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恩诺沙星及其代谢产物在中华绒螯蟹血淋巴中的比较药代动力学
引用本文:郑宗林,叶金明,李代金,杨先乐,胡鲲,唐俊.恩诺沙星及其代谢产物在中华绒螯蟹血淋巴中的比较药代动力学[J].海洋渔业,2011,33(1).
作者姓名:郑宗林  叶金明  李代金  杨先乐  胡鲲  唐俊
作者单位:1. 西南大学水产系,重庆,402460
2. 江苏省扬州市水产生产技术指导站,扬州,225000
3. 农业部渔业动植物病原库,上海海洋大学,上海,201306
基金项目:科技部项目"重要技术标准研究",国家科技攻关项目
摘    要:研究了不同水温(16℃、25℃)、不同给药剂量(10 mg/kg、20 mg/kg)和不同给药方式(肌注、口灌)等条件下,恩诺沙星及其代谢产物环丙沙星在中华绒螯蟹体内的药代动力学,比较了不同条件下药物在蟹血淋巴中的吸收、分布和代谢的差异。结果表明,恩诺沙星在蟹血淋巴中的药-时数据符合开放式二室模型。16℃时以10 mg/kg剂量肌注给药后,恩诺沙星在蟹血淋巴的主要药代动力学参数为:AUC96.818 mg/(L.h),Cmax6.54μg/mL,t1/2α0.851 h,t1/2β95.415 h;25℃时以10 mg/kg剂量肌注给药后,恩诺沙星的主要药代动力学参数为:AUC168.457 mg/(L.h),Cmax7.12μg/mL,t1/2α0.58h,t1/2β88.833 h;25℃时以20 mg/kg剂量肌注给药后,恩诺沙星的主要药代动力学参数为:AUC155.612 mg/(L.h),Cmax11.045μg/mL,t1/2α5.239h,t1/2β88.378 h;25℃时以10 mg/kg剂量口灌给药后,恩诺沙星的主要药代动力学参数为:AUC86.525 mg/(L.h),Cmax3.469μg/mL,t1/2α8.071h,t1/2β61.842 h。不同条件下,恩诺沙星在蟹血淋巴中的主要药代动力学参数差异较大。恩诺沙星的活性代谢产物环丙沙星在各种给药条件下的蟹血淋巴中均能检出,但含量均处于较低值,且药-时数据不能用房室模型拟合,表明恩诺沙星在蟹体内只有极少部分代谢为环丙沙星。

关 键 词:恩诺沙星  环丙沙星  中华绒螯蟹  高效液相色谱  药代动力学

On comparative pharmacokinetic of Enrofloxacin in Hemolymph of Chinese mitten-handed crab,Eriocheir sinensis
ZHENG Zong-lin,YE Jin-ming,LI Dai-jin,YANG Xian-le,HU Kun,TANG Jun.On comparative pharmacokinetic of Enrofloxacin in Hemolymph of Chinese mitten-handed crab,Eriocheir sinensis[J].Marine Fisheries,2011,33(1).
Authors:ZHENG Zong-lin  YE Jin-ming  LI Dai-jin  YANG Xian-le  HU Kun  TANG Jun
Abstract:Several comparative pharmacokinetic data such as absorption,distribution and metabolism had been studied on enrofloxacin(ENR) in Chinese mitten-handed crab,Eriocheir sinensis with different water temperature,dose and dosage regime(oral administration and intramuscular injection).Results indicated that the hemolymph concentration-time data of Enrofloxacin in Eriocheir sinensis were best described by a two-compartment open model under different conditions.The main pharmacokinetics parameters by intramuscular administration with 10 mg/kg b.w.at 16 ℃: AUC 96.818mg /(L·h),Cmax 6.54 μg/mL,t1/2α 0.851h,t1/2β 95.415 h;the main pharmacokinetics parameters by intramuscular administration with 10 mg/kg b.w.at 25 ℃: AUC 168.457 mg /(L·h),Cmax 7.12 μg/mL,t1/2α 0.58h,t1/2β 88.833 h;the main pharmacokinetics parameters by intramuscular administration with 20 mg/kg b.w.at 25 ℃: AUC 155.612 mg /(L·h),Cmax 11.045 μg/mL,t1/2α 5.239 h,t1/2β 88.378 h;the main pharmacokinetics parameters by oral administration with 10 mg/kg b.w.at 25 ℃: AUC 86.525 mg /L·h,Cmax 3.469 μg/mL,t1/2α8.071 h,t1/2β 61.842h.Results showed that the main pharmacokinetic parameters under different conditions were significantly different.The active metabolite ciprofloxacin(CIP) was checked in hemolymph of Eriocheir sinensis in all experiments,but all compartment models were not suitable for concentration-time data,and the concentration was very low,which indicated the poor capability of Eriocheir sinensis metabolizing enrofloxacin into ciprofloxacin.
Keywords:Enrofloxacin  Ciprofloxacin  Eriocheir sinensis  RP-HPLC  Pharmacokinetics
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