首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Calcium-binding casein phosphopeptides-loaded chitosan oligosaccharides core-shell microparticles for controlled calcium delivery: Fabrication, characterization, and in vivo release studies
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Calcium-binding casein phosphopeptides-loaded chitosan oligosaccharides core-shell microparticles for controlled calcium delivery: Fabrication, characterization, and in vivo release studies

机译:钙粘合酪蛋白蛋白磷酸磷酸壳聚糖寡糖用于受控钙递送的核 - 壳微粒:制备,表征和体内释放研究

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摘要

Core-shell microparticles based on food-grade biopolymers are of particular interest for biological components delivery owing to their unique controlled release property. Here, we introduce a method to fabricate calciumbinding casein phosphopeptides (CPP)-loaded core-shell microparticles for oral calcium delivery, based on ionic gelation interactions between chitosan oligosaccharides (COS) and tripolyphosphate (TPP). The fabrication method, textural properties, calcium binding capacity, pH-dependent stability, thermal properties, intermolecular forces, morphology characterizations, the controlled calcium release and calcium absorption properties in vitro and vivo of core-shell microparticles were studied. The results showed that COS was successfully crosslinked through TPP while CPP-Ca was incorporated in it, and microparticles showed appropriate textural properties, calcium-loaded capacity, and thermal properties. Morphology observations showed the core structures were successfully coatedwith outer-layer COS shell. Additionally, the calciumrelease and absorption studies in vitro and in vivo exhibited CPP-Ca-loaded microparticles could achieve controlled calcium release and sustained calcium uptake. Therefore, the fabricated CPP-Ca-loaded core-shell microparticles could function as promising calcium supplements for enhancing calcium bioavailability. (C) 2019 Elsevier B.V. All rights reserved.
机译:由于其独特的控释性,基于食品级生物聚合物的核心壳微粒对生物成分的递送特别感兴趣。这里,我们介绍一种制造钙屈辛酪蛋白肽(CPP) - 基于壳聚糖寡糖(COS)和三聚磷酸酯(TPP)之间的离子凝胶相互作用的口服钙递送来制造钙纤维蛋白磷酸肽(CPP)的核壳微粒。研究了制备方法,纹理性质,钙结合能力,pH依赖性稳定性,热性质,分子间力,形态学表征,体外和体内核 - 壳微粒体外和体内的钙释放和钙吸收性能。结果表明,COS通过TPP成功交联,而CPP-CA掺入其中,并且微粒显示出适当的纹理性质,钙载能力和热性能。形态学观察显示核心结构成功涂覆外层COS壳。另外,体外和体内的钙释放和吸收研究表现出CPP-Ca-Loaded微粒可以实现控制的钙释放和持续的钙吸收。因此,制造的CPP-Ca-Loaded核心壳微粒可以用作提高生物利用度的有前途的钙补充剂。 (c)2019 Elsevier B.v.保留所有权利。

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