| Literature DB >> 25192821 |
I P Monteiro1, D Gabriel2, B P Timko2, M Hashimoto2, S Karajanagi3, R Tong2, A P Marques4, R L Reis4, D S Kohane5.
Abstract
We have developed a bilayered dermal-epidermal scaffold for application in the treatment of full-thickness skin defects. The dermal component gels in situ and adapts to the lesion shape, delivering human dermal fibroblasts in a matrix of fibrin and cross-linked hyaluronic acid modified with a cell adhesion-promoting peptide. Fibroblasts were able to form a tridimensional matrix due to material features such as tailored mechanical properties, presence of protease-degradable elements and cell-binding ligands. The epidermal component is a robust membrane containing cross-linked hyaluronic acid and poly-l-lysine, on which keratinocytes were able to attach and to form a monolayer. Amine-aldehyde bonding at the interface between the two components allows the formation of a tightly bound composite scaffold. Both parts of the scaffold were designed to provide cell-type-specific cues to allow for cell proliferation and form a construct that mimics the skin environment.Entities:
Keywords: Amine–aldehyde bonding; Bilayered; Hyaluronic acid; Skin defects
Mesh:
Year: 2014 PMID: 25192821 PMCID: PMC4254066 DOI: 10.1016/j.actbio.2014.08.029
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947