Document Detail


Breaking the bonds: non-viral vectors become chemically dynamic.
MedLine Citation:
PMID:  17955026     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The delivery of a variety of nucleic acids such as plasmid DNA (pDNA) and small interfering RNA (siRNA) to mammalian cells is both an important research tool and potential therapeutic approach. Synthetic vehicles (SVs) that include lipoplexes and polyplexes, are widely used for non-viral delivery. A promising method of improving the efficacy of this approach is to create SVs that are chemically dynamic, so that delivery is enabled by the cleavage of chemical bonds upon exposure to various physiological environments or external stimuli. An example of this approach is the use of masked endosomolytic agents (MEAs) that improve the release of nucleic acids from endosomes, a key step during transport. When the MEA enters the acidic environment of the endosome, a pH-labile bond is broken, releasing the agent';s endosomolytic capability. Another challenge has been to develop SVs that enable in vivo delivery. Recently, an MEA that was used within dynamic polyconjugates (DPCs) enabled the efficient delivery of siRNA into hepatocytes in vivo. The use of labile bonds to mask endosomolytic agents, provides a critical design feature, because it enables efficient in vivo delivery without sacrificing endosomolytic function for release into the cytoplasm.
Authors:
Jon A Wolff; David B Rozema
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Publication Detail:
Type:  Journal Article; Review     Date:  2007-10-23
Journal Detail:
Title:  Molecular therapy : the journal of the American Society of Gene Therapy     Volume:  16     ISSN:  1525-0024     ISO Abbreviation:  Mol. Ther.     Publication Date:  2008 Jan 
Date Detail:
Created Date:  2007-12-21     Completed Date:  2008-05-13     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100890581     Medline TA:  Mol Ther     Country:  United States    
Other Details:
Languages:  eng     Pagination:  8-15     Citation Subset:  IM    
Affiliation:
Waisman Center, Department of Pediatrics and Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, USA. jwolff@wisc.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Drug Delivery Systems
Gene Transfer Techniques*
Genetic Vectors / administration & dosage*,  chemical synthesis*
Humans
RNA, Small Interfering / administration & dosage
Chemical
Reg. No./Substance:
0/RNA, Small Interfering

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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