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本文引用的文献

1
pH-Responsive Polymers as Gene Carriers.作为基因载体的pH响应性聚合物
Macromol Rapid Commun. 2010 Jul 1;31(13):1122-33. doi: 10.1002/marc.200900867. Epub 2010 May 4.
2
High loading efficiency and sustained release of siRNA encapsulated in PLGA nanoparticles: quality by design optimization and characterization.载药量高且能持续释放 siRNA 的 PLGA 纳米粒:基于质量源于设计的优化和表征。
Eur J Pharm Biopharm. 2011 Jan;77(1):26-35. doi: 10.1016/j.ejpb.2010.11.008. Epub 2010 Nov 18.
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Mimicry of protein function with cell-penetrating peptides.利用细胞穿透肽模拟蛋白质功能。
Methods Mol Biol. 2011;683:233-47. doi: 10.1007/978-1-60761-919-2_17.
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Tocopheryl oligochitosan-based self assembling oligomersomes for siRNA delivery.基于生育酚低聚糖壳聚糖的自组装寡聚物囊泡用于 siRNA 的递送。
Biomaterials. 2011 Jan;32(3):849-57. doi: 10.1016/j.biomaterials.2010.09.027.
5
Pulmonary gene silencing in transgenic EGFP mice using aerosolised chitosan/siRNA nanoparticles.利用雾化壳聚糖/ siRNA 纳米粒在转基因 EGFP 小鼠中进行肺部基因沉默。
Pharm Res. 2010 Dec;27(12):2520-7. doi: 10.1007/s11095-010-0255-y. Epub 2010 Sep 8.
6
STAT3 silencing in dendritic cells by siRNA polyplexes encapsulated in PLGA nanoparticles for the modulation of anticancer immune response.通过包裹在 PLGA 纳米粒中的 siRNA 多聚物沉默树突状细胞中的 STAT3 以调节抗肿瘤免疫反应。
Mol Pharm. 2010 Oct 4;7(5):1643-54. doi: 10.1021/mp100067u. Epub 2010 Sep 14.
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Evaluation of cationic nanoparticles of biodegradable copolymers as siRNA delivery system for hepatitis B treatment.评价可生物降解共聚物的阳离子纳米颗粒作为治疗乙型肝炎的 siRNA 递送系统。
Int J Pharm. 2010 Nov 15;400(1-2):194-200. doi: 10.1016/j.ijpharm.2010.08.026. Epub 2010 Aug 27.
8
RVG peptide tethered bioreducible polyethylenimine for gene delivery to brain.RVG 肽连接的生物还原性聚乙烯亚胺用于脑内基因递送。
J Control Release. 2011 Oct 10;155(1):18-25. doi: 10.1016/j.jconrel.2010.08.011. Epub 2010 Aug 25.
9
Silica nanoparticles as a delivery system for nucleic acid-based reagents.二氧化硅纳米颗粒作为基于核酸的试剂的递送系统。
J Mater Chem. 2009 Jan 1;19(35):6308-6316. doi: 10.1039/b904197d.
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Engineered design of mesoporous silica nanoparticles to deliver doxorubicin and P-glycoprotein siRNA to overcome drug resistance in a cancer cell line.介孔二氧化硅纳米粒子的工程设计,以递送阿霉素和 P-糖蛋白 siRNA,以克服癌细胞系中的药物耐药性。
ACS Nano. 2010 Aug 24;4(8):4539-50. doi: 10.1021/nn100690m.

聚合物在小干扰 RNA 递送中的应用。

Polymers in small-interfering RNA delivery.

机构信息

Department of Chemistry, BK School of Molecular Science, Polymer Research Institute, Pohang University of Science and Technology, Pohang, Korea.

出版信息

Nucleic Acid Ther. 2011 Jun;21(3):133-47. doi: 10.1089/nat.2011.0293.

DOI:10.1089/nat.2011.0293
PMID:21749290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3198620/
Abstract

This review will cover the current strategies that are being adopted to efficiently deliver small interfering RNA using nonviral vectors, including the use of polymers such as polyethylenimine, poly(lactic-co-glycolic acid), polypeptides, chitosan, cyclodextrin, dendrimers, and polymers-containing different nanoparticles. The article will provide a brief and concise account of underlying principle of these polymeric vectors and their structural and functional modifications which were intended to serve different purposes to affect efficient therapeutic outcome of small-interfering RNA delivery. The modifications of these polymeric vectors will be discussed with reference to stimuli-responsiveness, target specific delivery, and incorporation of nanoconstructs such as carbon nanotubes, gold nanoparticles, and silica nanoparticles. The emergence of small-interfering RNA as the potential therapeutic agent and its mode of action will also be mentioned in a nutshell.

摘要

这篇综述将涵盖目前正在采用的有效使用非病毒载体传递小干扰 RNA 的策略,包括使用聚合物如聚乙烯亚胺、聚(乳酸-共-乙醇酸)、多肽、壳聚糖、环糊精、树枝状聚合物和含有不同纳米粒子的聚合物。本文将简要介绍这些聚合物载体的基本原理及其结构和功能修饰,这些修饰旨在用于不同目的,以影响小干扰 RNA 传递的有效治疗结果。将参照刺激响应性、靶向特异性传递以及碳纳米管、金纳米粒子和硅纳米粒子等纳米结构的掺入来讨论这些聚合物载体的修饰。小干扰 RNA 作为潜在治疗剂及其作用模式也将简要提及。