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一种用于同时测定大鼠药代动力学中梓醇苷 I 及其代谢物梓醇苷 II 的灵敏高效液相色谱-串联质谱法。

A Sample and Sensitive HPLC-MS/MS Method for Simultaneous Determination of Ziyuglycoside I and Its Metabolite Ziyuglycoside II in Rat Pharmacokinetics.

机构信息

National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herb Medicine, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.

State Key Laboratory of Innovative Drug and Efficient Energy-Saving Pharmaceutical Equipment, Jiangxi University of Traditional Chinese Medicine, Nanchang 330006, China.

出版信息

Molecules. 2018 Feb 28;23(3):543. doi: 10.3390/molecules23030543.

Abstract

Ziyuglycoside I (ZGS1) is a promising drug candidate for the treatment of leucopenia. Currently, information on ZGS1 and its in vivo metabolite ziyuglycoside II (ZGS2) is limited. The objective of this study was to investigate the pharmacokinetics, tissue distribution, and excretion of ziyuglycoside I (ZGS1) and its metabolite ziyuglycoside II (ZGS2) in rats. In our study, a simple and sensitive high-performance liquid chromatography-mass spectrometry (HPLC-MS/MS) method was established for simultaneous determination of ZGS1 and its metabolite for Sprague-Dawley rat pharmacokinetics studies. The method was validated following internationally-approved guidelines. The results presented in this study indicated that subcutaneous administration of ZGS1 prolonged its extension time and increased the area under the curve (AUC) of ZGS2 during 0 to t minutes. In summary, in this study, the pharmacokinetic characteristics of ZGS1 and its metabolite ZGS2 were defined and its tissue distribution, and excretion in rats were described. Our finding may be beneficial for leucopenia drug that focus on ZGS1.

摘要

梓醇苷 I(ZGS1)是一种很有前途的治疗白细胞减少症的药物候选物。目前,关于 ZGS1 及其体内代谢物梓醇苷 II(ZGS2)的信息有限。本研究旨在研究梓醇苷 I(ZGS1)及其代谢物梓醇苷 II(ZGS2)在大鼠体内的药代动力学、组织分布和排泄情况。在我们的研究中,建立了一种简单灵敏的高效液相色谱-质谱联用(HPLC-MS/MS)方法,用于同时测定 ZGS1 及其代谢物用于 Sprague-Dawley 大鼠药代动力学研究。该方法按照国际认可的指南进行了验证。本研究结果表明,ZGS1 的皮下给药延长了其半衰期,并在 0 至 t 分钟期间增加了 ZGS2 的曲线下面积(AUC)。总之,在这项研究中,定义了 ZGS1 及其代谢物 ZGS2 的药代动力学特征,并描述了它们在大鼠中的组织分布和排泄情况。我们的发现可能对以 ZGS1 为重点的白细胞减少症药物有帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a93/6017276/f4487248fc3b/molecules-23-00543-g001.jpg

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