核酸递送的纳米方法:障碍、解决方案和当前前景。

Joan Castaneda Gonzalez, Ki Wan Park, Dallin Brian Evans, Rishi Sharma, Om Sahaym, Shamila Gopalakrishnan, Aqib Iqbal Dar, Tulio A Valdez, Anjali Sharma
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引用次数: 0

摘要

核酸(NA)疗法通过将治疗基因传递到靶细胞中,在治疗多种遗传疾病方面具有巨大的潜力。然而,安全有效地将这些基因运送到预定位置存在重大挑战。病毒载体虽然有效,但存在免疫原性和诱变等风险。这引起了人们对非病毒的、基于纳米颗粒的NA递送系统的兴趣。这篇综述文章描述了NA递送的各种生理障碍,并探讨了基于纳米颗粒的NA递送系统,包括生物工程纳米颗粒、肽、脂质纳米颗粒和聚合物纳米颗粒,强调了它们克服NA递送体内障碍的独特特性。虽然这些基于纳米颗粒的NA递送系统为病毒载体提供了一个有希望的替代方案,但需要解决与细胞毒性、可重复性合成和成本相关的挑战。本文还讨论了NA递送的当前临床前景,强调需要更安全、可扩展和具有成本效益的解决方案。纳米颗粒在NA治疗中具有广阔的前景,有可能开发出临床相关的、无毒的、稳定的和非免疫原性的递送载体,为更广泛的治疗应用和改善临床结果铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nano Approaches to Nucleic Acid Delivery: Barriers, Solutions, and Current Landscape.

Nucleic acid (NA) therapy holds tremendous potential for treating a wide range of genetic diseases by the delivery of therapeutic genes into target cells. However, significant challenges exist in safely and effectively delivering these genes to their intended locations. Viral vectors, though efficient, pose risks such as immunogenicity and mutagenesis. This has resulted in growing interest in non-viral, nanoparticle-based NA delivery systems. This review article describes various physiological barriers to NA delivery and explores nanoparticle-based NA delivery systems, including bioengineered nanoparticles, peptides, lipid nanoparticles, and polymeric nanoparticles, highlighting their unique features to overcome in vivo barriers for NA delivery. While these nanoparticle-based NA delivery systems offer a promising alternative to viral vectors, challenges related to cytotoxicity, reproducible synthesis, and cost need to be addressed. The current clinical landscape of NA delivery is also discussed, emphasizing the need for safer, scalable, and cost-effective solutions. Nanoparticles represent a promising future in NA therapy, with the possibility of developing clinically relevant, non-toxic, stable, and non-immunogenic delivery vehicles, paving the way for broader therapeutic applications and improved clinical outcomes.

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