静脉注射恩诺沙星对 1-6 月龄和 12 月龄绵羊的药代动力学比较

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Devran Coskun, Orhan Corum, Duygu Durna Corum, Kamil Uney
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引用次数: 0

摘要

背景:恩诺沙星(ENR)是一种氟喹诺酮类抗生素,已被批准用于所有年龄段的绵羊。身体成分和代谢能力会随着年龄的增长而发生变化。这些变化可能会改变药物的药代动力学,从而改变药物的效果。因此,需要在目标年龄动物中确定药物的药代动力学:测定ENR及其活性代谢产物环丙沙星(CIP)在不同年龄的绵羊体内单次静脉注射10毫克/千克剂量ENR后的药代动力学。研究方法研究分别在绵羊一岁、六个月和十二个月大时进行。通过颈静脉给所有年龄段的绵羊静脉注射单剂量 10 毫克/千克 ENR。采用高效液相色谱-紫外法测定ENR和CIP的血浆浓度,并采用非室分析法进行分析。结果:在一个月大的绵羊血浆中检测到 ENR 的时间为 36 小时,在其他年龄段的绵羊血浆中检测到 ENR 的时间为 24 小时。在所有年龄组中,血浆中检测到 CIP 的时间均不超过 24 小时。一个月大绵羊的 t1/2ʎz 和 Vdss 明显高于六个月大和十二个月大的绵羊。不同年龄组的 ClT 和 AUC 值没有差异。一个月大的绵羊的 AUC0-∞CIP/AUC0-∞ENR 比率高于六个月大和十二个月大的绵羊。结论与绵羊衰老相关的最重要的药代动力学变化是 ENR 的 Vdss 和 t1/2 ʎz 下降,以及 ENR 与 CIP 的代谢比率降低。药代动力学/药效学数据显示,在所有年龄段的绵羊中,静脉注射 10 毫克/千克剂量的 ENR 对大肠杆菌、多杀性念珠菌和支原体 (>125) 的最佳 AUC0-24/MIC90 比率为 0.37 µg/mL ,对金黄色葡萄球菌 (>30) 的最佳 AUC0-24/MIC90 比率为 0.5 µg/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Pharmacokinetics of İntravenous Enrofloxacin in One- Six- And Twelve-Month-Old Sheep
Background: Enrofloxacin (ENR) is a fluoroquinolone antibiotic approved for use in sheep of all ages. The body composition and metabolic capability change with age. These changes may alter the pharmacokinetics of drugs and thus their effect. Therefore, the pharmacokinetics of drugs need to be established in target-age animals Objective: To determine the pharmacokinetics of ENR and its active metabolite, ciprofloxacin (CIP), following a single intravenous administration of ENR at a dose of 10 mg/kg in different ages of sheep. Methods: The study was carried out in the one-, six- and twelve-month age period of the sheep. A single dose of 10 mg/kg ENR was administered intravenously through the jugular vein to sheep in all age periods. ENR and CIP plasma concentrations were determined using HPLC–UV and analyzed using a non-compartmental method. Results: ENR was detected in the plasma until 36 h in one-month-old and up to 24 h in other ages. CIP was detected in the plasma up to 24 h in all age groups. The t1/2ʎz and Vdss were significantly higher in one-month-old sheep than in six and twelve-months old sheep. There was no difference in ClT and AUC values in different age groups. AUC0-∞CIP/AUC0-∞ENR ratios were higher in one-month-old than in six- and twelve-months sheep. Conclusion: The most important pharmacokinetic changes associated with aging in sheep are decreased Vdss and t1/2ʎz of ENR and the low ratio metabolizing of ENR to CIP. Pharmacokinetic/pharmacodynamic data showed that ENR after IV administration of 10 mg/kg dose provided the optimal AUC0–24/MIC90 ratios for E. coli, P. multocida and Mycoplasma spp. (>125) with MIC of 0.37 µg/mL and for S. aureus (>30) with MIC of 0.5 µg/mL in all ages of sheep.
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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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