Suppr超能文献

具有特定消化酶活性的纳米结构生物材料用于控制亲脂性生物活性分子的胃肠道吸收。

Nanostructuring Biomaterials with Specific Activities towards Digestive Enzymes for Controlled Gastrointestinal Absorption of Lipophilic Bioactive Molecules.

机构信息

School of Pharmacy and Medical Sciences, University of South Australia, City East Campus, Adelaide, South Australia 5001, Australia.

Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand.

出版信息

Adv Colloid Interface Sci. 2016 Nov;237:52-75. doi: 10.1016/j.cis.2016.10.003. Epub 2016 Oct 22.

Abstract

This review describes the development of novel lipid-based biomaterials that modulate fat digestion for the enhanced uptake of encapsulated lipophilic bioactive compounds (e.g. drugs and vitamins). Specific focus is directed towards analysing how key material characteristics affect the biological function of digestive lipases and manipulate lipolytic digestion. The mechanism of lipase action is a complex, interfacial process, whereby hydrolysis can be controlled by the ability for lipase to access and adsorb to the lipid-in-water interface. However, significant conjecture exists within the literature regarding parameters that influence the activities of digestive lipases. Important findings from recent investigations that strategically examined the interplay between the interfacial composition of the lipid microenvironment and lipolysis kinetics in simulated biophysical environments are presented. The correlation between lipolysis and the rate of solubilisation and absorption of lipophilic compounds in the gastrointestinal tract (GIT) is detailed. Greater insights into the mechanism of lipase action have provided a new approach for designing colloidal carriers that orally deliver poorly soluble compounds, directly impacting the pharmaceutical and food industries.

摘要

本文综述了新型基于脂质的生物材料的发展,这些材料可调节脂肪消化,从而增强脂溶性生物活性化合物(如药物和维生素)的包封摄取。本研究特别关注分析关键材料特性如何影响消化脂肪酶的生物学功能,并操纵脂肪的消化。脂肪酶的作用机制是一个复杂的界面过程,脂肪酶水解的能力可以通过脂肪酶能够进入和吸附到油水界面的能力来控制。然而,文献中对于影响消化脂肪酶活性的参数存在很大的推测。本文介绍了在模拟生物物理环境中,最近对脂质微环境的界面组成和脂肪酶动力学之间相互作用进行了策略性研究的重要发现。详细阐述了脂肪消化与脂溶性化合物在胃肠道(GIT)中溶解和吸收速率之间的相关性。对脂肪酶作用机制的深入了解为设计口服传递难溶性化合物的胶体载体提供了新方法,直接影响了制药和食品行业。

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