Biofilm infection will cause chronic inflammation and hinder the normal healing process of wound. Here, based on the self-assembly of three designed amphiphilic pentapeptides named EK, GG, and DR, pH-switchable antibacterial hydrogels with amphiphilic fiber network are used for the eradication of biofilms and the rescue of delayed healing in infected wounds. These pentapeptides-based hydrogels exhibit an acidic pHswitchable antimicrobial effect and are biocompatible at neutral pH. Additionally, supramolecular nanofiber networks with physical cross-linking with thermosensitive polymers (PNIPAm) and loaded antibacterial oregano oil are further developed. In vitro experiments indicate that the antimicrobial activity of hydrogels comes from the disassembly of acidic pH-dependent nanofiber network and activated release of pentapeptides and oregano oil, which achieves synergistic biofilm eradication. Remarkably, DRbased supramolecular hydrogel improves the healing efficiency of the full-thickness wound of skin in vivo, which is manifested by increased wound closure rate, reduced inflammatory response, faster angiogenesis, and collagen deposition in the wound, exhibiting great potential as wound dressing. The proposed synergistic strategy of inhibiting biofilm formation and activating healing may provide an efficient method for the treatment of clinically infected wounds.
Supermacroporous
hydrogels have attracted wide concern due to their
comfort and breathability in wearable health-monitoring applications.
Size controllable supermacroporous structure and excellent mechanical
properties are the most important for its application. However, they
are normally fabricated by the cryogelation method, which is difficult
to control pore size and maintain flexibility. Here, yeast fermentation-inspired
gelatin hydrogels with a controllable supermacroporous structure and
excellent mechanical properties were fabricated for the first time.
The pore size can be controlled by adjusting the content of glucose
and yeast, the ratio of glucose to yeast, fermentation time, and gelatin
content during fermentation. The hydrogels demonstrated a controllable
pore size range from 100 to 400 μm and rapid swelling characteristics.
The mechanical properties were maintained by soaking ammonium sulfate
solution for 12 h, showing maximum tensile and compressive strains
over 300 and 99%, respectively. This novel approach can be easily
applied to the preparation of supermacroporous and high ductility
hydrogels under mild conditions. Furthermore, conductive hydrogels
combined supermacroporous structures with conductive polyaniline and
reduced oxidized graphene, and silver nanowires were prepared as wearable
flexible sensors. The obtained sensors maintain well-distributed porosity,
breathability, and mechanical flexibility, also showing excellent
conductivity of 2.4 S m–1. Finally, the sensors
were successfully applied to detect physiological signals and human–computer
interaction.
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