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药物的肠道靶向:合理设计方法与挑战。

Intestinal targeting of drugs: rational design approaches and challenges.

机构信息

Cardiovascular, Metabolic, and Endocrine Diseases Chemistry, Pfizer Worldwide Research and Development, Cambridge, MA 02139, USA.

出版信息

Curr Top Med Chem. 2013;13(7):776-802. doi: 10.2174/1568026611313070002.

Abstract

Targeting drugs to the gastrointestinal tract has been and continues to be an active area of research. Gut-targeting is an effective means of increasing the local concentration of active substance at the desired site of action while minimizing concentrations elsewhere in the body that could lead to unwanted side-effects. Several approaches to intestinal targeting exist. Physicochemical property manipulation can drive molecules to large, polar, low absorption space or alternatively to lipophilic, high clearance space in order to minimize systemic exposure. Design of compounds that are substrates for transporters within the gastrointestinal tract, either uptake or efflux, or at the hepato-biliary interface, may help to increase intestinal concentration. Prodrug strategies have been shown to be effective particularly for colon targeting, and several different technology formulation approaches are currently being researched. This review provides examples of various approaches to intestinal targeting, and discusses challenges and areas in need of future scientific advances.

摘要

将药物靶向胃肠道一直是并且仍然是一个活跃的研究领域。肠道靶向是一种有效的方法,可以增加活性物质在所需作用部位的局部浓度,同时最大限度地减少可能导致不良反应的其他部位的浓度。有几种肠道靶向的方法。物理化学性质的改变可以将分子导向大的、极性的、低吸收空间,或者相反地导向亲脂性的、高清除空间,以最大限度地减少全身暴露。设计在胃肠道内的转运体(无论是摄取还是外排)或肝胆界面作为底物的化合物,可以帮助增加肠道浓度。前药策略已被证明对结肠靶向特别有效,目前正在研究几种不同的技术制剂方法。本文提供了各种肠道靶向方法的例子,并讨论了未来科学进步所需的挑战和领域。

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