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通过基质固相分散和液相色谱-质谱联用技术测定牛奶和鸡蛋中12种磺胺类抗菌药物的快速确证分析方法

Rapid confirmatory assay for determining 12 sulfonamide antimicrobials in milk and eggs by matrix solid-phase dispersion and liquid chromatography-mass spectrometry.

作者信息

Bogialli Sara, Curini Roberta, Di Corcia Antonio, Nazzari Manuela, Polci Maria Letizia

机构信息

Dipartimento diChimica, Università La Sapienza, Piazza Aldo Moro 5, 00185 Roma, Italy.

出版信息

J Agric Food Chem. 2003 Jul 16;51(15):4225-32. doi: 10.1021/jf0343837.

Abstract

A rapid confirmatory method for determining 12 sulfonamide (SAs) antibacterials in whole milk and eggs is presented. This method is based on the matrix solid-phase dispersion technique with hot water as extractant followed by liquid chromatography (LC)-mass spectrometry (MS). The LC-MS instrument was equipped with an electrospray ion source and a single quadrupole. After 4 mL of a milk sample containing the analytes had been deposited on sand (crystobalite), this material was packed into an extraction cell. SAs were extracted by flowing 4 mL of water through the cell heated at 75 degrees C. With some modifications, this procedure was applied also to eggs. After pH adjustment and filtration, 0.5 mL of the final extracts was then injected into the LC column. MS data acquisition was performed in the positive-ion mode and by monitoring at least three ions for each target compound. The in-source collision-induced dissociation process produced confirmatory ions. At the 50 ng/g level, recovery of the analytes in milk and eggs was 77-92% with relative standard deviations ranging between 1 and 11%. Estimated limits of quantification (S/N = 10) were 1-3 ng/g of SAs in milk and 2-6 ng/g in eggs. With both matrices, attempts to reduce the analysis time by using a short chromatographic run time caused severe ion signal suppression for the early-eluted SAs. This effect was traced to competition effects by polar endogenous coextractives, maybe proteinaceous species, which are eluted in the first part of the chromatographic run. This unwelcome effect was almost completely removed by simply adopting more selective chromatographic conditions.

摘要

本文介绍了一种快速确证方法,用于测定全脂牛奶和鸡蛋中的12种磺胺类抗菌药物。该方法基于基质固相分散技术,以热水为萃取剂,随后进行液相色谱(LC)-质谱(MS)分析。LC-MS仪器配备了电喷雾离子源和单四极杆。将4 mL含有分析物的牛奶样品沉积在沙子(方石英)上后,将该材料装入萃取池中。通过使4 mL水在75℃加热的萃取池中流动来萃取磺胺类药物。经过一些修改,该程序也适用于鸡蛋。在调节pH值并过滤后,将0.5 mL最终提取物注入LC柱。MS数据采集在正离子模式下进行,对每种目标化合物监测至少三个离子。源内碰撞诱导解离过程产生确证离子。在50 ng/g水平下,牛奶和鸡蛋中分析物的回收率为77-92%,相对标准偏差在1%至11%之间。估计定量限(S/N = 10)在牛奶中为1-3 ng/g磺胺类药物,在鸡蛋中为2-6 ng/g。对于这两种基质,试图通过使用短色谱运行时间来缩短分析时间,会导致早期洗脱的磺胺类药物出现严重的离子信号抑制。这种效应可追溯到极性内源性共萃取物(可能是蛋白质类物质)的竞争效应,它们在色谱运行的第一部分被洗脱。通过简单地采用更具选择性的色谱条件,这种不良效应几乎完全消除。

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