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. Author manuscript; available in PMC: 2013 Jul 1.
Published in final edited form as: Biochem Pharmacol. 2012 Aug 28;85(1):1–11. doi: 10.1016/j.bcp.2012.08.018

Table 1.

Vectors and systems for gene targeting and myocardial delivery


Advantages Disadvantages
Non-Viral Plasmids Simplified construction, versatility of expression cassette size, favorable biosafety risk profiles Low transduction efficiency, transient expression

Liposomes Allow for targeting at the cell surface, ultrasound manipulation possible, favorable biosafety risk profiles More complex construction, usually requires competent blood flow, transient expression

Viral Replication Deficient Adenoviruses Large DNA packaging possible, enters both dividing and non-dividing cells, well suited for myocardial delivery Serotype immunogenicity, potential cytotoxicity, transient expression

Adeno-associated Virus Greater stability than Adenovirus, enters both dividing and non- dividing cells, well suited for myocardial delivery, longer periods of expression, reduced immunogenicity DNA insertion possible causing oncogenic potential, smaller DNA packaging

Lentivirus Integrates into host DNA for long term expression, minimal immunogenicity Smaller DNA packaging, high tropism for dividing cells, insertional mutagenesis