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Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications
Published on: February 7, 2021
NIR-triggered photothermal nanocomposite hydrogels integrating polydopamine carbon dots and dynamic multi-networks
Huanxuan Huang1, Shiyang Liao2, Dong Zhang1
1Shanghai Key Laboratory of Advanced Polymeric Materials, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China. mdlang@ecust.edu.cn.
Abstract:
Accelerating the regeneration of infected wounds necessitates a multifaceted therapeutic intervention that simultaneously eradicates bacterial pathogens, adapts seamlessly to dynamic tissue deformations, and provides uninterrupted barrier protection, ultimately fostering a pro-healing microenvironment. To address these requirements, a dynamic multi-network nanocomposite hydrogel (OG/PCDs) was developed that couples on-demand photothermal therapy with orchestrated tissue remodeling. Specifically, polydopamine carbon dots (PDA-CDs) with exceptional near-infrared (NIR) photothermal conversion efficiency were initially synthesized as broad-spectrum antimicrobial agents. By combining intrinsic physical membrane disruption with NIR-triggered photothermal ablation, the PDA-CDs exhibit potent antibacterial activity while effectively mitigating the risk of bacterial resistance development. Subsequently, the OG/PCDs hydrogel was rationally engineered via the integration of dynamic Schiff base linkages, boronate ester bonds, and UV-triggered free-radical polymerization. Benefiting from its sophisticated architecture, the resulting hydrogel exhibited rapid autonomous self-healing capabilities, reliable tissue adhesion, and an intelligent pH-responsive release profile tailored for acidic infective microenvironments. Crucially, the hydrogel inherits the superior photothermal performance of PDA-CDs, enabling the efficient elimination of both planktonic bacteria and resilient biofilms. In vivo evaluations using an S. aureus-infected wound model demonstrated that the NIR-activated OG/PCDs hydrogel effectively sterilized the wound bed (>99% bacterial eradication) and significantly accelerated tissue remodeling, culminating in an impressive 98.42% wound closure rate over 14 days. Overall, by synergizing targeted photothermal antimicrobial efficacy with dynamic structural adaptability, the nanocomposite hydrogel presents a promising therapeutic platform to combat bacterial infections and facilitate tissue regeneration.