Cationic liposomes as gene transfer vectors: Barriers to successful application in gene therapy

ORCiD

Nejat Düzgüneş: 0000-0001-6159-1391

Department

Biomedical Sciences

Document Type

Article

Publication Title

Current Opinion in Molecular Therapeutics

ISSN

1464-8431

Volume

1

Issue

2

First Page

147

Last Page

157

Publication Date

4-1-1999

Abstract

Despite extensive research in the last decade on the use of cationic liposomes as gene transfer vectors and the development of elegant strategies to enhance their biological activity, these systems are still far from being viable alternatives to the use of viral vectors in gene therapy. Here, we highlight the most recent and relevant discoveries in this field, describe the main factors that influence the performance of cationic liposomes, and elucidate the barriers faced by these carrier systems as well as the mechanisms by which they mediate intracellular gene delivery.

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