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Title: | Oxidized ionic polysaccharide hydrogels: review on derived scaffolds characteristics and tissue engineering applications |
Authors: | Pandey, Murali Monohar |
Keywords: | Pharmacy Alginate Chitosan Gellan gum Hyaluronic acid liposomes Periodate oxidation |
Issue Date: | Nov-2024 |
Publisher: | Elsevier |
Abstract: | Polysaccharide-based hydrogels have gained prominence due to their non-toxicity, biocompatibility, and structural adaptability for constructing tissue engineering scaffolds. Polysaccharide crosslinking is necessary for hydrogel stability in vivo. The periodate oxidation enables the modification of native polysaccharide characteristics for wound healing and tissue engineering applications. It produces dialdehydes, which are used to crosslink biocompatible amine-containing macromolecules such as chitosan, gelatin, adipic acid dihydrazide, silk fibroin, and peptides via imine/hydrazone linkages. Crosslinked oxidized ionic polysaccharide hydrogels have been studied for wound healing, cardiac and liver tissue engineering, bone, cartilage, corneal tissue regeneration, abdominal wall repair, nucleus pulposus regeneration, and osteoarthritis. Several modified hydrogel systems have been synthesized using antibiotics and inorganic substances to improve porosity, mechanical and viscoelastic properties, desired swelling propensity, and antibacterial efficacy. Thus, the injectable hydrogels provide a host-tissue-mimetic environment with high cell adhesion and viability, making them appropriate for scarless wound healing and tissue engineering applications. This review describes the oxidation procedure for alginate, hyaluronic acid, gellan gum, pectin, xanthan gum and chitosan, as well as the characteristics of the resulting materials. Furthermore, a critical review of scientific advances in wound healing and tissue engineering applications has been provided. |
URI: | https://www.sciencedirect.com/science/article/pii/S0141813024068983 http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18141 |
Appears in Collections: | Department of Pharmacy |
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