4.4 Article

Preparation of biocompatible wound dressings with dual release of antibiotic and platelet-rich plasma for enhancing infected wound healing

Journal

JOURNAL OF BIOMATERIALS APPLICATIONS
Volume 36, Issue 2, Pages 219-236

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/0885328221996013

Keywords

Carboxymethyl chitosan; microspheres; platelet-rich plasma; wound infections

Funding

  1. military logistics research project: preparation of composite absorbable wound adjuvant loaded with platelet gel dressing [CWH17C019]
  2. Research on key technologies of emergency blood transfusion equipment and blood products [BGZ15C002]
  3. Medical Scientific Research Foundation of Guangdong Province of China: Study on the mechanism of platelet-rich fibrin inhibiting bacterial biofilm [A2019194]

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In this study, a dual release dressing was developed, which can treat infected wounds and accelerate the healing process, showing good antibacterial effects against various bacteria and regulating pro-inflammatory and anti-inflammatory factors.
The ever-growing threats of bacterial infection and chronic wound healing have provoked an urgent need for novel antibacterial wound dressings. In this study, we developed a wound dressing for the treatment of infected wounds, which can reduce the inflammatory period (through the use of gentamycin sulfate (GS)) and enhance the granulation stage (through the addition of platelet-rich plasma (PRP)). Herein, the sustained antimicrobial CMC/GMs@GS/PRP wound dressings were developed by using gelatin microspheres (GMs) loading GS and PRP, covalent bonding to carboxymethyl chitosan (CMC). The prepared dressings exhibited high water uptake capability, appropriate porosity, excellent mechanical properties, sustain release of PRP and GS. Meanwhile, the wound dressing showed good biocompatibility and excellent antibacterial ability against Gram-negative and Gram-positive bacteria. Moreover, in vivo experiments further demonstrated that the prepared dressings could accelerate the healing process of E. coli and S. aureus-infected full-thickness wounds in vivo, reepithelialization, collagen deposition and angiogenesis. In addition, the treatment of CMC/GMs@GS/PRP wound dressing could reduce bacterial count, inhibit pro-inflammatory factors (TNF-alpha, IL-1 beta and IL-6), and enhance anti-inflammatory factors (TGF-beta 1). The findings of this study suggested that biocompatible wound dressings with dual release of GS and PRP have great potential in the treatment of chronic and infected wounds.

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