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两种硫酸头孢喹肟乳房内注入剂在牛奶中的药代动力学及相对生物利用度研究

Pharmacokinetics and relative bioavailability study of two cefquinome sulfate intramammary infusions in cow milk.

作者信息

Li Shuang, Yu Na, Tang Yaoxin, Liu Chunshuang, Zhang Ying, Chen Xiaojie, Wu Hao, Li Xiubo, Liu Yiming

机构信息

National Feed Drug Reference Laboratories, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, China.

Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, Tianjin, China.

出版信息

Front Vet Sci. 2024 Mar 11;11:1384076. doi: 10.3389/fvets.2024.1384076. eCollection 2024.

Abstract

In this study, two intramammary infusions of cefquinome sulfate were investigated for pharmacokinetics and bioavailability. Twelve lactating cows for each group were administered an effective dose of 75 mg/gland for cefquinome, with milk samples collected at various time intervals. The concentrations of cefquinome in milk at different times were determined by the UPLC-MS/MS method. Analyses of noncompartmental pharmacokinetics were conducted on the concentration of cefquinome in milk. Mean pharmacokinetic parameters of group A and group B following intramammary administration were as follows: AUC 300558.57 ± 25052.78 ng/mL and 266551.3 ± 50654.85 ng/mL, C 51786.35 ± 11948.4 ng/mL and 59763.7 ± 8403.2 ng/mL, T 5.69 ± 0.62 h and 5.25 ± 1.62 h, MRT 7.43 ± 0.79 h and 4.8 ± 0.78 h, respectively. Pharmacokinetic experiments showed that the relative bioavailability of group B was 88.69% that of group A. From our findings, group B (3 g: 75 mg) shows a quicker drug elimination process than group A (8 g: 75 mg), which suggests that the withdrawal period for the new formulation may be shorter.

摘要

在本研究中,对硫酸头孢喹肟进行两次乳房内灌注以研究其药代动力学和生物利用度。每组12头泌乳奶牛,给予头孢喹肟有效剂量75mg/乳区,并在不同时间间隔采集乳样。采用超高效液相色谱-串联质谱法测定不同时间牛奶中头孢喹肟的浓度。对牛奶中头孢喹肟的浓度进行非房室药代动力学分析。乳房内给药后A组和B组的平均药代动力学参数如下:AUC分别为300558.57±25052.78ng/mL和266551.3±50654.85ng/mL,C分别为51786.35±11948.4ng/mL和59763.7±8403.2ng/mL,T分别为5.69±0.62h和5.25±1.62h,MRT分别为7.43±0.79h和4.8±0.78h。药代动力学实验表明,B组的相对生物利用度为A组的88.69%。根据我们的研究结果,B组(3g:75mg)的药物消除过程比A组(8g:75mg)更快,这表明新制剂的停药期可能更短。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b92/10962211/aac50e807212/fvets-11-1384076-g001.jpg

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