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用于加速候选药物早期开发的临时制备的控释制剂。

Extemporaneously prepared controlled release formulations for accelerating the early phase development of drug candidates.

作者信息

Thombre Avinash G, Berchielli Alfred, Rogers Janyce F

机构信息

Pfizer Inc., Center for Discovery and Development Sciences, Eastern Point Road, Groton, CT 06340, USA.

Pfizer Inc., Center for Discovery and Development Sciences, Eastern Point Road, Groton, CT 06340, USA.

出版信息

Drug Discov Today. 2014 May;19(5):694-700. doi: 10.1016/j.drudis.2014.02.001. Epub 2014 Feb 19.

Abstract

Extemporaneous drug preparations, which are compounded by a pharmacist at a clinical site, are commonly used in early clinical studies to evaluate the performance of drug candidates. However, the types of formulations compounded have been limited to relatively simple preparations such as solutions, suspensions and active ingredients filled into capsules. This article describes the preparation of advanced formulations, specifically extemporaneously prepared matrix tablets and osmotic capsules, which can be used to evaluate the feasibility of controlled release for exploratory new drug candidates or new formulations of existing drugs with a differentiated medical advantage. Extemporaneously prepared dosage forms enable the rapid assessment (i.e. reduced cycle time) of new formulation ideas with minimal quantity of the active pharmaceutical ingredient needed to demonstrate proof-of-concept.

摘要

由药剂师在临床场所配制的临时药物制剂,常用于早期临床研究以评估候选药物的性能。然而,所配制的制剂类型仅限于相对简单的制剂,如溶液、混悬液以及填充于胶囊中的活性成分。本文描述了先进制剂的制备,特别是临时制备的基质片剂和渗透胶囊,它们可用于评估具有探索性的新药候选物或具有差异化医学优势的现有药物新制剂的控释可行性。临时制备的剂型能够以最少的活性药物成分用量快速评估(即缩短周期时间)新的制剂理念,以证明概念验证。

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