Nanostructured porous Si-based nanoparticles for targeted drug delivery.

Biomatter Pub Date : 2012-10-01 DOI:10.4161/biom.22347
Mohammad-Ali Shahbazi, Barbara Herranz, Hélder A Santos
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引用次数: 102

Abstract

One of the backbones in nanomedicine is to deliver drugs specifically to unhealthy cells. Drug nanocarriers can cross physiological barriers and access different tissues, which after proper surface biofunctionalization can enhance cell specificity for cancer therapy. Recent developments have highlighted the potential of mesoporous silica (PSiO(2)) and silicon (PSi) nanoparticles for targeted drug delivery. In this review, we outline and discuss the most recent advances on the applications and developments of cancer therapies by means of PSiO(2) and PSi nanomaterials. Bio-engineering and fine tuning of anti-cancer drug vehicles, high flexibility and potential for sophisticated release mechanisms make these nanostructures promising candidates for "smart" cancer therapies. As a result of their physicochemical properties they can be controllably loaded with large amounts of drugs and coupled to homing molecules to facilitate active targeting. The main emphasis of this review will be on the in vitro and in vivo studies.

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靶向药物递送的纳米结构多孔硅基纳米颗粒。
纳米医学的支柱之一是将药物特异性地输送到不健康的细胞。药物纳米载体可以跨越生理屏障,进入不同的组织,经过适当的表面生物功能化,可以增强细胞特异性,用于癌症治疗。最近的发展突出了介孔二氧化硅(PSiO(2))和硅(PSi)纳米颗粒用于靶向药物递送的潜力。在这篇综述中,我们概述和讨论了PSiO(2)和PSi纳米材料在癌症治疗中的应用和发展的最新进展。生物工程和抗癌药物载体的微调、高灵活性和复杂释放机制的潜力使这些纳米结构成为“智能”癌症治疗的有希望的候选者。由于它们的物理化学性质,它们可以被控制地装载大量药物,并与归巢分子偶联,以促进主动靶向。本综述的重点将放在体外和体内研究上。
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