کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5561283 1562117 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Derivation of an oral Maximum Allowable Dose Level for Bisphenol A
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Derivation of an oral Maximum Allowable Dose Level for Bisphenol A
چکیده انگلیسی


- Bisphenol A is classified by California as “known to cause reproductive toxicity”.
- California derived a dermal Maximum Allowable Dose Level (MADL) for Bisphenol A.
- We derived an oral MADL of 157 μg/d based on the Delclos et al. (2014) study.
- This oral MADL provides a similar margin of safety as most regulatory guidelines.

Bisphenol A (BPA) is a high production volume chemical that is used in plastics and epoxy coatings. In 2015, California's Office of Environmental Health Hazard Assessment (OEHHA) added BPA to the Proposition 65 list of chemicals “known to cause reproductive toxicity” based on its Developmental and Reproductive Toxicant Identification Committee's (DART-IC) conclusion that BPA has been shown to cause female reproductive toxicity. A critical factor in determining compliance with Proposition 65 is a Maximum Allowable Dose Level (MADL), which is the exposure level at which a chemical would have no observable reproductive effect even if a person were exposed to 1000 times that level. We performed a comprehensive review of the literature, including the studies reviewed by DART-IC, and derived an oral MADL. Of all the studies we identified, Delclos et al. (2014) is of sufficient quality, has the lowest no observed effect level (NOEL), and results in the most conservative MADL of 157 μg/d. This is generally supported by other studies, including those that were considered by DART-IC. Also, the oral MADL provides a similar margin of safety as OEHHA's dermal MADL and other regulatory guidelines. Taken together, the scientific data support an oral MADL of 157 μg/d.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Regulatory Toxicology and Pharmacology - Volume 86, June 2017, Pages 312-318
نویسندگان
, , , , , , , , ,