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Surface decoration of selenium nanoparticles by mushroom polysaccharides-protein complexes to achieve enhanced cellular uptake and antiproliferative activity

机译:蘑菇多糖-蛋白质复合物对硒纳米颗粒的表面修饰,以增强细胞摄取和抗增殖活性

摘要

By using mushroom polysaccharides-protein complexes (PSP) as the capping agent, size controllable and highly stable selenium nanoparticles (SeNPs) have been successfully created in a simple redox system of sodium selenite and ascorbic acid. SeNPs were capped with PSP through strong physical adsorption of hydroxyl groups of polysaccharides and imino groups of proteins on the surface of SeNPs. PSP surface decoration significantly enhanced the cellular uptake of SeNPs through endocytosis. Treatment with PSP-SeNPs significantly inhibited the growth of MCF-7 human breast cacinoma cells through induction of apoptosis with the involvement of PARP cleavage and caspase activation. Moreover, PSP-SeNPs not only significantly induced dose-dependent disruption of mitochondrial membrane potential in MCF-7 cells after 24 h treatment, but it also enhanced reactive oxygen species (ROS) generation as early as 15 min, indicating that ROS-mediated mitochondrial dysfunction may play an important role in PSP-SeNPs-induced apoptosis. Our results suggest that PSP-SeNPs may be a candidate for further evaluation as a chemopreventive agent for human cancers, and the strategy to use PSP as a surface decorator could be a highly efficient way to enhance the cellular uptake and anticancer efficacy of nanomaterials.
机译:通过使用蘑菇多糖-蛋白质复合物(PSP)作为封端剂,已在亚硒酸钠和抗坏血酸的简单氧化还原系统中成功制备了尺寸可控且高度稳定的硒纳米颗粒(SeNP)。通过在SeNPs表面强力吸附多糖的羟基和蛋白质的亚氨基,SeNPs被PSP封端。 PSP表面修饰通过内吞作用显着增强了SeNPs的细胞摄取。 PSP-SeNPs的治疗通过PARP裂解和caspase激活的诱导细胞凋亡来显着抑制MCF-7人乳腺癌细胞的生长。此外,PSP-SeNPs不仅在24 h处理后显着诱导MCF-7细胞线粒体膜电位的剂量依赖性破坏,而且在15分钟之内也增强了活性氧(ROS)的生成,表明ROS介导的线粒体功能障碍可能在PSP-SeNPs诱导的细胞凋亡中起重要作用。我们的结果表明,PSP-SeNPs可能作为人类癌症的化学预防剂进行进一步评估,而使用PSP作为表面修饰剂的策略可能是提高细胞吸收和纳米材料抗癌功效的高效方法。

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