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口服药饵给药方案期间及之后虹鳟鱼中土霉素的药代动力学

Oxytetracycline pharmacokinetics in rainbow trout during and after an orally administered medicated feed regimen.

作者信息

Miller Ron A, Pelsor Francis R, Kane Andrew S, Reimschuessel Renate

机构信息

U.S. Food and Drug Administration, Center for Veterinary Medicine, Office of New Animal Drug Evaluation, 7500 Standish Place, Rockville, Maryland 20855, USA.

出版信息

J Aquat Anim Health. 2012 Jun;24(2):121-8. doi: 10.1080/08997659.2012.675933.

Abstract

The pharmacokinetic-pharmacodynamic predictor of antimicrobial activity for tetracyclines is reported to be the area under the concentration-time curve at steady state (AUC(ss)) divided by the minimal inhibitory concentration of the targeted pathogen. Here, we estimate AUC(ss) values for oxytetracycline (OTC) in serum of rainbow trout Oncorhynchus mykiss by using a destructive sampling study design. Seventy-two rainbow trout were fed OTC-medicated feed at 74.7 +/- 1.5 mg/kg (mean +/- SD) body weight (BW) by oral gavage for 10 consecutive days. Serum was collected from nine fish at 1, 3, 6, 8, 10, 12, 15, and 22 d after dosing began. Serum OTC concentrations were measured by high-performance liquid chromatography with a 0.01-microg/mL limit of detection. The average OTC AUC(ss) was 29.2 microg x h/mL and was estimated using nonlinear mixed-effects modeling and bootstrap resampling techniques. The elimination half-life was estimated as 85.0 h, and the fraction of steady state achieved was estimated as 0.85. The calculated AUC(ss) (24.8 microg x h/mL) following 10 d of oral dosing with 75 mg OTC/kg BW was less than the estimated AUC(ss). Results suggest that the pharmacokinetics of OTC exposure, including the AUC(ss), is better evaluated by using multiday dosimetry than by using a standard single-dose protocol.

摘要

据报道,四环素类抗菌活性的药代动力学-药效学预测指标是稳态浓度-时间曲线下面积(AUC(ss))除以目标病原体的最低抑菌浓度。在此,我们通过采用破坏性采样研究设计,估算虹鳟鱼(Oncorhynchus mykiss)血清中土霉素(OTC)的AUC(ss)值。72条虹鳟鱼通过口服灌胃,连续10天投喂含74.7±1.5毫克/千克(平均±标准差)体重(BW)的OTC药饵。给药开始后第1、3、6、8、10、12、15和22天,从9条鱼采集血清。血清OTC浓度采用高效液相色谱法测定,检测限为0.01微克/毫升。平均OTC AUC(ss)为29.2微克·小时/毫升,采用非线性混合效应模型和自助重采样技术估算。消除半衰期估计为85.0小时,达到稳态的分数估计为0.85。75毫克OTC/千克体重口服给药10天后计算的AUC(ss)(24.8微克·小时/毫升)低于估算的AUC(ss)。结果表明,与使用标准单剂量方案相比,采用多日剂量法能更好地评估OTC暴露的药代动力学,包括AUC(ss)。

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