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采用除磷脂预处理的液相色谱串联质谱法同时测定人血液中的双甲脒、杀虫脒、速灭威及其代谢物

Simultaneous determination of amitraz, chlordimeform, formetanate and metabolites in human blood by liquid chromatography tandem mass spectrometry with phospholipid-removal pretreatment.

作者信息

Gao Xue, Sun Yongbin, You Haidan, Dai Yannan, Guo Hao, Zhao Qingbiao

机构信息

Chongqing Key Lab of Catalysis & Functional Organic Molecules, Chongqing Technology and Business University, China.

Division of Pharmaceutics, National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Traditional Chinese Medicine, Nanchang, China.

出版信息

Biomed Chromatogr. 2019 Apr;33(4):e4477. doi: 10.1002/bmc.4477. Epub 2019 Feb 4.

Abstract

In this study, a reliable ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method coupled with an easy, fast and effective sample pretreatment procedure was developed for simultaneous determination of amitraz, chlordimeform, formetanate and their metabolites in human blood. With the procedures of protein precipitation and a phospholipid-removal step, the endogenous compound interference was significantly reduced, and matrix effects were significantly reduced. The linear ranges of matrix-matched standard curves were from 0.5 to 1000 ng/mL with coefficients of determination >0.996. Very low limits of detection (0.05-0.12 ng/mL) and limits of quantitation (0.15-0.4 ng/mL) were achieved. Reasonable recoveries ranging from 88.1 to 103.5% were obtained. The intra-day RSDs ranging from 3.2 to 8.6% and inter-day RSDs ranging from 4.8 to 9.2% indicated good precision. With the introduction of a phospholipid-removal step, the ME ranged from 90.1 to 98.5%. The established method was successfully applied to the analysis of a blood sample from a formetanate poisoning case. This method possesses the advantages of high sensitivity, reduced matrix effects and rapidity.

摘要

在本研究中,建立了一种可靠的超高效液相色谱串联质谱(UPLC-MS/MS)方法,并结合简便、快速且有效的样品前处理程序,用于同时测定人血中双甲脒、杀虫脒、速灭威及其代谢物。通过蛋白质沉淀和去除磷脂步骤,内源性化合物干扰显著降低,基质效应也显著降低。基质匹配标准曲线的线性范围为0.5至1000 ng/mL,测定系数>0.996。实现了极低的检测限(0.05 - 0.12 ng/mL)和定量限(0.15 - 0.4 ng/mL)。获得了88.1%至103.5%的合理回收率。日内相对标准偏差范围为3.2%至8.6%,日间相对标准偏差范围为4.8%至9.2%,表明精密度良好。引入去除磷脂步骤后,基质效应范围为90.1%至98.5%。所建立的方法成功应用于一例速灭威中毒病例血样的分析。该方法具有灵敏度高、基质效应降低和快速等优点。

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