摘要
目的研究芸香甙在兔体内的药代动力学。方法家兔一次静注芸香甙5mg·kg-1后,利用荧光分光光度法测定不同时间的血药浓度。应用3P87药动学软件程序对数据进行计算机处理。结果芸香甙的药时(C-T)方程为:C=85.9789e-0.9044T+34.5105e-0.0587T+4.3838e-0.0046T。芸香甙的主要药代动力学参数如下:T1/2a:(0.7609±0.1066)min,T1/2b:(12.5667±3.7139)min,T1/2c:(162.5651±50.6035)min,K12:(0.5123±0.1316)min-1,K21:(0.3298±0.0737)min-1,K13:(0.0739±0.0182)min-1,K31:(0.0100±0.0037)min-1,K10:(0.0774±0.0160)min-1,Vc:(0.0404±0.0044)L·kg-1,AUC:(1679.7583±480.6045)mg·L-1·min-1,CL(s):(0.0031±0.0008)L·kg-1·min-1。结论芸香甙在兔体内的C-T变化符合三室开放模型;芸香甙在体内的分布、消除迅速。
AIM To study the pharmacokinetics of rutoside in rabbits. METHODS After administration of rutoside (5 mg·kg-1, iv), the plasma concentration at different times were determined by fluorescence spectrophotometry. The data were proccssed with 3P87 pharmacokinetic procedure. RESULTS The concentrationtime (CT) equation is: C=859789 e-0.9044 T+345105 e-0.0587 T+43838 e-0.0046 T. The pharmacokinetic parameters are as follows: T1/2a:(07609±01066) min,T1/2b:(125667±37139) min,T1/2c:(1625651±506035) min,K12:(05123±01316) min-1,K21:(03298±00737) min-1,K13:(00739±00182) min-1,K31:(00100±00037) min-1,K10:(00774±00160) min-1, Vc:(00404±00044) L·kg-1,AUC:(16797583±4806045) mg·L-1·min,CLs:(00031±00008) L·kg-1·min-1. CONCLUSION In the body of rabbit, the CT change of rutoside conforms to an open three compartment model, the distribution and the elimination of rutoside are rapid.
出处
《中国药理学通报》
CAS
CSCD
北大核心
1998年第2期178-180,共3页
Chinese Pharmacological Bulletin
关键词
芸香甙
药代动力学
开放三室模型
参数
rutoside
pharmacokinetics
open three compartment model
parameter