In vitro to in vivo extrapolation for high throughput prioritization and decision making

In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To realize this potential, methods are needed to relate in vitro effects to in vivo responses, i.e., in vitro to in vivo extrapolation (IVIVE). Curren...

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Published inToxicology in vitro Vol. 47; pp. 213 - 227
Main Authors Bell, Shannon M., Chang, Xiaoqing, Wambaugh, John F., Allen, David G., Bartels, Mike, Brouwer, Kim L.R., Casey, Warren M., Choksi, Neepa, Ferguson, Stephen S., Fraczkiewicz, Grazyna, Jarabek, Annie M., Ke, Alice, Lumen, Annie, Lynn, Scott G., Paini, Alicia, Price, Paul S., Ring, Caroline, Simon, Ted W., Sipes, Nisha S., Sprankle, Catherine S., Strickland, Judy, Troutman, John, Wetmore, Barbara A., Kleinstreuer, Nicole C.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.03.2018
Elsevier Science Ltd
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Abstract In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To realize this potential, methods are needed to relate in vitro effects to in vivo responses, i.e., in vitro to in vivo extrapolation (IVIVE). Currently available IVIVE approaches need to be refined before they can be utilized for regulatory decision-making. To explore the capabilities and limitations of IVIVE within this context, the U.S. Environmental Protection Agency Office of Research and Development and the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods co-organized a workshop and webinar series. Here, we integrate content from the webinars and workshop to discuss activities and resources that would promote inclusion of IVIVE in regulatory decision-making. We discuss properties of models that successfully generate predictions of in vivo doses from effective in vitro concentration, including the experimental systems that provide input parameters for these models, areas of success, and areas for improvement to reduce model uncertainty. Finally, we provide case studies on the uses of IVIVE in safety assessments, which highlight the respective differences, information requirements, and outcomes across various approaches when applied for decision-making. •In vitro to in vivo extrapolation uses a model relating active in vitro concentrations to an in vivo response-inducing dose•Models for regulatory use will vary depending on needs: prioritization vs. hazard assessment•Transparency and reporting standards for models are critical during implementation
AbstractList In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To realize this potential, methods are needed to relate in vitro effects to in vivo responses, i.e., in vitro to in vivo extrapolation (IVIVE). Currently available IVIVE approaches need to be refined before they can be utilized for regulatory decision-making. To explore the capabilities and limitations of IVIVE within this context, the U.S. Environmental Protection Agency Office of Research and Development and the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods co-organized a workshop and webinar series. Here, we integrate content from the webinars and workshop to discuss activities and resources that would promote inclusion of IVIVE in regulatory decision-making. We discuss properties of models that successfully generate predictions of in vivo doses from effective in vitro concentration, including the experimental systems that provide input parameters for these models, areas of success, and areas for improvement to reduce model uncertainty. Finally, we provide case studies on the uses of IVIVE in safety assessments, which highlight the respective differences, information requirements, and outcomes across various approaches when applied for decision-making.In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To realize this potential, methods are needed to relate in vitro effects to in vivo responses, i.e., in vitro to in vivo extrapolation (IVIVE). Currently available IVIVE approaches need to be refined before they can be utilized for regulatory decision-making. To explore the capabilities and limitations of IVIVE within this context, the U.S. Environmental Protection Agency Office of Research and Development and the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods co-organized a workshop and webinar series. Here, we integrate content from the webinars and workshop to discuss activities and resources that would promote inclusion of IVIVE in regulatory decision-making. We discuss properties of models that successfully generate predictions of in vivo doses from effective in vitro concentration, including the experimental systems that provide input parameters for these models, areas of success, and areas for improvement to reduce model uncertainty. Finally, we provide case studies on the uses of IVIVE in safety assessments, which highlight the respective differences, information requirements, and outcomes across various approaches when applied for decision-making.
In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To realize this potential, methods are needed to relate in vitro effects to in vivo responses, i.e., in vitro to in vivo extrapolation (IVIVE). Currently available IVIVE approaches need to be refined before they can be utilized for regulatory decision-making. To explore the capabilities and limitations of IVIVE within this context, the U.S. Environmental Protection Agency Office of Research and Development and the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods co-organized a workshop and webinar series. Here, we integrate content from the webinars and workshop to discuss activities and resources that would promote inclusion of IVIVE in regulatory decision-making. We discuss properties of models that successfully generate predictions of in vivo doses from effective in vitro concentration, including the experimental systems that provide input parameters for these models, areas of success, and areas for improvement to reduce model uncertainty. Finally, we provide case studies on the uses of IVIVE in safety assessments, which highlight the respective differences, information requirements, and outcomes across various approaches when applied for decision-making. •In vitro to in vivo extrapolation uses a model relating active in vitro concentrations to an in vivo response-inducing dose•Models for regulatory use will vary depending on needs: prioritization vs. hazard assessment•Transparency and reporting standards for models are critical during implementation
In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To realize this potential, methods are needed to relate in vitro effects to in vivo responses, i.e., in vitro to in vivo extrapolation (IVIVE). Currently available IVIVE approaches need to be refined before they can be utilized for regulatory decision-making. To explore the capabilities and limitations of IVIVE within this context, the U.S. Environmental Protection Agency Office of Research and Development and the National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods co-organized a workshop and webinar series. Here, we integrate content from the webinars and workshop to discuss activities and resources that would promote inclusion of IVIVE in regulatory decision-making. We discuss properties of models that successfully generate predictions of in vivo doses from effective in vitro concentration, including the experimental systems that provide input parameters for these models, areas of success, and areas for improvement to reduce model uncertainty. Finally, we provide case studies on the uses of IVIVE in safety assessments, which highlight the respective differences, information requirements, and outcomes across various approaches when applied for decision-making.
Author Brouwer, Kim L.R.
Lumen, Annie
Sprankle, Catherine S.
Allen, David G.
Ring, Caroline
Wetmore, Barbara A.
Ke, Alice
Price, Paul S.
Chang, Xiaoqing
Choksi, Neepa
Strickland, Judy
Simon, Ted W.
Casey, Warren M.
Fraczkiewicz, Grazyna
Kleinstreuer, Nicole C.
Bartels, Mike
Ferguson, Stephen S.
Bell, Shannon M.
Lynn, Scott G.
Troutman, John
Wambaugh, John F.
Paini, Alicia
Sipes, Nisha S.
Jarabek, Annie M.
AuthorAffiliation g Simulations Plus, Inc., 42505 10 th St. West, Lancaster, CA 93534, USA
e National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods, National Institute of Environmental Health Sciences, P.O. Box 12233, Research Triangle Park, NC 27709, USA
h Simcyp Limited (a Certara company), John Street, Sheffield S2 4SU, United Kingdom
b U.S. Environmental Protection Agency, 109 T.W. Alexander Dr., Research Triangle Park, NC 27709, USA
f National Toxicology Program, National Institute of Environmental Health Sciences, P.O. Box 12233, Research Triangle Park, NC 27709, USA
c Dow Chemical Company, Saginaw, MI , USA
d UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Campus Box 7569, Chapel Hill, NC 27599, USA
m Ted Simon LLC, 4184 Johnston Road, Winston, GA 30187, USA
a Integrated Laboratory Systems, Inc., P.O. Box 13501, Research Triangle Park, NC 27709, USA
n Central Product Safety, The Procter & Gamble Company, Cincinnati, OH 45202
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– name: l Oak Ridge Institute for Science and Education, P.O. Box 2008, Oak Ridge, TN 37831, USA
– name: i National Center for Toxicological Research, U.S. Food and Drug Administration, 3900 NCTR Road, Jefferson, AR 72079, USA
– name: b U.S. Environmental Protection Agency, 109 T.W. Alexander Dr., Research Triangle Park, NC 27709, USA
– name: g Simulations Plus, Inc., 42505 10 th St. West, Lancaster, CA 93534, USA
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/29203341$$D View this record in MEDLINE/PubMed
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U.S. Environmental Protection Agency, 109 T.W. Alexander Dr., Research Triangle Park, NC 27709, USA. Wetmore.barbara@epa.gov.
ToxStrategies, Austin, TX (78759), USA. cring@toxstrategies.com.
http://ToxMetrics.com, 2407 Wilmington Drive, Midland, MI 48642 USA. mjbartels@toxmetrics.com.
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Snippet In vitro chemical safety testing methods offer the potential for efficient and economical tools to provide relevant assessments of human health risk. To...
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SubjectTerms Animal Use Alternatives - trends
Animals
Assessments
Biocompatibility
Case studies
Chemical Safety - instrumentation
Chemical Safety - legislation & jurisprudence
Chemical Safety - methods
Chemical Safety - trends
Computational Biology
Computational toxicology
Computer Simulation
Decision making
Decision Making, Computer-Assisted
Decision Making, Organizational
Environmental protection
Expert Systems
Extrapolation
Guidelines as Topic
Health Priorities - trends
Health risks
High throughput testing
High-Throughput Screening Assays - trends
Humans
In vitro methods and tests
In vivo methods and tests
IVIVE
Models, Biological
National Institute of Environmental Health Sciences (U.S.)
Organic chemistry
R&D
Research & development
Risk assessment
Safety
System effectiveness
Toxicity
Toxicity testing
Toxicity Tests - instrumentation
Toxicity Tests - methods
Toxicity Tests - trends
Toxicokinetic
Toxicology
United States
United States Dept. of Health and Human Services
United States Environmental Protection Agency
Title In vitro to in vivo extrapolation for high throughput prioritization and decision making
URI https://dx.doi.org/10.1016/j.tiv.2017.11.016
https://www.ncbi.nlm.nih.gov/pubmed/29203341
https://www.proquest.com/docview/2067365440
https://www.proquest.com/docview/1973025088
https://pubmed.ncbi.nlm.nih.gov/PMC7393693
Volume 47
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