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用于递送小干扰RNA的自组装β-葡聚糖纳米药物

Self-Assembling β-Glucan Nanomedicine for the Delivery of siRNA.

作者信息

Lee Kyungwoo, Min Daejin, Choi Yonghyun, Yoon Semi, Jang Jaehee, Hwang Jangsun, Jeon Hojeong, Cho Yong Woo, Choi Jonghoon

机构信息

School of Integrative Engineering, Chung-Ang University, Seoul 06974, Korea.

Center for Biomaterials, Korea Institute of Science and Technology, Seoul 02792, Korea.

出版信息

Biomedicines. 2020 Nov 12;8(11):497. doi: 10.3390/biomedicines8110497.

DOI:10.3390/biomedicines8110497
PMID:33198404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7698166/
Abstract

We aimed to design and manufacture a transporter capable of delivering small interfering RNAs (siRNAs) into the skin without causing any damage. β-glucans are unique chiral polysaccharides with well-defined immunological properties and supramolecular wrapping ability. However, the chiral properties of these polymers have hardly been applied in drug delivery systems. In this study, β-glucan nanoparticles were designed and manufactured to deliver genetic material to the target cells. The β-glucan molecules were self-assembled with an siRNA into nanoparticles of 300-400 nm in diameter via a conformational transition process, in order to construct a gene delivery system. The assembled gene nanocarriers were associated with high gene-loading ability. The expression and efficiency of siRNA were verified after its delivery via β-glucan. Our results provide evidence that β-glucan nanoparticles can be effectively used to deliver siRNA into the cells.

摘要

我们旨在设计并制造一种能够将小干扰RNA(siRNA)递送至皮肤且不会造成任何损伤的转运体。β-葡聚糖是具有明确免疫特性和超分子包裹能力的独特手性多糖。然而,这些聚合物的手性特性在药物递送系统中几乎未得到应用。在本研究中,设计并制造了β-葡聚糖纳米颗粒以将遗传物质递送至靶细胞。β-葡聚糖分子通过构象转变过程与siRNA自组装成直径为300 - 400 nm的纳米颗粒,以构建基因递送系统。组装后的基因纳米载体具有高基因负载能力。在通过β-葡聚糖递送siRNA后,验证了其表达和效率。我们的结果提供了证据,表明β-葡聚糖纳米颗粒可有效地用于将siRNA递送至细胞中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/759b19b6fd2a/biomedicines-08-00497-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/861f9efd7f66/biomedicines-08-00497-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/72d7267bd257/biomedicines-08-00497-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/628ca882abd6/biomedicines-08-00497-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/388c7fa3302b/biomedicines-08-00497-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/759b19b6fd2a/biomedicines-08-00497-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/861f9efd7f66/biomedicines-08-00497-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/72d7267bd257/biomedicines-08-00497-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/628ca882abd6/biomedicines-08-00497-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/388c7fa3302b/biomedicines-08-00497-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39e6/7698166/759b19b6fd2a/biomedicines-08-00497-g005.jpg

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