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[分散固相萃取-液相色谱-串联质谱法同时快速测定化妆品中81种糖皮质激素]

[Simultaneous rapid determination of 81 glucocorticoids in cosmetics by dispersive solid phase extraction and liquid chromatography-tandem mass spectrometry].

作者信息

Luo Huitai, Huang Xiaolan, Wu Huiqin, Zhang Qiuyan, Zhu Zhixin, Huang Fang, Lin Xiaoshan, Ma Yefen, Deng Xin

机构信息

Guangdong Provincial Key Laboratory of Emergency Test for Dangerous Chemicals, China National Analytical Center(Guangzhou), Guangzhou 510070, China.

出版信息

Se Pu. 2017 Aug 8;35(8):816-825. doi: 10.3724/SP.J.1123.2017.04005.

Abstract

A novel method was developed for the simultaneous rapid determination of 81 illegally added glucocorticoids (GCs) in cosmetics using dispersive-solid phase extraction (d-SPE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). The analytes were extracted by acetonitrile after dispersing with water, and then purified using the C and primary secondary amine (PSA). The chromatographic separations were performed on a Poroshell 120 PFP column (100 mm×2.1 mm, 2.7 μ m) under multiple chromatographic retention modes. Acetonitrile and 0.2% (v/v) acetic acid aqueous solution were used as mobile phases with gradient elution, and all the 10 groups of isomers were baseline separated. The qualitative identification and quantitative analysis of the 81 GCs were operated in the electrospray ionization positive mode using dynamic multiple reaction monitoring (DMRM). The 81 GCs finally were quantified by internal standard method. The correlation coefficients of linear calibration curves were greater than 0.99 in the corresponding mass concentration ranges. The average recoveries of the 81 GCs at three spiked levels ranged from 68.8% to 105.3% with relative standard deviations (RSDs) of 2.9%-13.1% (=6). The LODs ( ≥ 3) and LOQs ( ≥ 10) were 0.002-0.006 μ g/g and 0.005-0.020 μ g/g, respectively. A number of 137 cosmetic samples submitted by customers were screened. Sixteen positive samples were found, and the contents of GCs were from 16.9 μ g/g to 158 μ g/g. The results showed that the new method is simple, rapid, sensitive and reliable, and it is suitable for qualitative and quantitative screening analysis of the 81 GCs in cosmetics simultaneously.

摘要

建立了一种采用分散固相萃取(d-SPE)和液相色谱-串联质谱(LC-MS/MS)同时快速测定化妆品中81种非法添加糖皮质激素(GCs)的新方法。用乙腈在加水分散后萃取分析物,然后用C18和伯仲胺(PSA)进行净化。在Poroshell 120 PFP柱(100 mm×2.1 mm,2.7μm)上采用多种色谱保留模式进行色谱分离。以乙腈和0.2%(v/v)乙酸水溶液为流动相进行梯度洗脱,10组异构体均实现基线分离。采用电喷雾电离正模式,通过动态多反应监测(DMRM)对81种GCs进行定性鉴定和定量分析。最终采用内标法对81种GCs进行定量。在相应质量浓度范围内,线性校准曲线的相关系数大于0.99。81种GCs在3个加标水平下的平均回收率为68.8%~105.3%,相对标准偏差(RSDs)为2.9%~13.1%(n = 6)。方法的检出限(LODs,n≥3)和定量限(LOQs,n≥10)分别为0.002~0.006μg/g和0.005~0.020μg/g。对客户提交的137份化妆品样品进行了筛查。发现16份阳性样品,GCs含量为16.9μg/g至158μg/g。结果表明,该新方法简便、快速、灵敏、可靠,适用于化妆品中81种GCs的同时定性和定量筛查分析。

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