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多次给药后运动纯种马体内愈创甘油醚的药代动力学

Pharmacokinetics of guaifenesin following administration of multiple doses to exercised Thoroughbred horses.

作者信息

Knych H K, Stanley S D, Benson D, Arthur R M

机构信息

K.L. Maddy Analytical Chemistry Laboratory, School of Veterinary Medicine, University of California, Davis, CA, USA.

Department of Veterinary Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, CA, USA.

出版信息

J Vet Pharmacol Ther. 2016 Aug;39(4):416-9. doi: 10.1111/jvp.12287. Epub 2016 Jan 14.

Abstract

Guaifenesin is an expectorant commonly used in performance horses to aid in the clearance of mucus from the airways. Guaifenesin is also a centrally acting skeletal muscle relaxant and as such is a prohibited drug with withdrawal necessary prior to competition. To the authors' knowledge, there are no reports in the literature describing single or multiple oral administrations of guaifenesin in the horse to determine a regulatory threshold and related withdrawal time. Therefore, the objective of the current study was to describe the pharmacokinetics of guaifenesin following oral administration in order to provide data upon which appropriate regulatory recommendations can be established. Nine exercised Thoroughbred horses were administered 2 g of guaifenesin orally BID for a total of five doses. Blood samples were collected immediately prior to drug administration and at various times postadministration. Serum guaifenesin concentrations were determined and pharmacokinetic parameters calculated. Guaifenesin was rapidly absorbed (Tmax of 15 min) following oral administration. The Cmax was 681.3 ± 323.8 ng/mL and 1080 ± 732.8 following the first and last dose, respectively. The serum elimination half-life was 2.62 ± 1.24 h. Average serum guaifenesin concentrations remained above the LOQ of the assay (0.5 ng/mL) by 48 h postadministration of the final dose in 3 of 9 horses.

摘要

愈创甘油醚是一种常用的祛痰剂,用于赛马以帮助清除气道中的黏液。愈创甘油醚也是一种中枢性骨骼肌松弛剂,因此是一种违禁药物,比赛前需要停药。据作者所知,文献中没有关于在马身上单次或多次口服愈创甘油醚以确定监管阈值和相关停药时间的报道。因此,本研究的目的是描述口服愈创甘油醚后的药代动力学,以便提供数据来制定适当的监管建议。对9匹运动型纯种马口服2克愈创甘油醚,每日两次,共给药5次。在给药前及给药后的不同时间采集血样。测定血清愈创甘油醚浓度并计算药代动力学参数。口服愈创甘油醚后吸收迅速(达峰时间为15分钟)。首次给药和末次给药后的血药峰浓度分别为681.3±323.8纳克/毫升和1080±732.8纳克/毫升。血清消除半衰期为2.62±1.24小时。在9匹马中的3匹马末次给药后48小时,血清愈创甘油醚平均浓度仍高于检测限(0.5纳克/毫升)。

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