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环丙沙星在泰迪山羊单次肌内注射后的药代动力学及给药方案

Pharmacokinetics and dosage regimen of ciprofloxacin following single intramuscular administration in Teddy goats.

作者信息

Iqbal Zahid, Javed Ijaz, Basit Abdul, Jan Ibadullah, Khan Amir Ali

机构信息

Department of Pharmacology, Isra University, Hyderabad, Pakistan.

出版信息

Pak J Pharm Sci. 2011 Jan;24(1):69-74.

Abstract

The objective of this study was to determine the pharmacokinetics and dosage regimen of ciprofloxacin in Teddy goats. Ciprofloxacin was administered intramuscularly at 5 mg/kg body weight in each of eight animals. Following drug administration, blood samples were collected at different time intervals and analyzed for ciprofloxacin using HPLC. Pharmacokinetic parameters were calculated using two compartment open model. Peak plasma concentration (Cmax) of ciprofloxacin, 1.77±0.20 µg/ml was achieved at 0.90±0.04 hours (Tmax). Values for half-life of absorption (t1/2 abs), distribution (t1/2 α) and elimination (t1/2 β) were 0.52±0.04, 0.52±0.04 and 2.62±0.39 hours, respectively. The value for apparent volume of distribution (Vd) was 3.76±0.92 l/kg, area-under-the-curve (AUC) 5.89±0.91 µg.hr/ml and total body clearance (CL) was 1.09±0.11 l/hr/kg. Based on these results, it was concluded that calculated dose should be higher than the dose recommended by the manufacturer to treat susceptible bacteria in goats.

摘要

本研究的目的是确定环丙沙星在泰迪山羊体内的药代动力学和给药方案。对八只动物每只均按5mg/kg体重肌肉注射环丙沙星。给药后,在不同时间间隔采集血样,并用高效液相色谱法分析环丙沙星。使用二室开放模型计算药代动力学参数。环丙沙星的血浆峰浓度(Cmax)为1.77±0.20µg/ml,在0.90±0.04小时(Tmax)达到。吸收半衰期(t1/2 abs)、分布半衰期(t1/2α)和消除半衰期(t1/2β)的值分别为0.52±0.04、0.52±0.04和2.62±0.39小时。表观分布容积(Vd)值为3.76±0.92 l/kg,曲线下面积(AUC)为5.89±0.91µg.hr/ml,总体清除率(CL)为1.09±0.11 l/hr/kg。基于这些结果,得出结论:为治疗山羊体内的敏感细菌,计算所得剂量应高于制造商推荐的剂量。

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