Suppr超能文献

非吸烟健康志愿者血浆和唾液中可替宁的药代动力学。

The pharmacokinetics of cotinine in plasma and saliva from non-smoking healthy volunteers.

作者信息

Curvall M, Elwin C E, Kazemi-Vala E, Warholm C, Enzell C R

机构信息

Research Department, Swedish Tobacco Co., Stockholm.

出版信息

Eur J Clin Pharmacol. 1990;38(3):281-7. doi: 10.1007/BF00315031.

Abstract

Cotinine is a major metabolite of nicotine in man. Its disposition kinetics has been followed in plasma and saliva from nine nonsmokers, 23 to 56 years of age. Cotinine 5, 10 and 20 mg was given intravenously and orally to each subject, and plasma, saliva and urine samples were collected for 96 h. The kinetics of cotinine was best described by a multicompartment model with three distinct phases both in plasma and saliva. Regardless of the mode of administration, there was no indication of dose-dependent kinetics. Mean total plasma clearance was 63.8 ml.h-1.kg-1 and mean renal clearance was 4.7 ml.h-1.kg-1, i.e. only 10% of the dose was excreted unchanged in the urine. The volume of distribution, as calculated from the plasma curves, was slightly greater than the body weight, 1.1 l.kg-1. The concentration of cotinine was 20 to 40% higher in unstimulated mixed saliva than in plasma during the absorption, distribution and elimination phases. As the clearance and distribution values in saliva were directly proportional to the corresponding values in plasma, similar terminal half-life values were obtained in the two body fluids, 15.5 and 16.8 h for plasma and saliva, respectively. Thus the kinetics of cotinine is linear after intravenous and after oral dosing, and salivary concentrations give the same information about cotinine disposition in the body as do plasma concentrations.

摘要

可替宁是人体中尼古丁的主要代谢产物。对9名年龄在23至56岁之间的非吸烟者的血浆和唾液中的可替宁处置动力学进行了跟踪研究。给每位受试者静脉注射和口服5毫克、10毫克和20毫克的可替宁,并在96小时内收集血浆、唾液和尿液样本。可替宁的动力学在血浆和唾液中均可用具有三个不同阶段的多室模型来最佳描述。无论给药方式如何,均未显示出剂量依赖性动力学。平均总血浆清除率为63.8毫升·小时⁻¹·千克⁻¹,平均肾清除率为4.7毫升·小时⁻¹·千克⁻¹,即只有10%的剂量以原形从尿液中排出。根据血浆曲线计算的分布容积略大于体重,为1.1升·千克⁻¹。在吸收、分布和消除阶段,未刺激的混合唾液中的可替宁浓度比血浆中的高20%至40%。由于唾液中的清除率和分布值与血浆中的相应值成正比,因此在这两种体液中获得了相似的终末半衰期值,血浆和唾液分别为15.5小时和16.8小时。因此,可替宁在静脉注射和口服给药后的动力学是线性的,唾液浓度与血浆浓度一样,能提供关于可替宁在体内处置的相同信息。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验