Advanced Corneal Hydrogels: From Passive Replacement to Active Regeneration and Intelligent Interaction
Wang X., Zhou W., Xue H., Xue W., Gao G., Zhu B.
Narrative Review on Chronic Wound, Scar, published in Adv Sci (Weinh) (2026) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Narrative Review
- Journal
- Adv Sci (Weinh) (2026)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41736701
- PMCID
- PMC13045501
- DOI
- 10.1002/advs.202522362
Abstract (original English)
Hydrogels represent a transformative solution for corneal pathologies, offering the advantages of transparency, biocompatibility, and structural tunability to address the global donor tissue shortage. This review establishes a comprehensive framework for material design by delineating critical requirements, including optical clarity, mechanical anisotropy, and stable wet adhesion within dynamic ocular environments. The performances of natural, synthetic, and decellularized-matrix hydrogels are systematically compared to elucidate the structure-property relationships essential for recapitulating native corneal physiology. Beyond passive substitution, the transition toward bioactive regeneration is examined through analyses of scarless wound healing, sustained drug delivery, and stimuli-responsive implants. Furthermore, the integration of advanced technologies is evaluated with a focus on three-/four-dimensional bioprinting for hierarchical architectural reconstruction and hydrogel-based wearable bioelectronics for real-time sensing. Finally, pivotal clinical translation bottlenecks, ranging from sterilization to long-term immunocompatibility, are identified to guide the development of next-generation personalized and intelligent corneal devices.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
How we grade evidenceBrowse all related research
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