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非离子型表面活性剂囊泡用于 RNAi 治疗药物的递送。

Nonionic surfactant vesicles for delivery of RNAi therapeutics.

机构信息

Pharmaceutical Development of Green Innovation Group, Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.

出版信息

Nanomedicine (Lond). 2013 Nov;8(11):1865-73. doi: 10.2217/nnm.13.155.

DOI:10.2217/nnm.13.155
PMID:24156490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3971008/
Abstract

RNAi is a promising potential therapeutic approach for many diseases. A major barrier to its clinical translation is the lack of efficient delivery systems for siRNA. Among nonviral vectors, nonionic surfactant vesicles (niosomes) have shown a great deal of promise in terms of their efficacy and toxicity profiles. Nonionic surfactants have been shown to be a superior alternative to phospholipids in several studies. There is a large selection of surfactants with various properties that have been incorporated into niosomes. Therefore, there is great potential for innovation in terms of nisome composition. This article summarizes recent advancements in niosome technology for the delivery of siRNA.

摘要

RNAi 是一种有前途的潜在治疗方法,可用于许多疾病。其临床转化的主要障碍是缺乏有效的 siRNA 递送系统。在非病毒载体中,非离子表面活性剂囊泡(niosomes)在功效和毒性特征方面显示出巨大的潜力。在几项研究中,非离子表面活性剂已被证明是磷脂的优越替代品。有多种具有不同性质的表面活性剂已被纳入 niosomes。因此,在 niosome 组成方面有很大的创新潜力。本文总结了最近在用于递送 siRNA 的 niosome 技术方面的进展。

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本文引用的文献

1
Nanodesign of olein vesicles for the topical delivery of the antioxidant resveratrol.油质体的纳米设计用于局部递送抗氧化剂白藜芦醇。
J Pharm Pharmacol. 2013 Aug;65(8):1158-67. doi: 10.1111/jphp.12093. Epub 2013 Jun 20.
2
Delivery systems and local administration routes for therapeutic siRNA.治疗性 siRNA 的递药系统和局部给药途径。
Pharm Res. 2013 Apr;30(4):915-31. doi: 10.1007/s11095-013-0971-1. Epub 2013 Jan 24.
3
Characterization of long-circulating cationic nanoparticle formulations consisting of a two-stage PEGylation step for the delivery of siRNA in a breast cancer tumor model.由两阶段聚乙二醇化步骤组成的长循环阳离子纳米颗粒制剂的表征,用于在乳腺癌肿瘤模型中递送 siRNA。
J Pharm Sci. 2013 Jan;102(1):227-36. doi: 10.1002/jps.23351. Epub 2012 Nov 6.
4
Comparative cellular pharmacokinetics and pharmacodynamics of siRNA delivery by SPANosomes and by cationic liposomes.SPANosomes 和阳离子脂质体介导的 siRNA 递呈的细胞药代动力学和药效学比较。
Nanomedicine. 2013 May;9(4):504-13. doi: 10.1016/j.nano.2012.10.002. Epub 2012 Oct 29.
5
Doxorubicin loaded magneto-niosomes for targeted drug delivery.载多柔比星的磁介体纳米囊用于靶向药物递送。
Colloids Surf B Biointerfaces. 2013 Feb 1;102:803-7. doi: 10.1016/j.colsurfb.2012.09.019. Epub 2012 Sep 18.
6
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Adv Drug Deliv Rev. 2013 Jan;65(1):36-48. doi: 10.1016/j.addr.2012.09.037. Epub 2012 Oct 1.
7
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Adv Colloid Interface Sci. 2012 Nov 15;183-184:46-54. doi: 10.1016/j.cis.2012.08.002. Epub 2012 Aug 17.
8
Cationic niosomes composed of spermine-based cationic lipids mediate high gene transfection efficiency.基于 spermine 的阳离子脂质组成的阳离子脂质体介导高基因转染效率。
J Drug Target. 2012 Nov;20(9):783-92. doi: 10.3109/1061186X.2012.716846. Epub 2012 Aug 29.
9
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10
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