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大鼠血浆及肺/脑组织中奥希替尼浓度的测定。

Determination of osimertinib concentration in rat plasma and lung/brain tissues.

作者信息

Zuo Yalan, Yang Peidan, Yang Ruixia, Hou Juan, Feng Rui, Liang Ping, Liu Jiang

机构信息

Department of Pharmacy, The Fourth Hospital of Hebei Medical University Shijiazhuang 050000, Hebei, China.

College of Pharmacy, Hebei Medical University Shijiazhuang 050000, Hebei, China.

出版信息

Am J Transl Res. 2024 Dec 15;16(12):8008-8022. doi: 10.62347/SYZD2489. eCollection 2024.

Abstract

OBJECTIVES

The aim of this study was to establish an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the detection of osimertinib in rat plasma, lung and brain tissues.

METHODS

Forty-eight rats were randomly divided into an experimental group (receiving osimertinib at doses of 5, 8, and 10 mg/kg) and a control group. After continuous intragastric administration for 15 days, samples of blood, lung, and brain tissue were collected. Chromatographic separation was achieved using a BEH C18 column with gradient elution, employing a mobile phase of water (containing 0.1% (v/v) formic acid) and acetonitrile. The concentration of osimertinib in the samples was determined using an AB SCIEX 5500 triple quadrupole mass spectrometer operated in positive electrospray ionization (ESI+) and multiple reaction monitoring (MRM) mode.

RESULTS

A UPLC-MS/MS analytical method for determining osimertinib concentrations was successfully established and validated. A linear relationship was observed for osimertinib concentrations in plasma within the range of 1-300 ng/mL, and in lung and brain tissues within the range of 0.5-50 ng/mL. The selectivity, accuracy, precision, matrix effect, extraction recovery, and stability all meet the requirements of methodological validation criteria.

CONCLUSIONS

A rapid and sensitive UPLC-MS/MS method was developed and validated for quantifying osimertinib concentrations in rat plasma, lung, and brain tissues, providing a valuable tool for pharmacokinetic and tissue distribution studies.

摘要

目的

本研究旨在建立一种超高效液相色谱-串联质谱(UPLC-MS/MS)法,用于检测大鼠血浆、肺组织和脑组织中的奥希替尼。

方法

将48只大鼠随机分为实验组(分别接受5、8和10 mg/kg剂量的奥希替尼)和对照组。连续灌胃给药15天后,采集血液、肺组织和脑组织样本。采用BEH C18色谱柱,以水(含0.1%(v/v)甲酸)和乙腈为流动相进行梯度洗脱实现色谱分离。使用AB SCIEX 5500三重四极杆质谱仪,在正电喷雾电离(ESI+)和多反应监测(MRM)模式下测定样本中奥希替尼的浓度。

结果

成功建立并验证了一种用于测定奥希替尼浓度的UPLC-MS/MS分析方法。奥希替尼在血浆中浓度范围为1-300 ng/mL、在肺组织和脑组织中浓度范围为0.5-50 ng/mL时呈现线性关系。选择性、准确度、精密度、基质效应、提取回收率和稳定性均符合方法学验证标准的要求。

结论

开发并验证了一种快速灵敏的UPLC-MS/MS方法,用于定量大鼠血浆、肺组织和脑组织中的奥希替尼浓度,为药代动力学和组织分布研究提供了有价值的工具。

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