|
Type of modification | Material | Active substance | Biomedical or pharmaceutical application | Dosage form | Reference |
|
Oxidation | Oxidized-NaALG | Limbal epithelial stem cells | Improvement of corneal wound healing therapy | Hydrogel
| Wright et al. [10] |
Flurbiprofen | Sustained oral delivery | Beads | Maiti et al. [11] |
|
Reductive-amination of oxidized alginate | ALG-g-poly(ethylene glycol) | Human foreskin fibroblasts | Specific cell microencapsulation | Microspheres | Mahou et al. [12] |
|
Sulfation | Sulfated ALG | — | Reduction of secretion inflammatory cytokines, improvement of the biocompatibility | Microspheres | Arlov et al. [13] |
|
Phosphorylation | Phosphorylated ALG | — | Mineralization of hydroxyapatite and participation in the chelation process for tissue engineering | Gel | Coleman et al. [14] |
|
Graft copolymerization | NaALG-co-polyacrylamide | Famotidine | Sustained release gastroretentive carrier | Hydrogel | Tripathi and Mishra [15] |
Starch--poly(acrylic acid)-NaALG | Diclofenac sodium | pH-sensitive matrices for the oral drug delivery | Hydrogel beads | Chang [16] |
ALG-glycidyl methacrylate
| Human endothelial cell lines HUVEC and L929 | Thermal polymerizable injectable hydrogel for tissue engineering, especially for myocardial repair | Hydrogel | Wang et al. [17]
|
Galactosylated ALG | Hepatocytes | Cell carrier with mechanical stability and selective permeability | Microcapsules | Tian et al. [18] |
α-Cyclodextrin-ALG conjugate | Sphingomonas cloacae | Immobilization of bacteria | Beads | Pluemsab et al. [19] |
β-Cyclodextrin-ALG conjugate | Ondansetron | Controlled drug delivery systems | Gel | Izawa et al. [20] |
|
Esterification | Propylene glycol ALG | Lysozyme | Protein encapsulation with a sustained release | Microparticles | Hurteaux et al. [21] |
|