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基于动力学的消费者从化妆品中接触水杨酸的安全评估表明,没有发育毒性健康风险的证据。

A kinetic-based safety assessment of consumer exposure to salicylic acid from cosmetic products demonstrates no evidence of a health risk from developmental toxicity.

机构信息

Johnson & Johnson Consumer Inc., Skillman, NJ, USA.

L'Oreal Research and Development, Worldwide Safety Evaluation, 9 Rue Pierre Dreyfus, 92110 Clichy, France.

出版信息

Regul Toxicol Pharmacol. 2018 Apr;94:245-251. doi: 10.1016/j.yrtph.2018.01.026. Epub 2018 Feb 21.

DOI:10.1016/j.yrtph.2018.01.026
PMID:29410076
Abstract

Salicylic acid (SA) has a long history of safe use as ingredient in topical cosmetic products. In 2016, the Committee for Risk Assessment of the European Chemicals Agency proposed to classify SA as a Category 2 reproductive toxicant based on adverse developmental effects in animal toxicity studies. This hazard-based classification (based on mg/kg doses) requires a reassessment of the safety of the current SA concentrations in cosmetic consumer products. Herein, a safety reassessment was performed in which margins of safety were calculated based on literature data on the NOAEL plasma exposure levels from animal reproductive toxicity studies with ASA (rapidly converts to SA in plasma), human SA plasma levels from oral exposure to ASA and human dermal exposure to SA-containing cosmetic products. In addition, a literature review was performed, which shows that there are no adverse developmental effects despite extensive human clinical oral use of ASA up to the maximum recommended therapeutic doses. The plasma exposure-based safety assessment for SA combined with an absence of any clinical health risk with oral ASA use in the literature supports that there is an acceptable margin of safety for the consumer exposure to SA as authorized in the current EU cosmetic regulation.

摘要

水杨酸(SA)作为一种成分被安全地用于局部美容产品已有很长的历史。2016 年,欧洲化学品管理局风险评估委员会根据动物毒性研究中发育不良的影响,提议将 SA 归类为 2B 类生殖毒性物质。这种基于危害的分类(基于 mg/kg 剂量)需要重新评估当前化妆品消费产品中 SA 浓度的安全性。在此,进行了安全性重新评估,根据动物生殖毒性研究中 ASA(在血浆中迅速转化为 SA)的 NOAEL 血浆暴露水平、口服暴露于 ASA 后的人 SA 血浆水平以及含有 SA 的人皮肤接触化妆品产品的文献数据,计算了安全边际。此外,还进行了文献综述,结果表明,尽管广泛的人类临床口服使用 ASA 达到最大推荐治疗剂量,但没有发育不良的影响。基于血浆暴露的 SA 安全性评估以及文献中口服 ASA 使用不存在任何临床健康风险表明,当前欧盟化妆品法规中授权的消费者接触 SA 具有可接受的安全边际。

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