| Literature DB >> 28447455 |
Na Li1, Heng-Cong Luo1,2, Meng Ren1, Li-Ming Zhang, Wei Wang1, Cheng-Lin Pan, Li-Qun Yang, Guo-Juan Lao1, Jun-Jie Deng, Kai-Jin Mai, Kan Sun1, Chuan Yang1, Li Yan1.
Abstract
Overexpression of matrix metalloproteinase-9 (MMP-9) is critical for diabetic chronic wounds involved in the refractory wound healing process. We aimed to develop a strategy through RNAi to decrease MMP-9 expression and improve diabetic wound healing. We had explored β-CD-(D3)7 as a gene carrier to take siRNA and effectively interfere with MMP-9 expression. It has been proven that β-CD-(D3)7 could be used as an effective siRNA delivery system. In this study, we want to know about the efficiency and safety of β-CD-(D3)7/MMP-9 siRNA for improving wound healing in diabetic rats. β-CD-(D3)7/MMP-9 siRNA treated animals show lower levels of MMP-9 expression, which induce faster wound-close rates. Histological evaluation indicates that β-CD-(D3)7/MMP-9 siRNA significantly increases the content of collagen around the injured tissues. The number of neutrophilic ganulocytes was significantly decreased through treatment of β-CD-(D3)7/MMP-9 siRNA. In vivo fluorescence imaging assessment shows that β-CD-(D3)7/MMP-9 siRNA could not cause organ damage and organ accumulation. The results suggest that β-CD-(D3)7/MMP-9 siRNA might be developed as a novel topical agent for the diabetic wounds treatment.Entities:
Keywords: RNA interference; diabetic wound healing; matrix metalloproteinase-9; siRNA; β-CD-(D3)7
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Year: 2017 PMID: 28447455 DOI: 10.1021/acsami.7b02809
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229