Physical methods of nucleic acid transfer: general concepts and applications

J Villemejane, LM Mir - British journal of pharmacology, 2009 - Wiley Online Library
J Villemejane, LM Mir
British journal of pharmacology, 2009Wiley Online Library
Physical methods of gene (and/or drug) transfer need to combine two effects to deliver the
therapeutic material into cells. The physical methods must induce reversible alterations in
the plasma membrane to allow the direct passage of the molecules of interest into the cell
cytosol. They must also bring the nucleic acids in contact with the permeabilized plasma
membrane or facilitate access to the inside of the cell. These two effects can be achieved in
one or more steps, depending upon the methods employed. In this review, we describe and …
Physical methods of gene (and/or drug) transfer need to combine two effects to deliver the therapeutic material into cells. The physical methods must induce reversible alterations in the plasma membrane to allow the direct passage of the molecules of interest into the cell cytosol. They must also bring the nucleic acids in contact with the permeabilized plasma membrane or facilitate access to the inside of the cell. These two effects can be achieved in one or more steps, depending upon the methods employed. In this review, we describe and compare several physical methods: biolistics, jet injection, hydrodynamic injection, ultrasound, magnetic field and electric pulse mediated gene transfer. We describe the physical mechanisms underlying these approaches and discuss the advantages and limitations of each approach as well as its potential application in research or in preclinical and clinical trials. We also provide conclusions, comparisons, and projections for future developments. While some of these methods are already in use in man, some are still under development or are used only within clinical trials for gene transfer. The possibilities offered by these methods are, however, not restricted to the transfer of genes and the complementary uses of these technologies are also discussed. As these methods of gene transfer may bypass some of the side effects linked to viral or biochemical approaches, they may find their place in specific clinical applications in the future.
This article is part of a themed section on Vector Design and Drug Delivery. For a list of all articles in this section see the end of this paper, or visit: http://www3.interscience.wiley.com/journal/121548564/issueyear?year=2009
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