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硅藻土纳米硅用于药物输送。

Diatomite silica nanoparticles for drug delivery.

机构信息

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples 80131, Italy.

Institute for Microelectronics and Microsystems, National Council of Research, Naples 80131, Italy ; Department of Pharmacy, University of Naples Federico II, Naples 80131, Italy.

出版信息

Nanoscale Res Lett. 2014 Jul 3;9(1):329. doi: 10.1186/1556-276X-9-329. eCollection 2014.

Abstract

UNLABELLED

Diatomite is a natural fossil material of sedimentary origin, constituted by fragments of diatom siliceous skeletons. In this preliminary work, the properties of diatomite nanoparticles as potential system for the delivery of drugs in cancer cells were exploited. A purification procedure, based on thermal treatments in strong acid solutions, was used to remove inorganic and organic impurities from diatomite and to make them a safe material for medical applications. The micrometric diatomite powder was reduced in nanoparticles by mechanical crushing, sonication, and filtering. Morphological analysis performed by dynamic light scattering and transmission electron microscopy reveals a particles size included between 100 and 300 nm. Diatomite nanoparticles were functionalized by 3-aminopropyltriethoxysilane and labeled by tetramethylrhodamine isothiocyanate. Different concentrations of chemically modified nanoparticles were incubated with cancer cells and confocal microscopy was performed. Imaging analysis showed an efficient cellular uptake and homogeneous distribution of nanoparticles in cytoplasm and nucleus, thus suggesting their potentiality as nanocarriers for drug delivery.

PACS

87.85.J81.05.Rm; 61.46. + w.

摘要

未标记

硅藻土是一种天然的化石物质,由硅质硅藻骨架的碎片组成。在这项初步工作中,利用硅藻土纳米颗粒作为癌细胞中药物传递的潜在系统的特性。基于在强酸溶液中的热处理的纯化程序,用于从硅藻土中去除无机和有机杂质,并使它们成为用于医疗应用的安全材料。通过机械粉碎、超声和过滤将微米级的硅藻土粉末减小到纳米颗粒。通过动态光散射和透射电子显微镜进行的形态分析显示出粒径在 100 至 300nm 之间。用 3-氨丙基三乙氧基硅烷对硅藻土纳米颗粒进行功能化,并通过四甲基罗丹明异硫氰酸酯进行标记。用不同浓度的化学修饰纳米颗粒孵育癌细胞,并进行共焦显微镜检查。成像分析显示出纳米颗粒在细胞质和核内的有效细胞摄取和均匀分布,因此表明它们作为药物传递的纳米载体的潜力。

PACS

87.85.J81.05.Rm; 61.46. + w.

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