ArticleBioactive materials2026
Skin-mimetic bilayer hydrogel enhances spatiotemporal coordination of neuro-immune-vascular interactions to accelerate diabetic wound healing.
Article in Bioactive materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Harnessing spatiotemporal melatonin delivery from engineered platforms for targeted microenvironment remodeling in peripheral neuropathy.Materials today. Bio · 2026Review
- Inflammation and wound healing: a comprehensive overview of mechanisms, therapeutic strategies, and translational perspectives.Biomarker research · 2026Review
- Integrative neuromodulation in diabetic foot infections: electroacupuncture-driven macrophage reprogramming and synergy with antimicrobial biomaterials.Frontiers in cellular and infection microbiology · 2026Review
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Diabetic wound healing is a complex spatiotemporal process that requires stage-specific interventions to address disrupted neuro-immune interactions and impaired angiogenesis. However, achieving such precise coordination with a single regenerative dressing remains a considerable challenge. Drawing inspiration from native skin physiology, we have developed an intelligent, conductive, skin-mimetic bilayer hydrogel that spatially segregates functions and temporally orchestrates the repair process. This design features a robust, anisotropic upper layer that provides protection and serves as an efficient conduit for electrical stimulation, combined with a responsive lower layer that adheres to the wound and enables on-demand drug delivery. Specifically, the lower hydrogel releases calcitonin gene-related peptide in response to the early inflammatory microenvironment, effectively suppressing the pro-inflammatory M1 macrophage phenotype and promoting its transition to the pro-repair M2 phenotype. Subsequently, the conductive upper layer sustains the release of magnesium ions and synergizes with electrical stimulation to significantly enhance endothelial cell migration and tube formation via activation of the VEGF signaling pathway. Transcriptomic analysis reveals that this combination fosters a pro-regenerative microenvironment by enriching pathways related to extracellular matrix organization and angiogenesis. This skin-mimetic structure-to-function design offers a practical strategy for staged, precise wound repair in diabetes and provides a generalizable framework for chronic tissue regeneration.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.