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验证和实施液相色谱/串联质谱法测定人血浆中总游离 RO4929097 的浓度,RO4929097 是一种针对 Notch 信号通路的 γ-分泌酶抑制剂。

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.

机构信息

Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jun 1;879(19):1537-43. doi: 10.1016/j.jchromb.2011.03.045. Epub 2011 Mar 31.

Abstract

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 C(18) 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 0.2 ml/min for 6 min. The lower limits of quantitation (LLOQs) were 5 ng/ml for the total RO4929097 in plasma and 0.5 ng/ml for the unbound drug in phosphate buffer solution (PBS). Calibration curves were linear over RO4929097 concentration range of 5-2000 ng/ml in plasma for the total drug and 0.5-200 ng/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.

摘要

建立并验证了一种反相高效液相色谱-串联质谱(LC-MS/MS)法,用于定量测定人血浆中的总游离 RO4929097(一种针对 Notch 信号的γ-分泌酶抑制剂)。样品制备采用乙酸乙酯进行液液萃取。色谱分离在 Waters X-Terra™ MS C(18)柱上进行,采用甲醇/0.45%甲酸水溶液(60:40,v/v)作为等度流动相,流速为 0.2ml/min,洗脱时间为 6min。总 RO4929097 的定量下限(LLOQ)为血浆中的 5ng/ml,游离药物在磷酸盐缓冲液(PBS)中的 LLOQ 为 0.5ng/ml。总药物在血浆中的浓度范围为 5-2000ng/ml,游离药物在 PBS 中的浓度范围为 0.5-200ng/ml,RO4929097 的校准曲线均呈线性。日内和日间准确度和精密度均符合生物分析方法的一般可接受标准(<15%)。该方法已成功用于描述癌症患者口服 RO4929097 后的总游离和血浆药代动力学特征。

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