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载辅酶 Q10 的微胶囊,由单硬脂酸甘油酯和大豆分离蛋白-亚麻籽胶稳定:特性、体外释放和消化行为。

Coenzyme Q10-loaded microcapsules stabilized by glyceryl monostearate and soy protein isolates-flaxseed gum: Characterization, in vitro release and digestive behavior.

机构信息

School of Biology and Food Engineering, Changshu Institute of Technology, Changshu 215500, China; The East China Science and Technology Research Institute of Changshu Company Limited, Changshu 215500, China.

School of Biology and Food Engineering, Changshu Institute of Technology, Changshu 215500, China.

出版信息

Int J Biol Macromol. 2024 Oct;278(Pt 1):134680. doi: 10.1016/j.ijbiomac.2024.134680. Epub 2024 Aug 12.

Abstract

This study aimed to stabilize microcapsules with core materials of glyceryl monostearate (GMS) and octyl and decyl glycerate, and wall materials of soy protein isolates (SPI) and flaxseed gum (FG) by complex coacervation method to overcome the drawbacks of coenzyme Q10 (CoQ10). It was demonstrated by the study that the obtained microcapsules were irregular aggregates. Differential scanning calorimetry and x-ray diffraction patterns indicated that CoQ10 was entrapped inside the disordered semisolid cores of microcapsules. The CoQ10 loading and encapsulation efficiency analysis revealed that GMS and FG helped CoQ10 better encapsulated inside the microcapsules. The in vitro release curve showed a "burst" release of CoQ10 absorbed on the surface of microcapsules for the first 180 min, followed by a sustained release of the encapsulated CoQ10. GMS and FG contributed to the sustained release and the release mechanism of the microcapsules was Fickian diffusion. The in vitro simulated digestion demonstrated that the constructed microcapsules improved the bio-accessibility of CoQ10. Finally, due to the protection of GMS and FG, microcapsules had good storage stability. In conclusion, this study emphasized the potential of using new microcapsules to deliver and protect lipophilic ingredients, providing valuable information for developing functional foods with higher bioavailability.

摘要

本研究旨在通过复凝聚法稳定以甘油单硬脂酸酯(GMS)和辛基、癸基甘油酯为芯材,大豆分离蛋白(SPI)和亚麻籽胶(FG)为壁材的微胶囊,以克服辅酶 Q10(CoQ10)的缺点。研究表明,所得到的微胶囊是不规则的聚集体。差示扫描量热法和 X 射线衍射图谱表明,CoQ10 被包埋在微胶囊无序的半固态芯材内部。CoQ10 的负载和包封效率分析表明,GMS 和 FG 有助于更好地将 CoQ10 包封在微胶囊内。体外释放曲线显示,CoQ10 在微胶囊表面的吸收在最初的 180 分钟内呈现“突释”释放,随后是包封的 CoQ10 的持续释放。GMS 和 FG 有助于持续释放,微胶囊的释放机制为菲克扩散。体外模拟消化表明,构建的微胶囊提高了 CoQ10 的生物可及性。最后,由于 GMS 和 FG 的保护,微胶囊具有良好的储存稳定性。总之,本研究强调了使用新型微胶囊来输送和保护脂溶性成分的潜力,为开发具有更高生物利用度的功能性食品提供了有价值的信息。

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