Wong See Kiat, Lawrencia Dora, Supramaniam Janarthanan, Goh Bey Hing, Manickam Sivakumar, Wong Tin Wui, Pang Cheng Heng, Tang Siah Ying
Chemical Engineering Discipline, School of Engineering, Monash University Malaysia, Subang Jaya, Malaysia.
Biofunctional Molecule Exploratory Research Group, School of Pharmacy, Monash University Malaysia, Subang Jaya, Malaysia.
Front Nutr. 2021 Oct 4;8:752207. doi: 10.3389/fnut.2021.752207. eCollection 2021.
The present work aimed to investigate the swelling behavior, digestion, and release of a hydrophobic bioactive compound, thymoquinone (TQ), loaded in Pickering emulsion incorporated in alginate-chitosan hydrogel beads using a simulated gastrointestinal model. In this study, oil-in-water Pickering emulsions of uniform micron droplet sizes were formulated using 20% red palm olein and 0.5% (w/v) cellulose nanocrystals-soy protein isolate (CNC/SPI) complex followed by encapsulation within beads. FT-IR was used to characterize the bonding between the alginate, chitosan, and Pickering emulsion. 2% (w/v) alginate-1% (w/v) chitosan hydrogel beads were found to be spherical with higher stability against structural deformation. The alginate-chitosan beads displayed excellent stability in simulated gastric fluid (SGF) with a low water uptake of ~19%. The hydrogel beads demonstrated a high swelling degree (85%) with a superior water uptake capacity of ~593% during intestinal digestion in simulated intestinal fluid (SIF). After exposure to SIF, the microstructure transformation was observed, causing erosion and degradation of alginate/chitosan wall materials. The release profile of TQ up to 83% was achieved in intestinal digestion, and the release behavior was dominated by diffusion via the bead swelling process. These results provided useful insight into the design of food-grade colloidal delivery systems using protein-polysaccharide complex-stabilized Pickering emulsions incorporated in alginate-chitosan hydrogel beads.
本研究旨在利用模拟胃肠道模型,研究负载于藻酸盐-壳聚糖水凝胶珠粒中、包含在皮克林乳液中的疏水性生物活性化合物百里醌(TQ)的溶胀行为、消化和释放情况。在本研究中,使用20%的红棕榈油精和0.5%(w/v)的纤维素纳米晶体-大豆分离蛋白(CNC/SPI)复合物制备了均匀微米级液滴尺寸的水包油型皮克林乳液,随后将其包封在珠粒中。采用傅里叶变换红外光谱(FT-IR)对藻酸盐、壳聚糖和皮克林乳液之间的键合进行表征。发现2%(w/v)藻酸盐-1%(w/v)壳聚糖水凝胶珠粒呈球形且对结构变形具有更高的稳定性。藻酸盐-壳聚糖珠粒在模拟胃液(SGF)中表现出优异的稳定性,吸水率低至约19%。在模拟肠液(SIF)中进行肠道消化时,水凝胶珠粒表现出高溶胀度(85%)和高达约593%的优异吸水能力。暴露于SIF后,观察到微观结构转变,导致藻酸盐/壳聚糖壁材发生侵蚀和降解。在肠道消化过程中,TQ的释放率高达83%,释放行为主要由通过珠粒溶胀过程的扩散主导。这些结果为使用包含在藻酸盐-壳聚糖水凝胶珠粒中的蛋白质-多糖复合物稳定的皮克林乳液设计食品级胶体递送系统提供了有用的见解。