School of Modern Industry for Selenium Science and Engineering, Wuhan Polytechnic University, Wuhan 430023, PR China.
Key Laboratory for Deep Processing of Major Grain and Oil, Ministry of Education, Hubei Key Laboratory for Processing and Transformation of Agricultural Products, Wuhan Polytechnic University, Wuhan 430023, PR China.
Int J Biol Macromol. 2024 Nov;280(Pt 2):135586. doi: 10.1016/j.ijbiomac.2024.135586. Epub 2024 Sep 12.
To develop a promising selenium supplement that overcomes the instability and poor water dispersibility of selenium nanoparticles (SeNPs), we synthesized a series of amphiphilic octenyl succinic anhydride starch (OSAS) through esterification. As the degree of substitution (DS) increased, the particle size of OSAS micelles and the critical micelle concentration (CMC) decreased. FTIR and XRD analysis confirmed the successful introduction of octenyl succinic anhydride groups onto starch. Subsequently, OSAS micelles were used as carriers to synthesize SeNPs via in situ chemical reduction, forming SeNPs-loaded self-assembled starch nano-micelles (OSAS-SeNPs). The OSAS-SeNPs exhibited spherical dispersion in water with an average diameter of 116.1 ± 2.3 nm, contributed to enhanced hydrophobic interactions. TEM images showed a core-shell structure with SeNPs as the core and OSAS as the shell. FTIR results indicated hydrogen bonding interactions between OSAS and SeNPs. Due to the negatively charged OSAS shell and hydrogen bonding (OH⋯Se), OSAS-SeNPs remained non-aggregated for one month at room temperature, demonstrating remarkable stability. This study suggests that using OSAS can address the synthesis and stability issues of SeNPs, making it a potential selenium supplement candidate for further evaluation as an anticancer agent.
为了开发一种有前景的硒补充剂,克服硒纳米颗粒(SeNPs)的不稳定性和差的水分散性,我们通过酯化合成了一系列两亲性辛烯基琥珀酸淀粉(OSAS)。随着取代度(DS)的增加,OSAS 胶束的粒径和临界胶束浓度(CMC)降低。傅里叶变换红外光谱(FTIR)和 X 射线衍射(XRD)分析证实了成功地将辛烯基琥珀酸酐基团引入到淀粉上。随后,OSAS 胶束被用作载体,通过原位化学还原法合成 SeNPs,形成负载 SeNPs 的自组装淀粉纳米胶束(OSAS-SeNPs)。OSAS-SeNPs 在水中呈现出球形分散,平均直径为 116.1±2.3nm,有助于增强疏水性相互作用。TEM 图像显示了具有 SeNPs 为核和 OSAS 为壳的核壳结构。FTIR 结果表明 OSAS 与 SeNPs 之间存在氢键相互作用。由于带负电荷的 OSAS 壳和氢键(OH⋯Se),OSAS-SeNPs 在室温下一个月内保持非聚集状态,表现出显著的稳定性。这项研究表明,使用 OSAS 可以解决 SeNPs 的合成和稳定性问题,使其成为作为抗癌剂进一步评估的潜在硒补充剂候选物。