Advanced Functional Materials· 2026Q1
Programmable Temperature‐Capped Dressing for Enhanced Wound Healing, Bacterial Clearance, and Inflammatory Modulation
- 0citations
- Q1SCImago
- 2026year
Short summary
A new bilayer hydrogel dressing uses a PNIPAM upper layer to create programmable temperature caps (45°C for infection, 41°C for repair), enhancing wound healing and bacterial clearance (>99%) while reducing thermal damage.
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Key points
- A detachable bilayer hydrogel dressing features a PNIPAM upper layer for programmable temperature capping (45°C and 41°C) and a MXene/ciprofloxacin lower layer for synergistic antibacterial therapy.
- The dressing achieved rapid and effective antibacterial activity (>99%) against E. coli and S. aureus.
- In an infected rat wound model, the dressing accelerated wound closure, reduced inflammatory markers (TNF-α, IL-6, p-NF-κB p65), and modulated angiogenic remodeling (VEGF/CD31).
- The MXene network enables in situ temperature monitoring, with a proof-of-concept for autonomous feedback regulation via a closed-loop laser control system.
AI-generated from the title and abstract; the full text is not read.
Abstract
ABSTRACT Reconciling efficient bacterial eradication with tissue safety remains a challenge in photothermal therapy (PTT) because of open‐loop thermal actuation. Herein, we propose a detachable bilayer hydrogel dressing comprising a poly(N‐isopropylacrylamide) (PNIPAM)‐based protective upper layer as a self‐regulating thermal cap, and a Ti 3 C 2 T x MXene/ciprofloxacin (CIP) therapeutic lower layer providing synergistic antibacterial therapy. Sequential replacement of the protection layer enables programmed temperature caps of 45°C for early infection control and 41°C for subsequent repair. Synergistic MXene/CIP effects achieve rapid and effective antibacterial activity (>99%) against both Escherichia coli and Staphylococcus aureus . In an infected rat wound model, the programmable temperature‐capped dressing shortens high‐temperature exposure, attenuates TNF‐α/IL‐6/p‐NF‐κB p65 expression, modulates VEGF/CD31‐associated angiogenic remodeling, and accelerates closure compared with controls. Furthermore, the percolated MXene network endows the therapeutic layer with stable negative temperature coefficient (NTC) behavior. To explore this extended electronic utility, we demonstrated the dressing's capability for in situ temperature monitoring. Additionally, a benchtop closed‐loop laser control system was constructed to serve as a proof‐of‐concept for future autonomous feedback regulation. Overall, this bioelectronic hybrid platform advances PTT from conventional open‐loop heating toward a thermally capped and feedback‐compatible therapeutic strategy, offering a versatile paradigm for safer infected wound management.
The authors' abstract, as published at the source. Advanced Functional Materials, 2026 · DOI ↗
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Field: Rehabilitation
RehabilitationMedicine