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. Author manuscript; available in PMC: 2023 Apr 24.
Published in final edited form as: Mol Diagn Ther. 2022 Dec 13;27(2):129–140. doi: 10.1007/s40291-022-00625-y

Table 1.

Non-viral vectors to deliver genes into injured hearts.

Delivery method Target gene Species Reference
DNA plasmid VEGF A-165 Human, Pig, Sheep [6668]
PEGylated-NP Schisandrin B Rat [77]
PEGylated-NP Baicalin Rat [78]
PEGylated-NP Puerarin Rat [79]
PLGA-NP Cyclosporine A Mouse [80]
PLGA-NP Irbesartan Mouse [81]
PLGA-NP Pitavastatin Mouse, Rat, Pig [8284]
PLGA-NP VEGF Mouse [85]
PLGA-NP IGF1 Mouse [86]
Conjugate chitosan-graft-PEI-eprosartan VEGF Rat [87]
PDMA EGFP Mouse [88]
Hydrogel miR-302 Mouse [91]
Hydrogel miR-199a-3p Rat [92]
Hydrogel miR-21–5p Pig [93]
UTM VEGF Mouse [94]

PEGylated-NP, nanoparticles with polyethylene glycol; PLGA-NP, a copolymer (lactic-co-glycolic acid); PEI, polyethylenimine; PDMA, a cationic poly(beta-amino ester); UTM, the ultrasound-targeted microbubble; VEGF, vascular endothelial growth factor; IGF, insulin-like growth factor; EGFP, enhanced green fluorescent protein.