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超高效液相色谱-四极杆-飞行时间高分辨质谱法快速筛查及确证化妆品中73种常见禁用化合物

[Fast screening and confirmation of 73 common prohibited compounds in cosmetics by ultra performance liquid chromatography-quadrupole-time-of-flight high resolution mass spectrometry].

作者信息

Li Yangjie, Huang Jiaying, Fang Jihui, Huang Zhiye

机构信息

Guangdong Institute for Drug Control, National Medical Products Administration Key Laboratory for Safety Risk Assessment of Cosmetics, Guangzhou 510000, China.

出版信息

Se Pu. 2022 May 8;40(5):433-442. doi: 10.3724/SP.J.1123.2021.09010.

DOI:10.3724/SP.J.1123.2021.09010
PMID:35478002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9404159/
Abstract

A high throughput screening method based on ultra performance liquid chromatography-quadrupole-time-of-flight high resolution mass spectrometry (UPLC-Q-TOF HRMS) was developed for the simultaneous and rapid confirmation of 73 prohibited compounds in cosmetics. The sample was dispersed in a saturated sodium chloride solution and ultrasonically extracted using acetonitrile containing 0.2% (v/v) formic acid. The resultant solution was centrifuged and then cleaned using dispersive solid phase extraction using a primary secondary amine (PSA) sorbent. The purified solution was centrifuged, and the supernatant was filtered through a 0.22 μm membrane before determination. The optimal pretreatment method was determined by comparing the recovery rates obtained using different extraction solvents and different amounts of purifying agents. The chromatographic separation conditions and mass spectrometry scanning mode were also optimized. Chromatographic separation was performed on an Acquity UPLC HSS T3 column (100 mm×2.1 mm, 1.8 μm) with gradient elution using 0.1% (v/v) formic acid aqueous solution and methanol as mobile phases. The eluent from the column was further detected using Q-TOF HRMS with the high resolution multiple reaction monitoring (MRM HR) scanning mode. Retention time, precise mass of parent ion, isotope abundance ratio, and precise mass of fragment ions were the parameters considered for rapid untargeted screening and confirmation. The matrix effects of water- and cream-based cosmetics were investigated. The matrix effects could be addressed using the matrix matched standard curve method. The correlation coefficients for the 73 prohibited compounds were all >0.99 in the corresponding linear concentration range. The limits of detection (LODs) were in the range of 5-150 μg/kg, and the limits of quantification (LOQs) were in the range of 15-450 μg/kg. Average recoveries were in the range of 60.3%-130.3% at three spiked levels, and the intra-day and inter-day precisions were 0.8%-10.0% (=6) and 1.1%-15.0% (=3), respectively. A total of 692 cosmetics samples were screened; 16 positive samples were detected, namely, sulfamethoxazole, meprednisone, lincomycin, 4-acetamidophenol, trimethoprim, alfacalcidol, betamethasone 17-valerate, brimonidine, chloramphenicol, chlorpheniramine, clobetasol propionate, crotamiton, econazole, ketoconazole, prednisone 21-acetate, and prednisone, with content in the range of 0.5-1136.1 mg/kg. The optimized method is accurate, fast, and simple, and it is suitable for the routine detection and rapid screening of common prohibited compounds in cosmetics. In addition, a screening and confirmation library was established for the 650 prohibited compounds using SCIEX OS and Library View software, using information-dependent acquisition (IDA)-MS/MS mode for MS data acquisition. The database contains multiple types of information, including formulas, theoretical exact mass, retention time, precise mass of parent ion, isotope abundance ratio, and fragment ion distribution. The library can be used for the simultaneous and rapid confirmation of prohibited compounds in cosmetics.

摘要

建立了一种基于超高效液相色谱 - 四极杆 - 飞行时间高分辨率质谱(UPLC - Q - TOF HRMS)的高通量筛选方法,用于同时快速确证化妆品中的73种禁用化合物。样品分散于饱和氯化钠溶液中,用含0.2%(v/v)甲酸的乙腈超声提取。所得溶液离心后,采用伯仲胺(PSA)吸附剂通过分散固相萃取进行净化。净化后的溶液再次离心,上清液经0.22μm滤膜过滤后进行测定。通过比较不同萃取溶剂和不同用量净化剂的回收率确定了最佳预处理方法。同时对色谱分离条件和质谱扫描模式进行了优化。色谱分离在Acquity UPLC HSS T3柱(100 mm×2.1 mm,1.8μm)上进行,以0.1%(v/v)甲酸水溶液和甲醇为流动相进行梯度洗脱。柱流出物采用高分辨率多反应监测(MRM HR)扫描模式通过Q - TOF HRMS进一步检测。保留时间、母离子精确质量、同位素丰度比和碎片离子精确质量是用于快速非靶向筛选和确证的参数。研究了水性和膏状化妆品的基质效应。基质效应可采用基质匹配标准曲线法解决。73种禁用化合物在相应线性浓度范围内的相关系数均>0.99。检测限(LOD)在5 - 150μg/kg范围内,定量限(LOQ)在15 - 450μg/kg范围内。在三个加标水平下,平均回收率在60.3% - 130.3%范围内,日内和日间精密度分别为0.8% - 10.0%(n = 6)和1.1% - 15.0%(n = 3)。共筛选了692份化妆品样品;检测到16份阳性样品,分别为磺胺甲恶唑、甲泼尼龙、林可霉素、对乙酰氨基酚、甲氧苄啶、阿法骨化醇、倍他米松17 - 戊酸酯、溴莫尼定、氯霉素、氯苯那敏、丙酸氯倍他索、克罗米通、益康唑、酮康唑、醋酸泼尼松龙和泼尼松,含量在0.5 - 1136.1mg/kg范围内。该优化方法准确、快速、简便,适用于化妆品中常见禁用化合物的常规检测和快速筛选。此外,使用SCIEX OS和Library View软件,采用信息依赖采集(IDA) - MS/MS模式采集质谱数据,为650种禁用化合物建立了筛选和确证库。该数据库包含多种类型信息,包括分子式、理论精确质量、保留时间、母离子精确质量、同位素丰度比和碎片离子分布。该库可用于同时快速确证化妆品中的禁用化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/02220c6a3e29/cjc-40-05-433-img_5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/3e9a99217889/cjc-40-05-433-img_1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/02220c6a3e29/cjc-40-05-433-img_5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/3e9a99217889/cjc-40-05-433-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/6c5228aec431/cjc-40-05-433-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/74e83cc3ac80/cjc-40-05-433-img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06d0/9404159/fb720f4c8a1a/cjc-40-05-433-img_4.jpg
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Se Pu. 2020 Dec 8;38(12):1423-1430. doi: 10.3724/SP.J.1123.2020.06017.
2
[High-throughput screening and quantitative analysis method of 112 pharmaceutical and personal care products in water based on ultra-high performance liquid chromatography with high-resolution mass spectrometry].基于超高效液相色谱-高分辨率质谱联用的水中112种药品及个人护理用品高通量筛选与定量分析方法
Se Pu. 2018 Nov 1;36(11):1147-1157. doi: 10.3724/SP.J.1123.2018.06029.
3
[Rapid determination of 87 prohibited ingredients in cosmetics by ultra performance liquid chromatography-tandem mass spectrometry].
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4
[Simultaneous determination of 28 fragrance components in cosmetics by gas chromatography-tandem mass spectrometry].[气相色谱-串联质谱法同时测定化妆品中的28种香料成分]
Se Pu. 2023 Jan;41(1):76-86. doi: 10.3724/SP.J.1123.2022.03043.
[Rapid determination of 66 antibiotics in cosmetics using ultra high performance liquid chromatography-linear ion trap/Orbitrap mass spectrometry].[超高效液相色谱-线性离子阱/轨道阱质谱法快速测定化妆品中的66种抗生素]
Se Pu. 2018 Jul 8;36(7):643-650. doi: 10.3724/SP.J.1123.2018.01041.
4
[Simultaneous determination of 121 veterinary drugs in pork by QuEChERS and ultra performance liquid chromatography-tandem mass spectrometry].[采用QuEChERS和超高效液相色谱-串联质谱法同时测定猪肉中121种兽药]
Se Pu. 2015 Dec;33(12):1242-50. doi: 10.3724/sp.j.1123.2015.09016.
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[Determination of residues of pesticides and veterinary drugs in milk by ultra performance liquid chromatography coupled with quadrupole-time of flight mass spectrometry].超高效液相色谱-四极杆飞行时间质谱法测定牛奶中农药和兽药残留量
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