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头孢他啶在绵羊体内的药代动力学及其在组织和腹膜液中的渗透情况。

Pharmacokinetics of ceftazidime in sheep and its penetration into tissue and peritoneal fluids.

作者信息

Rule R, Rubio M, Perelli M C

机构信息

CIC Provincia de Buenos Aires, Cátedra de Farmacología, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, La Plata, Argentina.

出版信息

Res Vet Sci. 1991 Nov;51(3):233-8. doi: 10.1016/0034-5288(91)90069-z.

DOI:10.1016/0034-5288(91)90069-z
PMID:1780573
Abstract

Serum, tissue and peritoneal fluid concentrations of ceftazidime were studied in ewes after intravenous, intramuscular and subcutaneous administration at 50 mg kg-1 bodyweight. Tissue and peritoneal cages were implanted in the animals studied. After intravenous bolus administration, the mean serum concentration versus time profile was best described by a two-compartment open model. The distribution rate constant (alpha) was 3.5 +/- 1.1 h-1 and the half-life (t 1/2 alpha) 0.22 +/- 0.09 hour. The elimination rate constant (beta) was 0.43 +/- 0.04 h-1 and half-life (t 1/2 beta) 1.6 +/- 0.2 hours. The area under the curve was 275.7 +/- 84.0 micrograms.ml-1 h. The volume of distribution as steady state was 356.1 +/- 208.0 ml kg-1. The penetration ratio into tissue fluid was 62.6 +/- 15.1 per cent and into peritoneal fluid 61.1 +/- 16.5 per cent. After intramuscular injection, the elimination half-life was 1.7 +/- 0.2 hours, the area under the curve was 228.7 +/- 43.3 micrograms.ml-1 h. and the elimination rate constant was 0.42 +/- 0.05 h-1. The penetration ratio into tissue fluid was 68.5 +/- 37.3 per cent and into peritoneal fluid 73.3 +/- 34.4 per cent. After subcutaneous injection, the elimination half-life was 1.8 +/- 0.5 hours, the area under the curve was 231.8 +/- 65.6 micrograms.ml-1 h. and the elimination constant was 0.41 +/- 0.10 h-1. The penetration ratio into tissue fluid was 47.2 +/- 3.5 per cent and into peritoneal fluid 58.1 +/- 15.6 per cent.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

以50mg/kg体重对母羊进行静脉内、肌肉内和皮下给药后,研究了头孢他啶在血清、组织和腹水中的浓度。在受试动物体内植入组织和腹水收集装置。静脉推注给药后,血清浓度-时间曲线最佳拟合为二室开放模型。分布速率常数(α)为3.5±1.1 h-1,半衰期(t 1/2α)为0.22±0.09小时。消除速率常数(β)为0.43±0.04 h-1,半衰期(t 1/2β)为1.6±0.2小时。曲线下面积为275.7±84.0μg·ml-1·h。稳态分布容积为356.1±208.0 ml/kg。组织液渗透比为62.6±15.1%,腹水渗透比为61.1±16.5%。肌肉注射后,消除半衰期为1.7±0.2小时,曲线下面积为228.7±43.3μg·ml-1·h,消除速率常数为0.42±0.05 h-1。组织液渗透比为68.5±37.3%,腹水渗透比为73.3±34.4%。皮下注射后,消除半衰期为1.8±0.5小时,曲线下面积为231.8±65.6μg·ml-1·h,消除常数为0.41±0.10 h-1。组织液渗透比为47.2±3.5%,腹水渗透比为58.1±15.6%。(摘要截取自250字)

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