Olomukoro Aghogho A, Lüthy Lucas, Flug Tom, Gionfriddo Emanuela
Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, NY, 14260-3000, USA.
CTC Analytics AG, Industriestrasse 20, 4222, Zwingen, Switzerland.
Anal Bioanal Chem. 2025 May 24. doi: 10.1007/s00216-025-05908-x.
Research efforts have primarily focused on identifying per- and polyfluoroalkyl substances (PFAS) in common environmental media like water, air, soil, and biological samples. However, there is limited research on PFAS detection in complex samples such as personal care products, including cosmetics. PFAS are used in cosmetics for emulsification, surfactant action, and stabilization, and have been detected in products such as foundation, powders, and nail polish. The complexity of cosmetic formulations, with various additives, makes the analysis of these samples extremely challenging. This study aimed to explore and develop convenient extraction methods to accurately quantify eight anionic PFAS in mascara products. Solid-phase microextraction (SPME) and automated micro solid-phase extraction (µSPE) were evaluated, and quantification was performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Six mascara products, including waterproof and non-waterproof types, were analyzed, optimizing methanol-water mixtures as dispersive media to maximize PFAS recovery. Elution solution composition, volume, and dispensing speed were optimized for the µSPE method to ensure quantitative elution of the PFAS from the extraction phase. For the SPME method, the extraction time was optimized to account for the varying diffusion behavior of PFAS in the mixed-phase medium. Both extraction methods were evaluated in terms of greenness and practicality, with SPME achieving the best overall scores. Method validation demonstrated good linearity (0.025 to 25 ng/g) for both protocols, with µSPE providing lower limits of quantification (LOQ) for the most hydrophobic PFAS. 6:2 diPAP was quantified in real samples at concentrations ranging from 1.26 to 3.48 ng/g in 4 of the 9 mascaras tested.
研究工作主要集中在识别水、空气、土壤和生物样本等常见环境介质中的全氟和多氟烷基物质(PFAS)。然而,对于个人护理产品(包括化妆品)等复杂样本中PFAS的检测研究有限。PFAS被用于化妆品中以起到乳化、表面活性剂作用和稳定作用,并且已在粉底、散粉和指甲油等产品中被检测到。化妆品配方的复杂性以及各种添加剂使得对这些样本的分析极具挑战性。本研究旨在探索和开发便捷的提取方法,以准确量化睫毛膏产品中的八种阴离子PFAS。对固相微萃取(SPME)和自动微量固相萃取(µSPE)进行了评估,并使用液相色谱 - 串联质谱(LC - MS/MS)进行定量分析。分析了六种睫毛膏产品,包括防水型和非防水型,优化了甲醇 - 水混合物作为分散介质以最大化PFAS的回收率。针对µSPE方法,对洗脱液组成、体积和 dispense速度进行了优化,以确保PFAS从萃取相中定量洗脱。对于SPME方法,优化了萃取时间以考虑PFAS在混合相介质中不同的扩散行为。从绿色度和实用性方面对两种萃取方法进行了评估,SPME获得了最佳总体评分。方法验证表明两种方案均具有良好的线性(0.025至25 ng/g),µSPE为大多数疏水性PFAS提供了更低的定量限(LOQ)。在测试的9种睫毛膏中的4种实际样本中,6:2二磷酸全氟辛烷磺酸(6:2 diPAP)的定量浓度范围为1.26至3.48 ng/g。