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QuEChERS-超高效液相色谱-串联质谱法同时测定保健食品中21种非法添加化学药物
引用本文:郑佳,郗存显,曹淑瑞,王国民,唐柏彬,王智,母昭德.QuEChERS-超高效液相色谱-串联质谱法同时测定保健食品中21种非法添加化学药物[J].色谱,2017,35(12):1257-1265.
作者姓名:郑佳  郗存显  曹淑瑞  王国民  唐柏彬  王智  母昭德
作者单位:1. 重庆医科大学药学院, 重庆 400016; 2. 重庆出入境检验检疫局重庆市进出口食品安全工程技术研究中心, 重庆 400020; 3. 重庆市生物化学与分子药理学重点实验室, 重庆 400016
基金项目:国家质量监督检验检疫总局科技计划项目(2016IK296);重庆市科学技术委员会青-科学基金专项项目(cstc2014kjrc-qnrc00002).
摘    要:建立了QuEChERS-超高效液相色谱-串联质谱测定改善睡眠类和提高免疫力类保健食品中21种非法添加化学药物的分析方法。口服液、保健酒分别用乙腈和乙腈-水-甲酸(60∶39∶1,v/v/v)振荡提取,QuEChERS法净化;采用Acquity UPLCTMBEH C18色谱柱(50 mm×2.1 mm,1.7μm)分离,以乙腈和2 mmol/L乙酸铵溶液(含0.1%(v/v)甲酸)为流动相进行梯度洗脱;在电喷雾离子源正离子模式(ESI+)下电离,多反应监测(MRM)模式检测。结果表明,21种化学药物在1~100μg/L范围内线性关系良好,相关系数(R2)均≥0.992,检出限(LOD)为0.07~3.41μg/kg,定量限(LOQ)为0.22~11.36μg/kg。3种加标水平(10、20和100μg/kg)下,21种化学药物在口服液和保健酒中的平均加标回收率分别为61.4%~116.5%和67.4%~98.4%;相对标准偏差(RSD)分别为0.2%~13.4%和0.2%~11.8%。该法简便,灵敏性高,实用性强,可用于改善睡眠和提高免疫力类保健食品中21种非法添加化学药物的检测。

关 键 词:超高效液相色谱-串联质谱  QuEChERS  化学药物  保健食品
收稿时间:2017-09-18

Determination of 21 illegally added chemical drugs in health foods using ultra performance liquid chromatography-tandem mass spectrometry coupled with QuEChERS
ZHENG Jia,XI Cunxian,CAO Shurui,WANG Guomin,TANG Bobin,WANG Zhi,MU Zhaode.Determination of 21 illegally added chemical drugs in health foods using ultra performance liquid chromatography-tandem mass spectrometry coupled with QuEChERS[J].Chinese Journal of Chromatography,2017,35(12):1257-1265.
Authors:ZHENG Jia  XI Cunxian  CAO Shurui  WANG Guomin  TANG Bobin  WANG Zhi  MU Zhaode
Institution:1. College of Pharmacy, Chongqing Medical University, Chongqing 400016, China; 2. Chongqing Entry-Exit Inspection and Quarantine Bureau Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing 400020, China; 3. Chongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing 400016, China
Abstract:A method for the simultaneous determination of 21 illegally added chemical drugs in improving sleep and immunity health foods using ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was developed. Oral liquid and health wine samples were shaken with acetonitrile and acetonitrile-water-formic acid (60:39:1, v/v/v), respectively, then purified by QuEChERS method. The extracts were separated on an Acquity UPLCTM BEH C18 column (50 mm×2.1 mm, 1.7 μm) with gradient elution of acetonitrile and 2 mmol/L ammonium acetate solution containing 0.1% (v/v) formic acid as mobile phases. The electrospray ionization in positive ion mode was used for analysis in multiple reaction monitoring (MRM) mode. The results showed that the target drugs had a good linear relationship in the range of 1-100 μg/L with the correlation coefficients (R2) ≥ 0.992. The limits of detection (LODs) and limits of quantification (LOQs) were 0.07-3.41 μg/kg and 0.22-11.36 μg/kg, respectively. The average recoveries of the 21 chemical drugs in oral liquid and health wine were in the range of 61.4%-116.5% and 67.4%-98.4% with the relative standard deviations (RSDs) of 0.2%-13.4% and 0.2%-11.8%, respectively. The developed method is sensitive and reliable. It has been successfully used for the detection of illegally added chemical drugs in real samples.
Keywords:ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)  QuEChERS  chemical drugs  health foods
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