Liu Yingze, Su Chong, Zhang Yuyao, Zhang Di, Li Yaoshuang, Gu Jingkai, Wang Ensi, Sun Dong
School of Pharmaceutical Sciences, Jilin University, Changchun, 130012, PR China; Beijing Institute of Drug Metabolism, Beijing, 102209, PR China.
Zhuhai United Laboratories co.,LTD, PR China.
Anal Biochem. 2021 Dec 15;635:114435. doi: 10.1016/j.ab.2021.114435. Epub 2021 Oct 29.
A high-throughput quantitative analytical method based on Direct Analysis in Real Time tandem mass spectrometry (DART-MS/MS) has been developed and validated for the determination of diazepam in rat plasma, whereby analyzing of each sample needs merely 25 μL plasma, simple solid phase extraction sample preparation and 15 s acquisition time. The multiple reaction monitoring (MRM) transitions at m/z 285.2 → 193.1 and 316.0 → 270.0 were selected for the monitoring of diazepam and its internal standard clonazepam respectively. A good linearity within the range of 10-2000 ng/mL, an intra- and inter-day precisions within <7.78% as to an accuracy ranging from 1.04% to 7.92% have been achieved. The method has been successfully applied to the pharmacokinetic study of diazepam in rats' plasma after a single intragastric administration at a dose of 10 mg/kg. The results indicate that this method fulfills the requirements of the bioanalysis in sensitivity and accuracy. It shows considerable promise for application of DART-MS to the quantitative investigation of other drugs.
已开发并验证了一种基于实时直接分析串联质谱法(DART-MS/MS)的高通量定量分析方法,用于测定大鼠血浆中的地西泮。该方法分析每个样品仅需25μL血浆,样品制备采用简单的固相萃取,采集时间为15秒。选择m/z 285.2→193.1和316.0→270.0的多反应监测(MRM)跃迁分别监测地西泮及其内标氯硝西泮。在10 - 2000 ng/mL范围内具有良好的线性,日内和日间精密度均<7.78%,准确度范围为1.04%至7.9%。该方法已成功应用于大鼠单次灌胃给药10 mg/kg后血浆中地西泮的药代动力学研究。结果表明,该方法在灵敏度和准确度方面满足生物分析的要求。它显示出DART-MS在其他药物定量研究中的应用前景。