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甲苯磺酸在红耳龟(滑龟指名亚种)体内的药代动力学

Pharmacokinetics of tolfenamic acid in red-eared slider turtles (Trachemys scripta elegans).

作者信息

Corum Orhan, Atik Orkun, Durna Corum Duygu, Er Ayse, Uney Kamil

机构信息

Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Kastamonu, Kastamonu, Turkey.

Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Afyonkocatepe, Afyon, Turkey.

出版信息

Vet Anaesth Analg. 2019 Sep;46(5):699-706. doi: 10.1016/j.vaa.2019.05.009. Epub 2019 Jun 8.

Abstract

OBJECTIVE

To determine the pharmacokinetics of tolfenamic acid (TA) after different routes of administration [intravenous (IV) and intramuscular (IM), 2 mg kg] and doses (IV, 2 and 4 mg kg) in red-eared slider turtles (Trachemys scripta elegans).

STUDY DESIGN

Randomized experimental trial.

ANIMALS

Sixteen healthy red-eared slider turtles.

METHODS

Turtles were randomly assigned to two groups (n = 8 each). Group 1 received TA at a dose of 2 mg kg IV and then IM, after a washout period of 30 days. Group 2 received 4 mg kg TA IV. A noncompartmental analysis was used to calculate pharmacokinetic variables.

RESULTS

No local and/or systemic adverse drug effects were observed in any turtle. Elimination half-life and mean residence time following IM administration at 2 mg kg were significantly longer than those following IV administration. The bioavailability following IM administration was complete. The area under the plasma concentration-time curve, elimination half-life, mean residence time and total clearance were significantly different between the dose groups.

CONCLUSIONS AND CLINICAL RELEVANCE

The absence of adverse reactions in the turtles of the study of TA along with the favourable pharmacokinetic properties (the long half-life and the complete bioavailability) of TA administered at the single doses of 2 and 4 mg kg suggest the possibility of its effective use in turtles. However, further studies are required to establish a multiple dosage regimen of TA and to evaluate the clinical efficacy of administering TA.

摘要

目的

确定在红耳龟(滑龟)中不同给药途径(静脉注射和肌肉注射,2毫克/千克)和剂量(静脉注射,2和4毫克/千克)后托芬那酸(TA)的药代动力学。

研究设计

随机实验性试验。

动物

16只健康红耳龟。

方法

将龟随机分为两组(每组n = 8)。第1组在30天的洗脱期后,先静脉注射2毫克/千克剂量的TA,然后肌肉注射。第2组静脉注射4毫克/千克TA。采用非房室分析计算药代动力学变量。

结果

在任何龟中均未观察到局部和/或全身药物不良反应。肌肉注射2毫克/千克剂量后的消除半衰期和平均驻留时间显著长于静脉注射后的。肌肉注射后的生物利用度是完全的。剂量组之间的血浆浓度-时间曲线下面积、消除半衰期、平均驻留时间和总清除率有显著差异。

结论及临床意义

在TA研究的龟中未出现不良反应,以及单剂量2和4毫克/千克的TA具有良好的药代动力学特性(长半衰期和完全生物利用度),提示其在龟中有效使用的可能性。然而,需要进一步研究来确定TA的多剂量方案并评估TA给药的临床疗效。

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