首页> 外文期刊>Analytical and bioanalytical chemistry >Development of a high-throughput method for the determination of itraconazole and its hydroxy metabolite in human plasma, employing automated liquid-liquid extraction based on 96-well format plates and LC/MS/MS
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Development of a high-throughput method for the determination of itraconazole and its hydroxy metabolite in human plasma, employing automated liquid-liquid extraction based on 96-well format plates and LC/MS/MS

机译:基于96孔板和LC / MS / MS的自动液-液萃取技术开发了一种测定人血浆中伊曲康唑及其羟基代谢物的高通量方法

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A semi-automated liquid chromatography-tandem mass spectrometry (LC/MS/MS) method was developed for the simultaneous quantification of the antifungal drug itraconazole (ITZ) and its coactive metabolite bydroxyltraconazole (OH-ITZ) in human plasma. The plasma samples underwent liquid-liquid extraction (LLE) in 2.2 mL 96 deepwell plates. ITZ, OH-ITZ and the internal standard (IS) R51012 were extracted from plasma, using a mixture of acetonitrile (ACN) and methyl t-butyl ether (MTBE) as the organic solvent. This specific mixture, due to its composition, had a significant impact on the performance of the assay. All liquid transfer steps, including preparation of calibration standards and quality control samples as well as the addition of the IS, were performed automatically using robotic liquid handling workstations for parallel sample processing. After vortexing, centrifugation and freezing, the supernatant organic solvent was evaporated. The analytes and IS were dissolved in a small volume of a reconstitution Solution, an aliquot of which was analyzed by combined reversed phase LC/MS/MS, with positive ion electrospray ionization and a Turbolon Spray interface, using multiple reactions monitoring (MRM). The method was shown to be sensitive and specific to both ITZ and OH-ITZ, it revealed excellent linearity for the range of concentrations 2-500 ng mL(-1) for ITZ and 41000 ng mL(-1) for OH-ITZ, it was very accurate and it gave very good inter- and intra-day precisions. The proposed high-throughput method was employed in a bioequivalence study after per os administration of two 100 mg tablets of ITZ, and it allowed this study to be completed in under four days.
机译:建立了一种半自动化液相色谱-串联质谱法(LC / MS / MS),用于同时定量人血浆中抗真菌药伊曲康唑(ITZ)及其活性代谢物的量。血浆样品在2.2 mL 96深孔板中进行液-液萃取(LLE)。使用乙腈(ACN)和甲基叔丁基醚(MTBE)的混合物作为有机溶剂,从血浆中提取ITZ,OH-ITZ和内标(IS)R51012。由于其组成,这种特定的混合物对测定的性能有重大影响。所有液体转移步骤,包括校准标准品和质量控制样品的准备以及IS的添加,都是使用机器人液体处理工作站自动进行并行样品处理的。涡旋,离心和冷冻后,蒸发上清液有机溶剂。将分析物和IS溶解在少量的重构溶液中,使用多重反应监控(MRM),通过组合的反相LC / MS / MS,正离子电喷雾电离和Turbolon喷雾界面对等分试样进行分析。结果表明该方法对ITZ和OH-ITZ均具有灵敏性和特异性,对于ITZ浓度范围为2-500 ng mL(-1)和OH-ITZ浓度范围为41000 ng mL(-1),它显示出极好的线性,它非常准确,而且日间和日间精度都很高。口服2片ITZ片剂后,建议的高通量方法用于生物等效性研究,并且该研究可在4天之内完成。

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