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绵羊静脉注射和肌肉注射氯霉素后的药代动力学

Chloramphenicol pharmacokinetics after intravenous and intramuscular administration in sheep.

作者信息

Mestorino O N, Errecalde J O

机构信息

Department of Pharmacology and Toxicology, Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, Buenos Aires, Argentina.

出版信息

Zentralbl Veterinarmed A. 1998 Apr;45(3):175-80. doi: 10.1111/j.1439-0442.1998.tb00814.x.

Abstract

The pharmacokinetics of chloramphenicol were studied after intravenous and intramuscular administration of 50 mg/kg body weight in Merino sheep. After intravenous administration, the drug was rapidly distributed extravascularly with a half-life of 10.5 +/- 8.83 min. Extensive distribution was confirmed by an apparent volume of distribution at steady state (1.5 +/- 0.43 1/kg). The elimination half-life was 3.24 +/- 0.60 h. After intramuscular injection, the absorption half-life was 44.33 +/- 19.21 min with a bioavailability of 65%. A maximum serum concentration of 15.57 +/- 3.95 micrograms/ml was determined 2 h after administration. Serum concentrations above 5 micrograms/ml were maintained for approximately 12 h with an elimination half-life of 5.75 +/- 1.25 h, longer than the half-life obtained after intravenous administration. In conclusion, the intramuscular administration of chloramphenical at a dose rate of 50 mg/kg permitted the maintenance of inhibitory concentrations of the antibiotic for the majority of Salmonella and Pasteurella isolates for at least 12 h.

摘要

在美利奴绵羊中静脉注射和肌肉注射50mg/kg体重的氯霉素后,对其药代动力学进行了研究。静脉注射后,药物迅速向血管外分布,半衰期为10.5±8.83分钟。稳态时的表观分布容积(1.5±0.43L/kg)证实了药物的广泛分布。消除半衰期为3.24±0.60小时。肌肉注射后,吸收半衰期为44.33±19.21分钟,生物利用度为65%。给药后2小时测定的最大血清浓度为15.57±3.95μg/ml。血清浓度高于5μg/ml可维持约12小时,消除半衰期为5.75±1.25小时,长于静脉注射后的半衰期。总之,以50mg/kg的剂量率肌肉注射氯霉素,可使大多数沙门氏菌和巴氏杆菌分离株的抗生素抑制浓度维持至少12小时。

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