虾青素
牛血清白蛋白
化学
Zeta电位
傅里叶变换红外光谱
化学工程
壳聚糖
动态光散射
纳米颗粒
纳米载体
氢键
疏水效应
圆二色性
自组装
多糖
色谱法
有机化学
药物输送
结晶学
分子
生物化学
工程类
类胡萝卜素
作者
Yingyuan Zhao,Junxia Liu,Shengmeng Zhang,Zhaoxuan Wang,Huihui Jia,Hiroaki Oda,Ruifang Li
标识
DOI:10.1016/j.ijbiomac.2022.11.006
摘要
Astaxanthin is a natural liposoluble ketocarotenoid with various biological activities. Hydrophobic astaxanthin with C2h symmetry can self-assembly form H-type aggregates and J-type aggregates in hydrated polar solvents. However, astaxanthin and its aggregates are limited by its water insolubility and chemical instability. Here, the biological macromolecules bovine serum albumin (BSA) and chitosan were chosen as protein-polysaccharides based delivery systems for astaxanthin aggregates by molecular self-assembly method. The precise prepared H-ABC-NPs and J-ABC-NPs suspensions were both near spheres with hydrodynamic size around 281 ± 9 nm and 368 ± 5 nm and zeta potentials around +26 mV and +30 mV, respectively. Two types of astaxanthin aggregates were distinguished, water-dispersible, and stable in nanocarriers through UV-vis spectra observation. The encapsulation efficiency of the astaxanthin in ABC-NPs was above 90 %. Fourier transform infrared spectroscopy (FTIR) and circular dichroism (CD) analyses indicated that the dominant driving forces of ABC-NPs formation mainly included electrostatic, hydrophobic interactions and hydrogen bonding. These results offer an elegant opportunity for the protein-polysaccharides delivery systems, and provide an important perspective for applying novel water-dispersed astaxanthin aggregates products in nutrition and medicine industry.
科研通智能强力驱动
Strongly Powered by AbleSci AI