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不同剂量静脉注射卡洛芬在山羊体内的药代动力学

Pharmacokinetics of Carprofen Administered Intravenously at Different Doses in Goats.

作者信息

Corum Orhan, Oguz Halis, Hitit Mustafa, Durna Corum Duygu, Coskun Devran, Erdogan Teslime, Bahcivan Emre, Uney Kamil

机构信息

Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Hatay Mustafa Kemal, Hatay 31060, Türkiye.

Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Selcuk, Konya 42003, Türkiye.

出版信息

Vet Sci. 2025 Sep 2;12(9):852. doi: 10.3390/vetsci12090852.

DOI:10.3390/vetsci12090852
PMID:41012777
Abstract

This investigation focuses on understanding the pharmacokinetic behavior of intravenously administered carprofen at doses of 0.7, 1.4, and 4 mg/kg in goats. Eighteen animals were randomly assigned into three groups, with six goats per group, and blood samples were collected at 22 time points post-administration. Plasma concentrations were analyzed using a validated HPLC-UV method, and key pharmacokinetic parameters were derived using non-compartmental analysis. Results show that, at 0.7 mg/kg, carprofen exhibited the total clearance (Cl) of 2.19 mL/h/kg, volume of distribution at steady state (V) of 126.56 mL/kg, area under the curve (AUC) of 321.00 h*µg/mL, and elimination half-life (t) of 44.32 h. When comparing doses, an increase in Cl was observed at 4 mg/kg, and the volume of distribution increased at both 1.4 and 4 mg/kg dosages. Additionally, a reduction in dose-normalized AUC was evident at the highest dose. Data showed that the effect of the drug may be prolonged as the dose increases. These differences between dose groups may be clinically insignificant after the single administration of all doses. Carprofen can be used at all three dose levels in goats; however, vigilance regarding the potential side effects and drug residues is essential, especially during repeated treatments.

摘要

本研究着重于了解静脉注射剂量为0.7、1.4和4mg/kg的卡洛芬在山羊体内的药代动力学行为。18只动物被随机分为三组,每组6只山羊,并在给药后的22个时间点采集血样。使用经过验证的高效液相色谱-紫外检测法分析血浆浓度,并采用非房室分析法得出关键药代动力学参数。结果显示,在0.7mg/kg剂量下,卡洛芬的总清除率(Cl)为2.19mL/h/kg,稳态分布容积(V)为126.56mL/kg,曲线下面积(AUC)为321.00h*µg/mL,消除半衰期(t)为44.32h。比较不同剂量时,在4mg/kg剂量下观察到清除率增加,在1.4和4mg/kg剂量下分布容积均增加。此外,最高剂量下剂量标准化的AUC明显降低。数据表明,药物的作用可能会随着剂量增加而延长。单次给予所有剂量后,各剂量组之间的这些差异在临床上可能无显著意义。卡洛芬可在山羊的所有三个剂量水平使用;然而,尤其是在重复治疗期间,对潜在副作用和药物残留保持警惕至关重要。

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本文引用的文献

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Effect of Xylazine on Pharmacokinetics and Physiological Efficacy of Intravenous Carprofen in Castrated Goats Kids.赛拉嗪对去势山羊幼崽静脉注射卡洛芬的药代动力学和生理功效的影响。
Animals (Basel). 2023 Aug 24;13(17):2700. doi: 10.3390/ani13172700.
2
Pharmacokinetics and bioavailability of carprofen in sheep.卡洛芬在绵羊体内的药代动力学和生物利用度。
J Vet Pharmacol Ther. 2022 Nov;45(6):543-549. doi: 10.1111/jvp.13085. Epub 2022 Jun 29.
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Pharmacokinetics of carprofen following single and repeated intravenous administrations of different doses in sheep.
在绵羊中单次和重复静脉给予不同剂量后的卡洛芬药代动力学。
J Vet Pharmacol Ther. 2022 Sep;45(5):481-487. doi: 10.1111/jvp.13079. Epub 2022 Jun 24.
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Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route.猪作为测试新型抗炎药物制剂的动物模型:卡洛芬的药代动力学及肌肉注射途径的生物利用度
Pharmaceutics. 2022 May 12;14(5):1045. doi: 10.3390/pharmaceutics14051045.
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Pharmacokinetics and Bioavailability of Carprofen in Rainbow Trout () Broodstock.卡洛芬在虹鳟亲鱼中的药代动力学和生物利用度
Pharmaceutics. 2021 Jun 30;13(7):990. doi: 10.3390/pharmaceutics13070990.
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Pharmacokinetics of meloxicam, carprofen, and tolfenamic acid after intramuscular and oral administration in Japanese quails (Coturnix coturnix japonica).美洛昔康、卡洛芬和托芬那酸在日本鹌鹑( Coturnix coturnix japonica )肌肉注射和口服后的药代动力学。
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