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使用颊部分隔作为药物吸收相互作用的模型。

The use of buccal partitioning as a model of drug absorption interactions.

作者信息

McElnay J C, Mooney C

出版信息

J Clin Hosp Pharm. 1983 Jun;8(2):137-42. doi: 10.1111/j.1365-2710.1983.tb01043.x.

Abstract

Bioavailability describes both the rate and extent of drug absorption. The buccal absorption technique is a useful method for the examination of changed extent of drug absorption resulting from drug absorption interactions. The present work examined the usefulness of drug recovery profiles (after buccal absorption) in evaluating the rate of drug absorption. Recovery data, in the case of propranolol, did not change markedly after marked changes in the drug absorption rate, indicating that recovery profiles are a poor monitoring tool for changed absorption rates. The rate of drug absorption can be found using the buccal absorption method; however, this involves several different experiments on different days and, also, data must be found by measuring the drug in the absorption solution which also contains the interactant. The latter agent may interfere with drug assay procedures. The present work involved the model drug propranolol. Other drugs perhaps may behave differently.

摘要

生物利用度描述了药物吸收的速率和程度。颊部吸收技术是一种用于检查因药物吸收相互作用导致的药物吸收程度变化的有用方法。目前的研究考察了药物回收曲线(颊部吸收后)在评估药物吸收速率方面的实用性。就普萘洛尔而言,在药物吸收速率发生显著变化后,回收数据并未明显改变,这表明回收曲线对于变化的吸收速率是一种较差的监测工具。可以使用颊部吸收法来测定药物吸收速率;然而,这需要在不同日期进行几个不同的实验,而且,还必须通过测量吸收溶液中的药物来获取数据,而该吸收溶液中也含有相互作用剂。后一种试剂可能会干扰药物分析程序。目前的研究涉及模型药物普萘洛尔。其他药物的表现可能有所不同。

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