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An Injectable CMCS/γ-PGA/PRP Bioadhesive With Antibacterial, Adhesive, and Regenerative Properties for Infected Wound Healing.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology2026-03-28PubMed
Total: 77.5Innovation: 9Impact: 0Rigor: 0Citation: 0

Summary

This preclinical study reports a tri-functional injectable CMCS/γ-PGA/PRP bioadhesive achieving >99.9% bacterial kill, rapid wet-tissue adhesion, and sustained growth factor release. In infected rat wounds, one application produced sterile sealing and full epithelialization by day 6 with enhanced collagen deposition and M2 macrophage polarization.

Key Findings

  • >99.9% bactericidal efficacy against Escherichia coli and Staphylococcus aureus
  • Instantaneous wet-tissue adhesion exceeding 3 kPa
  • Sustained gradient release of PDGF, TGF-β, and VEGF
  • Infected rat wounds achieved sterile sealing and complete epithelialization within 6 days
  • 1.5-fold increase in collagen deposition and M2 macrophage polarization

Clinical Implications

If validated in humans, this bioadhesive could provide a one-step alternative for managing contaminated traumatic and surgical wounds in plastic and reconstructive settings, potentially lowering infection rates and accelerating healing.

Why It Matters

Condensing suture, antibiotics, and dressing into a single bioadhesive platform could streamline care for contaminated wounds and reduce complications. The mechanistic integration of antimicrobial action and pro-regenerative signaling is a notable advance.

Limitations

  • Preclinical animal data without human clinical validation
  • Long-term safety, biofilm robustness, and head-to-head comparisons with standard of care are not reported

Future Directions

Conduct GLP toxicology, dose-ranging, and randomized clinical trials in contaminated traumatic and surgical wounds; evaluate performance against polymicrobial biofilms and in immunocompromised hosts.

Study Information

Study Type
Basic/Mechanistic Research (preclinical in vivo)
Research Domain
Treatment
Evidence Level
V - Preclinical animal study without clinical outcomes; hypothesis-generating evidence
Study Design
OTHER