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用于控制铁释放、增强铁吸收和生物利用度的铁传递系统。

Iron delivery systems for controlled release of iron and enhancement of iron absorption and bioavailability.

机构信息

School of Food Science and Technology, National Engineering Research Center of Seafood, Dalian Polytechnic University, Dalian, P. R. China.

Collaborative Innovation Center of Seafood Deep Processing, Dalian Polytechnic University, Dalian, P. R. China.

出版信息

Crit Rev Food Sci Nutr. 2023;63(29):10197-10216. doi: 10.1080/10408398.2022.2076652. Epub 2022 May 19.

Abstract

Iron deficiency is a global nutritional problem, and adding iron salts directly to food will have certain side effects on the human body. Therefore, there is growing interest in food-grade iron delivery systems. This review provides an overview of iron delivery systems, with emphasis on the controlled release of iron during gastrointestinal digestion, as well as the enhancement of iron absorption and bioavailability. Iron-bearing proteins are easily degraded by digestive enzymes and absorbed through receptor-mediated endocytosis. Instead, protein aggregates are slowly degraded in the stomach, which delays iron release and serves as a potential iron supplement. Amino acids, peptides and polysaccharides can bind iron through iron binding sites, but the formed compounds are prone to dissociation in the stomach. Moreover, peptides and polysaccharides can deliver iron by mediating the formation of ferric oxyhydroxide which is absorbed through endocytosis or bivalent transporter 1. In addition, liposomes are unstable during gastric digestion and iron is released in large quantities. Complexes formed by polysaccharides and proteins, and microcapsules formed by polysaccharides can delay the release of iron in the gastric environment and prolong iron release in the intestinal environment. This review is conducive to the development of iron functional ingredients and dietary supplements.

摘要

缺铁是一个全球性的营养问题,直接将铁盐添加到食物中会对人体产生一定的副作用。因此,人们对食品级铁传递系统越来越感兴趣。本综述概述了铁传递系统,重点介绍了铁在胃肠道消化过程中的控制释放,以及铁吸收和生物利用度的增强。含铁蛋白很容易被消化酶降解,并通过受体介导的内吞作用吸收。相反,蛋白质聚集体在胃中缓慢降解,从而延迟铁的释放,成为潜在的铁补充剂。氨基酸、肽和多糖可以通过铁结合位点与铁结合,但形成的化合物在胃中容易解离。此外,肽和多糖可以通过介导形成通过内吞作用或二价转运体 1 吸收的高铁羟氧化物来输送铁。此外,脂质体在胃消化过程中不稳定,铁大量释放。多糖和蛋白质形成的复合物以及多糖形成的微胶囊可以在胃环境中延迟铁的释放,并延长铁在肠道环境中的释放。本综述有助于铁功能成分和膳食补充剂的开发。

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