Author/Authors :
Monteiro، نويسنده , , I.P. and Gabriel، نويسنده , , D. and Timko، نويسنده , , B.P. and Hashimoto، نويسنده , , M. and Karajanagi، نويسنده , , S. and Tong، نويسنده , , R. and Marques، نويسنده , , A.P. and Reis، نويسنده , , R.L. and Kohane، نويسنده , , D.S.، نويسنده ,
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.
Keywords :
Amine–aldehyde bonding , Bilayered , Hyaluronic acid , Skin defects