首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Validation and implementation of a liquid chromatography/tandem mass spectrometry assay for quantitation of the total and unbound RO4929097, a γ-secretase inhibitor targeting Notch signaling, in human plasma
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Validation and implementation of a liquid chromatography/tandem mass spectrometry assay for quantitation of the total and unbound RO4929097, a γ-secretase inhibitor targeting Notch signaling, in human plasma

机译:液相色谱/串联质谱分析法在人血浆中定量和定量未结合的靶向Notch信号的γ-分泌酶抑制剂RO4929097的验证和实施

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摘要

A reversed-phased liquid chromatography with tandem mass spectrometry (LC-MS/MS) method was developed and validated for quantitation of the total and unbound RO4929097, a γ-secretase inhibitor targeting Notch signaling, in human plasma. Sample preparation involved a liquid-liquid extraction with ethyl acetate. Chromatographic separation was achieved on a Waters X-Terra? MS C18 column with an isocratic mobile phase consisting of methanol/0.45% formic acid in water (60:40, v/v) running at a flow rate of 0.2ml/min for 6min. The lower limits of quantitation (LLOQs) were 5ng/ml for the total RO4929097 in plasma and 0.5ng/ml for the unbound drug in phosphate buffer solution (PBS). Calibration curves were linear over RO4929097 concentration range of 5-2000ng/ml in plasma for the total drug and 0.5-200ng/ml in PBS for the unbound drug. The intra-day and inter-day accuracy and precision were within the generally accepted criteria for bioanalytical method (<15%). The method has been successfully employed to characterize the total and unbound plasma pharmacokinetics of RO4929097 after its oral administration in cancer patients.
机译:已开发了一种采用串联质谱(LC-MS / MS)的反相液相色谱法,并已进行了定量,可用于定量测定人血浆中总的和未结合的靶向Notch信号的γ-分泌酶抑制剂RO4929097。样品制备涉及用乙酸乙酯进行液-液萃取。色谱分离是在Waters X-Terra?上完成的。 MS C18色谱柱,其等度流动相由甲醇/0.45%甲酸的水溶液(60:40,v / v)组成,以0.2ml / min的流速运行6分钟。血浆中总RO4929097的定量下限(LLOQs)为5ng / ml,磷酸盐缓冲液(PBS)中的未结合药物的定量下限为0.5ng / ml。对于总药物,血浆中RO4929097浓度范围为5-2000ng / ml,对于未结合药物而言,PBS中0.5-200ng / ml的校准曲线为线性。日内和日间准确性和精密度均在生物分析方法公认的标准之内(<15%)。该方法已成功用于表征RO4929097在癌症患者中口服后的总和未结合血浆药代动力学。

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