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

机译:基质固相分散-液相色谱-质谱法快速测定牛奶和鸡蛋中的12种磺胺类抗生素

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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 degreesC. 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. [References: 29]
机译:介绍了一种用于确定全脂牛奶和鸡蛋中12种磺酰胺(SAs)抗菌剂的快速确证方法。该方法基于基质固相分散技术,以热水为萃取剂,然后进行液相色谱(LC)-质谱(MS)。 LC-MS仪器配备了电喷雾离子源和单个四极杆。在将4 mL含有分析物的牛奶样品沉积在沙子(方石英)上后,将该材料装填到萃取池中。通过使4 mL的水流过加热到75摄氏度的电池来提取SA。经过一些修改,此过程也适用于鸡蛋。调节pH值并过滤后,将0.5 mL最终提取物注入LC色谱柱。 MS数据采集是在阳离子模式下进行的,并且通过监测每种目标化合物的至少三个离子来进行。源内碰撞诱导的离解过程产生了确认离子。在50 ng / g的水平下,牛奶和鸡蛋中分析物的回收率为77-92%,相对标准偏差为1-11%。估计的定量限(S / N = 10)是牛奶中SA的1-3 ng / g和鸡蛋中2-6 ng / g的SA。对于这两种基质,尝试通过使用较短的色谱运行时间来减少分析时间会严重抑制早期洗脱SA的离子信号。这种作用可追溯到极性内源性共提取物(可能是蛋白质类)的竞争作用,它们在色谱运行的第一部分被洗脱。通过采用更具选择性的色谱条件,几乎可以完全消除这种不受欢迎的效果。 [参考:29]

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