Lin Dongdong, Su Jiaqi, Chen Shuai, Wei Jiao, Zhang Liang, Li Xiude, Yuan Fang
School of Physical Science and Technology, Qian Xuesen Collaborative Research Center of Astrochemistry and Space Life Sciences, Ningbo University, Ningbo, China.
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Key Laboratory of Functional Dairy, Ministry of Education, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing, China.
Front Nutr. 2022 Jul 19;9:965600. doi: 10.3389/fnut.2022.965600. eCollection 2022.
The complexation of protein and polysaccharide has shown considerable potential for the encapsulation of functional food components. In this work, propylene glycol alginate (PGA) molecules with different molecular weights (100, 500, and 2,000 kDa) were prepared through HO oxidation, which were further combined with β-lactoglobulin nanoparticles (β-lgNPs) to form PGA-β-lgNPs complexes for the delivery of curcumin (Cur). Results showed that the depolymerization of PGA molecule was resulted from the breakage of glycosidic bonds in the main chain, and the depolymerization rate of PGA molecule depended on the reaction time, temperature, solution pH and HO concentration. As the increasing molecular weight of PGA, the particle size, zeta-potential and turbidity of the complexes were obviously increased. The formation of PGA/β-lgNPs complexes was mainly driven by non-covalent interaction, including electrostatic gravitational interaction, hydrogen bonding and hydrophobic effect. Interestingly, the difference in the molecular weight of PGA also led to significantly differences in the micro-morphology of the complexes, as PGA with a high molecular weight (2,000 kDa) generated the formation of a "fruit-tree" shaped structure, whereas PGA with relatively low molecular weight (100 and 500 kDa) led to spherical particles with a "core-shell" structure. In addition, the incorporation of PGA molecules into β-lgNPs dispersion also contributed to the improvement in the encapsulation efficiency of Cur as well as physicochemical stability of β-lgNPs, and PGA with a higher molecular weight was confirmed with a better effect. Findings in the current work may help to further understand the effect of molecular weight of polysaccharide on the physical and structural properties as well as effectiveness as delivery systems of polysaccharide-protein complexes, providing for the possibility for the design and development of more efficient carriers for bioactive compounds in food system.
蛋白质与多糖的络合在功能性食品成分的包封方面显示出巨大潜力。在本研究中,通过HO氧化制备了不同分子量(100、500和2000 kDa)的海藻酸丙二醇酯(PGA)分子,并将其与β-乳球蛋白纳米颗粒(β-lgNPs)进一步结合,形成用于递送姜黄素(Cur)的PGA-β-lgNPs复合物。结果表明,PGA分子的解聚是由主链中糖苷键的断裂引起的,PGA分子的解聚速率取决于反应时间、温度、溶液pH值和HO浓度。随着PGA分子量的增加,复合物的粒径、zeta电位和浊度明显增大。PGA/β-lgNPs复合物的形成主要由非共价相互作用驱动,包括静电引力相互作用、氢键和疏水作用。有趣的是,PGA分子量的差异也导致复合物微观形态的显著差异,高分子量(2000 kDa)的PGA形成了“果树”形结构,而分子量相对较低(100和500 kDa)的PGA则导致具有“核壳”结构的球形颗粒。此外,将PGA分子掺入β-lgNPs分散体中也有助于提高Cur的包封效率以及β-lgNPs的物理化学稳定性,且已证实高分子量的PGA效果更好。当前研究结果可能有助于进一步了解多糖分子量对多糖-蛋白质复合物的物理和结构性质以及作为递送系统的有效性的影响,为食品体系中生物活性化合物更高效载体的设计和开发提供了可能性。