Table 2.
Effect | Mechanism of Action | Key Findings |
---|---|---|
Angiogenesis inhibition [92] |
Endothelial cell migration inhibition Downregulation of pro-angiogenic factors |
CMCS inhibited 2D and 3D migration of HUVECs, decreased CD34 expression in hepatocarcinoma tissues, and controlled serum levels of TIMP-1 and VEGF |
Angiogenesis promotion [93] |
Stimulation of growth factors | CMCS loaded with bioactive glass or magnesium ions stimulated the expression of VEGF and bFGF |
Antibacterial [106] | Bacterial membrane disruption | CMCS hydrogels with silver nanoparticles showed >95% reduced rates against S. aureus and E. coli after 50 laundering cycles |
Osteogenesis promotion [108] |
Regulation of bone-related proteins | CMCS increased osteocalcin content and the OPG/RANKL ratio in a rabbit knee replacement model |
Controlled drug release [73] |
pH-responsive swelling | CMCS/starch hydrogels with CuO nanoparticles showed pH-dependent swelling and controlled release of amoxicillin |
Collagen deposition [23] |
Stimulation of fibroblast activity | CMCS/HA/Ag hydrogels promoted collagen fiber deposition in partial-thickness burn wounds |
Anti-fungal activity [85] |
Fungal growth inhibition | CMCS delayed growth of C. albicans, C. krusei, and C. glabrata |
Gene therapy enhancement [88] |
Reduction in host immune response | CMCS allowed for repeated administration and long-term transgene expression of IL-10 in a hepatic fibrosis model |
Anti-inflammatory [87,108,109,110] | Cytokine modulation Antioxidant effect |
CMCS hydrogels suppressed pro-inflammatory cytokines, increased anti-inflammatory mediators, and scavenged reactive oxygen species |
Wound healing [113] | Promotion of fibroblast activity Cytokine modulation |
CMCS/plantamajoside hydrogel increased cell viability, migration, and collagen deposition, reduced expression of IL-1β, IL-6, and TNF-α, and increased IL-10 expression |