摘要
大鼠ｉｖ本品的时量曲线属二室开放模型。给大鼠ｉｖ本品５及１０ｍｇ·ｋｇ－１后，药物自血浆的清除呈线性动力学。该药给大鼠ｉｖ及ｉｇ后，体内分布广、消除迅速，原形药可进入脑组织。本品自大鼠尿、粪、胆汁的排出量均很少。
Areverse-phaseHPLCmethodfordeterminationofvinpocetineinbiologicalsamp
les was developed.The method was simple,highly specific and accurate.
After iv administrationof vinpocetine in rats , the plasma
concentration- time curves of vinpocetine was found to be fitted to
atwo-compartment open model. Dosing 5 and l0 mg· kg-1 vinpocetine in
rats,the elimination of thedrug from plasma accorded with linear
kinetics and the elimination half-lives were shown to be 1. 76±0.27
h.The volumesofdistribution were 7.30±0.49 L·kg-1(5 mg·kg-1)and 6.
07±0.67 L·kg-1(10 mg· kg-1)respectively.The drug levels were high
in the lung, spleen,liver and kidney,moderate in brain,fat and testis
and low in heart,muscle and blood. Our results demonstrate
thatvinpocetine was eliminated in a rapid rate and distributed widely
in the body. The bioavailability ofvinpocetine after ig
administration was 5 4.54%in rats.A small amount of unchanged
vinpocetinewas detected in urine, feces and bile after iv and ig
administration.
出处
《药学学报》
CAS
CSCD
北大核心
1994年第2期81-85,共5页
Acta Pharmaceutica Sinica
