Bibliographic Details
| Title: |
Chitosan Nanofibrous Dressing Increased Angiogenesis and Anti-inflammatory Response in an Acute Wound Model in Rats: A Comparative Study. |
| Authors: |
Salkovskiy, Yury1 (AUTHOR) ysalkovskiy@unomaha.edu, Ghanbari, Mahboubeh1 (AUTHOR), Jara, Carlos P.2 (AUTHOR), Cartwright, Sara2 (AUTHOR), Mondal, Pinaki2 (AUTHOR), Freel, Colman3 (AUTHOR), Razian, Sayed Ahmadreza1 (AUTHOR), MacTaggart, Jason2 (AUTHOR), Carlson, Mark A.2 (AUTHOR) |
| Source: |
Annals of Biomedical Engineering. Dec2025, Vol. 53 Issue 12, p3415-3434. 20p. |
| Subjects: |
Chitosan, Wound healing, Skin regeneration, Inflammation, Antimicrobial bandages, Rats, Neovascularization |
| Abstract: |
Purpose: Chitosan-based materials are promising for wound healing because of their antibacterial efficacy, biocompatibility, and biodegradability, though their healing mechanisms remain unclear. This study explores the cellular and molecular mechanisms of wound healing with chitosan nanofibrous dressings. Methods: Thirty-nine Sprague Dawley rats were divided into three groups based on the type of dressings administered: (1) chitosan nanofibrous dressing + transparent film, (2) commercial scaffold + transparent film, and (3) transparent film alone (control). Full-thickness wounds (2 cm × 2 cm) were created on the dorsum, splinted, and covered with dressings. Evaluations at 7, 14, and 21 days included histological analysis, and measurements of TNF-α and iNOS levels in the wounds. Results: On day 21, epithelialization was significantly higher in the chitosan group than in the scaffold group (87.5% vs. 42.0%, p = 0.03). TNF-α levels were lower in both treatment groups compared to the controls. In the chitosan group, the CD68+/CD163+ ratio was lower than in the scaffold group (0.28 vs. 0.62, p = 0.037), and blood vessel formation was greater than in the controls. Conclusion: These results suggest that chitosan nanofibrous dressings enhance acute wound healing in rats by promoting re-epithelialization, neovasculogenesis, and maintaining low TNF-α levels in the later phases of healing. [ABSTRACT FROM AUTHOR] |
|
Copyright of Annals of Biomedical Engineering is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
| Database: |
Engineering Source |