4.7 Article

Polyhexamethylene guanidine hydrochloride modified sodium alginate nonwoven with potent antibacterial and hemostatic properties for infected full-thickness wound healing

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 209, Issue -, Pages 2142-2150

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.04.194

Keywords

Surface modification; Sodium alginate nonwoven; Polyhexamethylene guanidine; Antibacterial performance; Blood clotting; Infected wound healing

Funding

  1. National Natural Science Foundation of China [51803128, 52073186]
  2. National Natural Science Foundation of China [51803128, 52073186]
  3. Fundamental Research Funds for the Central Universities [51803128]
  4. Strategic Cooperation Projects of Yi Bin City and Sichuan University [52073186]
  5. Lu Zhou City and Sichuan University [20826041D4160]
  6. Sui Ning City and Sichuan University [2020CDYB-6]
  7. State Key Laboratory of Polymer Materials Engineering [2021CDLZ-14]
  8. Funding of Engineering Characteristic Team, Sichuan University [2021CDSN-03]
  9. [sklpme2021-3-01]
  10. [2020SCUNG122]

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An antibacterial and hemostatic wound dressing has been developed with excellent liquid absorption capacity, water vapor permeability, and ideal antibacterial activity. The dressing promotes blood clotting by activating platelets and demonstrates ideal biocompatibility. Its use on infected wounds improves wound closure and tissue regeneration.
The development of multifunctional wound dressings has always been considered as a promising strategy to promote blood coagulation, inhibit bacterial infection, and accelerate wound healing. Herein, an antibacterial and hemostatic dressing (SA-PHMG) was developed based on sodium alginate (SA) nonwoven and polyhexamethylene guanidine hydrochloride (PHMG) through a completely green industrial route, including dipping, padding, and drying. According to studies, SA-PHMG dressings exhibited excellent liquid absorption capacity and water vapor permeability. Moreover, bactericidal assays have demonstrated that SA-PHMG dressings have ideal antibacterial activity against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and mixed bacteria, maintaining potent antibacterial activity even after 10 cycles of antibacterial trials or 50 times of washing or soaping. The in vitro evaluation of the hemostatic effect indicated that the SA-PHMG could significantly promote blood clotting by activating platelets, and in vitro and in vivo hemolysis, cytotoxicity and skin irritation studies demonstrated the ideal biocompatibility of the dressings. In addition, better wound closure and tissue regeneration were recorded using SA-PHMG nonwoven as the dressing based on an infected full-thickness wound model. In conclusion, this antibacterial, hemostatic, biocompatible, and environmentally friendly SA-PHMG nonwoven exhibit the potential for infected wound healing.

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