一种可持续的创新方法,用于测定身体乳霜中的对羟基苯甲酸酯,以进行暴露和风险评估。

IF 3 4区 医学 Q1 MEDICINE, LEGAL
Thalita da Silva Ramos, Karina Borba Gonçalves, Luiz Paulo de Aguiar Marciano, Mariana Azevedo Rosa, Isarita Martins
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引用次数: 0

摘要

对羟基苯甲酸甲酯(MeP)、对羟基苯甲酸乙酯(EtP)、对羟基苯甲酸丙酯(PrP)和对羟基苯甲酸丁酯(BuP)是化妆品、药品和食品中使用最广泛的防腐剂。由于过度使用含有对羟基苯甲酸酯的产品配方,这些化合物与毒性作用有关。对羟基苯甲酸酯的毒性可能与内分泌紊乱有关,因为它们能够模拟雌二醇的作用。本文开发并采用了一种简单、可持续、稳健且创新的分散液-液微萃取(DLLME)技术来提取身体乳霜样品中的这些异生物,旨在计算安全系数(MoS)以评估暴露风险。该方法的线性关系良好(r> 0.99),检出限较低(0.01-0.04 % w/w),精密度和准确度令人满意(分别为 4.33-10.47 和 -14.25-13.85)。在分析的 10 个样品中,有 7 个样品的对羟基苯甲酸酯含量符合欧洲法律规定的可接受浓度。PrP 的 MoS 值(37.58)表明其安全性有所降低,这表明使用个人护理产品可能会导致全身接触 PrP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A sustainable and innovative method to determine parabens in body creams for exposure and risk assessment

Methylparaben (MeP), ethylparaben (EtP), propylparaben (PrP), and butylparaben (BuP) are among the most widely used preservatives in cosmetics, drugs, and foods. These compounds have been associated with toxic effects due to the overuse of products with parabens in their formulation. The toxicity of parabens may be correlated to endocrine disruption, owing to their ability to mimic the actions of estradiol. In this paper, a simple, sustainable, robust, and innovative dispersive liquid-liquid microextraction (DLLME) technique was developed and employed to extract these xenobiotics from body cream samples, aiming to calculate the margin of safety (MoS) to assess the risk of exposure. The validated method presented suitable linearity (r > 0.99), lower limits of detection (ranging from 0.01 to 0.04 % w/w), and satisfactory precision and accuracy (ranging from 4.33 to 10.47, and from −14.25 to 13.85, respectively). Seven of the ten analysed samples presented paraben contents within the acceptable concentration according to European legislation. The MoS value obtained for PrP (37.58) suggested its reduced safety, indicating that PrP may significantly contribute to systemic exposure resulting from the use of personal care products.

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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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