Dietary fibre hydrogels: Tunable polydextrose-sodium alginate networks for bioactive compound delivery
Yuqing He1, Wei Gao1, Zhijun Zhang2
1Shandong Key Laboratory of Healthy Food Resources Exploration and Creation, School of Food Sciences and Engineering, Qilu University of Technology, Shandong Academy of Sciences, Jinan, 250353, China; State Key Laboratory of Green Papermaking and Resource Cycling, Qilu University of Technology, Shandong Academy of Sciences, Jinan, 250353, China.
Abstract:
Herein, we developed a versatile composite hydrogel by combining two dietary fibres, polydextrose (PDX) and sodium alginate (SA), at varying mass ratios (from 9:1 to 6:4). The microstructure of the prepared hydrogels evolved from an irregular macroporous network to a highly ordered honeycomb-like structure with increasing SA content. Fourier transform infrared spectroscopy and X-ray diffraction analysis revealed that PDX-SA composite hydrogels were formed through ionic cross-linking and hydrogen bonding. The incorporation of SA significantly enhanced the swelling capacity, colloidal stability (indicated by a high negative zeta potential), and water retention capacity (indicated by low syneresis) of the hydrogels while reducing their initial gel strength. The composite hydrogel with a PDX:SA ratio of 6:4 (PDX-SA-4) exhibited optimal overall properties, including a uniform microstructure, high swelling ratio (38.32% at 8 h), and excellent suspension stability (zeta potential: -33.92 mV). Furthermore, anthocyanins (ACNs) were effectively loaded into PDX-SA-4, exhibiting a concentration-dependent release profile in vitro. Notably, in vitro digestion experiments revealed that PDX-SA-ACNs synergistic lipid-regulating hydrogel effectively inhibited lipid digestion. These findings indicate that PDX-SA composite hydrogels, with tunable physicochemical properties, can be used to develop functional foods and delivery systems capable of modulating satiety and inhibiting lipid absorption.


