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一种缓释型茶碱产品在猫体内的药代动力学

Pharmacokinetics of an extended-release theophylline product in cats.

作者信息

Guenther-Yenke Christine L, McKiernan Brendan C, Papich Mark G, Powell Elizabeth

机构信息

Wheat Ridge Veterinary Specialists, Wheat Ridge Animal Hospital, 3695 Kipling St, Wheat Ridge, CO 80033, USA.

出版信息

J Am Vet Med Assoc. 2007 Sep 15;231(6):900-6. doi: 10.2460/javma.231.6.900.

Abstract

OBJECTIVE

To evaluate the pharmacokinetics of a brand of extended-release theophylline tablets and capsules in healthy cats.

DESIGN

Randomized 3-way crossover study.

ANIMALS

6 healthy cats.

PROCEDURES

A single dose of aminophylline (10 mg/kg [4.5 mg/lb], IV), a 100-mg extended-release theophylline tablet, or a 125-mg extended-release theophylline capsule was administered to all cats. Plasma samples were collected via preplaced central catheters throughout a 36-hour period. Plasma samples were frozen until analyzed by use of a fluorescence polarization monoclonal immunoassay.

RESULTS

All cats tolerated drug administration and plasma collection with no adverse effects. Peak concentrations were reached for both orally administered products between 8 and 12 hours after administration. Bioavailability was excellent. Plasma concentrations were within the human therapeutic concentration of 5 to 20 microg/mL.

CONCLUSIONS AND CLINICAL RELEVANCE

Daily administration of the brand of theophylline tablets and capsules used in this study at 15 mg/kg (6.8 mg/lb) and 19 mg/kg (8.6 mg/lb), respectively, maintained plasma concentrations within the desired therapeutic range in healthy cats.

摘要

目的

评估某品牌的缓释茶碱片和胶囊在健康猫体内的药代动力学。

设计

随机三交叉研究。

动物

6只健康猫。

步骤

给所有猫静脉注射单剂量氨茶碱(10 mg/kg [4.5 mg/lb])、一片100 mg的缓释茶碱片或一粒125 mg的缓释茶碱胶囊。在36小时内通过预先放置的中心静脉导管采集血样。血样冷冻保存,直至采用荧光偏振单克隆免疫分析法进行分析。

结果

所有猫对给药和采血耐受,未出现不良反应。口服给药产品在给药后8至12小时达到峰值浓度。生物利用度良好。血浆浓度处于人类治疗浓度5至20 μg/mL范围内。

结论及临床意义

本研究中使用的品牌的茶碱片和胶囊分别按15 mg/kg(6.8 mg/lb)和19 mg/kg(8.6 mg/lb)每日给药,可使健康猫的血浆浓度维持在所需治疗范围内。

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