Simultaneous Screening of 172 Veterinary Drugs by Modified QuEChERS-LC–MS/MS in TCM Galli Gigerii Endothelium Corneum

IF 1.3 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of chromatographic science Pub Date : 2024-04-05 DOI:10.1093/chromsci/bmae014
Qing Hu, Jian Sun, Hong Yu, Rui Feng, Jingxian Zhang, Heng Zhou, Shen Ji
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Abstract

An analytical method was developed for the screening of 172 veterinary drugs in traditional Chinese medicine Galli Gigerii Endothelium Corneum by high-performance liquid chromatography tandem mass spectrometry. The samples were pretreated by a modified QuEChERS method. A Zorbax Eclipse plus C18 column (1.8 μm, 3.0 × 150 mm2, Agilent) was used for the separation of analytes by gradient elution. All analytes were detected by electrospray ionization mass spectrometry with multiple reaction monitoring mode. Good linearity with R ≥ 0.99 was exhibited for all analytes within the respective range. The recoveries of all monitored analytes ranged from 55.4 to 127.6% at three spiked levels (limit of quantitation—LOQ, 2-fold LOQ, 10-fold LOQ), with relative standard deviations <17.8%. The estimated LOQ levels were 0.2–20 μg/kg. The application of this method provides a reference for the safety control of traditional Chinese medicines.
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利用改良的 QuEChERS-LC-MS/MS 技术同时筛选中药五倍子内皮角质层中的 172 种兽药
建立了高效液相色谱-串联质谱法筛选中药五倍子中172种兽药的分析方法。样品经改良的 QuEChERS 方法预处理。采用 Zorbax Eclipse plus C18 色谱柱(1.8 μm,3.0 × 150 mm2,安捷伦)进行梯度洗脱分离。所有分析物均采用多反应监测模式的电喷雾离子化质谱检测。在相应的检测范围内,所有分析物的线性关系良好,R ≥ 0.99。在三个加标水平(定量限、2 倍定量限、10 倍定量限)下,所有监测分析物的回收率为 55.4% 至 127.6%,相对标准偏差为 17.8%。估计的 LOQ 水平为 0.2-20 μg/kg。该方法的应用为中药的安全性控制提供了参考。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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