A novel polysaccharide gel bead enabled oral enzyme delivery with sustained release in small intestine

• Published in: Food hydrocolloids Vol. 84; pp. 68 - 74
• Main Authors: Wang, Yi-Wei, Chen, Li-Ye, An, Feng-Ping, Chang, Man-Qian, Song, Hong-Bo
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01.11.2018
• Subjects: beta-galactosidase; bioactive compounds; bioactive properties; coatings; encapsulation; enzyme activity; food composition; Fourier transform infrared spectroscopy; FTIR; gastric juice; hydrocolloids; Hydrogel; hydrogels; in vitro studies; kappa carrageenan; Release; scanning electron microscopes; scanning electron microscopy; SEM; small intestine; sodium; Swelling; therapeutics; SEM; Hydrogel; Swelling; FTIR; Release
• ISSN: 0268-005X; 1873-7137
• DOI: 10.1016/j.foodhyd.2018.05.039

We report a novel oral delivery system based on sodium alginate/κ-carrageenan binary polysaccharide gel bead. β-galactase was selected as a model molecule to evaluate the capacity of the beads as delivery system. After enzyme encapsulation, the hydrogel beads were subsequently coated with κ-carrageenan (κ-CG) and ε-polylysine (ε-PL). Scanning electron microscope (SEM) images revealed the microstructural differences between the beads synthesized with and without ε-PL coating. Fourier transform infrared spectroscopy (FTIR) spectra further proofed the successful coating of ε-PL and κ-CG. Releasing studies showed that the enzyme releasing time is significantly prolonged by ε-PL coating. In vitro experiments showed that, the hydrogel beads synthesized with 0.6% ε-PL were stable and compact in the simulated gastric fluid environment with negligible swelling, which can protect the loaded enzyme effectively. More than 94.6% lactase activity can be retained after treated with simulated gastric fluid (pH 4) for 2 h. After transferred into simulated small intestinal fluid for 14 h (pH 7.4), as much as 89.6% of the enzyme can be released from the beads. It is worthy to note that the activity of the released enzyme retained 76.0% of total enzyme activity. These unique properties of the hydrogel beads enabled the effectively maintenance of enzyme bioactivity and thus enhanced the enzyme delivery and therapeutic efficiency. The reported delivery system is an ideal oral delivery system for bioactive food compounds, especially for compounds that are unstable in gastric environment. [Display omitted] •Polylysine coating on hydrogel bead was achieved via electrostatic interactions.•β-galactase in coated beads had a good resistance against gastric acid damage.•Coated beads showed a significantly improved oral release behavior.•Usability after drying demonstrated potential applications in food industry.