Adenovirus in a Synthetic Membrane Wrapper: An Example of Hybrid Vigor?

Even though more than two decades have passed since the first report of lipofection, there is still a compelling need for the development of new vector approaches to realize the enormous potential of this field.

There are no non-viral systems that are anywhere close to achieving the same level of sophisticated functional integration into their design as viruses.

Any effective nucleic acid carrier system will ultimately need to address the issues of safe manufacture in large volumes, with reproducible production and shelf stability, and at low cost before gaining clinical acceptance.

The most pressing needs for the development of efficient non-viral carrier systems are improvements in targeting efficiency and selectivity.

David H. Thompson*
Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, Indiana 47907
ACS Nano, 2008, 2 (5), pp 821–826
DOI: 10.1021/nn800279s
Publication Date (Web): May 27, 2008
Copyright © 2008 American Chemical Society
* Address correspondence to davethom@purdue.edu.

Abstract

Abstract Image

Nucleic acid delivery applications require the development of carrier systems that are effective, selective, and non-toxic. Many different viral and non-viral approaches, including the use of retroviruses, adenoviruses, liposomes, and dendrimers, have been investigated. Unfortunately, issues still remain with regard to the safety and efficiency of these delivery vehicles. In this Perspective, the challenges of designing a stable vector that is capable of effective gene therapy are highlighted. Progress in the area is also presented, including the work of Kostarelos and co-workers appearing in this issue of ACS Nano, in which they describe a novel delivery vehicle that consists of lipid envelopes encasing viral nanoparticles.

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This article has been cited by 2 ACS Journal articles (2 most recent appear below).

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History

  • Published In Issue May 27, 2008
  • Article ASAPMay 27, 2008

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