Freeze-dried chitosan–dipotassium hydrogen orthophosphate (CS/DHO) scaffold |
|
The CS/DHO/PL biomaterial possessed the ability to release PL proteins in a sustained manner for up to 5 days in response to the changing pH
The CS/DHO/PL scaffold did not exhibit cytotoxicity towards HSFs 2
|
[69] |
Electrospun sodium alginate/pullulan scaffold (SA/PUL) |
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The SA/PUL/PL biomaterial released significantly higher amounts of protein when compared to the SA/PUL biomaterial coated with PL
Both the SA/PUL/PL and SA/PUL biomaterial coated with PL promoted the viability and proliferation of human fibroblasts in vitro
|
[135] |
Electrospun fibrin/poly(ether)urethane scaffold |
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The biomaterial exhibited an initial burn release of GFs on day 1, followed by sustained release during the next 7 days
The biomaterial supported the viability of the mouse fibroblasts in vitro
The biomaterial accelerated wound closure after 14 days in mice
|
[136] |
Freeze-dried collagen/sulfated hyaluronan scaffold (collagen/sHA3) |
|
|
[137] |
3D-printed carboxylmethyl chitosan/oxidized alginate grafted catechol scaffold (CMCs/O-AlgCat) |
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The CMCs/O-AlgCat biomaterial released GFS in a sustained manner up to 10 days
The CMCs/O-AlgCat biomaterial supported the viability and proliferation of the mouse fibroblasts in vitro
The CMCs/O-AlgCat biomaterial promoted the healing of infected burn wounds in rats
|
[138] |