Hopf Nancy B, De Luca Hélène P, Borgatta Myriam, Koch Holger M, Pälmke Claudia, Benedetti Manon, Berthet Aurélie, Reale Elena
Center for Primary Care and Public Health (Unisanté), University of Lausanne, Route de la Corniche 2, Epalinges, Lausanne 1066, Switzerland; Swiss Center for Applied Human Toxicology (SCAHT), Basel.
Center for Primary Care and Public Health (Unisanté), University of Lausanne, Route de la Corniche 2, Epalinges, Lausanne 1066, Switzerland; Swiss Center for Applied Human Toxicology (SCAHT), Basel.
Toxicol Lett. 2024 Jul;398:38-48. doi: 10.1016/j.toxlet.2024.05.016. Epub 2024 Jun 14.
Population studies reveal widespread exposure to phthalates. Understanding their absorption, distribution, metabolism, and excretion is vital to reduce exposure. However, data on skin absorption remain limited. We thus aim to characterize the skin permeation of three phthalates in a mixture, neat or in emulsion; di(2-ethylhexyl) phthalate (d4-DEHP), dibutyl phthalate (d4-DBP), and diethyl phthalate (d4-DEP), by comparing in vitro human skin (800 µm) permeation (24 hours) results using flow-through diffusion cells with urine results obtained from volunteers exposed to the same mixture applied to a forearm (40 cm). Metabolites were analyzed in receptor fluids and urine. Phthalates crossed the skin barrier and metabolized into monoesters before elimination. Increased permeation was observed for phthalates in emulsion compared to neat substances, with polyethylene glycol (PEG) in the receptor fluid enhancing emulsion permeation, but not affecting neat substances. In vitro results mirrored in vivo findings: DEP showed rapid permeation (J: ∼2 ug/cm/h) and urinary excretion peaking at six hours post-application, whereas DBP exhibited slower kinetics (J: ∼0.1 ug/cm/h), with a urinary peak at 15-17 hours post-application. DEHP had minimal permeation (J: ∼0.0002 ug/cm/h) with no observable urinary peak. These findings underscore the importance of comprehending phthalate skin absorption for effective exposure mitigation strategies.
人群研究表明,邻苯二甲酸盐的暴露十分普遍。了解它们的吸收、分布、代谢和排泄对于减少暴露至关重要。然而,关于皮肤吸收的数据仍然有限。因此,我们旨在通过比较体外人皮肤(800微米)在流通扩散池中24小时的渗透结果与志愿者前臂(40厘米)涂抹相同混合物后尿液中的结果,来表征三种邻苯二甲酸盐在纯品或乳液中的皮肤渗透情况。这三种邻苯二甲酸盐分别是邻苯二甲酸二(2-乙基己基)酯(d4-DEHP)、邻苯二甲酸二丁酯(d4-DBP)和邻苯二甲酸二乙酯(d4-DEP)。对受体液和尿液中的代谢物进行了分析。邻苯二甲酸盐穿过皮肤屏障,在排出之前代谢为单酯。与纯物质相比,乳液中的邻苯二甲酸盐渗透增加,受体液中的聚乙二醇(PEG)增强了乳液的渗透,但不影响纯物质。体外结果与体内发现相符:DEP显示出快速渗透(通量J:约2微克/平方厘米/小时),尿液排泄在涂抹后6小时达到峰值,而DBP的动力学较慢(通量J:约0.1微克/平方厘米/小时),尿液峰值出现在涂抹后15-17小时。DEHP的渗透最小(通量J:约0.0002微克/平方厘米/小时),没有可观察到的尿液峰值。这些发现强调了理解邻苯二甲酸盐皮肤吸收对于有效暴露缓解策略的重要性。