MMP-9 responsive dipeptide-tempted natural protein hydrogel-based wound dressings for accelerated healing action of infected diabetic wound.
Anti-inflammatory
In vivo diabetic wound
L-carnosine
Matrix metalloproteinase-9
Silk protein
Journal
International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578
Informations de publication
Date de publication:
15 Jun 2020
15 Jun 2020
Historique:
received:
27
09
2019
revised:
25
10
2019
accepted:
25
10
2019
pubmed:
23
11
2019
medline:
10
2
2021
entrez:
23
11
2019
Statut:
ppublish
Résumé
The infected diabetic wound ulcer is a significant problem for the diabetic patients, which leads to removal of affected foot site due to its delayed/non-healing tissues. The poly-microbial infections and active matrix metalloproteinases (MMP) are the significant influencing factors to delayed healing in diabetic mice. The main purposes of present investigation are to evaluation the targeted inactivation of MMP and avoid polymicrobial infections by using a combined therapeutic effect of metal chelating dipeptide (L-carnosine) and curcumin with the biocompatible silk protein hydrogel (L-car@cur/SF) dressing in the infected diabetic wound ulcer. The in vitro biological assay methods, such as, cell viability, anti-oxidant activity, anti-inflammatory macrophage cells and inhibition collagenase exhibited that the designed hydrogel matrix to be human cell compatible and could be accelerate for significant diabetic healing potential. The activation of cur/SF matrix by the L-carnosine was persuading the inactivation of matrix metalloproteinase-9 (MMP-9) through its potent chelating effects of Zn
Identifiants
pubmed: 31756486
pii: S0141-8130(19)37862-6
doi: 10.1016/j.ijbiomac.2019.10.236
pii:
doi:
Substances chimiques
Antioxidants
0
Dipeptides
0
Hydrogels
0
Carnosine
8HO6PVN24W
Matrix Metalloproteinase 9
EC 3.4.24.35
Curcumin
IT942ZTH98
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1058-1069Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.