脂类消化
壳聚糖
皮克林乳液
多糖
化学
Zeta电位
化学工程
油滴
乳状液
水解
脂滴
絮凝作用
表面电荷
消化(炼金术)
粒径
色谱法
脂肪酶
生物化学
有机化学
纳米颗粒
酶
物理化学
工程类
作者
Ana Letícia Rodrigues Costa,Andresa Gomes,Guilherme de Figueiredo Furtado,Heloisa Tibolla,Florência Cecília Menegalli,Rosiane Lopes Cunha
标识
DOI:10.1016/j.carbpol.2019.115344
摘要
An in vitro digestibility protocol was used to elucidate the role of different emulsifying polysaccharides particles on the lipid digestion rate of oil-in-water Pickering emulsions. Emulsions stabilized by cellulose crystals (CCrys), cellulose nanofibers (CNFs), chitosan particles and a conventional emulsifier (Tween 80) were evaluated concerning microstructure, droplet size, zeta potential and free fatty acids released during digestion. After gastric step, the high positive charge of chitosan-stabilized emulsions favored the droplets disaggregation resulting in a mild effect of bridging flocculation by particles sharing and displacement of the size curve distribution toward lower size. After passing through the intestinal condition, these emulsions presented few droplets and chitosan aggregates with a monomodal size distribution and high mean droplet size (D4,3 = 197 ± 8 μm). On the other hand, Tween 80, CCrys and CNFs were able to inhibit lipid digestion and no changes on mean droplet size were observed following intestinal step. CNFs-stabilized emulsion showed the lowest lipid digestion, whereas the strong adherence of the CCrys particles onto the droplet interface became them resistant to displacement by surface-active components (i.e. bile salts and lipase enzyme). On the other hand, a slow lipid hydrolysis could be observed in chitosan-stabilized emulsions promoted by competition between chitosan aggregates and intestinal fluids by the oil droplet interface. Studying the emulsions stabilized using different polysaccharides particles on gastrointestinal conditions we could elucidate important features for their potential application as control systems of lipid digestion rate, as well as, as delivery systems of lipophilic compounds.
科研通智能强力驱动
Strongly Powered by AbleSci AI