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酮洛芬在尼罗罗非鱼( )和虹鳟鱼( )中的药代动力学。

Pharmacokinetics of Ketoprofen in Nile Tilapia () and Rainbow Trout ().

作者信息

Greene Whitney, Mylniczenko Natalie D, Storms Timothy, Burns Charlene M, Lewbart Gregory A, Byrd Lynne, Papich Mark G

机构信息

Mote Marine Laboratory and Aquarium, Sarasota, FL, United States.

John G. Shedd Aquarium, Chicago, IL, United States.

出版信息

Front Vet Sci. 2020 Oct 7;7:585324. doi: 10.3389/fvets.2020.585324. eCollection 2020.

Abstract

The objective of this study was to document the pharmacokinetics of ketoprofen following 3 mg/kg intramuscular (IM) and intravenous (IV) injections in rainbow trout () and 8 mg/kg intramuscular (IM) injection in Nile tilapia (. Plasma was collected laterally from the tail vein for drug analysis at various time intervals up to 72 h following the injection of ketoprofen. In trout, area under the curve (AUC) levels were 115.24 μg hr/mL for IM and 135.69 μg hr/mL for IV groups with a half-life of 4.40 and 3.91 h, respectively. In both trout and tilapia, there were detectable ketoprofen concentrations in most fish for 24 h post-injection. In tilapia, there was a large difference between the R- and S-enantiomers, suggesting either chiral inversion from R- to S-enantiomer or more rapid clearance of the R-enantiomer. AUC values of the S- and R-enantiomers were 510 and 194 μg hr/Ml, respectively, corresponding to a faster clearance for the R-enantiomer. This study shows that there were very high plasma concentrations of ketoprofen in trout and tilapia with no adverse effects observed. Future studies on the efficacy, frequency of dosing, analgesia, adverse effects, and route of administration are warranted.

摘要

本研究的目的是记录酮洛芬在虹鳟鱼中3mg/kg肌肉注射(IM)和静脉注射(IV)以及尼罗罗非鱼中8mg/kg肌肉注射后的药代动力学。在注射酮洛芬后的72小时内,于不同时间间隔从尾静脉侧向采集血浆用于药物分析。在虹鳟鱼中,肌肉注射组的曲线下面积(AUC)水平为115.24μg·hr/mL,静脉注射组为135.69μg·hr/mL,半衰期分别为4.40小时和3.91小时。在虹鳟鱼和尼罗罗非鱼中,大多数鱼在注射后24小时内均可检测到酮洛芬浓度。在尼罗罗非鱼中,R-和S-对映体之间存在很大差异,这表明可能存在从R-对映体到手性转化为S-对映体的情况,或者R-对映体的清除更快。S-和R-对映体的AUC值分别为510和194μg·hr/Ml,这表明R-对映体的清除更快。本研究表明,虹鳟鱼和尼罗罗非鱼中的酮洛芬血浆浓度非常高,但未观察到不良反应。有必要对其疗效、给药频率、镇痛效果、不良反应和给药途径进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f451/7579418/fb0dd479020a/fvets-07-585324-g0001.jpg

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