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Fabrication of Hyaluronan-Poly(vinylphosphonic acid)-Chitosan Hydrogel for Wound Healing Application
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A new hydrogel made of hyaluronan, poly(vinylphosphonic acid), and chitosan (HA/PVPA/CS hydrogel) was fabricated and characterized to be used for skin wound healing application. Firstly, the component ratio of hydrogel was studied to optimize the reaction effectiveness. Next, its microstructure was observed by light microscope. The chemical interaction in hydrogel was evaluated by nuclear magnetic resonance spectroscopy and Fourier transform-infrared spectroscopy. Then, a study on its degradation rate was performed. After that, antibacterial activity of the hydrogel was examined by agar diffusion method. Finally,in vivostudy was performed to evaluate hydrogel’s biocompatibility. The results showed that the optimized hydrogel had a three-dimensional highly porous structure with the pore size ranging from about 25 µm to less than 125 µm. Besides, with a degradation time of two weeks, it could give enough time for the formation of extracellular matrix framework during remodeling stages. Furthermore, the antibacterial test showed that hydrogel has antimicrobial activity againstE. coli.Finally,in vivostudy indicated that the hydrogel was not rejected by the immune system and could enhance wound healing process. Overall, HA/PVPA/CS hydrogel was successfully fabricated and results implied its potential for wound healing applications.
Title: Fabrication of Hyaluronan-Poly(vinylphosphonic acid)-Chitosan Hydrogel for Wound Healing Application
Description:
A new hydrogel made of hyaluronan, poly(vinylphosphonic acid), and chitosan (HA/PVPA/CS hydrogel) was fabricated and characterized to be used for skin wound healing application.
Firstly, the component ratio of hydrogel was studied to optimize the reaction effectiveness.
Next, its microstructure was observed by light microscope.
The chemical interaction in hydrogel was evaluated by nuclear magnetic resonance spectroscopy and Fourier transform-infrared spectroscopy.
Then, a study on its degradation rate was performed.
After that, antibacterial activity of the hydrogel was examined by agar diffusion method.
Finally,in vivostudy was performed to evaluate hydrogel’s biocompatibility.
The results showed that the optimized hydrogel had a three-dimensional highly porous structure with the pore size ranging from about 25 µm to less than 125 µm.
Besides, with a degradation time of two weeks, it could give enough time for the formation of extracellular matrix framework during remodeling stages.
Furthermore, the antibacterial test showed that hydrogel has antimicrobial activity againstE.
coli.
Finally,in vivostudy indicated that the hydrogel was not rejected by the immune system and could enhance wound healing process.
Overall, HA/PVPA/CS hydrogel was successfully fabricated and results implied its potential for wound healing applications.
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