鸡静注和口服盐酸沙拉沙星的药物动力学研究  被引量:7

PHARMACOKINETICS OF SARFLOXACIN HYDROCHLORIDE IN CHICKENS AFITER INTRAVENOUS AND ORAL ADMINISTRATION

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作  者:操继跃[1,2] 邱银生 王大菊[1,2] 周利娟 周诗其 徐群英[1,2] 严汉池[1,2] 江美安 

机构地区:[1]华中农业大学牧医学院 [2]湖北省医药工业研究院

出  处:《华中农业大学学报》1999年第3期248-251,共4页Journal of Huazhong Agricultural University

摘  要:伊利莎蛋鸡8只单次快速静脉注射盐酸沙拉星10mg/kg(以沙拉沙星计)后,利用高效液相色谱法测定血清中沙拉星的浓度。房室模型分析表明:血药浓度-时间数据适合无吸收因素二室模型,其消除半衰期(tβ)、表观分布容积(Vd)、总体清除率(CLB)和药时曲线下面积(AUC)分别为(2.47±0.87Oh、(5.10±2.25)L/kg、(1.42±0.24)L/kg·h和(7.27±1.37)μg/ml·h。伊利莎蛋鸡8只口服盐酸沙拉沙星溶液10mg/kg(以沙拉沙星计)后,药物在体内呈现有吸收单室模型,其吸收半衰期(tka)、消除半衰期(tke)、血药达峰时间(Tmax)、药峰浓度(Cmax)和药时曲线下面积分别为(0.32±0.15)h、(3.68±0.89)h、(1.25±0.35)h、(0.86±0.28)μg/ml和(5.53±1.95)μg/ml·h。鸡内服盐酸沙拉沙星混悬剂(以淀粉混)10mg/kg(以沙拉沙星计)后,药物吸收不规则,统计矩理论分析表明:药时曲线零阶矩(AUC)、药时曲线一阶矩(MRT,平均驻留时间)和消除半衰期(tke)分别为(1.03±0.27)μg/ml·h、(6.22±0.76?A dose of 10 mg sarafloxaxin/kg body weight was administered intravenously to 8 healthy chickens. Serum sarafloxacin concentrations were determined using HPLC method. The serum concentration time date of sarafloxacin were best described by a two compartment open model. The elimination half life( t 1/2β ), the volume of distribution [ V d(area)], the total body clearance ( C l B) and the area under the curve ( AUC ) were 2.47±0.87 h, 510±2.25 L/kg, 1.42±0.24 L/kg.h and 7.27±1.37 μg/mg.h., respectively. Solution formulation of the drug was given to 8 healthy chickens at a dosage of 10 mg per kilgram of body weight orally. Serum sarafloxacin pharmacokinetic parameters were calculated using a one compartment open model. The absorption and elimination half lives were 0.32±0.15 h and 3.68±0.9 h respectively. The peak of serum concentration ( C max ) and the time to reach C max ( T max ) were 0.86±0.28 μg/ml and 1.25±0.35 h, respectively. The bioavailability( F ) was 76.03%. Following oral adminstration of the drug (suspension formulation) at a dose of 10mg sarafloxacin/kg body weight, the serum concentration time data were analysed by statistical matrix method. The area under the curve( AUC ), the mean residual time( MRT ) and the elimination half life were 1.03±0.27 μg/ml.h, 6.22±0.76 h and 2.81±0.59 h. The bioavailability( F ) was 14.22 % only.

关 键 词:盐酸沙拉沙星 药物动力学  抗菌素 口服 静注 

分 类 号:S859.796[农业科学—临床兽医学] S854.52[农业科学—兽医学]

 

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