Eleutherin、Eleutherin和Eleutherol在大鼠体内药动学和组织分布的UPLC-MS/MS方法的建立

Pengcheng Guo, Jie-yu Chen, Jing Su, F. Raza, Bin Hao, Xinyi Wu, Yi-Qing Cheng, M. Qiu
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引用次数: 1

摘要

刺黄球是一种经典的傣族传统药物,在云南被广泛用于冠心病的临床治疗。萘醌是刺五菊治疗冠心病的主要活性化合物,主要含有异刺五菊苷、刺五菊苷和刺五菊醇。本研究旨在研究异戊二烯醚苷、戊二烯醚苷和戊二烯醚醇的体内参数。本实验采用雄性SD大鼠口服三种化合物,并采集血液和组织标本。建立了一种新的超高效液相色谱-串联质谱(UPLC-MS/MS)方法来测定化合物的绝对口服生物利用度和组织分布特征。选择乙腈和0.1% (v/v)甲酸溶液为色谱流动相。采用C18柱。方法以倍他米松为内标。采用扫描型多反应监测仪在正离子模式下进行MS/MS检测。我们的数据显示该方法的线性,r大于0.9983。异戊二烯醚苷、戊二烯醚苷和戊二烯醇的定量下限分别为1.00、3.84和0.498 ng/mL。总精密度小于12.68%,加样回收率为85.44 ~ 103.83%,血浆中化合物的准确度为91.56 ~ 110.75%。稳定性分析表明,在不同条件下,它们在血浆中的稳定性为87.83 ~ 114.62%。口服异刺甲醚、刺甲醚和刺甲醚醇的半衰期分别为6.11、7.30和3.07小时。绝对口服生物利用度分别为5.38%、4.64%和2.47%。3种成分在小肠中的分布最高。综上所述,所建立的方法可成功用于SD大鼠体内三组分参数的测定。本工作为今后棘球菊新药的开发提供参考。
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Development of a UPLC-MS/MS Method for Pharmacokinetic and Tissue Distribution of Isoeleutherin, Eleutherin, and Eleutherol in Bulbus eleutherinis in Rats
Bulbus eleutherinis is a classical traditional Dai medicine, and has been widely used in clinical treatment of coronary heart disease (CHD) in Yunnan, China. Naphthoquinone, as the main active compound in Bulbus eleutherinis in treating CHD, mainly contain isoeleutherin, eleutherin, and eleutherol. This study aimed to investigate the in vivo parameters of isoeleutherin, eleutherin, and eleutherol. In this work, male Sprague Dawley (SD) rats were treated with the three compounds by oral administration, and then blood and tissue samples were collected. A novel UPLC-MS/MS (ultra-performance liquid chromatography-tandem mass spectrometry) method has been developed to determine the absolute oral bioavailability, and the tissue distribution profile of the compounds. Acetonitrile and 0.1% (v/v) solution of formic acid were selected as the mobile phase of the chromatogram. C18 column was employed. Betamethasone was used as an internal standard in the method. The detection was performed with a multireaction monitor of scan type in positive ion mode by MS/MS. Our data showed linearity of the method with r over 0.9983. Lower limits of quantification of isoeleutherin, eleutherin, and eleutherol were 1.00, 3.84, and 0.498 ng/mL, respectively. The overall precision of the compounds was less than 12.68%, recoveries ranged from 85.44 to 103.83%, and the accuracy of the compounds in plasma was between 91.56 and 110.75%. The stability assay showed that they were stable (87.83–114.62%) under different conditions in plasma. For oral administration, the half-lives of isoeleutherin, eleutherin, and eleutherol was 6.11, 7.30, and 3.07 hours, respectively. The absolute oral bioavailabilities were 5.38, 4.64, and 2.47%, respectively. Moreover, the three components had the highest distribution in small intestine. In conclusion, the established method was successfully applied to the determination of the in vivo parameters of the three components in SD rats. This work provides a reference for the development of new drugs of Bulbus eleutherinis in the future.
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