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A phase II study of the gamma secretase inhibitor RO4929097 in patients with previously treated metastatic pancreatic adenocarcinoma.γ-分泌酶抑制剂RO4929097用于既往接受过治疗的转移性胰腺腺癌患者的II期研究。
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4
A phase Ib combination study of RO4929097, a gamma-secretase inhibitor, and temsirolimus in patients with advanced solid tumors.RO4929097(一种γ-分泌酶抑制剂)联合替西罗莫司治疗晚期实体瘤患者的 Ib 期联合研究。
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本文引用的文献

1
Simultaneous determination of ABT-888, a poly (ADP-ribose) polymerase inhibitor, and its metabolite in human plasma by liquid chromatography/tandem mass spectrometry.采用液相色谱/串联质谱法同时测定人血浆中的多聚(ADP-核糖)聚合酶抑制剂 ABT-888 及其代谢物。
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Feb 1;878(3-4):333-9. doi: 10.1016/j.jchromb.2009.11.037. Epub 2009 Nov 27.
2
Preclinical profile of a potent gamma-secretase inhibitor targeting notch signaling with in vivo efficacy and pharmacodynamic properties.一种靶向Notch信号传导、具有体内疗效和药效学特性的强效γ-分泌酶抑制剂的临床前概况。
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A Notch updated.一个经过更新的Notch。
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The molecular programme of tumour reversion: the steps beyond malignant transformation.肿瘤逆转的分子程序:恶性转化之外的步骤。
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Rational targeting of Notch signaling in cancer.癌症中Notch信号通路的合理靶向治疗
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Key elements of bioanalytical method validation for small molecules.小分子生物分析方法验证的关键要素。
AAPS J. 2007 Mar 30;9(1):E109-14. doi: 10.1208/aapsj0901011.
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Binding of gefitinib, an inhibitor of epidermal growth factor receptor-tyrosine kinase, to plasma proteins and blood cells: in vitro and in cancer patients.表皮生长因子受体 - 酪氨酸激酶抑制剂吉非替尼与血浆蛋白及血细胞的结合:体外研究及癌症患者体内研究
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Characterization of tissue specific expression of Notch-1 in human tissues.
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Notch signaling: cell fate control and signal integration in development.Notch信号通路:发育过程中的细胞命运控制与信号整合
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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.

DOI:10.1016/j.jchromb.2011.03.045
PMID:21497565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3771103/
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。