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在儿童患者用即释口服剂型开发中应用体外生物药剂学方法。

Application of in vitro biopharmaceutical methods in development of immediate release oral dosage forms intended for paediatric patients.

机构信息

Pharmacy, Pharmacology and Therapeutics Section, University of Birmingham, Birmingham, UK.

出版信息

Eur J Pharm Biopharm. 2013 Nov;85(3 Pt B):833-42. doi: 10.1016/j.ejpb.2013.04.015. Epub 2013 May 9.

Abstract

Biopharmaceutics is routinely used in the design and development of medicines to generate science based evidence to predict in vivo performance; the application of this knowledge specifically to paediatric medicines development is yet to be explored. The aim of this review is to present the current status of available biopharmaceutical tools and tests including solubility, permeability and dissolution that may be appropriate for use in the development of immediate release oral paediatric medicines. The existing tools used in adults are discussed together with any limitations for their use within paediatric populations. The results of this review highlight several knowledge gaps in current methodologies in paediatric biopharmaceutics. The authors provide recommendations based on existing knowledge to adapt tests to better represent paediatric patient populations and also provide suggestions for future research that may lead to better tools to evaluate paediatric medicines.

摘要

生物药剂学在药品的设计和开发中被常规应用,以产生基于科学的证据来预测体内性能;然而,这一知识在儿科药品开发中的具体应用仍有待探索。本综述的目的是介绍目前可用于开发即释型口服儿科药品的生物药剂学工具和测试的现状,包括溶解度、渗透性和溶解率。本文讨论了成人中使用的现有工具,以及它们在儿科人群中使用的任何限制。本综述的结果突出了儿科生物药剂学中当前方法学的几个知识空白。作者根据现有知识提出了一些建议,以调整测试方法,更好地代表儿科患者群体,同时也为未来可能开发出更好的儿科药品评估工具的研究提供了建议。

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