Biological evaluation of collagen-chitosan scaffolds for dermis tissue engineering

Three-dimensional collagen-chitosan scaffolds were fabricated with type I collagen and chitosan through freeze drying and glutaraldehyde cross-linking. Dermal fibroblasts were isolated from neonatal Sprague-Dawley rat skin by dispase II/collagenase I digestion. The fibroblasts were then seeded into the scaffolds to construct tissue-engineered dermis. The microstructure of the scaffolds as well as the fibroblasts' proliferation, cytokine secretion and cell cycle were investigated. Flow cytometry analysis indicated that cells in the scaffolds proliferated steadily. IL-6 concentration measurement by the ELISA test suggested that the scaffolds could promote secretion of the fibroblasts' cytokine. These results show that the fibroblasts and the scaffolds interact well with each other, and the fibroblasts have better proliferation ability and biological activity in the scaffolds than in monolayer culture. The scaffolds are a promising candidate for tissue repair and regeneration with enhanced biostability and good cytocompatibility.