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HPLC-MS/MS 法研究口服去氟喹替尼在大鼠体内的药代动力学。

Pharmacokinetic study of deufruquintinibs in rats by HPLC-MS/MS after oral administration.

机构信息

College of Medical Science, China Three Gorges University, Yichang, China.

Affiliated Renhe Hospital of China Three Gorges University, Yichang, China.

出版信息

Biomed Chromatogr. 2022 Nov;36(11):e5459. doi: 10.1002/bmc.5459. Epub 2022 Jul 31.

Abstract

A sensitive and specific high-performance liquid chromatography-tandem mass spectrometry method was established to quantitatively determine the pharmacokinetics of fruquintinib (HMPL-013) and its derivatives [deufruquintinib-3D (HMPL-013-3D), deufruquintinib-6D (HMPL-013-6D) and deufruquintinib-9D (HMPL-013-9D)] in rats. Detection was performed on a triple quadrupole mass spectrometer in multiple reaction monitoring mode. The method established in this assay was successfully applied to a pharmacokinetic study of HMPL-013 and HMPL-013-Ds after oral administration. These results showed that HMPL-013-Ds had longer half-life and larger area under the plasma concentration-time curve than HMPL-013, especially HMPL-013-6D, which provides a significant basis for innovative ideas for drug structure transformation to reduce drug administration frequency and dosage.

摘要

建立了一种灵敏、特异的高效液相色谱-串联质谱法,用于定量测定 fruquintinib(HMPL-013)及其衍生物[去呋喃基 quinintinib-3D(HMPL-013-3D)、去呋喃基 quinintinib-6D(HMPL-013-6D)和去呋喃基 quinintinib-9D(HMPL-013-9D)]在大鼠体内的药代动力学。检测采用三重四极杆质谱仪在多重反应监测模式下进行。该方法成功应用于 HMPL-013 和 HMPL-013-Ds 口服后的药代动力学研究。这些结果表明,HMPL-013-Ds 的半衰期比 HMPL-013 更长,血浆浓度-时间曲线下面积更大,尤其是 HMPL-013-6D,这为药物结构转化以降低给药频率和剂量的创新思路提供了重要依据。

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