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绵羊以两种不同速率口服西美昔布后的血浆概况。

Plasma profile of cimicoxib in sheep after oral administration at two different rates.

作者信息

Di Salvo A, Giorgi M, Lee H K, Vercelli C, Rueca F, Marinucci M Trabalza, Rocca G Della

机构信息

.

出版信息

Pol J Vet Sci. 2017 Sep 26;20(3):535-538. doi: 10.1515/pjvs-2017-0065.

Abstract

Sheep are often subjected to painful procedures and thus they need to be treated with analgesics. Nevertheless, knowledges about pharmacokinetic features of these drugs in this species are poor. The aim of this study was to evaluate plasma behaviour of cimicoxib in sheep after a single oral administration at two different dose rates (4 and 6 mg/kg). Maximum plasma concentrations of cimicoxib were equal to 273.78 (median value; range 189.00-567.32) and 565.01 (range 308.27-822.59) ng/mL after treatment with 4 and 6 mg/kg, respectively. The time of maximum concentration (Tmax) was achieved between 4 and 10 hours following treatment at the lower dose, and between 6 and 10 hours after the administration of the higher dose, with one sheep achieving the concentration peak at 0.75 hours. The slow absorption and the great individual variability in plasma concentration, probably due to ruminal effects, suggest that cimicoxib is not suitable for oral treatment in sheep.

摘要

绵羊经常要接受痛苦的手术,因此需要用镇痛药进行治疗。然而,关于这些药物在该物种中的药代动力学特征的知识却很匮乏。本研究的目的是评估西咪考昔在绵羊单次口服两种不同剂量率(4和6毫克/千克)后的血浆行为。用4毫克/千克和6毫克/千克治疗后,西咪考昔的最大血浆浓度分别等于273.78(中位数;范围189.00 - 567.32)和565.01(范围308.27 - 822.59)纳克/毫升。较低剂量治疗后,在4至10小时之间达到最大浓度时间(Tmax),较高剂量给药后在6至10小时之间达到,有一只绵羊在0.75小时达到浓度峰值。吸收缓慢以及血浆浓度存在很大的个体差异,可能是由于瘤胃效应,这表明西咪考昔不适合用于绵羊的口服治疗。

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