华西药学杂志
華西藥學雜誌
화서약학잡지
WEST CHINA JOURNAL OF PHARMACEUTICAL SCIENCES
2001年
1期
31-33
,共3页
黄林清%周世文%周素琴%张诗平%汤建林%黄永平%邱磊
黃林清%週世文%週素琴%張詩平%湯建林%黃永平%邱磊
황림청%주세문%주소금%장시평%탕건림%황영평%구뢰
维拉帕米%硫唑嘌呤%药代动力学%相互作用
維拉帕米%硫唑嘌呤%藥代動力學%相互作用
유랍파미%류서표령%약대동역학%상호작용
目的:研究维拉帕米对硫唑嘌呤代谢物6-巯嘌呤药动学的影响。方法:采用高效液相色谱法(HPLC),以8只健康家兔为实验对象,对硫唑嘌呤单用及与维拉帕米合用后血中硫唑嘌呤代谢物6-巯嘌呤浓度(6-MP)及药动学参数的变化进行观察。结果:合用维拉帕米后,6-MP的表观分布容积(Vd)增加3倍,AUC降低65.8%,清除率(Cls)增加3倍,t1/2β延长1.5倍,其它药动学参数无显著影响。结论:维拉帕米使硫唑嘌呤代谢物6-巯嘌呤的血药浓度明显降低及清除率明显增加。
目的:研究維拉帕米對硫唑嘌呤代謝物6-巰嘌呤藥動學的影響。方法:採用高效液相色譜法(HPLC),以8隻健康傢兔為實驗對象,對硫唑嘌呤單用及與維拉帕米閤用後血中硫唑嘌呤代謝物6-巰嘌呤濃度(6-MP)及藥動學參數的變化進行觀察。結果:閤用維拉帕米後,6-MP的錶觀分佈容積(Vd)增加3倍,AUC降低65.8%,清除率(Cls)增加3倍,t1/2β延長1.5倍,其它藥動學參數無顯著影響。結論:維拉帕米使硫唑嘌呤代謝物6-巰嘌呤的血藥濃度明顯降低及清除率明顯增加。
목적:연구유랍파미대류서표령대사물6-구표령약동학적영향。방법:채용고효액상색보법(HPLC),이8지건강가토위실험대상,대류서표령단용급여유랍파미합용후혈중류서표령대사물6-구표령농도(6-MP)급약동학삼수적변화진행관찰。결과:합용유랍파미후,6-MP적표관분포용적(Vd)증가3배,AUC강저65.8%,청제솔(Cls)증가3배,t1/2β연장1.5배,기타약동학삼수무현저영향。결론:유랍파미사류서표령대사물6-구표령적혈약농도명현강저급청제솔명현증가。
OBJECTIVE:To study effects of verapamil on 6-mercaptopurine pharmacokinetics. METHODS:Serum concentration of 6-mercaptopurine (6-MP) , a active metobilite of azathiopurine (Azp) , was determined by HPLC,and the pharmacokinetic parameters were researched after single administration of Azp and co-administration verapamil(Vp) in 8 rabbits.RESULTS:The results indicated that Vd and Cls of 6-MP increased 3 times , T1/2β raised 1.5 times , AUC decreased 65.8 percent , and other pharmacokinetic parameters have no significant differences after co-administration Vp in 8 rabbits.CONCLUSION:6-MP serum concentration was decreased and clearance rate increased evidently after co-administration verapamil in rabbits.