\u2014looking to see whether an adverse outcome, for example, a tumor, has developed.\u00a0 Here the scientist is observing the downstream consequence of a chemical\u2019s interference with the proper function of one or more <a href=\"http:\/\/www.genome.gov\/27530687\">biological pathways<\/a>.\u00a0 In contrast, HT methods mostly focus on \u201ccatching\u201d an early indicator of hazard:\u00a0 the perturbation of the pathway(s) itself, rather than the ultimate consequence of that perturbation.\u00a0 This requires much less time: \u00a0Not only does the effect happen sooner, but it can often be observed in something less than the whole animal, e.g., in a culture of cells or even a solution of cell components.<br \/>\nThat also means that many chemicals can be put through a battery of HT assays simultaneously.\u00a0 Indeed, thousands of chemicals can be analyzed in hundreds of assays all in a period of time far shorter than would be required to detect adverse outcomes in laboratory animals.\u00a0 Given the massive <a href=\"http:\/\/ehp03.niehs.nih.gov\/article\/fetchArticle.action?articleURI=info%3Adoi%2F10.1289%2Fehp.0800168\">backlog of chemicals with little or no safety data<\/a>, the speed of HT tools could be very valuable, at least in screening and prioritizing chemicals by level of potential concern.<\/li>\n<li><span style=\"text-decoration: underline;\">Human relevance<\/span>.\u00a0 Because of the ethical problems associated with human testing, as well as the simple fact that we live so long, traditional toxicological methods use laboratory animals to assess the toxicity a chemical may present to a human.\u00a0 According to the seminal National Academy of Sciences report <a href=\"http:\/\/dels.nas.edu\/Report\/Toxicity-Testing-Twenty-first\/11970\">\u201cToxicity Testing in the 21<sup>st<\/sup> Century: A Vision and a Strategy,\u201d<\/a> use of such animal \u201cmodels\u201d is possible because in general human biology is similar to that of test animals.\u00a0 While animal studies have served as important and useful tools in predicting the hazards a chemical may present to a human, an extrapolation is still needed at some level from animal data to estimating risk in humans.\u00a0 And there are cases where the toxicity a chemical presents is <em>not<\/em> shared between a lab animal and human.\u00a0 For example, <a href=\"http:\/\/cerhr.niehs.nih.gov\/common\/thalidomide.html\">thalidomide<\/a> is toxic to human fetuses, but rats are resistant to its effects.<br \/>\nEPA\u2019s ToxCast HT assays employ human cells, grown in culture, in addition to animal cells.\u00a0 That means potentially greater confidence that effects observed in the human cells could happen in a whole person.\u00a0 Additionally, this could lower the likelihood of a cross-species \u201cfalse negative,\u201d that is, missing an effect because it happens not to occur in the lab animal chosen for a given test but would occur in a human \u2013 or, conversely, a \u201cfalse positive,\u201d that is, seeing an effect in the animal model that for some reason would not occur in people.\u00a0 (Note that false negatives or false positives may arise for entirely different reasons in HT assays.\u00a0 But that\u2019s a discussion for a future blog post.)<\/li>\n<li><span style=\"text-decoration: underline;\">Multiple cell types and life stages.<\/span>\u00a0 In addition to advantages resulting from testing on human cells in general, HT methods also offer the potential to look for different kinds of toxicity by testing chemicals on different cell types (e.g. liver cells, kidney cells, etc). \u00a0This can shed light on a chemical\u2019s ability to disrupt a process that only takes place in certain organs.\u00a0 Some HT assays even use <a href=\"http:\/\/www.bioseekinc.com\/technology\/backgrounder.htm\">combinations of cell types<\/a> \u00a0taken directly from human tissues, in an effort to mimic responses of, and interactions between, cells types that are <a href=\"http:\/\/www.bioseekinc.com\/technology\/biomap_whitepaper.pdf\">involved in the body\u2019s reaction to a particular disease or disorder<\/a> (<em>e.g.,<\/em> asthma).<br \/>\nA particularly exciting <em>potential<\/em> application of HT tests is in evaluating chemical effects on early life stages, including fetal development.\u00a0 For example, the <a href=\"http:\/\/tivs-center.uh.edu\/research-partners\/index.php\">Texas-Indiana Virtual STAR Center<\/a> is using mouse <a href=\"http:\/\/stemcells.nih.gov\/info\/basics\/basics3.asp\">embryonic stem cells<\/a> to determine <a href=\"http:\/\/www.epa.gov\/ncct\/v-Embryo\/research.html#embryonic\">how chemicals may affect key biological pathways during early fetal development<\/a>.\u00a0 While this kind of research is still at an early stage (no pun intended), the potential to effectively screen chemicals for developmental toxicity using HT tests would greatly strengthen chemical safety assessments.<\/li>\n<li><span style=\"text-decoration: underline;\">Exposure Relevance.<\/span>\u00a0 Chemical testing in laboratory animals is typically done at high dosing concentrations to ensure that, if an adverse effect is caused, it can be detected in a relatively small number of animals in a relatively short period of time.\u00a0 These concentrations are often much higher than what a person would actually experience. \u00a0Methods are then used to extrapolate the data from such high-dose exposure to lower concentrations more representative of \u201creal-world\u201d exposure.\u00a0 The high- to low-dose extrapolation process has been always been contentious; for example, are effects seen at high doses merely artifacts of the high doses, or real effects that would still be seen at lower doses?\u00a0 An advantage of HT methods is that a wide range of doses, including low doses, can be directly tested and in enough samples that statistically meaningful results can be obtained.\u00a0 Such capabilities may also assist in resolving disputes around chemicals\u2019 ability to cause different effects at low doses than they cause at high doses.<\/li>\n<li><span style=\"text-decoration: underline;\">Assessing Mixtures<\/span>.\u00a0 We don\u2019t live in bubbles where exposures to chemicals occur one at a time.\u00a0 Rather, we are exposed to multiple chemicals over the same time period with overlapping durations.\u00a0 <a href=\"http:\/\/www.cdc.gov\/exposurereport\/executive_summary.html\">Human biomonitoring data<\/a> reveal the presence of hundreds of chemicals inside our bodies, from <a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2011\/01\/14\/new-study-demands-far-more-than-a-pregnant-pause-expectant-women-carry-dozens-of-toxic-chemicals-in-their-bodies\/\">fetushood<\/a> to adulthood.\u00a0 It is a challenge to put hazard data generated in separate lab tests for individual chemicals into this real-world context of multiple, simultaneous chemical exposures.\u00a0 In addition, testing all of the various combinations of chemicals in traditional tests would require far more lab animals and be enormously time-consuming and expensive.\u00a0 High-throughput assays offer a means to test large numbers of chemical mixtures, at multiple doses, and to look for effects at multiple time points.<\/li>\n<li><span style=\"text-decoration: underline;\">Green Chemistry.<\/span>\u00a0 HT methods find their way into green chemistry applications, too.\u00a0 High-throughput technologies hold promise for informing safer chemical, selection, design and engineering.\u00a0 These assays could flag potential toxicity concerns for new chemicals during early research, design, and development phases.\u00a0 Many of the HT technologies used in ToxCast and related programs in fact originate from the <a href=\"http:\/\/pharmalicensing.com\/public\/articles\/view\/1005568086_3befc0562a952\">pharmaceutical industry<\/a>, where they have been used for many years in drug discovery to screen out drug candidates that appear ineffective or show indications of hazard, and to push forward into further evaluation and development drugs that show potential for market approval.\u00a0 Efforts are already underway to integrate HT tools into green chemical design.\u00a0 A <a href=\"http:\/\/www.niehs.nih.gov\/news\/newsletter\/2011\/april\/science-scientists\/index.cfm\">workshop held just this March<\/a>, brought expert scientists together to discuss a new paradigm in safer chemical design that relies in part on HT and other computational technologies.<\/li>\n<li><span style=\"text-decoration: underline;\">Crisis Situations.<\/span>\u00a0 In crisis situations where there is limited time to evaluate a chemical or mixture before its use, we might be able to rely on batteries of quick high-throughput tests to make a more informed decision.\u00a0 However, even in these situations care should be taken to clearly communicate any limitations and uncertainties associated with these decisions and the data informing them.\u00a0 For example, EPA used some of its ToxCast assays to examine <a href=\"http:\/\/www.epa.gov\/bpspill\/reports\/ComparativeToxTest.Final.6.30.10.pdf\">potential endocrine-disrupting effects of dispersant chemicals used to clean up the BP oil spill<\/a>.\u00a0 Given the crisis state of the situation (and putting aside the fact that the testing came <em>after<\/em> millions of gallons of the dispersants had already been used, begging the question of why more thorough testing hadn\u2019t been conducted well before then), this information was helpful.\u00a0 However, EDF expressed concern (see <a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2010\/07\/02\/not-so-fast-why-dispersants-epa-ranks-as-practically-non-toxic-are-still-a-concern\/\">here<\/a> and <a href=\"https:\/\/blogs.edf.org\/nanotechnology\/2010\/06\/30\/hurry-up-and-wait-not-much-new-revealed-by-epas-initial-round-of-dispersant-toxicity-testing\/\">here<\/a>) regarding the poor communication of the results of such assays in a manner that effectively exonerated these chemicals from having<em> any<\/em> endocrine-disrupting activity \u2013 let alone other effects \u2013 despite the significant limitations of the available assays.\u00a0 The important lesson here is that the new technologies shouldn\u2019t be given explicit credit beyond their actual capabilities in any situation crisis or otherwise.<\/li>\n<\/ul>\n<p>Which brings us to the end of this post with a good segue to the next one in this series.\u00a0 The many potential benefits of HT methods are enticing and certainly give ample justification for the substantial effort and resources federal agencies are investing to bring them to bear.\u00a0\u00a0 But we still have a ways to go from current research and development activities on HT and other cutting-edge tools, to full-throttle use of them in decision-making, regulatory or otherwise.<\/p>\n<p>In the next post, I\u2019ll look at a number of the challenges these methods entail that must be overcome if they are to become the basis for the ideal chemical testing future.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Jennifer McPartland, Ph.D., is a Health Scientist. Parts in this series:\u00a0\u00a0\u00a0\u00a0\u00a0 Part 1\u00a0\u00a0\u00a0\u00a0 Part 2\u00a0\u00a0\u00a0\u00a0 Part 3\u00a0\u00a0\u00a0\u00a0 Part 4 This is the third in a series of blog posts on new approaches that federal agencies are exploring to improve how chemicals are evaluated for safety.\u00a0 Previous posts primarily focused on the scientific principles underlying these &#8230;<\/p>\n","protected":false},"author":5105,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[56094,5009],"tags":[39168,39167,39986,39171,91637],"coauthors":[114134],"class_list":["post-1367","post","type-post","status-publish","format-standard","hentry","category-new-testing-methods","category-health-science","tag-biomonitoring","tag-computational-toxicology","tag-endocrine-disruption","tag-exposure-vs-hazard","tag-toxcast"],"acf":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/posts\/1367","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/users\/5105"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/comments?post=1367"}],"version-history":[{"count":1,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/posts\/1367\/revisions"}],"predecessor-version":[{"id":13676,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/posts\/1367\/revisions\/13676"}],"wp:attachment":[{"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/media?parent=1367"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/categories?post=1367"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/tags?post=1367"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/blogs.edf.org\/health\/wp-json\/wp\/v2\/coauthors?post=1367"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}