Aliabbasi Neda, Emam-Djomeh Zahra, Askari Gholamreza, Salami Maryam
Transfer Phenomena Laboratory (TPL), Department of Food Science, Technology and Engineering, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran.
J Sci Food Agric. 2023 Feb;103(3):1484-1498. doi: 10.1002/jsfa.12246. Epub 2022 Nov 2.
Protein gels are used for different purposes, such as providing good texture, serving as fat replacers, and enhancing the nutritional and functional characteristics of foods. They can also deliver controlled release agents for sensitive drugs. The objective of this study was to investigate the impact of κ-carrageenan (kcr) concentration (0, 1.5, 3, and 4.5 mg g ) on the morphological and physicochemical properties and release behavior of glucono-δ-lactone (GDL)-induced pinto bean protein aggregate (PBA) gels.
When κ-carrageenan concentration increased from 0 to 1.5 and 3 mg.g , the firmness of the samples increased significantly, by 2.04 and 3.7 fold, respectively (P < 0.05). A compact and homogenous network with considerable strength and maximum water-holding capacity (97.52 ± 1.17%) was obtained with the addition of 3 mg g κ-carrageenan to the gel system. Further increasing the κ-carrageenan concentration to 4.5 mg g produced a coarse gel structure with higher storage modulus (G'), firmness (6.30-fold), thermal stability, and entrapment efficiency (85.6%). Depending on the κ-carrageenan concentration, various microstructures from protein continuous phase to κ-carrageenan continuous phase were observed. The release test indicated that 70.25% of the loaded curcumin was released in the simulated gastrointestinal tract for pure PBA gels. In contrast, for binary gels containing 4.5 mg g κ-carrageenan, curcumin was protected in the upper gastrointestinal tract, and 64.45% of loaded curcumin was delivered to the colon.
Our study showed that κ-carrageenan/PBA gels had high entrapment efficiency and could protect curcumin in the upper gastrointestinal tract. The hydrogels are therefore very valuable for colon-targeting delivery purposes. © 2022 Society of Chemical Industry.
蛋白质凝胶有不同用途,比如提供良好质地、用作脂肪替代物以及增强食品的营养和功能特性。它们还能为敏感药物提供控释剂。本研究的目的是探究κ-卡拉胶(kcr)浓度(0、1.5、3和4.5毫克/克)对葡萄糖酸-δ-内酯(GDL)诱导的斑豆蛋白聚集体(PBA)凝胶的形态、理化性质及释放行为的影响。
当κ-卡拉胶浓度从0增加到1.5毫克/克和3毫克/克时,样品的硬度显著增加,分别增加了2.04倍和3.7倍(P < 0.05)。向凝胶体系中添加3毫克/克κ-卡拉胶可得到具有相当强度和最大持水能力(97.52±1.17%)的致密均匀网络。将κ-卡拉胶浓度进一步提高到4.5毫克/克会产生具有更高储能模量(G')、硬度(6.30倍)、热稳定性和包封率(85.6%)的粗糙凝胶结构。根据κ-卡拉胶浓度的不同,观察到从蛋白质连续相到κ-卡拉胶连续相的各种微观结构。释放试验表明,对于纯PBA凝胶,70.25%的负载姜黄素在模拟胃肠道中释放。相比之下,对于含有4.5毫克/克κ-卡拉胶的二元凝胶,姜黄素在上胃肠道中受到保护,64.45%的负载姜黄素被递送至结肠。
我们的研究表明,κ-卡拉胶/PBA凝胶具有高包封率,并且可以在上胃肠道中保护姜黄素。因此,这些水凝胶对于结肠靶向递送目的非常有价值。© 2022化学工业协会。