Central Agricultural Office Food and Feed Safety Directorate, Food Toxicology National Reference Laboratory, Mester utca 81, Budapest 1095, Hungary.
J Pharm Biomed Anal. 2010 Dec 1;53(4):919-28. doi: 10.1016/j.jpba.2010.06.026. Epub 2010 Jul 1.
A new method was developed to identify and quantify corticosteroids (prednisolone, methylprednisone, flumetasone, dexamethasone, and methylprednisolone) in raw bovine milk by liquid chromatography-tandem mass spectrometry (LC-MS/MS) utilizing mixed-mode polymeric strong cation exchange and reversed-phase (MCX) solid-phase extraction (SPE) to reduce ion effects in a multimode ion (MMI) source. The main advantage of this method over other commonly used methods includes the use of a single SPE cartridge with a low volume for sample preparation and fast separation on the HPLC system with reduced ion suppression. This study is the first to report the determination of methylprednisone, a metabolite of methylprednisolone, in bovine milk. This method was validated in accordance with the European Union (EU) Commission Decision 2002/657/EC. The recoveries vary between 90% and 105%. The within-laboratory reproducibility (precision) is less than 30%. The decision limits and detection capabilities were calculated along with LODs, which ranged from 0.02 to 0.07 microg/kg. The method was further enhanced by its successful adaptation to other LC-MS/MS systems equipped with the newly developed ion source, Agilent Jet Stream (AJS). After optimization of the AJS ion source and MS parameters, even lower LOD values were achieved (0.001-0.006 microg/kg) for the corticosteroids. Analytical results obtained with the AJS were characterized by an enhanced area response and similar noise level comparable to those obtained with conventional orthogonal atmospheric ionization (API).
建立了一种利用混合模式聚合物强阳离子交换和反相(MCX)固相萃取(SPE)技术,结合多模式离子源(MMI),在生牛乳中直接检测和定量分析皮质甾类药物(泼尼松龙、甲泼尼龙、氟替卡松、地塞米松和甲泼尼龙)的液相色谱-串联质谱(LC-MS/MS)新方法。与其他常用方法相比,该方法的主要优点包括:使用单个 SPE 小柱,样品制备体积小;在 HPLC 系统上进行快速分离,减少离子抑制。本研究首次报道了在牛乳中检测甲泼尼龙(甲泼尼龙的代谢物)。该方法按照欧盟委员会 2002/657/EC 号决议进行了验证。回收率在 90%到 105%之间。实验室内部重现性(精密度)小于 30%。计算了决定限和检测限,其值分别为 0.02-0.07μg/kg。该方法进一步通过成功适应配备新型离子源的其他 LC-MS/MS 系统得以增强,该离子源为安捷伦喷射流(AJS)。在优化 AJS 离子源和 MS 参数后,皮质甾类药物的检测限(LOD)甚至更低(0.001-0.006μg/kg)。用 AJS 获得的分析结果具有增强的峰面积响应和类似的噪声水平,与传统正交大气压电离(API)获得的结果相当。