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Nanoparticle-based delivery system for application of siRNA in vivo.

机译:基于纳米粒子的递送系统,可在体内应用siRNA。

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摘要

Small interfering RNAs (siRNAs) silence the expression of specific target genes by mediating RNA interference (RNAi) in mammalian cells. siRNAs have not only been widely used as a valuable tool for functional genomics research, but they also have demonstrated great potential in biomedical therapeutic applications for diseases caused by abnormal gene overexpression or mutation. One of the most important issues to overcome before full clinical application is the development of effective administration methods for siRNAs to the target tissue or cells in vivo, which is highly dependent on the delivery system. Currently, there are two major kinds of in vivo delivery systems: viral or nonviral. As one of the nonviral carrier systems, nanoparticles, combinations of liposomes and cationic polymer complexes, have exhibited improved in vivo stability, target specificity, and cell/tissue uptake and internalization of the encapsulated RNAi oligos, which result in more effective silencing with less cellular toxicity and immune stimulation. This review will discuss the latest advancements in nanoparticle-mediated RNAi delivery systems, including nano-materials, preparation, and characteristics. In conjunction, the clinical trial cases related to the nanoparticle-siRNA complexes will be highlighted. The safety issues of nanoparticles used in vivo will also be mentioned. Finally, this review will summarize the perspectives for future applications of nanoparticle-mediated RNAi delivery systems.
机译:小型干扰RNA(siRNA)通过介导哺乳动物细胞中的RNA干扰(RNAi)使特定靶基因的表达沉默。 siRNA不仅被广泛用作功能基因组学研究的有价值的工具,而且在由异常基因过表达或突变引起的疾病的生物医学治疗应用中也显示出巨大潜力。在完全临床应用之前要克服的最重要问题之一是开发对siRNA体内靶组织或细胞的有效给药方法,该方法高度依赖于递送系统。当前,有两种主要的体内递送系统:病毒或非病毒。作为一种非病毒载体系统,纳米颗粒,脂质体和阳离子聚合物复合物的组合已表现出改善的体内稳定性,靶标特异性以及被囊化的RNAi寡核苷酸的细胞/组织摄取和内在化,从而导致更有效的沉默和更少的细胞毒性和免疫刺激。这篇评论将讨论纳米粒子介导的RNAi递送系统的最新进展,包括纳米材料,制备和特性。结合在一起,将重点介绍与纳米粒子-siRNA复合物相关的临床试验案例。也将提及体内使用的纳米颗粒的安全性问题。最后,本综述将总结纳米粒子介导的RNAi递送系统未来应用的前景。

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