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酮洛芬在山羊单独重复给药或与头孢喹肟联合给药后的药代动力学

Ketoprofen Pharmacokinetics in Goats Following Repeated Treatment Alone or in Combination With Cefquinome.

作者信息

Durna Corum Duygu, Corum Orhan, Giorgi Mario, Kartal Serafettin, Turk Erdinc, Sakin Fatih, Donmez Huseyin, Uney Kamil

机构信息

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

Department of Veterinary Sciences, University of Pisa, Pisa, Italy.

出版信息

J Vet Pharmacol Ther. 2025 Jun 24. doi: 10.1111/jvp.70008.

Abstract

This work was aimed at investigating the pharmacokinetic changes after repeated administration of ketoprofen (3 mg/kg, IM, once a day for 5 days) to goats either alone or in combination with cefquinome (2 mg/kg, IM, once a day for 5 days). The study was carried out on six goats according to a balanced, open, two-phase, cross-pharmacokinetic design. The plasma ketoprofen concentrations were measured using HPLC-UV, and the pharmacokinetic data were estimated using a non-compartmental analysis. After the first dose of ketoprofen, the terminal elimination half-life (t), area under the plasma concentration-time curve (AUC), and peak plasma concentration (C) were 1.47 h, 12.23 h*μg/mL, and 6.06 μg/mL, respectively. The last dose of ketoprofen resulted in significant variations in t and AUC values compared to the first dose, but C was similar. Cefquinome administration caused significant differences in the t, AUC, and C of ketoprofen. There was no variation in T between the first and final doses or between treatment groups. The accumulation ratio of ketoprofen was 1.32 and 0.76 when used alone and in combination with cefquinome, respectively. Repeated administration of ketoprofen alone or with cefquinome altered its disposition; therefore, the efficacy of ketoprofen when used alone or in combination with cefquinome in goats should be determined, and the dosage regimen should be re-evaluated.

摘要

本研究旨在调查酮洛芬(3毫克/千克,肌肉注射,每天一次,共5天)单独或与头孢喹肟(2毫克/千克,肌肉注射,每天一次,共5天)联合重复给药于山羊后的药代动力学变化。该研究按照平衡、开放、两阶段、交叉药代动力学设计在六只山羊身上进行。使用高效液相色谱-紫外检测法测定血浆酮洛芬浓度,并采用非房室分析估算药代动力学数据。首次给予酮洛芬后,终末消除半衰期(t)、血浆浓度-时间曲线下面积(AUC)和血浆峰浓度(C)分别为1.47小时、12.23小时·微克/毫升和6.06微克/毫升。与首次给药相比,最后一次给药的酮洛芬在t和AUC值上有显著变化,但C值相似。头孢喹肟的给药导致酮洛芬的t、AUC和C有显著差异。首次和末次给药之间或治疗组之间的T无变化。单独使用和与头孢喹肟联合使用时,酮洛芬的蓄积比分别为1.32和0.76。单独或与头孢喹肟联合重复给药会改变酮洛芬的处置;因此,应确定酮洛芬单独或与头孢喹肟联合用于山羊时的疗效,并重新评估给药方案。

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