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[高效液相色谱-四极杆/静电场轨道阱高分辨质谱法快速筛查保健食品中的西布曲明及其五种衍生物]

[Rapid screening of sibutramine and five derivatives in health food by high performance liquid chromatography-quadrupole/electrostatic orbitrap high-resolution mass spectrometry].

作者信息

Hong Deng, Xie Wen, Hou Jianbo, Hu Xiaoli, Shi Yingzhu, Li Jie

机构信息

Zhejiang Academy of Science and Technology for Inspection and Quarantine, Hangzhou 311215, China.

出版信息

Se Pu. 2019 Nov 8;37(11):1173-1178. doi: 10.3724/SP.J.1123.2019.05017.

DOI:10.3724/SP.J.1123.2019.05017
PMID:31642269
Abstract

A rapid screening method was developed to determine sibutramine and five derivatives in health food by high performance liquid chromatography-quadrupole/electrostatic orbitrap high-resolution mass spectrometry (HPLC-Q/Orbitrap HRMS). The sample was extracted with methanol via ultrasonic-assisted extraction coupled with high-speed centrifugation. Separation was performed on a Hypersil Gold column (100 mm×2.1 mm, 3 μm) by gradient elution with methanol/water (containing 0.15%(v/v) formic acid) as the mobile phase. The positive full mass scan/date-dependent MS (Full MS/dd-MS) mode was used during MS detection, and quantification was achieved by resolution of the precursor mass. The analytes in the sample were separated, and accurate mass and MS fragment ions were simultaneously attained within 8 min. The results indicated that the obtained mass accuracy errors of the six analytes were less than 1×10. Good linearities were obtained in the range of 0.5-20.0 μg/L, and all correlation coefficients were higher than 0.999. The limits of quantification were 25 μg/kg and the recoveries were in the range of 93.5%-103.5% with relative standard deviations of 1.5%-7.7%. This simple-pretreatment, rapid, accurate, high-sensitivity, and high-selectivity method can be used in the rapid screening and quantitative analysis of sibutramine and its derivatives in health food.

摘要

建立了一种利用高效液相色谱-四极杆/静电轨道阱高分辨质谱(HPLC-Q/Orbitrap HRMS)测定保健食品中西布曲明及其5种衍生物的快速筛查方法。样品经甲醇超声辅助提取并高速离心。采用Hypersil Gold柱(100 mm×2.1 mm,3 μm),以甲醇/水(含0.15%(v/v)甲酸)为流动相进行梯度洗脱分离。质谱检测采用正离子全质量扫描/数据依赖型质谱(Full MS/dd-MS)模式,通过母离子质量分辨率进行定量。样品中的分析物在8分钟内实现分离,同时获得精确质量和质谱碎片离子。结果表明,6种分析物的质量准确度误差均小于1×10。在0.5 - 20.0 μg/L范围内线性良好,所有相关系数均高于0.999。定量限为25 μg/kg,回收率在93.5% - 103.5%之间,相对标准偏差为1.5% - 7.7%。该方法预处理简单、快速、准确、灵敏度高、选择性好,可用于保健食品中西布曲明及其衍生物的快速筛查和定量分析。

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引用本文的文献

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