Jiang Hongrui, Wang Xiaoyi, Han Lishu, Tang Chengjiang, He Jie, Min Douyong
College of Light Industry and Food Engineering, Guangxi University, 53004 Nanning, China.
College of Light Industry and Food Engineering, Guangxi University, 53004 Nanning, China.
Int J Biol Macromol. 2023 Aug 15;246:125620. doi: 10.1016/j.ijbiomac.2023.125620. Epub 2023 Jun 29.
High internal phase Pickering emulsions (HIPPEs) stabilized by food grade particles have received much attention as deliver vehicles for bioactives in recent years. In this study, ultrasonic treatment was conducted to regulate the size of silkworm pupa protein (SPP) particles, fabricating oil-in-water (O/W) HIPPEs with intestinal releasability. Briefly, the pretreated SPP and SPP-stabilized HIPPEs were characterized, and the targeting release was investigated using in vitro gastrointestinal simulations and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Results revealed ultrasonic treatment time was the key factor regulating emulsification performance and stability of HIPPEs. Optimized SPP particles were obtained based on their size and zeta potential of 152.67 nm and 26.77 mV, respectively. With ultrasonic treatment, the hydrophobic groups in the secondary structure of SPP were exposed, facilitating the formation of a stable oil-water interface for HIPPEs. Additionally, SPP-stabilized HIPPE showed high stable against the gastric digestion. The SPP with 70 kDa molecular weight, which was the major interfacial proteins of the HIPPE, can be hydrolyzed by intestinal digestive enzymes, enabling the intestine-targeted release of the emulsion. Overall, in the present study, a facile method was developed to stabilize HIPPEs using solo SPP with ultrasonic treatment to protect and deliver hydrophobic bioactive ingredients.
近年来,由食品级颗粒稳定的高内相比Pickering乳液(HIPPEs)作为生物活性物质的递送载体受到了广泛关注。在本研究中,进行了超声处理以调节蚕蛹蛋白(SPP)颗粒的大小,制备具有肠道释放能力的水包油(O/W)型HIPPEs。简要地说,对预处理的SPP和SPP稳定的HIPPEs进行了表征,并使用体外胃肠道模拟和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳研究了靶向释放。结果表明,超声处理时间是调节HIPPEs乳化性能和稳定性的关键因素。基于其尺寸和zeta电位分别为152.67 nm和26.77 mV获得了优化的SPP颗粒。通过超声处理,SPP二级结构中的疏水基团暴露出来,有利于形成稳定的HIPPEs油水界面。此外,SPP稳定的HIPPE对胃消化具有高度稳定性。分子量为70 kDa的SPP是HIPPE的主要界面蛋白,可被肠道消化酶水解,从而实现乳液的肠道靶向释放。总体而言,在本研究中,开发了一种简便的方法,通过超声处理使用单一SPP来稳定HIPPEs,以保护和递送疏水性生物活性成分。