In vivo and ex vivo percutaneous absorption of [14C]-bisphenol A in rats: a possible extrapolation to human absorption?
โ Scribed by Fabrice Marquet; Jean-Paul Payan; Dominique Beydon; Ludivine Wathier; Marie-Christine Grandclaude; Elisabeth Ferrari
- Book ID
- 105870989
- Publisher
- Springer-Verlag
- Year
- 2011
- Tongue
- English
- Weight
- 219 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0340-5761
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โฆ Synopsis
Bisphenol A (BPA) is a monomer used mainly in the synthesis of polycarbonates and epoxy resins. Percutaneous absorption is the second source of exposure, after inhalation, in the work environment. However, studies on this route of absorption are lacking or incomplete. In this study, percutaneous BPA absorption was measured in vivo and ex vivo in the rat, and ex vivo in humans. An approximately 12-fold difference in permeability between rat skin and human skin was found, with permeability being higher in the rat. In addition, inter- and intra-individual variability of up to tenfold was observed in humans. No accumulation of BPA in the skin was found during exposure. The skin clearance rate following exposure was estimated at 0.4ย ฮผg/cmยฒ/h. Ex vivo and in vivo percutaneous absorption fluxes of BPA in the rat were in the same range (about 2.0ย ฮผg/cmยฒ/h), suggesting that extrapolation to the in vivo situation in humans may be possible. The European tolerable daily intake (TDI) of BPA is 50ย ฮผg/kg body weight. However, many research projects have highlighted the significant effects of BPA in rodents at doses lower than 10ย ฮผg/kg/day. A 1-h occupational exposure over 2,000ย cmยฒ (forearms and hands) may lead to a BPA absorption of 4ย ฮผg/kg/day. This is 8% of the European TDI and is very close to the value at which effects have been observed in animals. This absorption must therefore be taken into account when evaluating risks of BPA exposure, at least until more relevant results on the toxicity of BPA in humans are available.
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The effect of surfactants on percutaneous absorption of naproxen was studied using rat in vivo models. The in vivo normalized relative absorption rates were in good agreement with the in vitro relative flux. An antipyretic model in the rat could not show relatively small increases in percutaneous ab