Rhein-chitosan in situ hydrogel promotes wound healing in diabetic mice
Chronic inflammation and infection often lead to delayed healing in skin wounds of patients with diabetes, presenting a significant challenge in clinical wound repair. In an effort to tackle this issue, we explored the utilization of the natural compounds Rhein and chitosan in the creation of a cros...
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Veröffentlicht in: | International journal of biological macromolecules 2024-10, Vol.277 (Pt 4), p.134472, Article 134472 |
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Sprache: | eng |
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Zusammenfassung: | Chronic inflammation and infection often lead to delayed healing in skin wounds of patients with diabetes, presenting a significant challenge in clinical wound repair. In an effort to tackle this issue, we explored the utilization of the natural compounds Rhein and chitosan in the creation of a crosslinked in situ gel. Developed as Rhein-chitosan in situ hydrogel (CS-Rh gel), this formulation has the ability to gel at body temperature, making it suitable for irregular wounds of varying shapes. Our experimental investigations have demonstrated its excellent biocompatibility, controlled release of Rhein, biodegradability, anti-inflammatory properties, antibacterial effect, as well as its ability to enhance keratinocyte proliferation and migration. Furthermore, in vivo studies have confirmed that CS-Rh gel can effectively mitigate tissue inflammation, promote collagen deposition, and significantly accelerate wound healing in diabetic mice within a short timeframe of two weeks. Consequently, this innovative approach holds promise as a viable therapeutic strategy for supporting the healing of diabetic wounds in a clinical setting.
•Rhein and chitosan are natural substances that offer superior biocompatibility and more affordable prices compared to other materials.•The CS-RH gel's temperature-sensitive property allows it to fill various irregular wounds in situ.•CS-RH gel can expedite wound healing in diabetic mice through various mechanisms, including antibacterial and anti-inflammatory properties, as well as by promoting keratinocyte proliferation and migration. |
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ISSN: | 0141-8130 1879-0003 1879-0003 |
DOI: | 10.1016/j.ijbiomac.2024.134472 |