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. 2021 Mar 31;10(5):234–256. doi: 10.1089/wound.2019.1094

Table 2.

Nanoparticles for drug delivery of wound healing drugs or biomolecules for the treatment of diabetic wounds in animal models

NP Composition Formulation Biomolecule Animal Model Area (cm2) Time* (Days) References
PLGA In (PVA-borate) hydrogel Insulin Rat+diabetes 1 0.3 16 78
In poly(ether)urethane– polydimethylsiloxane/fibrin-based scaffolds VEGF and bFGF Mice+diabetes 2 (db/db) 0.5 15 80
VEGF Mice+diabetes 2 (db/db) 0.5 19 77
EGF Rat+diabetes 1 2.5 21 81
In carbopol 980 Ferulic acid (FA) Rat+diabetes 1 2.5 cm excision 14 79
Lipid TNFα Mice+diabetes 2 (db/db) 0.5 16 82
Lecithin In pluronic gel Deferoxamine Rat+diabetes 1 4 11 83
Protamine In calcium alginate hydrogel/hyaluronan oligosaccharide Rat+diabetes 1 3 16 87
ELP In fibrin gel KGF Mice+diabetes 2 (db/db) 1 14 84
In fibrin gel SDF-1 Mice+diabetes 2 (db/db) 1 28 86
In fibrin gel SDF-1 Mice+diabetes 2 (db/db) 1 28 86
Chitosan Collagen/alginate Curcumin Rat+diabetes 1 4 15 156

Diabetes type 1 was inducted with aloxan (rabbits) or streptozocin (mice and rats) (*times for complete wound closure or more than 90% of full thickness wounds).

bFGF, basic fibroblast growth factor; ELP, elastin-like protein; KGF, keratinocyte growth factor; STF-1, stromal cell-derived factor-1; TNFα, tumor necrosis factor alpha.