Aptamer guided delivery of nucleic acid-based nanoparticles

M. Panigaj, J. Reiser
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引用次数: 8

Abstract

Abstract Targeted delivery of bioactive compounds is a key part of successful therapies. In this context, nucleic acid and protein-based aptamers have been shown to bind therapeutically relevant targets including receptors. In the last decade, nucleic acid-based therapeutics coupled to aptamers have emerged as a viable strategy for cell specific delivery. Additionally, recent developments in nucleic acid nanotechnology offer an abundance of possibilities to rationally design aptamer targeted RNA or DNA nanoparticles involving combinatorial use of various intrinsic functionalities. Although a host of issues including stability, safety and intracellular trafficking remain to be addressed, aptamers as simple functional chimeras or as parts of multifunctional self-assembled RNA/DNA nanostructures hold great potential for clinical applications.
核酸基纳米粒子的适体引导递送
生物活性化合物的靶向递送是成功治疗的关键部分。在这种情况下,核酸和基于蛋白质的适体已被证明可以结合包括受体在内的治疗相关靶标。在过去的十年中,以核酸为基础的治疗偶联适体已经成为细胞特异性递送的可行策略。此外,核酸纳米技术的最新发展为合理设计适配体靶向RNA或DNA纳米粒子提供了丰富的可能性,包括组合使用各种内在功能。尽管包括稳定性、安全性和细胞内运输在内的许多问题仍有待解决,适体作为简单的功能嵌合体或作为多功能自组装RNA/DNA纳米结构的一部分,在临床应用中具有巨大的潜力。
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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