奥拉西坦在大鼠和小鼠的药代动力学研究  

PHARMACOKINETICS OF OXIRACETAM IN RATS AND MICE

作　　者：刘昌孝[1,2] 顾以保[1,2] 李全胜[1,2] 

机构地区：[1]国家医药管理局天津药物研究院 [2]天津药物动力学与临床药理研究室

出　　处：《药学学报》1999年第2期85-89,共5页Acta Pharmaceutica Sinica

基　　金：国家"七.五"攻关项目

摘　　要：目的：研究奥拉西坦（ＯＲＣ）在大鼠和小鼠的药代动力学。方法：采用ＨＰＬＣ法测定生物样品中ＯＲＣ浓度，在大鼠和小鼠进行其药代动力学、吸收、分布、排泄试验。结果：大鼠灌胃给ＯＲＣ１００，２００和４００ｍｇ·ｋｇ－１后表明，本品ｐｏ吸收速率快，达峰时间短，药物自血清消除较快。小鼠１次ｉｇ给药１００ｍｇ·ｋｇ－１后，８０％以上药物在给药后３ｈ内由消化道消失；药物吸收后能分布到各种组织脏器，给药后３６ｈ累计尿排泄原形药物量约为药物剂量的８０％；蛋白结合率低，平均结合率为１０５％。结论：奥拉西坦是一吸收快、消除快、主要以原形药物由尿排泄、蛋白结合率低的药物。AIM: To study the pharmacokinetics, absorption, distribution and excretion of oxiracetam(ORC) in rats and mice. METHODS: The drug concentration was determined by using an HPLC system with pre treatment column for biological samples. RESULTS: The concentration time curves in rat serum showed an open one compartment model after ig doses of 100, 200 and 400 mg·kg -1 . The half life of absorption phase( T 1/2ka ) and peak time ( T peak)were found to be 0 11～0 36 h and 0 79～1 41 h, respectively. The elimination half life( T 1/2ke ) and mean residence time(MRT) were 3 18～4 05 h and 3 38～4 18 h, respectively. The mouse test with ig dose of 100 mg·kg -1 showed that 80% of the administered dosage was eliminated from the gastro intestinal tract 3 h after administration. One hour after dosing, ORC was widely distributed to various tissues and the tissue drug levels from high to low were heart, liver, kindey, brain, muscle, spleenm, intestine, stomach, testis, fat, lungs and ovary. ORC was excreted by about 80% of the administered dosage from urine within a 36 h period. Plasma protein binding ratio of ORC was found to be 10 5% at the concentration range of 50～200 μg·ml -1 . CONCLUSION: ORC is well absorbed when given orally and rapidly eliminated via the urine. The protein binding was found to be low.

关 键 词：奥拉西坦 药物代谢动力学 蛋白结合率 

分 类 号：R971[医药卫生—药品] R969.1[医药卫生—药学]