Biotinylated GHK peptide incorporated collagenous matrix: A novel biomaterial for dermal wound healing in rats
Matrikines are small peptide fragments of extracellular matrix proteins that display potent tissue repair activities. Difficulties in achieving sustained delivery of bioactive concentration of matrikines in the affected area limits their therapeutic use. The present study evaluates the effects bioti...
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Veröffentlicht in: | Journal of biomedical materials research 2005-05, Vol.73B (2), p.383-391 |
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Sprache: | eng |
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Zusammenfassung: | Matrikines are small peptide fragments of extracellular matrix proteins that display potent tissue repair activities. Difficulties in achieving sustained delivery of bioactive concentration of matrikines in the affected area limits their therapeutic use. The present study evaluates the effects biotinylated matrikine peptide (bio‐glycyl‐histidyl‐lysine) incorporated collagen membrane for dermal wound healing processes in rats. Biotinylated peptide incorporated collagen matrix (PIC) showed better healing when compared to wounds treated with collagen matrix [CF (collagen film)] and without collagen [CR (control)]. Binding studies indicate that biotinylated GHK (Bio‐GHK) binds effectively to the collagen matrix and red blood cell (RBC) membrane when compared with t‐butyloxycarbonyl substituted GHK (Boc‐GHK). Wound contraction, increased cell proliferation, and high expression of antioxidant enzymes in PIC treated group indicate enhanced wound healing activity when compared to CF and CR groups. Interestingly Bio‐GHK incorporated collagen increases the copper concentration by ninefold at the wound site indicating the wound healing property of Bio‐GHK can also be linked with both copper localization and matrikine activities. These results demonstrate the possibility of using Bio‐GHK incorporated collagen film as a therapeutic agent in the wound healing process. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater |
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ISSN: | 1552-4973 0021-9304 1552-4981 |
DOI: | 10.1002/jbm.b.30246 |