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氟苯尼考在肉鸡体内的组织浓度及药代动力学

Tissue concentrations and pharmacokinetics of florfenicol in broiler chickens.

作者信息

Afifi N A, Abo el-Sooud K A

机构信息

Department of Pharmacology, Faculty of Veterinary Medicine, Giza, Egypt.

出版信息

Br Poult Sci. 1997 Sep;38(4):425-8. doi: 10.1080/00071669708418013.

Abstract
  1. Florfenicol (30 mg/kg body weight) was administered to broiler chickens via intravenous (i.v.), intramuscular (i.m.) and oral routes to study its plasma concentrations, kinetic behaviour, systemic bioavailability and tissue content. 2. Following a single i.v. injection, the kinetic disposition of florfenicol followed a 2-compartmental open model with an elimination half-life of 173 min, total body clearance of 26.9 ml/kg/min and a steady state volume of distribution of 5.11 l/kg. 3. The highest plasma concentrations of florfenicol were 3.82 and 3.20 micrograms/ml following single i.m. and oral administration, respectively. The systemic bioavailability was 96.6% and 55.3% after i.m. and oral administration. The plasma protein binding of florfenicol was 18.5%. 4. Following its administration, the highest tissue concentrations of the drug were found in the kidney bile, lung, muscle, intestine, heart, liver, spleen and plasma. Low concentrations of the drug were found in brain, bone marrow and fat. No florfenicol residues were detected in tissues and plasma after 72 h except in the bile from where it disappeared after 96 h.
摘要
  1. 将氟苯尼考(30毫克/千克体重)通过静脉注射(i.v.)、肌肉注射(i.m.)和口服途径给予肉鸡,以研究其血浆浓度、动力学行为、全身生物利用度和组织含量。2. 单次静脉注射后,氟苯尼考的动力学处置符合二室开放模型,消除半衰期为173分钟,全身清除率为26.9毫升/千克/分钟,稳态分布容积为5.11升/千克。3. 单次肌肉注射和口服给药后,氟苯尼考的最高血浆浓度分别为3.82和3.20微克/毫升。肌肉注射和口服给药后的全身生物利用度分别为96.6%和55.3%。氟苯尼考的血浆蛋白结合率为18.5%。4. 给药后,该药物在肾脏、胆汁、肺、肌肉、肠道、心脏、肝脏、脾脏和血浆中的组织浓度最高。在大脑、骨髓和脂肪中发现该药物浓度较低。72小时后,除胆汁外,组织和血浆中未检测到氟苯尼考残留,胆汁中的氟苯尼考在96小时后消失。

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