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. 2008 Feb 20;99(5):856–862. doi: 10.1111/j.1349-7006.2008.00774.x

Table 1.

Non‐viral methods for in vivo gene transfer

Vector Route of injection Stimulus or additional treatment Characteristics References
Naked DNA Extracellular space None Localized transgene expression Muscle( 15 , 17 ), liver( 16 , 17 ), spleen, 17 ), kidney( 17 ), brain( 18 ), tumor( 19 , 20 , 21 , 22 )
High applicability to various targets
Naked DNA Extracellular or intravascular space Electric pulse Localized transgene expression Muscle( 17 , 26 ), liver( 17 , 27 ), spleen( 17 ), kidney( 17 ), tumor( 25 )
High applicability to various targets
Possible tissue damage caused by electric pulses
Naked DNA Extracellular or intravascular space Ultrasound Localized transgene expression Tumor( 29 ), carotid artery( 30 ), femoral artery( 31 )
High applicability to various targets
Naked DNA Intravascular space Massage Localized transgene expression Liver( 32 , 33 )
Applicability to other organs not reported
Naked DNA Intravascular space Occlusion of blood flow Localized transgene expression Liver( 35 , 37 ), diaphragm( 38 )
Surgery required for the occlusion
Naked DNA Intravascular space Pre‐injection of cationic liposomes Lung‐selective transgene expression Lung endothelial cells( 36 )
Reduced immunostimulatory response compared with DNA–cationic liposome complexes
Naked DNA Intravascular space Large volume injection at high speed Extremely high transgene expression Whole body( 2 , 4 , 39 )
Possible tissue damage
DNA–cationic liposome complex Extracellular or intravascular space None Low‐level transgene expression in vivo Lung endothelial cells( 46 )
High induction of inflammatory cytokines upon administration
DNA–cationic polymer complex Extracellular or intravascular space None Low‐level transgene expression in vivo Lung endothelial cells( 45 )
Concerns about cytotoxicity of cationic polymers