| Literature DB >> 29706001 |
Yili Qu1,2, Cong Cao3, Qingqing Wu4, Ai Huang1, Ying Song1, Hongling Li1, Yi Zuo5, Chenyu Chu1, Jidong Li5, Yi Man1,6.
Abstract
The major challenges associated with skin regeneration can include hindered vascularization and an insufficient degree of epithelization. In view of the complexity of these processes and the control signals on which they depend, one possible solution to these limitations could be simulating normal skin development and wound repair via the exogenous delivery of multiple cytokines. Here, we report the use of keratinocyte growth factor (KGF or FGF-7) and basic fibroblast growth factor (bFGF or FGF-2) released chemically modified collagen membranes to facilitate skin wound healing. The results from in vitro studies confirmed that this system resulted in higher cellular proliferation and faster cell migration. After transplanting the biomaterial onto an excisional wound healing model, the dual growth factor group, compared with the single growth factor groups and empty control group, showed more highly developed vascular networks and organized epidermal regeneration in the wounds. As a consequence, this experimental group showed mature epidermal coverage. Overall, this novel approach of releasing growth factors from a collagen membrane opens new avenues for fulfilling unmet clinical needs for wound care.Entities:
Keywords: basic fibroblast growth factor; collagen; controlled release; keratinocyte growth factor; skin regeneration; wound healing
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Year: 2018 PMID: 29706001 DOI: 10.1002/term.2691
Source DB: PubMed Journal: J Tissue Eng Regen Med ISSN: 1932-6254 Impact factor: 3.963