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超高效液相色谱-四极杆-飞行时间质谱法同时测定饲料中10种未经批准的镇静药物

[Simultaneous determination of 10 unapproved sedative drugs in feeds by ultra-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry].

作者信息

Xu Chengbao, Suo Ran, Zhang Feng, Chu Xiaogang, Ding Fei, Ling Yun, Yang Minli, Sun Li

机构信息

Agricultural University of Hebei, Baoding 071001, China.

出版信息

Se Pu. 2012 May;30(5):457-62. doi: 10.3724/sp.j.1123.2011.12032.

DOI:10.3724/sp.j.1123.2011.12032
PMID:22934407
Abstract

A new analytical method using ultra-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was developed for screening and confirmation of 10 unapproved sedative drugs in feeds. The samples were extracted using the solution of methanol-0.1 mol/L HCl (9:1, v/v), and the extracts were centrifuged and then directly purified through MCX cartridges. The identification and detection were achieved in positive electrospray ionization (ESI) mode using Q-TOF-MS. The potential of UPLC-Q-TOF MS for confirmatory analysis was shown by determining the accurate mass of all the compounds and fragment ions upon collision-induced-dissociation (CID) at different energies. The extra mass measurement errors for all the sedative drugs were found to be within 5 ppm. The calibration graphs were linear in the concentration range of 5-100 microg/L with the correlation coefficients more than 0.99 for the 10 drugs. The limits of quantification (LOQ, S/N = 10) were 8 microg/kg for nitrazepam, zolpidem and thioridazine; 10 microg/kg for thriazolam, estazolam, diazepam, promethazine, chlorpromazine and midazolam; 20 microg/kg for clozapine. The recoveries for all the compounds in feeds were 60.6%-108.5% with the relative standard deviations less than 10% at the spiked levels of LOQ, 2LOQ and 4LOQ.

摘要

建立了一种使用超高效液相色谱-四极杆-飞行时间质谱(UPLC-Q-TOF-MS)的新分析方法,用于筛查和确证饲料中10种未经批准的镇静药物。样品用甲醇-0.1 mol/L盐酸溶液(9:1,v/v)提取,提取物离心后直接通过MCX柱净化。采用Q-TOF-MS在正电喷雾电离(ESI)模式下进行鉴定和检测。通过在不同能量下碰撞诱导解离(CID)测定所有化合物和碎片离子的精确质量,显示了UPLC-Q-TOF MS用于确证分析的潜力。发现所有镇静药物的额外质量测量误差在5 ppm以内。10种药物的校准曲线在5-100 μg/L浓度范围内呈线性,相关系数大于0.99。硝西泮、唑吡坦和硫利达嗪的定量限(LOQ,S/N = 10)为8 μg/kg;三唑仑、艾司唑仑、地西泮、异丙嗪、氯丙嗪和咪达唑仑为10 μg/kg;氯氮平为20 μg/kg。在LOQ、2LOQ和4LOQ加标水平下,饲料中所有化合物的回收率为60.6%-108.5%,相对标准偏差小于10%。

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