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气相色谱-质谱法测定化妆品中13种防晒剂

[Determination of 13 sunscreen agents in cosmetics by gas chromatography-mass spectrometry].

作者信息

Lü Wen, Li Hongying, Liu Jie, Han Wei, Huang Wei

机构信息

Hubei Institute for Drug Control, Wuhan 430075, China.

出版信息

Se Pu. 2021 May;39(5):552-557. doi: 10.3724/SP.J.1123.2020.11003.

Abstract

Sunscreens can be categorized as physical and chemical types. Chemical sunscreens are widely used in cosmetics, and hence, their concentration in the desired products should be strictly monitored. Gas chromatography-mass spectrometry (GC-MS) is widely used for the analysis of cosmetics as it does not require organic mobile phases and allows for accurate qualitative and quantitative analyses. In this study, a method based on GC-MS was established for the determination of 13 sunscreen agents in cosmetics: ethylhexyl salicylate, homosalate, 4-methylbenzylidene camphor, ethylhexyl dimethyl para-aminobenzoic acid, ethylhexyl methoxycinnamate, octocrylene, butyl methoxydibenzoylmethane, diethylamino hydroxybenzoyl hexyl benzoate, 3-benzylidene camphor, benzophenone-3, camphor benzalkonium methosulfate, drometrizole trisiloxane, and isopentyl-4-methoxycinnamate. Accordingly, 0.5 g of the cosmetic product was dissolved in dichloromethane in a 50 mL volumetric flask and extracted ultrasonically for 15 min. Then, 1.0 mL of the extracting solution was withdrawn and diluted to 50.0 mL with dichloromethane. The mixture was filtered through a 0.22-μm membrane. A 1 μL aliquot of the dichloromethane solution was introduced onto the HP-5ms chromatographic column (30 m×250 μm×0.25 μm). The 13 components were separated under programed temperature elevation in the interval from 150 ℃ to 290 ℃. These components could be analyzed within 30 min after being ionized by the EI source, and their determination was achieved in selected ion monitoring (SIM) mode. The external standard method was employed for quantitative determination. Linear equations, linear correlation coefficients, and linear ranges were obtained by analyzing a series of mixed standard working solutions. The limits of detection (LODs, =3) and limits of quantification (LOQs, =10) of the 13 sunscreen agents were determined. The matrix effect and average recoveries of the 13 agents with six extraction solvents (dichloromethane, tetrahydrofuran, methanol, acetonitrile, -hexane, and acetone) were compared. Among these, dichloromethane showed a weak matrix effect and high average recovery. The matrix effect of dichloromethane was 90.1%-100.5%, and the average recovery was 96.3%. All the 13 sunscreen agents showed good linearity in their corresponding ranges. The correlation coefficients ( ) were higher than 0.998. The LODs and LOQs were in the ranges of 0.04 to 0.63 mg/g and 0.12 to 2.10 mg/g, respectively. Two types of cosmetics were selected to verify the accuracy and precision of the method at three levels. The average spiked recoveries of the 13 sunscreen agents in cream and lotion were 88.7%-103.6%, and 88.4%-102.3%, respectively; the corresponding relative standard deviations (RSDs, =6) were 1.7%-4.9% and 1.2%-3.9%. Whitening cosmetics are frequently added with sunscreen agents, which is a regulatory blind spot. Five batches of skin whitening products containing sunscreen agents were detected using this method. The contents of five sunscreen agents in skin whitening cosmetics ranged from 0.8% to 5.2%, which were lower than the relevant limits in China. Owing to its advantages of simple operation, high sensitivity, and good recovery, the proposed method is suitable for the qualitative and quantitative determination of 13 sunscreen agents in cosmetics. This method provides technical support for market supervision and laboratory testing.

摘要

防晒剂可分为物理型和化学型。化学防晒剂在化妆品中广泛使用,因此,应严格监测其在所需产品中的浓度。气相色谱 - 质谱联用仪(GC - MS)因其不需要有机流动相且能进行准确的定性和定量分析,而被广泛用于化妆品分析。在本研究中,建立了一种基于GC - MS的方法,用于测定化妆品中的13种防晒剂:水杨酸乙基己酯、胡莫柳酯、4 - 甲基亚苄基樟脑、二乙氨基羟苯甲酰基己酯、甲氧基肉桂酸乙基己酯、奥克立林、丁基甲氧基二苯甲酰甲烷、二乙氨基羟苯甲酰己酯苯甲酸酯、3 - 亚苄基樟脑、二苯甲酮 - 3、樟脑苯扎氯铵甲基硫酸酯、三硅氧烷二甲基辛酯和异戊基 - 4 - 甲氧基肉桂酸酯。相应地,将0.5 g化妆品样品溶解于50 mL容量瓶中的二氯甲烷中,并超声提取15 min。然后,取出1.0 mL提取液,用二氯甲烷稀释至50.0 mL。混合物通过0.22 - μm膜过滤。取1 μL二氯甲烷溶液注入HP - 5ms色谱柱(30 m×250 μm×0.25 μm)。13种成分在150℃至290℃的程序升温条件下分离。这些成分在经电子轰击电离源(EI源)电离后30 min内可进行分析,并在选择离子监测(SIM)模式下进行测定。采用外标法进行定量测定。通过分析一系列混合标准工作溶液获得线性方程、线性相关系数和线性范围。测定了13种防晒剂的检测限(LODs,n = 3)和定量限(LOQs,n = 10)。比较了13种防晒剂在六种萃取溶剂(二氯甲烷、四氢呋喃、甲醇、乙腈、正己烷和丙酮)中的基质效应和平均回收率。其中,二氯甲烷显示出较弱的基质效应和较高的平均回收率。二氯甲烷的基质效应为90.1% - 100.5%,平均回收率为96.3%。所有13种防晒剂在其相应范围内均表现出良好的线性。相关系数(r)高于0.998。检测限和定量限分别在0.04至0.63 mg/g和0.12至2.10 mg/g范围内。选择两种类型的化妆品在三个添加水平下验证该方法的准确性和精密度。面霜和乳液中13种防晒剂的平均加标回收率分别为88.7% - 103.6%和88.4% - 102.3%;相应的相对标准偏差(RSDs,n = 6)分别为1.7% - 4.9%和1.2% - 3.9%。美白化妆品常添加防晒剂,这是一个监管盲点。使用该方法检测了五批含有防晒剂的美白产品。美白化妆品中五种防晒剂的含量在0.8%至5.2%之间,低于中国的相关限值。由于该方法操作简单、灵敏度高且回收率良好,适用于化妆品中13种防晒剂的定性和定量测定。该方法为市场监管和实验室检测提供了技术支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdec/9404060/dd61f83c84a5/cjc-39-05-552-img_1.jpg

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