A gelatin/collagen/polycaprolactone scaffold for skin regeneration

A tissue-engineered skin substitute, based on gelatin ("G"), collagen ("C"), and poly(ε-caprolactone) (PCL; "P"), was developed. G/C/P biocomposites were fabricated by impregnation of lyophilized gelatin/collagen (GC) mats with PCL solutions, followed by solvent evapora...

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Veröffentlicht in:PeerJ (San Francisco, CA) CA), 2019-02, Vol.7, p.e6358-e6358, Article e6358
Hauptverfasser: Wei, Lin-Gwei, Chang, Hsin-I, Wang, Yiwei, Hsu, Shan-Hui, Dai, Lien-Guo, Fu, Keng-Yen, Dai, Niann-Tzyy
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Sprache:eng
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Zusammenfassung:A tissue-engineered skin substitute, based on gelatin ("G"), collagen ("C"), and poly(ε-caprolactone) (PCL; "P"), was developed. G/C/P biocomposites were fabricated by impregnation of lyophilized gelatin/collagen (GC) mats with PCL solutions, followed by solvent evaporation. Two different GC:PCL ratios (1:8 and 1:20) were used. Differential scanning calorimetry revealed that all G/C/P biocomposites had characteristic melting point of PCL at around 60 °C. Scanning electron microscopy showed that all biocomposites had similar fibrous structures. Good cytocompatibility was present in all G/C/P biocomposites when incubated with primary human epidermal keratinocytes (PHEK), human dermal fibroblasts (PHDF) and human adipose-derived stem cells (ASCs) . All G/C/P biocomposites exhibited similar cell growth and mechanical characteristics in comparison with C/P biocomposites. G/C/P biocomposites with a lower collagen content showed better cell proliferation than those with a higher collagen content . Due to reasonable mechanical strength and biocompatibility , G/C/P with a lower content of collagen and a higher content of PCL (GC P ) was selected for animal wound healing studies. According to our data, a significant promotion in wound healing and skin regeneration could be observed in GC P seeded with adipose-derived stem cells by Gomori's trichrome staining. This study may provide an effective and low-cost wound dressings to assist skin regeneration for clinical use.
ISSN:2167-8359
2167-8359
DOI:10.7717/peerj.6358