Carbon nanoparticles as transporters of melittin to glioma grade IV U87 cells in in vitro model

Paulina Biniecka, Ż. Bugajska, Karolina Daniluk, S. Jaworski
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引用次数: 4

Abstract

Carbon nanoparticles as transporters of melittin to glioma cells in in vitro model. Substances derived from nature have natural cytotoxic properties, melittin, the main component of bee venom is one of them. It has the ability to destroy any lipid bilayer, therefore to be used in a cancer treatment it needs to be targeted. The aim is to create the drug delivery system, which would efficiently deliver the active substance to glioma cells. Carbon nanoparticles are considered to be a good agent in biomedical applications, due to their biocompatibility and small sizes. In this study five types of nanoparticles were used: pristine graphene (GN), nanographene oxide (nGO), graphite (G), nanodiamond (UDD) and hierarchical nanoporous carbons (HNCs) to target the melittin to cancer cells. The visualization of the drug delivery complexes of melittin and nanoparticles was done with transmission electron microscopy, the influence of the complexes on cell morphology and structure was pictured with scanning electron microscope. Moreover, in order to check the viability of the cells treated with melittin and the complexes of melittin and nanoparticles the PrestoBlueTM assay was done, also to specify the way of the cell death the annexin V/PI assay was carried out. The results indicate that various nanoparticles behave differently in a complex with melittin. The UDD, GN and nGO nanoparticles resulted in higher mortality than the melittin itself. Creating and applying such complexes of melittin with nanoparticles in glioma cancer treatment may be a promising solution in the therapy.
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碳纳米颗粒作为蜂毒素向胶质瘤IV级U87细胞的转运体的体外模型研究
碳纳米颗粒作为蜂毒蛋白向胶质瘤细胞转运的体外模型研究。来源于自然界的物质具有天然的细胞毒性,蜂毒的主要成分蜂毒素就是其中之一。它有能力破坏任何脂质双分子层,因此要用于癌症治疗,它需要有针对性。其目的是创造药物输送系统,有效地将活性物质输送到胶质瘤细胞。碳纳米颗粒由于其生物相容性和体积小而被认为是生物医学应用的良好试剂。在这项研究中,使用了五种纳米颗粒:原始石墨烯(GN)、纳米氧化石墨烯(nGO)、石墨(G)、纳米金刚石(UDD)和分层纳米多孔碳(HNCs)来靶向癌细胞的蜂毒蛋白。利用透射电镜观察蜂毒素和纳米颗粒的给药配合物的结构,用扫描电镜观察配合物对细胞形态和结构的影响。此外,为了检查蜂毒素和蜂毒素与纳米颗粒复合物处理的细胞的活力,进行了PrestoBlueTM实验,并进行了膜联蛋白V/PI实验,以确定细胞死亡的方式。结果表明,不同的纳米颗粒在蜂毒蛋白的配合物中表现不同。UDD、GN和nGO纳米颗粒导致的死亡率高于蜂毒素本身。在神经胶质瘤治疗中,将蜂毒蛋白与纳米颗粒的复合物制备和应用可能是一种很有前途的治疗方案。
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