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Int J Biol Macromol ; 266(Pt 1): 131220, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38554920

RESUMO

Diabetic wound healing remains a healthcare challenge due to the overexpression of matrix metalloproteinase-9 (MMP-9) and the imbalance between angiogenic factors and vascular inhibitory factors. In this study, we developed a nanocomposite injectable collagen/chitosan hydrogel for the treatment of delayed diabetic wound healing, which can promote cell migration to the wound site (through the addition of phycocyanin) and reduce the expression of MMP-9 (through the use of ND-336) to improve the therapeutic effect of diabetic wound healing. Furthermore, different weight ratios of collagen and chitosan hydrogels were prepared to select the hydrogel with proper mechanical properties. In vitro experiments confirmed that all hydrogels have favorable biocompatibility and hemocompatibility. Notably, Gel 2, with a weight ratio of collagen and chitosan at 25:75, was found to have an excellent capability to facilitate cell migration and in vivo studies further proved that Gel 2 nanocomposite hydrogel had the best ability to improve diabetic wound healing by promoting cell migration and decreasing MMP-9 expression. The collagen/chitosan/genipin hydrogel loaded phycocyanin and ND-336 can be harnessed for non-toxic and efficient treatment of wound healing management of diabetes.


Assuntos
Quitosana , Colágeno , Hidrogéis , Iridoides , Metaloproteinase 9 da Matriz , Nanopartículas , Ficocianina , Cicatrização , Quitosana/química , Quitosana/farmacologia , Cicatrização/efeitos dos fármacos , Ficocianina/química , Ficocianina/farmacologia , Animais , Colágeno/química , Hidrogéis/química , Hidrogéis/farmacologia , Nanopartículas/química , Metaloproteinase 9 da Matriz/metabolismo , Diabetes Mellitus Experimental/tratamento farmacológico , Camundongos , Ratos , Masculino , Movimento Celular/efeitos dos fármacos , Humanos
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