journal article·2017-05-24

Efficiency and Safety of β-CD-(D3)7 as siRNA Carrier for Decreasing Matrix Metalloproteinase-9 Expression and Improving Wound Healing in Diabetic Rats

Na Li, Heng-Cong Luo, Meng Ren, Li-Ming Zhang, Wei Wang, Cheng-Lin Pan, Li-Qun Yang, Guo-Juan Lao, Jun-Jie Deng, Kai-jin Mai, Kan Sun, Chuan Yang, Li Yan

Publisher page

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-(D 3 ) 7 as a gene carrier to take siRNA and effectively interfere with MMP-9 expression. It has been proven that β-CD-(D 3 ) 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-(D 3 ) 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-(D 3 ) 7 /MMP-9 siRNA might be developed as a novel topical agent for the diabetic wounds treatment.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Wound Healing and Treatments · Silk-based biomaterials and applications · Periodontal Regeneration and Treatments

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Endocrinology, Sun Yat-sen Memorial Hospital, Guangdong Provincal Key Laboratory of Malignant Tumor Epigenetics and Gene Reguatioǹ Medical Research Center, Sun Yat-sen University, Guangzhou 510120, China

Department of Endocrinology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Guangzhou Municipality · Guangdong Province · Key Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes, Sun Yat-sen University · Key Laboratory of Malignant Tumor Molecular Mechanism and Translational Medicine, Guangzhou Bureau of Science and Information Technology

References (25)

Show source-provided references
1. 10.2337/diacare.28.2.46110.2337/diacare.28.2.461 ↗
2. 10.2337/dc08-076310.2337/dc08-0763 ↗
3. 10.1016/S1479-666X(07)80007-210.1016/S1479-666X(07)80007-2 ↗
4. 10.1177/153473461349050610.1177/1534734613490506 ↗
5. 10.1177/153473461453498010.1177/1534734614534980 ↗
6. 10.1016/j.jdiacomp.2012.12.00710.1016/j.jdiacomp.2012.12.007 ↗
7. 10.1111/j.1464-5491.2008.02414.x10.1111/j.1464-5491.2008.02414.x ↗
8. 10.7547/099048910.7547/0990489 ↗
9. Wu S. C. · Vasc. Health Risk Manage · 2007 · 3 · 65
10. 10.1016/j.addr.2015.10.00810.1016/j.addr.2015.10.008 ↗
11. 10.1016/j.ijpharm.2010.08.02210.1016/j.ijpharm.2010.08.022 ↗
12. 10.1038/gt.2010.6910.1038/gt.2010.69 ↗
13. 10.1016/j.jconrel.2010.02.00310.1016/j.jconrel.2010.02.003 ↗
14. 10.1016/j.biomaterials.2011.08.02610.1016/j.biomaterials.2011.08.026 ↗
15. 10.1016/j.jconrel.2016.06.03410.1016/j.jconrel.2016.06.034 ↗
16. 10.1039/c0jm03030a10.1039/c0jm03030a ↗
17. 10.2147/IJN.S6636810.2147/IJN.S66368 ↗
18. 10.1016/j.biomaterials.2009.07.03610.1016/j.biomaterials.2009.07.036 ↗
19. 10.1021/bc800072210.1021/bc8000722 ↗
20. 10.1016/S0142-9612(02)00445-310.1016/S0142-9612(02)00445-3 ↗
21. 10.1016/j.ejps.2004.01.00110.1016/j.ejps.2004.01.001 ↗
22. 10.1166/jbn.2016.215510.1166/jbn.2016.2155 ↗
23. 10.1021/bc000108410.1021/bc0001084 ↗
24. 10.1177/088532820708000510.1177/0885328207080005 ↗
25. 10.1002/dmrr.100410.1002/dmrr.1004 ↗