自愈水凝胶
透明质酸
材料科学
明胶
生物相容性
PLGA公司
肿胀 的
真皮成纤维细胞
组织工程
细胞包封
生物物理学
高分子化学
纳米颗粒
纳米技术
生物医学工程
成纤维细胞
化学
有机化学
复合材料
生物化学
体外
冶金
生物
医学
遗传学
作者
Daniele M. Catori,Laura C. E. da Silva,Matheus F. de Oliveira,Grace H. Nguyen,Joseph Christakiran Moses,Elizabeth J. Brisbois,Hitesh Handa,Marcelo G. de Oliveira
标识
DOI:10.1021/acsami.3c10030
摘要
An increasing number of studies have shown that the local release of nitric oxide (NO) from hydrogels stimulates tissue regeneration by modulating cell proliferation, angiogenesis, and inflammation. The potential biomedical uses of NO-releasing hydrogels can be expanded by enabling their application in a fluid state, followed by controlled gelation triggered by an external factor. In this study, we engineered a hydrogel composed of methacrylated hyaluronic acid (HAGMA) and thiolated gelatin (GELSH) with the capacity for in situ photo-cross-linking, coupled with localized NO release. To ensure a gradual and sustained NO release, we charged the hydrogels with poly(l-lactic-co-glycolic acid) (PLGA) nanoparticles functionalized with S-nitrosoglutathione (GSNO), safeguarding SNO group integrity during photo-cross-linking. The formation of thiol–ene bonds via the reaction between GELSH's thiol groups and HAGMA's vinyl groups substantially accelerated gelation (by a factor of 6) and increased the elastic modulus of hydrated hydrogels (by 1.9–2.4 times). HAGMA/GELSH hydrogels consistently released NO over a 14 day duration, with the release of NO depending on the hydrogels' equilibrium swelling degree, determined by the GELSH-to-HAGMA ratio. Biocompatibility assessments confirmed the suitability of these hydrogels for biological applications as they display low cytotoxicity and stimulated fibroblast adhesion and proliferation. In conclusion, in situ photo-cross-linkable HAGMA/GELSH hydrogels, loaded with PLGA-GSNO nanoparticles, present a promising avenue for achieving localized and sustained NO delivery in tissue regeneration applications.
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