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Determination of five macrolide antibiotic residues in raw milk using liquid chromatography-electrospray ionization tandem mass spectrometry

机译:液相色谱-电喷雾串联质谱法测定原料奶中五种大环内酯类抗生素残留

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摘要

A confirmatory method using liquid chromatography-electrospray ionization tandem mass spectrometry for determination of five macrolide antibiotics including spiramycin, tilmicosin, oleandomycin, erythromycin, and tylosin in raw milk is presented. Macrolides were extracted from raw milk by acetonitrile, and sample extracts were further cleaned up using solid-phase extraction cartridges. Data acquisition was achieved using multiple reaction monitoring, that is, two transitions, to provide a high degree of sensitivity and specificity. Matrix-matched standard calibration curves with the use of roxithromycin as an internal standard were utilized to achieve the best accuracy of the method. Both a conventional validation procedure and a designed experiment were applied to study the accuracy and precision of the method. The measurement uncertainty arising from accuracy and precision was estimated. The method accuracy, expressed as a percentage of overall recovery, was similar to 100%, and its intermediate precision was < 10%. LC-ESI/MS/MS method detection limits (S/N >= 3:1) of five macrolides were < 0.3 mu g/kg.
机译:提出了一种使用液相色谱-电喷雾串联质谱法测定生乳中5种大环内酯类抗生素的方法,其中包括螺旋霉素,替米考星,oleandomycin,erythromycin和tylosin。大环内酯类化合物通过乙腈从原料奶中提取,样品提取物使用固相萃取柱进一步净化。使用多个反应监控(即两个转换)可以实现数据采集,以提供高度的敏感性和特异性。以罗红霉素为内标,与基质匹配的标准校正曲线被用来获得该方法的最佳准确性。通过常规验证程序和设计实验来研究该方法的准确性和准确性。估算了由于精度和精度引起的测量不确定度。用总回收率表示的方法精度接近100%,中间精度<10%。 5种大环内酯类化合物的LC-ESI / MS / MS方法检出限(S / N> = 3:1)<0.3μg / kg。

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