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作 者:王欣然 尹伟成 王海燕[1] 路勇[1] WANG Xinran;YIN Weicheng;WANG Haiyan;LU Yong(National Institutes for Food and Drug Control,NMPA Key Laboratory for Researching and Evaluation of Cosmetics,Beijing 100050,China;Hunan Institute for Drug Control,Changsha 410000,China)
机构地区:[1]中国食品药品检定研究院,国家药品监督管理局化妆品研究与评价重点实验室,北京100050 [2]湖南省药品检验检测研究院,长沙410000
出 处:《分析试验室》2023年第4期564-568,共5页Chinese Journal of Analysis Laboratory
摘 要:建立了高效液相色谱-串联质谱(HPLC-MS/MS)测定化妆品中全氟辛基磺酸(PFOS)的方法。甲醇超声提取,HPLC-MS/MS法定量PFOS。采用Agilent Poroshell 120 EC-C18(100 mm×2.1 mm,2.7μm)色谱柱、以0.1%甲酸水溶液(A)-甲醇(B)为流动相进行梯度洗脱,负离子多反应监测(MRM)模式检测。结果显示,在1~100μg/L范围内PFOS线性关系良好,相关系数r^(2)>0.9998;检出限与定量限分别为0.015和0.050 mg/kg;平均回收率为98.7%~112.5%,相对标准偏差(RSDs)均小于5%。该方法适用于化妆品中PFOS的测定。A high performance liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)method was developed for the determination of perfluorooctane sulfonic acid(PFOS)in cosmetics.The cosmetic samples were extracted with methanol by ultrasonication,and PFOS was quantified by HPLC-MS/MS.The samples were detected in negative multiple reaction monitoring(MRM)mode using an Agilent Poroshell 120 EC-C18(100 mm×2.1 mm,2.7μm)column with a gradient elution using 0.1%formic acid aqueous solution(A)-methanol(B)as the mobile phase.The results showed that the linearity of PFOS was good in the range of 1-100μg/L with the correlation coefficient r^(2)larger than 0.9998;the limits of detection and limits of quantification were 0.015 and 0.050 mg/kg,respectively.The average recoveries were 98.7%-112.5%,and the relative standard deviations(RSDs)were less than 5%.The method is suitable for the determination of PFOS in cosmetics.
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