Institute of Food Science, Technology and Nutrition (ICTAN-CSIC), José Antonio Novais 10, 28040, Madrid, Spain.
Food Funct. 2021 Mar 15;12(5):2137-2147. doi: 10.1039/d0fo02922j.
Two drying methods (spray drying and heat drying) were used to entrap various natural compounds within a matrix of iota-carrageenan. The natural compounds were, namely, collagen hydrolysate (CH), pomegranate polyphenolic extract (PP) and shrimp lipid extract (SL). The resulting dry powders were compared in terms of water solubility, entrapment efficiency, hydrodynamic particle properties, ζ potential and antioxidant properties (ABTS radical scavenging capacity, ferric ion reducing power and Folin-reactive substances). Dry powders and plain compounds were incorporated into squid surimi gels, and after in vitro simulated gastrointestinal digestion (sGID), the residual antioxidant and angiotensin-converting enzyme (ACE)-inhibitory activities were evaluated. All powders showed antioxidant properties, electronegative ζ potential and great entrapment efficiency after rehydration (ranging from ∼70 to 97%). The heat-dried powders were composed of microparticles ranging from 177 to 380 μm resulting in low water solubility (21.6-36.1%), while the average particle size and solubility values of spray-dried preparations were 2.9-13.2 μm and >86%, respectively. In contrast to the plain compounds, the addition of any of the microparticle dried preparations allowed obtaining well-conformed surimi gels. The ACE-inhibitory capacity of the surimi gels after sGID was increased by the addition of any of the compounds studied, but to a lesser extent by their entrapment forms (except with the entrapped SL). The antioxidant activities of gels with the entrapped compounds were even lower than those of gels without bioactives in some cases. In conclusion, the addition of dried microparticles did not increase the biological activity as compared to the plain compounds; however, they were beneficial to ensure adequate gel consistency.
两种干燥方法(喷雾干燥和热干燥)被用于将各种天然化合物包埋在iota-卡拉胶基质中。这些天然化合物分别是胶原蛋白水解物(CH)、石榴多酚提取物(PP)和虾脂质提取物(SL)。所得干粉在水溶性、包埋效率、水动力颗粒特性、ζ电位和抗氧化性能(ABTS 自由基清除能力、铁离子还原能力和 Folin 反应物质)方面进行了比较。干粉和纯化合物被掺入鱿鱼鱼糜凝胶中,经过体外模拟胃肠道消化(sGID)后,评估了剩余的抗氧化和血管紧张素转换酶(ACE)抑制活性。所有粉末在复水后均表现出抗氧化特性、带负电荷的 ζ 电位和高包埋效率(范围为~70%至 97%)。热干燥粉末由 177 至 380 μm 的微颗粒组成,导致低水溶性(21.6-36.1%),而喷雾干燥制剂的平均粒径和溶解度值分别为 2.9-13.2 μm 和>86%。与纯化合物相比,任何微粉干燥制剂的添加都可以获得形态良好的鱼糜凝胶。sGID 后,添加任何研究化合物都可以增加鱼糜凝胶的 ACE 抑制能力,但以包埋形式添加的效果较小(除了包埋的 SL 外)。在某些情况下,含有包埋化合物的凝胶的抗氧化活性甚至低于不含生物活性物质的凝胶。总之,与纯化合物相比,添加干燥的微粉并没有增加生物活性;然而,它们有利于确保适当的凝胶一致性。