Synergistic Antimicrobial Glycyrrhizic Acid‐Based Functional Biosensing Composite for Sensitive Glucose Monitoring and Collaborative Wound Healing

High glucose blood and bacterial infection remain major issues for the slow healing of diabetic wounds, so developing functional biosensing composite with excellent antibacterial and remarkable glucose response sensitivity is necessary and prospective. Herein, by in situ synthesis AgNPs on the surface of self‐prepared PTIGA elastomers, PTIGA‐AgNPs conductive composites are obtained with efficient synergistic antibacterial effect, excellent mechanical and self‐healing properties. The strain of the composites can reach 1800%, and its self‐healing efficiency exceeds 90% at 60 °C within 8 h. Both elastomers and composites represent excellent biocompatibility and the antibacterial rate against E. coli and S. aureus exceeded 90%. Moreover, the biosensor assembled from the conductive composites exhibits excellent glucose response sensitivity and stability, with a sensitivity coefficient of 0.518 mA mm−1 in the range of 0.2–3.6 × 10−3 m glucose concentration, as well as a low detection limit of 0.08 × 10−3 m. Furthermore, based on the remarkable antibacterial performance and bioactivity derived from GA, the composites reduce the expression of pro‐inflammatory factors and promote the production of anti‐inflammatory factors, and effectively promote the regeneration of skin and granulation tissue of wounds in a diabetic full‐thickness skin defect model, demonstrating the enormous therapeutic potential in diabetic wound healing. Antibacterial PTIGA flexible substrates derived from glycyrrhizic acid (GA) and polycaprolactone triol (PT) are self‐synthesized. With the AgNPs being synthesized in situ by the autonomous reduction of GA, PTIGA‐AgNPs conductive composites with synergistic antibacterial and glucose‐responsive sites are prepared. The assembled PTIGA‐AgNPs biosensor exhibits remarkable application potential in blood glucose monitoring and promoting diabetic wound healing.