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高效液相色谱-串联质谱法测定化妆品中的三种甲基咪唑化合物

[Determination of three methylimidazole compounds in cosmetics by high performance liquid chromatography-tandem mass spectrometry].

作者信息

Cai Cui-Ling, Li Ju, Xi Jing, Hou Ying-Ye, Zeng Guang-Feng, Xie Jian-Jun, Wu Shu-Yue, Wang Lu

机构信息

Guangzhou Customs Technical Center, National Import and Export Food Quality Safety Risk Verification and Evaluation Laboratory (Cosmetics), Guangzhou 510623, China.

出版信息

Se Pu. 2024 Nov;42(11):1052-1058. doi: 10.3724/SP.J.1123.2023.11011.

DOI:10.3724/SP.J.1123.2023.11011
PMID:39449512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11519762/
Abstract

Methylimidazole compounds are byproducts formed during the caramel-coloring process and are used in various cosmetics. In addition metronidazole is an antibacterial and anti-inflammatory drug commonly used in modern medicine and is used in cosmetics to treat acne in the short-term. The illegal addition of metronidazole during cosmetics production can result in residual 2-methylimidazole (2-MEI), which, along with 4-methylimidazole (4-MEI), is a class 2B carcinogen. Therefore, establishing efficient, accurate, and sensitive analytical techniques for analyzing methylimidazole compounds in cosmetics is an urgent objective. In this study, a high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for simultaneously determining 1-methylimidazole (1-MEI), 2-MEI, and 4-MEI in cosmetics was developed. Cosmetics samples were extracted via ultrasonication in acetonitrile and purified using a mixed cation-exchange (MCX) solid-phase extraction (SPE) column, with subsequent drying under a stream of nitrogen and redissolution in acetonitrile. The resulting solution was then filtered through a 0.22 μm organic filter membrane for further testing. The analytes were separated using an XBridge shield RP chromatographic column (150 mm×4.6 mm, 3.5 μm) and isocratically eluted with 20 mmol/L ammonium formate solution (containing 0.1% formic acid)-acetonitrile (98∶2, v/v). The target compounds were ionized by electrospray ionization (ESI) source, analyzed in multi-reaction monitoring (MRM) mode, and quantified using the external standard method, with the peak area of the quantitative ion and the mass concentration of the compound taken as the longitudinal and transverse coordinates, respectively. Matrix-matching working curves were also constructed. 1-MEI exhibited good linear relationships in the range of 5-200 μg/L, with correlation coefficients ()≥0.9994, while 2-MEI and 4-MEI showed good linearities in the range of 2-100 μg/L with ≥0.9984. The three methylimidazole compounds exhibited limits of detection (LODs) and quantification (LOQs) of 10-30 μg/kg and 25-100 μg/kg, respectively. Under three spiked levels (LOQ, 2LOQ, 10LOQ), the recoveries of three methylimidazole compounds were 80.9%-107.9%, with relative standard deviations (RSDs, =6) of 1.2%-12.8%. The practicability of the method was examined using 48 cosmetic samples; 4-MEI was detected in nine samples at contents of 26-1000 μg/kg, while two samples contained 240 and 267 μg/kg of 2-MEI, respectively. 1-MEI was not detected in any of the 48 samples tested. The developed method is simple, fast, and highly sensitive, and provides methodological support for assessing risks and monitoring the three methylimidazole compounds in cosmetics through screening.

摘要

甲基咪唑类化合物是焦糖色素生产过程中形成的副产物,被用于各类化妆品中。此外,甲硝唑是现代医学中常用的一种抗菌消炎药,在化妆品中短期用于治疗痤疮。化妆品生产过程中非法添加甲硝唑会导致2-甲基咪唑(2-MEI)残留,2-甲基咪唑与4-甲基咪唑(4-MEI)一样,属于2B类致癌物。因此,建立高效、准确、灵敏的分析化妆品中甲基咪唑类化合物的技术是一项紧迫的任务。本研究建立了一种同时测定化妆品中1-甲基咪唑(1-MEI)、2-MEI和4-MEI的高效液相色谱-串联质谱(HPLC-MS/MS)方法。化妆品样品用乙腈超声提取,并用混合阳离子交换(MCX)固相萃取(SPE)柱净化,随后在氮气流下吹干并重新溶解于乙腈中。所得溶液经0.22μm有机滤膜过滤后进行进一步检测。采用XBridge shield RP色谱柱(150 mm×4.6 mm,3.5μm)分离分析物,并用20 mmol/L甲酸铵溶液(含0.1%甲酸)-乙腈(98∶2,v/v)等度洗脱。目标化合物通过电喷雾电离(ESI)源电离,在多反应监测(MRM)模式下进行分析,并采用外标法进行定量,以定量离子的峰面积和化合物的质量浓度分别作为纵、横坐标,同时构建基质匹配工作曲线。1-MEI在5-200μg/L范围内呈现良好的线性关系,相关系数()≥0.9994,而2-MEI和4-MEI在2-100μg/L范围内呈现良好的线性关系,≥0.9984。三种甲基咪唑类化合物的检测限(LOD)和定量限(LOQ)分别为10-30μg/kg和25-100μg/kg。在三个加标水平(LOQ、2LOQ、10LOQ)下,三种甲基咪唑类化合物的回收率为80.9%-107.9%相对标准偏差(RSD,=6)为1.2%-12.8%。用48份化妆品样品检验了该方法的实用性;在9份样品中检测到4-MEI,含量为26-1000μg/kg,而两份样品分别含有含量为240和267μg/kg的2-MEI。在所检测的48份样品中均未检测到1-MEI。所建立的方法简便、快速、灵敏度高,为通过筛查评估化妆品中三种甲基咪唑类化合物的风险和监测提供了方法学支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674a/11519762/96492d21647a/cjc-42-11-1052-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674a/11519762/1045761bf9a0/cjc-42-11-1052-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674a/11519762/96492d21647a/cjc-42-11-1052-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674a/11519762/1045761bf9a0/cjc-42-11-1052-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674a/11519762/96492d21647a/cjc-42-11-1052-img_2.jpg

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本文引用的文献

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