Pınarbaşı Nida, Zeren Firuze Ergin, Topuz Ayhan
Department of Food Engineering, Akdeniz University, Graduate School of Natural and Applied Sciences, Antalya, Türkiye.
Department of Food Engineering, Akdeniz University, Faculty of Engineering, Antalya, Türkiye.
J Food Sci. 2025 Aug;90(8):e70493. doi: 10.1111/1750-3841.70493.
The aim of this study was to enhance the stability and water solubility of ellagic acid (EA) from pomegranate peel by microencapsulation using various carriers, and to improve its biotransformation into urolithin A (Uro-A) and urolithin B (Uro-B) by a probiotic microorganism. The formulation of carrier materials, comprising maltodextrin, inulin, and gum Arabic, and the inlet air temperature of the spray-drying microencapsulation process were optimized to enhance the stability and water solubility of EA. In addition to the variable ratios of carrier materials, a fixed concentration of β-cyclodextrin (1.1%) was incorporated into carrier formulations to further improve the water solubility of EA. The optimal spray drying conditions were determined as an inlet air temperature of 158°C and a carrier composition ratio of maltodextrin:inulin:gum Arabic at 2:1:0, supplemented with 1.1% β-cyclodextrin. The EA concentration and water solubility of the microcapsules produced under the optimum conditions were 11.39 ± 0.35 g/100 g dry weight and 9.31 ± 0.78%, respectively. The optimized encapsulation process increased the water solubility of EA by 21.54 times compared to free EA. Microcapsules of EA produced under optimal conditions were evaluated through in vitro gastrointestinal digestion and compared with controls. Bifidobacterium pseudocatenulatum was used for microbial fermentation, and the conversion of EA to urolithins A and B was evaluated according to the microbial load and the length of the incubation time. Encapsulation was found to significantly enhance this biotransformation. The microcapsules were also characterized and tested under various storage conditions. PRACTICAL APPLICATIONS: Encapsulation of EA increases its stability and water solubility, making it a more effective bioactive compound. The study found that EA microcapsules produced under optimized spray-drying conditions significantly enhanced biotransformation to Uro-A and Uro-B when incubated with Bifidobacterium pseudocatenulatum. These results support the potential use of encapsulated EA in functional foods and dietary supplements to improve gut health and more effectively deliver bioactive compounds. Obtained results will be useful for science, food, and the nutraceutical industry.
本研究的目的是通过使用各种载体进行微囊化来提高石榴皮中鞣花酸(EA)的稳定性和水溶性,并通过益生菌微生物将其生物转化为尿石素A(Uro-A)和尿石素B(Uro-B)。对包含麦芽糊精、菊粉和阿拉伯胶的载体材料配方以及喷雾干燥微囊化过程的进风温度进行了优化,以提高EA的稳定性和水溶性。除了载体材料的可变比例外,还在载体配方中加入固定浓度的β-环糊精(1.1%),以进一步提高EA的水溶性。确定最佳喷雾干燥条件为进风温度158°C,麦芽糊精:菊粉:阿拉伯胶的载体组成比例为2:1:0,并添加1.1%的β-环糊精。在最佳条件下生产的微胶囊中EA浓度和水溶性分别为11.39±0.35 g/100 g干重和9.31±0.78%。与游离EA相比,优化后的包封工艺使EA的水溶性提高了21.54倍。对在最佳条件下生产的EA微胶囊进行体外胃肠消化评估,并与对照进行比较。使用假链双歧杆菌进行微生物发酵,并根据微生物负荷和孵育时间长度评估EA向尿石素A和B的转化。发现包封显著增强了这种生物转化。还对微胶囊在各种储存条件下进行了表征和测试。实际应用:EA的微囊化提高了其稳定性和水溶性,使其成为一种更有效的生物活性化合物。研究发现,在优化的喷雾干燥条件下生产的EA微胶囊与假链双歧杆菌孵育时,显著增强了向Uro-A和Uro-B的生物转化。这些结果支持了包封EA在功能性食品和膳食补充剂中的潜在用途,以改善肠道健康并更有效地递送生物活性化合物。所得结果将对科学、食品和营养保健品行业有用。