Review
Copyright ©The Author(s) 2023.
World J Diabetes. Apr 15, 2023; 14(4): 364-395
Published online Apr 15, 2023. doi: 10.4239/wjd.v14.i4.364
Table 5 Gene delivery vectors applied for the growth factor treatment of diabetic wounds
Therapeutic agents
Delivery system and route
Response on wound closure
Ref.
Plasmid KGF-1Intradermal injectionEnhanced wound closure at day 9[382]
Plasmid TGF-β1Intradermal injectionComplete wound closure by 7 d[162]
Plasmid TGF-β1Intradermal injection, ElectroporationEarly induction of closure by day 5[383]
Plasmid KGF-1Intradermal injection, ElectroporationEnhanced wound closure at day 12[384]
Minicircle-VEGFSubcutaneous injection, SonoporationComplete wound closure by 12 d[385]
Adenovirus encoding VEGFTopical application to wound bedComplete wound closure by 13 d[386]
Adenovirus encoding VEGFIntradermal injectionComplete wound closure by 27 d[387]
Adenovirus encoding PDGFIntralesional injectionResidual epithelial gap of 3 mm at day 7[388]
Adenovirus encoding VEGF‐CIntradermal injectionComplete wound closure by 21 d[222]
Lentivirus encoding PDGFInjected into base and wound marginNo effect[389]
Adeno-associated virus encoding VEGFIntradermal injectionComplete re-epithelialization at 28 d[390]
Bicistronic Adeno-associated virus encoding VEGF-A and FGF4Intradermal injectionComplete wound closure by 17 d[391]
RGDK‐lipopeptide:rhPDGF-B lipoplexSubcutaneous injectionComplete wound closure by 12 d[392]
Minicircle VEGFSubcutaneous injectionComplete wound closure by 12 d[393]