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静脉给予美洛昔康、酮洛芬和托芬那酸在石鸡中的药代动力学()。

Pharmacokinetics of intravenous meloxicam, ketoprofen and tolfenamic acid in chukar partridge ().

机构信息

Department of Pharmacology, Faculty of Pharmacy, University of Erzincan Binali Yıldırım, Erzincan, Turkey.

Departments of Pharmacology and Toxicology, Faculties of Veterinary Medicine, University of Kastamonu, Kastamonu, Turkey.

出版信息

Br Poult Sci. 2022 Feb;63(1):14-20. doi: 10.1080/00071668.2021.1990211. Epub 2021 Dec 6.

DOI:10.1080/00071668.2021.1990211
PMID:34633873
Abstract
  1. The aim of this study was to determine the pharmacokinetics of meloxicam (MLX, 1 mg/kg body weight (BW)), ketoprofen (KETO, 2 mg/kg BW), and tolfenamic acid (TA, 2 mg/kg BW) in chukar partridge () following intravenous (IV) administration.2. Twenty-four healthy chukar partridges were randomly divided into three equal groups (n = 8) as MLX, KETO and TA. Plasma concentrations of MLX, KETO and TA were measured using high-performance liquid chromatography-ultraviolet detection and analysed using non-compartmental analysis.3. No adverse effects were determined in chukar partridges after IV administration of MLX, KETO and TA. MLX, KETO and TA were detected in plasma up to 10, 12 and 12 h, respectively. The terminal elimination half-life of MLX, KETO and TA was 1.22, 1.77 and 1.95 h, respectively. MLX, KETO and TA exhibited volumes of distribution at a steady-state of 0.03, 0.23 and 0.41 l/kg BW, respectively. The total plasma clearance of MLX, KETO and TA was 0.02, 0.11 and 0.15 l/h/kg, respectively. The extraction ratios for MLX, KETO and TA were calculated as 0.002, 0.011 and 0.016, respectively.4. MLX, KETO and TA offer treatment in chukar partridges for various conditions with an absence of adverse reactions and properties such as short elimination half-life and low volume of distribution. However, there is a need to establish the safety and adverse effects of repeated administration, pharmacokinetics of other administration routes and pharmacological efficacy of MLX, KETO and TA in chukar partridges.
摘要
  1. 本研究旨在确定美洛昔康(MLX,1 毫克/公斤体重(BW))、酮洛芬(KETO,2 毫克/公斤 BW)和托芬那酸(TA,2 毫克/公斤 BW)在静脉注射(IV)给药后鹧鸪中的药代动力学。

  2. 24 只健康鹧鸪随机分为三组(n=8),分别为 MLX、KETO 和 TA。使用高效液相色谱-紫外检测法测定 MLX、KETO 和 TA 的血浆浓度,并采用非房室分析进行分析。

  3. 在鹧鸪 IV 给予 MLX、KETO 和 TA 后未确定不良反应。MLX、KETO 和 TA 在血浆中分别检测到 10、12 和 12 小时。MLX、KETO 和 TA 的终末消除半衰期分别为 1.22、1.77 和 1.95 小时。MLX、KETO 和 TA 在稳态时的分布容积分别为 0.03、0.23 和 0.41 l/kg BW。MLX、KETO 和 TA 的总血浆清除率分别为 0.02、0.11 和 0.15 l/h/kg。MLX、KETO 和 TA 的提取率分别计算为 0.002、0.011 和 0.016。

  4. MLX、KETO 和 TA 为鹧鸪的各种疾病提供治疗,无不良反应,具有半衰期短、分布容积低等特性。然而,需要确定重复给药的安全性和不良反应、其他给药途径的药代动力学以及 MLX、KETO 和 TA 在鹧鸪中的药效。

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