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Mechanisms and strategies for effective delivery of antisense and siRNA oligonucleotides.

作者信息

Juliano Rudy, Alam Md Rowshon, Dixit Vidula, Kang Hyumin

机构信息

Department of Pharmacology, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Nucleic Acids Res. 2008 Jul;36(12):4158-71. doi: 10.1093/nar/gkn342. Epub 2008 Jun 16.


DOI:10.1093/nar/gkn342
PMID:18558618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2475625/
Abstract

The potential use of antisense and siRNA oligonucleotides as therapeutic agents has elicited a great deal of interest. However, a major issue for oligonucleotide-based therapeutics involves effective intracellular delivery of the active molecules. In this Survey and Summary, we review recent reports on delivery strategies, including conjugates of oligonucleotides with various ligands, as well as use of nanocarrier approaches. These are discussed in the context of intracellular trafficking pathways and issues regarding in vivo biodistribution of molecules and nanoparticles. Molecular-sized chemical conjugates and supramolecular nanocarriers each display advantages and disadvantages in terms of effective and nontoxic delivery. Thus, choice of an optimal delivery modality will likely depend on the therapeutic context.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/1e589585d8a7/gkn342f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/ac2f6bd67d30/gkn342f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/74064628a5d4/gkn342f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/1e589585d8a7/gkn342f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/ac2f6bd67d30/gkn342f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/74064628a5d4/gkn342f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188c/2475625/1e589585d8a7/gkn342f3.jpg

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本文引用的文献

[1]
Integrins team up with tyrosine kinase receptors and plexins to control angiogenesis.

Curr Opin Hematol. 2008-5

[2]
Resolution of liver cirrhosis using vitamin A-coupled liposomes to deliver siRNA against a collagen-specific chaperone.

Nat Biotechnol. 2008-4

[3]
Sequence- and target-independent angiogenesis suppression by siRNA via TLR3.

Nature. 2008-4-3

[4]
Intracellular delivery of an anionic antisense oligonucleotide via receptor-mediated endocytosis.

Nucleic Acids Res. 2008-5

[5]
Efficient in vivo delivery of siRNA to the liver by conjugation of alpha-tocopherol.

Mol Ther. 2008-4

[6]
Reductively labile PRINT particles for the delivery of doxorubicin to HeLa cells.

J Am Chem Soc. 2008-4-16

[7]
Breathing life into polycations: functionalization with pH-responsive endosomolytic peptides and polyethylene glycol enables siRNA delivery.

J Am Chem Soc. 2008-3-19

[8]
Systemic leukocyte-directed siRNA delivery revealing cyclin D1 as an anti-inflammatory target.

Science. 2008-2-1

[9]
Molecular biology. The art of assembly.

Science. 2008-2-1

[10]
Monomolecular assembly of siRNA and poly(ethylene glycol)-peptide copolymers.

Biomacromolecules. 2008-2

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