Table 3.
Summary of key studies on bioscaffolds for corneal regeneration.
Study | Scaffold Type | Functionalization Methods | Cell Type(s) Used | Key Findings |
---|---|---|---|---|
Fagerholm P. et al. [18] | Collagen-based | None | Human corneal epithelial cells | Restored vision in animal models, good integration with host tissue |
Nosrati H. et al. [17] | Gelatin-based | RGD peptides | Corneal epithelial cells | Improved cell adhesion and proliferation |
Fagerholm P. et al. [18] | Decellularized porcine | Optimized SDS protocol | None | Maintained mechanical properties and transparency of decellularized corneal scaffolds |
Tayebi, T et al. [19] | Decellularized porcine | Enzymatic (trypsin and dispase) | None | Retained critical ECM components essential for cell attachment and function |
Yan, B et al. [21] | Collagen-based | None | MSCs | Improved wound healing and reduced scarring in a model of corneal alkali burn |
Yu, X et al. [28] | Collagen-based | Combined chemical and enzymatic approach | None | Improved decellularization, retaining critical ECM components for tissue engineering |
Teimouri, R et al. [23] | Poly(ethylene glycol)-based | None | Human corneal endothelial cells | Biodegradable and biocompatible hydrogel films for regeneration of corneal endothelium |
Fagerholm P. et al. [18] | Amniotic membrane-based | None | Keratocytes | A novel tissue-engineered corneal stromal equivalent |
Ahearne, M. et al. [10] | Silk fibroin-based | None | Human corneal endothelial cells | Human corneal endothelial cell growth on a silk fibroin membrane |
Tayebi et al. [19] | Chitosan-based | None | Various cell types | Supports cell attachment, proliferation, and bone regeneration |