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二氟沙星在猪和鸡体内的药代动力学特性及口服生物利用度

Pharmacokinetic properties and oral bioavailabilities of difloxacin in pig and chicken.

作者信息

Inui T, Taira T, Matsushita T, Endo T

机构信息

Pharmaceutical Development Research Laboratory, Tanabe Seiyaku Co., Ltd, Saitama, Japan.

出版信息

Xenobiotica. 1998 Sep;28(9):887-93. doi: 10.1080/004982598239128.

Abstract
  1. Pharmacokinetic properties of difloxacin have been studied in pig and chicken after intravenous and oral administration. 2. The serum concentrations of difloxacin in pig and chicken after intravenous administration were best described by a two-compartment open model, giving distribution half-lives of 0.50 and 0.66 h and elimination half-lives of 7.92 and 4.10 h for pig and chicken respectively. The steady-state distribution volumes were 1.70 and 3.06 l/kg for pig and chicken respectively. 3. After oral administration of 5 mg/kg to pig and chicken, the serum concentrations reached maximal levels of 3.61 and 0.96 microg/ml respectively at 1.25 and 1.40 h. The elimination half-lives were 11.8 and 7.35 h for pig and chicken respectively. 4. The bioavailabilities of difloxacin were calculated as 93.7 (pig) and 86.9% (chicken).
摘要
  1. 已对猪和鸡静脉注射及口服二氟沙星后的药代动力学特性进行了研究。2. 猪和鸡静脉注射二氟沙星后的血清浓度用二室开放模型能得到最佳描述,猪和鸡的分布半衰期分别为0.50小时和0.66小时,消除半衰期分别为7.92小时和4.10小时。猪和鸡的稳态分布容积分别为1.70升/千克和3.06升/千克。3. 猪和鸡口服5毫克/千克二氟沙星后,血清浓度分别在1.25小时和1.40小时达到最高水平,分别为3.61微克/毫升和0.96微克/毫升。猪和鸡的消除半衰期分别为11.8小时和7.35小时。4. 二氟沙星的生物利用度经计算分别为93.7%(猪)和86.9%(鸡)。

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