Your browser doesn't support javascript.
loading
A new approach methodology using kinetically-derived maximum dose levels in risk assessment - A case study with afidopyropen.
Loccisano, Anne E; Freeman, Elaine; Doi, Adriana; Frericks, Markus; Fegert, Ivana; Fabian, Eric; Riffle, Brandy.
Afiliação
  • Loccisano AE; Exponent Inc, Alexandria, VA, 22314, USA.
  • Freeman E; Exponent Inc, Washington, DC, 20036, USA.
  • Doi A; BASF Corporation Research Triangle Park, NC, 27709, USA.
  • Frericks M; BASF SE Regulatory Toxicology Crop Protection, Limburgerhof, Germany.
  • Fegert I; BASF SE Regulatory Toxicology Crop Protection, Limburgerhof, Germany.
  • Fabian E; BASF SE Experimental Toxicology and Ecology, Ludwigshafen, Germany.
  • Riffle B; BASF Corporation Research Triangle Park, NC, 27709, USA. Electronic address: brandy.riffle@basf.com.
Regul Toxicol Pharmacol ; 142: 105429, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37277056
We present a case study for afidopyropen (AF; insecticide) to characterize chronic dietary human health risk using a Risk 21-based approach. Our objective is to use a well-tested pesticidal active ingredient (AF) to show how a new approach methodology (NAM), using the kinetically-derived maximum dose (KMD) and with far less animal testing, can reliably identify a health-protective point of departure (PoD) for chronic dietary human health risk assessments (HHRA). Chronic dietary HHRA involves evaluation of both hazard and exposure information to characterize risk. Although both are important, emphasis has been placed on a checklist of required toxicological studies for hazard characterization, with human exposure information only considered after evaluation of hazard data. Most required studies are not used to define the human endpoint for HHRA. The information presented demonstrates a NAM that uses the KMD determined by saturation of a metabolic pathway, which can be used as an alternative POD. In these cases, the full toxicological database may not need to be generated. Demonstration that the compound is not genotoxic and that the KMD is protective of adverse effects in 90-day oral rat and reproductive/developmental studies is sufficient to support the use of the KMD as an alternative POD.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Praguicidas Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Praguicidas Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos