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中国临床药理学与治疗学 ›› 1998, Vol. 3 ›› Issue (1): 14-17.

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维脑路通及其各组分在7 例患者的药物动力学

袁成, 朱丽青, 王景祥, 曹晓芝1   

  1. 济南军区总医院临床药理科, 济南250031;
    1山东建材学院校医院
  • 收稿日期:1997-11-24 出版日期:1998-03-26 发布日期:2020-12-04
  • 作者简介:袁成, 男, 34 岁, 副主任药师, 主要从事临床药理学工作。王景祥, 男, 63 岁, 副主任药师, 科主任, 全军临床药理基地(济南)负责人。

Pharmacokinetics of venoruton and its compositions in patients with cardiouascular disorder

YUAN Cheng, ZHU Li-Qing,WANG Jing-Xiang, CAO Xiao-Zhi   

  1. Department of Pharmacology,General Hospital of Jinan Military Command, Jinan 250031
  • Received:1997-11-24 Online:1998-03-26 Published:2020-12-04

摘要: 目的 观察维脑路通及其各组分在人体内的药物动力学。方法 7 例患者静脉滴注维脑路通注射液600 mg 后, 用一种程序控制检测灵敏度的反相高效液相色谱法测定不同时间血清中维脑路通和各种羟乙基芦丁含量, 并分别计算其药物动力学。结果 维脑路通和一、二羟乙基芦丁在血清中的药物动力学为一室开放模型, 三、四羟乙基芦丁为二室开放模型, 各组分生物半衰期随羟乙基数目增加而缩短。结论 维脑路通的动力学过程与其组分并不呈现一致性。

关键词: 维脑路通, 羟乙基芦, 丁药物动力学, 高效液相色谱法

Abstract: Aim The pharmacokinetics of venoruton and its chief compositions, various hydro xyethyl-rutin was observed in seven patients with cardio vascular disorder.Methods After int ravenous injection of uenoruton, the serum drug concent rations at regulart ime were measured by HPLC method with programme-controled sensitivity and the pharmacokine tical parameters were computed by the prog ramme PKBP-N 1.Results Venoruton in the patients was found to conform to an opened sing le-compartment model with t1/2=5.8±1.7 h, Vc=111.1±32.0 L, AUC=37.5±10.8 mg/(h·L)and Cl=5.7±2.2 L/h.Hydroxyethyl rutin and dihydrox yethy l rutin confo rmed to the same model as venoruto n, but trihydrox yerthyl and tetrahydroxyethyl rutin conformed to an opened dubble-compartment model.The more hydroxyethy l number, the less t1/2.Conclusion Venoruton's pha rmacokinetics is different with that of its composition.This HPLC method built in the test is a suitable for determining venoruton in the body.

Key words: venoruton, hydorxyethy l-rutin, Pharmacokinetics, HPLC

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