摘要
按60mg kg的剂量给草鱼灌服呋喃唑酮,用高效液相色谱法检测用药后不同时间的血浆、肝脏、肾脏及肌肉中药物浓度,然后用MCPKP药代动力学软件处理药时数据,对药物在草鱼体内消除及组织残留进行研究.结果表明:单剂量口灌呋喃唑酮在草鱼血液中主要药动学参数为:AUC3.7569μg·h mL,Cmax0.5176μg mL,t1 2α1.5249h,t1 2β22.8632h,Tpeak2.2296h,k101.0158h-1,k120.1249h-1,k210.06547h-1;给药后72h肌肉和血浆中检测不到药物,7d后肝、肾中药物消除.
It is about studies on the depletion and residues of furazolidone in Ctenopharyngodon idelles after single administration. Tissues(plasma, muscle, liver and kidney) concentration of furazolidone were measured by HPLC. The plasma concentration-time data was analyzed with MCPKP practical pharmacokinetics software. The results showed that the main parameters in the blood of grass carp were :AUC 3.756 9 μg/mL, Cmax 0.517 6 μg/mL,t_(1/2α)1.524 9 h,t_(1/2β)22.863 2 h,T_(peak)2.229 6 h,k_(10) 1.015 8 h^(-1),k_(12) 0.124 9 h^(-1),k_(21)0.065 4 7 h^(-1),At seventy-two hours after dosing, the residues of furazolidone in plasma and muscle can not be detected, but the depletion of furazolidone in liver and kidney needs seven days.
出处
《湖北大学学报(自然科学版)》
CAS
2003年第4期346-349,共4页
Journal of Hubei University:Natural Science
基金
农业部渔业局重点项目(95-B-00-01)
湖南文理学院科研基金(编号:JJ0204)资助