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UPLC-MS/MS Analysis of Methotrexate in Human Plasma and Comparison with the Fluorescence Polarization Immunoassay

机译:血浆中甲氨蝶呤的UPLC-MS / MS分析及其与荧光偏振免疫测定法的比较

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Methotrexate (MTX) plasma concentration is routinely monitored to guide the dosage regimen of rescue drugs. This study aims to develop and validate an ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method for plasma MTX analysis, and to establish its agreement with the fluorescence polarization immunoassay (FPIA) in patients with high-dose MTX therapy. Separation was achieved by gradient elution with methanol and water (0.05% formic acid) at 40°C with a run time of 3 min. The intra- and inter-day inaccuracy and imprecision of the UPLC-MS/MS method were –4.25 to 3.1 and less than 7.63%, respectively. The IS-normalized recovery and matrix effect were 87.05 to 92.81 and 124.43 to 134.57%. The correlation coefficients between UPLC-MS/MS and FPIA were greater than 0.98. The UPLC-MS/MS method was in agreement with the FPIA at high levels of MTX (1.0 – 100 μmol/L), but not at low levels (0.01 – 1.0 μmol/L). Further studies are warranted to confirm these results.
机译:例行监测甲氨蝶呤(MTX)的血浆浓度,以指导急救药物的剂量方案。这项研究旨在开发和验证用于血浆MTX分析的超高效液相色谱串联质谱(UPLC-MS / MS)方法,并建立与大剂量MTX治疗患者的荧光偏振免疫测定(FPIA)的协议。通过在40°C下用甲醇和水(0.05%甲酸)进行3分钟的梯度洗脱来实现分离。 UPLC-MS / MS方法的日内和日间误差和不精确度分别为–4.25至3.1和小于7.63%。 IS归一化回收率和基质效应为87.05至92.81和124.43至134.57%。 UPLC-MS / MS与FPIA之间的相关系数大于0.98。在高水平MTX(1.0 – 100μmol/ L)处,UPLC-MS / MS方法与FPIA一致,但在低水平(0.01 – 1.0μmol/ L)处则与FPIA一致。有必要进一步研究以确认这些结果。

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