摘要
Timely hemostasis, bacterial inhibition, and accelerated tissue regeneration are core demands for clinical wound care. However, integrating robust wet adhesion and surface antifouling performance simultaneously remains a key bottleneck limiting conventional wound dressings. Herein, a carboxymethyl cellulose (CMC)-based drug-loaded hydrogel (DLCH) co-embedded with polyhexamethylene biguanide-loaded zeolite (PHMB@Zeo) and gelatin-dopamine-stabilized silver nanoparticles (Gel-DA-AgNPs) was rationally developed as the bottom functional therapeutic layer. Further, an asymmetric Janus drug-loaded hydrogel (JDLH) was fabricated by modifying DLCH surface with a hydrophobic HMDSO-TiO₂ antifouling coating. As the functional core, DLCH exhibits 45 kPa wet adhesion, 1353% stretchability, and sustained PHMB release over 240 h, achieving > 99% antibacterial activity against E. coli and S. aureus . Benefiting from DLCH's intrinsic superior properties, the resulting JDLH achieves rapid hemostasis at 41.33 ± 7.97 s and 46.33 ± 9.79 s in rat liver and heart non-compressible hemorrhage models, respectively. In vivo assays verify that JDLH accelerates full-thickness skin wound repair, reaching a 99.5% closure ratio on day 15 with boosted collagen deposition and angiogenesis. This work presents a portable Janus dressing with asymmetric adhesion, offering a practical advance for polysaccharide-based wound dressings and a promising candidate for emergency trauma and clinical wound care.
危险品化学品经营许可证(带存储)