School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Molecules. 2023 Mar 7;28(6):2426. doi: 10.3390/molecules28062426.
Recently, selenium nanoparticles have been drawing attention worldwide, and it is crucial to increase the stability of nano-Se. polysaccharides (MOP) are the main active component in radix. However, their low activity has limited their application. A novel selenium nanoparticle (Se-MOP) was prepared to solve these problems using MOP as a dispersant. The zeta potential was measured to evaluate the stability, and UV and ATR-FTIR were used to investigate the binding type of selenium and MOP. The morphology was observed by the TEM method. Furthermore, the inhibitory effect on five selected cancer cells (HepG2, MCF-7, AGS, PC9, and HCT8) was evaluated, showing remarkable inhibition of all five cancer cells. The mechanism of inhibition was also investigated by cell circle assay, and it was found that Se-MOP could induce cell circle G0/G1 phase arrest. Immune-enhancing activities were evaluated by measuring the proliferation and cytokines of mouse spleen lymphocytes in vitro and quantitative RT-PCR. The results indicated that single stimulation of Se-MOP and synergistic stimulation with PHA or LPS increased immune capacity and improved immune by increasing the expression of cytokines.
近年来,纳米硒受到了全世界的关注,提高纳米硒的稳定性至关重要。多糖(MOP)是 的主要活性成分。然而,其低活性限制了它们的应用。本研究采用 MOP 作为分散剂,制备了一种新型纳米硒(Se-MOP),以解决这些问题。通过测量 Zeta 电位评估其稳定性,通过 UV 和 ATR-FTIR 研究硒与 MOP 的结合类型。通过 TEM 方法观察形态。此外,还评估了对五种选定癌细胞(HepG2、MCF-7、AGS、PC9 和 HCT8)的抑制作用,结果表明对所有五种癌细胞均有显著抑制作用。还通过细胞周期试验研究了抑制机制,发现 Se-MOP 可诱导细胞周期 G0/G1 期阻滞。通过体外测量小鼠脾淋巴细胞的增殖和细胞因子以及定量 RT-PCR 评估免疫增强活性。结果表明,Se-MOP 的单独刺激以及与 PHA 或 LPS 的协同刺激均可通过增加细胞因子的表达来提高免疫能力和改善免疫。