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LC-ESI-MS/MS 法测定新型 FAK 抑制剂 defactinib 在小鼠血浆中的浓度及其在小鼠药代动力学研究中的应用。

LC-ESI-MS/MS determination of defactinib, a novel FAK inhibitor in mice plasma and its application to a pharmacokinetic study in mice.

机构信息

Medicinal Chemistry Department.

Drug Metabolism and Pharmacokinetics, Jubilant Biosys Ltd, Industrial Suburb, Yeshwanthpur, Bangalore 560 022, India.

出版信息

J Pharm Biomed Anal. 2018 Feb 5;149:358-364. doi: 10.1016/j.jpba.2017.11.022. Epub 2017 Nov 10.

Abstract

A sensitive, specific, selective and rapid LC-ESI-MS/MS method has been developed and validated for the quantification of defactinib in mice plasma using CN-tofacitinib as an internal standard (I.S.). Sample preparation was accomplished through a liquid-liquid extraction process. Baseline chromatographic resolution of defactinib and the I.S. was achieved on an Atlantis dC column using an isocratic mobile phase comprising 0.2% formic acid in water and acetonitrile (25:75, v/v) delivered at a flow rate of 0.5mL/min. Defactinib and the I.S. eluted at ∼1.59 and 0.99min, respectively. The total chromatographic run time was 2.50min. A linear response function was established in the concentration range of 0.13-106 ng/mL. Method validation was performed as per regulatory guidelines and the results met the acceptance criteria. The intra- and inter-day accuracy and precision were in the range of 5.57-13.3 and 8.63-12.1%, respectively. Defactinib was found to be stable under various stability conditions. This novel method has been applied to a pharmacokinetic study in mice.

摘要

一种灵敏、特异、选择性和快速的 LC-ESI-MS/MS 方法已经被开发并验证,用于定量检测小鼠血浆中的 defactinib,以 CN-tofacitinib 作为内标 (I.S.)。样品制备通过液液萃取法完成。在 Atlantis dC 柱上,采用包含 0.2%甲酸的水和乙腈(25:75,v/v)作为等度流动相,流速为 0.5mL/min,实现了 defactinib 和 I.S. 的基线色谱分离。defactinib 和 I.S. 分别在约 1.59 和 0.99min 洗脱。总色谱运行时间为 2.50min。在 0.13-106ng/mL 的浓度范围内建立了线性响应函数。方法验证符合法规指南的要求,结果符合验收标准。日内和日间准确度和精密度的范围分别为 5.57-13.3%和 8.63-12.1%。defactinib 在各种稳定性条件下均稳定。该新方法已应用于小鼠的药代动力学研究。

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