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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >A dried blood spots technique based LC-MS/MS method for the analysis of posaconazole in human whole blood samples
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A dried blood spots technique based LC-MS/MS method for the analysis of posaconazole in human whole blood samples

机译:基于干血斑技术的LC-MS / MS方法分析人全血样品中的泊沙康唑

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A rugged and robust liquid chromatographic tandem mass spectrometric (LC-MS/MS) method utilizing dried blood spots (DBS) was developed and validated for the analysis of posaconazole in human whole blood. Posaconazole fortified blood samples were spotted (15. μL) onto Ahlstrom Alh-226 DBS cards and dried for at least 2 h. Punched spots were then extracted by using a mixture of acetonitrile and water containing stable labeled internal standard (IS). Posaconazole and its IS were separated from endogenous matrix components on a Kinetex? C18 column under gradient conditions with a mobile phase A consisting of 0.1% formic acid and a mobile phase B consisting of 0.1% formic acid in acetonitrile/methanol (70/30, v/v). The analyte and IS were detected using a Sciex API 4000 triple quadrupole LC-MS/MS system equipped with a TurboIonSpray? source operated in the positive ion mode. The assay was linear over the concentration range of 5-5000 ng/mL. The inter-run accuracy and precision of the assay were -1.8% to 0.8% and 4.0% to 10.4%, respectively. Additional assessments unique to DBS were investigated including sample spot homogeneity, spot volume, and hematocrit. Blood spot homogeneity was maintained and accurate and precise quantitation results were obtained when using a blood spot volume of between 15 and 35. μL. Human blood samples with hematocrit values ranging between 25% and 41% gave acceptable quantitation results. The validation results indicate that the method is accurate, precise, sensitive, selective and reproducible.
机译:建立了一种利用干血斑(DBS)的坚固耐用的液相色谱串联质谱(LC-MS / MS)方法,并经过验证可用于分析人全血中的泊沙康唑。将泊沙康唑强化的血液样品点样(15.μL)到Ahlstrom Alh-226 DBS卡上,干燥至少2 h。然后使用含有稳定标记内标(IS)的乙腈和水的混合物提取穿孔的斑点。在Kinetex?上将泊沙康唑及其IS与内源性基质成分分离。在梯度条件下的C18色谱柱,其流动相A为0.1%甲酸,流动相B为0.1%甲酸的乙腈/甲醇溶液(70/30,v / v)。使用配备了TurboIonSpray?的Sciex API 4000三重四极杆LC-MS / MS系统检测分析物和IS。离子源以正离子模式运行。该测定在5-5000 ng / mL的浓度范围内呈线性。批间准确度和精密度分别为-1.8%至0.8%和4.0%至10.4%。研究了DBS独有的其他评估方法,包括样品斑点均一性,斑点体积和血细胞比容。当使用15至35μL的血斑体积时,可以保持血斑均匀性,并获得准确而精确的定量结果。血细胞比容值在25%到41%之间的人血样品给出了可接受的定量结果。验证结果表明该方法准确,准确,灵敏,选择性好且可重复。

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