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大鼠中莫诺苷的药代动力学及组织分布的高效液相色谱研究

HPLC study of pharmacokinetics and tissue distribution of morroniside in rats.

作者信息

Li Xiaona, Wang Qiao, Zhang Xiaowei, Sheng Xiaona, Zhou Yanan, Li Min, Jing Xiujuan, Li Deqiang, Zhang Lantong

机构信息

Department of Pharmaceutical Analysis, School of Pharmacy, Hebei Medical University, Shijiazhuang 050017, PR China.

出版信息

J Pharm Biomed Anal. 2007 Oct 18;45(2):349-55. doi: 10.1016/j.jpba.2007.05.013. Epub 2007 May 18.

Abstract

Morroniside is an important constituent of traditional Chinese medicines Fructus Corni with several bioactivities. An HPLC method for determination of morroniside in rat plasma and tissues was developed and the pharmacokinetic and tissue distribution characteristics of morroniside after intravenous and oral administrations were investigated. The bio-samples were prepared based on a simple protein precipitation and the separation of morroniside was achieved on a C(18) column with a mobile phase consisted of acetonitrile-methanol-0.1% formic acid (10:10:80, v/v) at a flow rate of 1.0 ml/min. Chromatograms were monitored at 239 nm and the temperature of column was kept at 25 degrees C. Pharmacokinetic study found that morroniside was absorbed and eliminated rapidly in rat and manifested linear dynamics at 10-40 mg/kg range and absolute bioavailability of morroniside was lower. Tissue distribution showed the highest level was observed in small intestine, then in kidney and stomach, but no morroniside was detected in brain, which indicated that small intestine, kidney and stomach were major distribution tissues of morroniside in rats, and morroniside had difficulty in crossing the blood-brain barrier. It was also found there was no long-term accumulation of morroniside in rat tissues.

摘要

山茱萸苷是传统中药山茱萸的一种重要成分,具有多种生物活性。建立了一种测定大鼠血浆和组织中山茱萸苷的高效液相色谱法,并研究了静脉注射和口服给药后山茱萸苷的药代动力学和组织分布特征。生物样品采用简单的蛋白沉淀法制备,山茱萸苷在C(18)柱上分离,流动相为乙腈-甲醇-0.1%甲酸(10:10:80, v/v),流速为1.0 ml/min。在239 nm处监测色谱图,柱温保持在25℃。药代动力学研究发现,山茱萸苷在大鼠体内吸收和消除迅速,在10-40 mg/kg范围内表现为线性动力学,山茱萸苷的绝对生物利用度较低。组织分布显示,小肠中含量最高,其次是肾脏和胃,但在脑中未检测到山茱萸苷,这表明小肠、肾脏和胃是大鼠山茱萸苷的主要分布组织,山茱萸苷难以通过血脑屏障。还发现山茱萸苷在大鼠组织中没有长期蓄积。

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