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反义寡核苷酸和小干扰RNA寡核苷酸治疗的生物学障碍。

Biological barriers to therapy with antisense and siRNA oligonucleotides.

作者信息

Juliano R, Bauman J, Kang H, Ming X

机构信息

UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599, USA.

出版信息

Mol Pharm. 2009 May-Jun;6(3):686-95. doi: 10.1021/mp900093r.

DOI:10.1021/mp900093r
PMID:19397332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2758224/
Abstract

Attaining the full therapeutic utility of antisense and siRNA oligonucleotides will require understanding of the biological barriers that stand between initial administration of these drugs and their final actions within cells. This review examines some of the key barriers that affect the biodistribution of oligonucleotides both in molecular form and when they are associated with nanocarriers. An understanding of the biological processes underlying these barriers will aid in the design of more effective delivery systems.

摘要

要实现反义寡核苷酸和小干扰RNA寡核苷酸的全部治疗效用,需要了解这些药物初始给药与它们在细胞内的最终作用之间存在的生物屏障。本综述探讨了一些影响寡核苷酸分子形式及其与纳米载体结合时生物分布的关键屏障。了解这些屏障背后的生物学过程将有助于设计更有效的递送系统。

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本文引用的文献

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siRNA as a tool for investigating organogenesis: The pitfalls and the promises.siRNA 作为研究器官发生的工具:陷阱与承诺。
Organogenesis. 2008 Jul;4(3):176-81. doi: 10.4161/org.4.3.6642.
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Increased RNAi is related to intracellular release of siRNA via a covalently attached signal peptide.RNA干扰增强与通过共价连接的信号肽实现的小干扰RNA的细胞内释放有关。
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Curr Pharm Des. 2008;14(34):3686-97. doi: 10.2174/138161208786898789.
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Cross-species comparison of in vivo PK/PD relationships for second-generation antisense oligonucleotides targeting apolipoprotein B-100.针对载脂蛋白B-100的第二代反义寡核苷酸体内药代动力学/药效学关系的跨物种比较。
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Exploring the full spectrum of macrophage activation.探索巨噬细胞激活的全谱。
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