<p>Diabetic wound healing remains a critical challenge due to a hyperglycemia-driven pathological change and lack of real-time diagnosis and monitoring, leading to delayed interventions and poor outcomes. We designed a pH-responsive multifunctional hydrogel (ZSC-SCHY) by encapsulating Scutellaria baicalensis-derived carbon quantum dots (SRC-CDs) into ZnS nanocages (ZS) within a carboxymethyl chitosan (CMCS)/sodium alginate (SA) hydrogel matrix. In vitro and in vivo evaluation showed that ZSC-SCHY dynamically converted the alkaline wound pH to a weakly acidic state. The pH-responsive fluorescence of SRC-CDs allowed real-time visual monitoring of wounds. Additionally, sustained release of Zn<sup>2+</sup> and H<sub>2</sub>S enhanced deep-tissue penetration and promoted angiogenesis. Notably, ZSC-SCHY significantly enhanced migration, proliferation, and synaptogenesis of Schwann cells, while also supporting endothelial cell functions and tissue remodeling. ZSC-SCHY presented an integrated theranostic platform that simultaneously overcame monitoring deficits and multifactorial pathology in diabetic wounds.</p> Graphical abstract <p></p>

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A pH-inspired hydrogel enables real-time monitoring and precise treatment of diabetic wounds

  • Yan Sun,
  • Xiangchen Su,
  • Xinrong Geng,
  • Mengdi Sun,
  • Ge Zhang,
  • Mingzhu Song,
  • Fang Li,
  • Ruizhen Lv,
  • Yuting Zhao,
  • Yijie Shi,
  • Liang Zhao

摘要

Diabetic wound healing remains a critical challenge due to a hyperglycemia-driven pathological change and lack of real-time diagnosis and monitoring, leading to delayed interventions and poor outcomes. We designed a pH-responsive multifunctional hydrogel (ZSC-SCHY) by encapsulating Scutellaria baicalensis-derived carbon quantum dots (SRC-CDs) into ZnS nanocages (ZS) within a carboxymethyl chitosan (CMCS)/sodium alginate (SA) hydrogel matrix. In vitro and in vivo evaluation showed that ZSC-SCHY dynamically converted the alkaline wound pH to a weakly acidic state. The pH-responsive fluorescence of SRC-CDs allowed real-time visual monitoring of wounds. Additionally, sustained release of Zn2+ and H2S enhanced deep-tissue penetration and promoted angiogenesis. Notably, ZSC-SCHY significantly enhanced migration, proliferation, and synaptogenesis of Schwann cells, while also supporting endothelial cell functions and tissue remodeling. ZSC-SCHY presented an integrated theranostic platform that simultaneously overcame monitoring deficits and multifactorial pathology in diabetic wounds.

Graphical abstract