丁香苦苷缓释片在家兔体内的药动学及生物等效性研究  

Study on Pharmacokinetics and Bioequivalence of Syingopicroside Sustained-release Tablets in Rabbits

作　　者：李生金[1] 李永吉[1] 吕邵娃[1] 孙爽[1] 许冬冬[1] 徐艳明[1] 董立财[1] 

机构地区：[1]黑龙江中医药大学药学院药剂学教研室,哈尔滨150040

出　　处：《中国实验方剂学杂志》2010年第13期4-6,共3页Chinese Journal of Experimental Traditional Medical Formulae

基　　金：哈尔滨市科技创新人才研究专项资金项目(2007RFXXS059)

摘　　要：目的:对自制丁香苦苷缓释片进行家兔体内的药动学及生物等效性评价。方法:6只健康家兔随机按照交叉试验方案设计,禁食12 h后单剂量口服缓释片剂(受试制剂T)和普通片剂(参比制剂R),于不同时间点在家兔耳缘静脉取血,处理后用高效液相色谱法检测血浆中丁香苦苷药物浓度,利用统计矩原理和可信区间法计算相关的药动学参数及判定两制剂是否生物等效。结果:受试制剂的相对生物利用度为132.6%,对比于受试制剂Tmax显著延长,峰形平缓;90%置信区间分别为AUC0-t:115.25%～144.44%,Cmax:51.33%～78.53%。结论:受试制剂与参比试剂做比较有良好的缓释效果。Objective： To evaluate the pharmacokinetics and bioequivalence of syingopicroside self-sustained-release tablets in rabbits.Method： The blood concent ration of syingopicroside of 6 rabbits was determined by HPLC and the pharmacokinetic parameters were calculated with statistical moment and confidence interval after administered random crossover with single dose of self-sustained-release syingopicroside tablets（test pharmaceutics,T） or the self-common tablets（reference pharmaceutics,R）.Result：The relative bioavailability of self-sustainedrelease syingopicroside tablets was 132.6%.In comparison with self-common tablets,the Tmaxextended significantly and the peak was prolonged gentle;the 90% confidence interval of AUC0-t was 115.25%-144.44%;the 90% confidence interval of Cmax was 51.33%-78.53%.Conclusion： A good slow-release effect was found when compared test formulation with the reference reagent.

关 键 词：丁香苦苷 缓释片 药物动力学 生物等效性 

分 类 号：R283.6[医药卫生—中药学]