National Institute for Quality Control in Health/Oswaldo Cruz Foundation (INCQS/FIOCRUZ), Av. Brasil 4365, Rio de Janeiro, RJ, Brazil.
Anal Chim Acta. 2009 Dec 10;656(1-2):72-84. doi: 10.1016/j.aca.2009.10.012. Epub 2009 Oct 17.
A liquid chromatography-electrospray ionization tandem mass spectrometric (LC-ESI-MS/MS) method for the analysis of several tetracyclines residues in bovine milk has been developed. Milk deproteinization/extraction of samples was performed with acidified acetonitrile. After diluting and purification by solid-phase extraction (SPE), the extracts were injected into the instrument operated in Multiple Reaction Monitoring (MRM) acquisition mode. The reversible epimerization at C-4 of oxytetracycline, tetracycline and chlortetracycline and the keto-enol tautomerism of chlortetracycline between C-11a and C-12 were considered for reliable quantification. Degradation was also taken in account and minimized for the same purpose. A central composite (response surface) design with desirability function was employed for the optimization of extraction and clean-up steps. The optimization improved the extraction efficiency of the more polar analytes reaching 93.9% for 4-epioxytetracycline and 95.8% for oxytetracycline at 100 microg L(-1). The validation was performed following the criteria established by Commission Decision 2002/657/EC.
建立了一种用于分析牛奶中几种四环素残留的液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)方法。样品经酸化乙腈沉淀/提取蛋白后,采用固相萃取(SPE)进行稀释和净化,提取液在多反应监测(MRM)采集模式下进样分析。考虑到四环素、土霉素和金霉素在 C-4 位的差向异构化以及金霉素在 C-11a 和 C-12 位的酮-烯醇互变异构,对其进行了可靠的定量分析。为了同样的目的,还考虑了降解并尽量减少了降解。采用具有可接受性函数的中心复合(响应面)设计对提取和净化步骤进行了优化。优化提高了极性较强分析物的提取效率,在 100μg/L 时,4-差向四环素的提取效率达到 93.9%,土霉素的提取效率达到 95.8%。验证按照委员会 2002/657/EC 号决定规定的标准进行。