Suppr超能文献

口服丹参-牡丹皮药对后正常、假手术和心肌缺血再灌注损伤大鼠体内 7 种生物活性成分的比较药代动力学。

Comparative pharmacokinetics of seven bioactive components in normal, sham-operated, and myocardial ischemia-reperfusion injury rats after oral administration of the Salvia Miltiorrhiza-Moutan Cortex herb pair.

机构信息

Department of Pharmacy, Hebei Province General Center, National Clinical Drug Monitoring Center, Shijiazhuang, China.

出版信息

Biomed Chromatogr. 2021 Mar;35(3):e5016. doi: 10.1002/bmc.5016. Epub 2020 Dec 2.

Abstract

Recently the Salvia Miltiorrhiza-Moutan Cortex (SM-MC) herb pair is considered as a promising Chinese medicinal mixture exhibiting a range of pharmacological activities, including treating cardiovascular disease due to its unique composition. In this study, we conducted the comparative pharmacokinetic analysis of seven main bioactive components of SM-MC in a different model rat. A straightforward ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) strategy that could simultaneously evaluate the levels of seven compounds was used to ensure the reliability of these pharmacokinetic analyses in rat plasma. The rat plasma samples were collected from normal, sham-operated, and myocardial ischemia-reperfusion injury (MIRI) groups at predetermined time points after the administration of SM-MC. The main pharmacokinetic parameters were detected and calculated. We successfully assessed the maximum concentration (C ), time to C (T ), the elimination rate constant (λ ), total half-life (t ), total body clearance (CL), and the area under the concentration-time curve from 0 to last sampling time (AUC ) and extrapolated to infinity (AUC ). To sum up, an optimized UPLC-MS/MS approach that could be used to rapidly, simultaneously, and sensitively detect seven bioactive compounds derived from SM-MC extract preparations was successfully developed, which may offer a pharmacokinetic basis for preclinical and clinical studies of SM-MC herb pair for treating MIRI.

摘要

最近,丹参-牡丹皮(SM-MC)药对被认为是一种很有前途的中药混合物,由于其独特的组成,具有多种药理活性,包括治疗心血管疾病。在本研究中,我们在不同模型大鼠中对 SM-MC 的七种主要生物活性成分进行了比较药代动力学分析。采用一种简单的超高效液相色谱-串联质谱(UPLC-MS/MS)策略,能够同时评估七种化合物的水平,以确保这些药代动力学分析在大鼠血浆中的可靠性。大鼠血浆样品分别从正常组、假手术组和心肌缺血再灌注损伤(MIRI)组在给药后预定时间点采集。检测并计算主要药代动力学参数。我们成功评估了最大浓度(C)、达到最大浓度的时间(T)、消除率常数(λ)、总半衰期(t)、总清除率(CL)和从 0 到最后采样时间的浓度-时间曲线下面积(AUC)和外推至无穷大(AUC)。总之,成功开发了一种优化的 UPLC-MS/MS 方法,可用于快速、同时、灵敏地检测 SM-MC 提取物中七种生物活性化合物,为 SM-MC 药对治疗 MIRI 的临床前和临床研究提供了药代动力学基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验