Application of mesoporous silica nanoparticles for drug delivery to cancer cells

B. Malaekeh-Nikouei, Mohammad Yahya Hanafi-Bojd
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引用次数: 0

Abstract

Cancer is one of the main causes of death worldwide. Chemotherapy is the most common method for cancer therapy which represent non-specific side effects on normal cells and tissues and drug resistance in cancer cells. There are two main mechanisms for Multi Drug Resistance (MDR) in cancer cells including: drug efflux pump and activation of anti-apoptotic pathways. Cancer chemotherapy disadvantages can be overcome by using nanoparticulate drug delivery systems like Mesoporous Silica Nanoparticles (MSNs) that have been used as drug delivery system since 2001. The present review included synthesis, targeted (active or passive) drug delivery to cancer cells, co-delivery of anticancer drugs and siRNA by MSNs and its toxicity. This review revealed that MSNs are good candidate for drug delivery to cancer cells due to its unique properties including: controllable pore and particle sizes, thermal and chemical stability, modifications of outer and inner surfaces of nanoparticles for drug and siRNA loading, attachment of ligand for targeted drug delivery, high drug loading capacity and controlled drug release, biocompatibility and biodegradation in aqueous medium.
介孔二氧化硅纳米粒子在癌症细胞给药中的应用
癌症是世界范围内死亡的主要原因之一。化疗是最常用的癌症治疗方法,它对正常细胞和组织有非特异性的副作用,对癌细胞有耐药性。肿瘤细胞发生多药耐药的机制主要包括药物外排泵和抗凋亡通路的激活。癌症化疗的缺点可以通过使用纳米颗粒药物传递系统来克服,如介孔二氧化硅纳米颗粒(MSNs),自2001年以来一直用作药物传递系统。本文综述了纳米微球的合成、靶向(主动或被动)给药、抗癌药物与siRNA的共递送及其毒性。本文综述表明,MSNs具有孔径和粒径可控、热稳定性和化学稳定性、纳米颗粒内外表面修饰可用于载药和siRNA、配体附着可靶向载药、高载药量和药物释放控制、在水介质中的生物相容性和生物降解等特点,是肿瘤细胞药物递送的良好候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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