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高效液相色谱-电喷雾串联质谱法对动物饲料中10种磺胺类药物的定性与定量分析

[Qualification and quantification of 10 sulfonamides in animal feedstuff by high performance liquid chromatography-electrospray tandem mass spectrometry].

作者信息

Qin Yan, Zhang Meijin, Lin Haidan

机构信息

Guangzhou Entry & Exit Inspection and Quarantine Bureau, Guangzhou 510623, China.

出版信息

Se Pu. 2005 Jul;23(4):397-400.

PMID:16250451
Abstract

The presence of sulfonamide (SA) residues in foods is largely due to the raising of animals with sulfonamide antibiotics added or polluted feedstuff. Because of interference from the matrices, the commonly used immunoassay or chromatographic method is not suitable for the analysis of multi-SAs in feedstuff. A high performance liquid chromatographic-electrospray tandem mass spectrometric (HPLC/ESI-MS-MS) method has been established for the simultaneous determination of multi-SAs including sulfadiazine (SD), sulfapyridine (SPD), sulfamerazine (SM1), sulfameter (SM), sulfamethazine (SM2), sulfamethoxypyridazine (SMP), sulfamethoxazole (SMZ), sulfamonomethoxine (SMM), sulfadimethoxine (SDM) and sulfaquinoxaline (SQX). After solvent extraction, solid phase extraction, dilution and reversed-phase HPLC separation, SAs were detected by ESI-MS-MS under multi-reaction monitoring mode. The qualification analysis was done by using retention time and distribution of diagnostic ion pairs, and the quantification was based on the peak intensity of common fragment ion m/z 156. The limits of quantification for 10 SAs were 0.5 - 2.0 microg/kg (S/N = 10). The correlation coefficient of linear calibration curve was over 0.9995 within the SAs concentration range 2.0 - 200 microg/L except for SDM and SQX. At the spiked level of 1.0 mg/kg, the average recoveries for the 10 SAs were between 70% and 92%, the relative standard deviations were under 10% for intra-day and under 15% for inter-day. Routine tests showed the method was fast, sensitive, specific, and practical for the SAs determination in feedstuff.

摘要

食品中磺胺类药物(SA)残留的存在主要是由于使用添加了磺胺类抗生素的饲料或受污染的饲料饲养动物所致。由于基质的干扰,常用的免疫分析或色谱方法不适用于饲料中多种磺胺类药物的分析。已建立了一种高效液相色谱 - 电喷雾串联质谱(HPLC/ESI-MS-MS)方法,用于同时测定多种磺胺类药物,包括磺胺嘧啶(SD)、磺胺吡啶(SPD)、磺胺甲基嘧啶(SM1)、磺胺对甲氧嘧啶(SM)、磺胺二甲嘧啶(SM2)、磺胺甲氧嗪(SMP)、磺胺甲恶唑(SMZ)、磺胺间甲氧嘧啶(SMM)、磺胺二甲氧嘧啶(SDM)和磺胺喹恶啉(SQX)。经溶剂萃取、固相萃取、稀释及反相高效液相色谱分离后,在多反应监测模式下通过电喷雾串联质谱检测磺胺类药物。通过保留时间和诊断离子对分布进行定性分析,基于共同碎片离子m/z 156的峰强度进行定量分析。10种磺胺类药物的定量限为0.5 - 2.0 μg/kg(信噪比 = 10)。除SDM和SQX外,在2.0 - 200 μg/L的磺胺类药物浓度范围内,线性校准曲线的相关系数均超过0.9995。在1.0 mg/kg的加标水平下,10种磺胺类药物的平均回收率在70%至92%之间,日内相对标准偏差低于10%,日间相对标准偏差低于15%。常规测试表明,该方法快速、灵敏、特异,适用于饲料中磺胺类药物的测定。

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