Chitosan composites and their research outcomes
Chitosan composite | Purpose | Scaffold type | Cell type used | In vitro cell response | In vivo response | Ref. |
---|---|---|---|---|---|---|
Chitosan/alginate-Hespiridin | Wound healing | Hydrogels | 3T3 murine fibroblast cell line | Cytocompatible, proliferative effect | Alg/Chit hydrogel—incomplete wound healing; Alg/Chit/10% hesperidin—no sign of inflammation and complete wound healing | [64] |
Chitin/chitosan/alginate/fucoidan | Functional wound dressing | Hydrogels | Human dermal fibroblast cells (DFCs) and dermal micro-vascular endothelial cells (DMVECs) | Stimulate cellular proliferation | Granulation and capillary formation on day 7 | [65] |
Chitosan/gelatin hydrogel incorporating PEGMA modified PCL nanofibers/curcumin | Skin regeneration | Hydrogels | L929 mouse fibroblast cells | Biocompatibility, more than 90% cellular viability, higher the PCP, lower the viability | - | [66] |
Chitosan/agarose | Skin substitute in regenerative medicine | Film | BJ human skin fibroblast cells | Non-cytotoxicity and strong cellular adhesion | - | [67] |
Chitosan/fibroin/poly (vinyl pyrrolidone) | Enhanced angiogenesis in wound healing | Hydrogels | - | - | Increased wound healing efficiency with increased fibroin content | [68] |
Polycaprolactone-hyaluronic acid/chitosan-zein | Tissue regeneration | Electrospun nanofiber | NHDF cells | Good cell viability for 7 days, good adhesive & proliferative capacity | - | [69] |
Chitosan-hyaluronic acid/VEGF loaded fibrin nanoparticles | Enhanced angiogenesis in wounds | Sponges | HDF cells and HUVEC cells | More than 85% cell viability | - | [70] |
Chitosan hydrogel/nanocapsules/nanoemulsion loaded with phenytoin | Wound healing | Hydrogel | - | - | Higher percent wound healing for the groups treated with allantoin (C+) and phenytoin-loaded nanocarriers on day 4 | [71] |
Gallic acid/chitosan/hyaluronic (GA-QCS/OHA hydrogels) | Infected wound healing | Hydrogels | L929 mouse fibroblast cells | Better proliferation within 5 days compared to the control group | Accelerated wound healing was obtained due to inhibiting the proinflammatory factor TNF-α and upregulating the vascularization factor CD31 | [72] |
Dual-dynamic-bond cross-linked ferric iron (Fe)/protocatechualdehyde (PA)/quaternized chitosan (QCS) | For closure of skin incisions and promotion of methicillin-resistant Staphylococcus aureus (MRSA)-infected wound healing | Hydrogel | L929 mouse fibroblast cells | Good cytocompatibility | Better incision closure. The activity of QCS and PA, and NIR-assisted ablation, synergistically enhanced the antibacterial capacity of the dressings against MRSA | [73] |
Quaternized chitosan-graft-polyaniline/oxidized dextran | Tissue engineering applications | Hydrogel | ADMSCs and C2C12 myoblast cells | Enhanced proliferation of C2C12 myoblasts | In Sprague-Dawley rats, in vivo hydrogel formation was confirmed | [74] |
Quaternized chitosan-g-polyaniline and benzaldehyde group functionalized poly(ethylene glycol)-co-poly(glycerol sebacate) | Full-thickness skin wound healing | Hydrogels | L929 mouse fibroblast cells | - | Excellent hemostatic performance on the hemorrhaging site | [75] |
Chitosan/xyloglucan composite | Accelerated wound healing | Hydrogels | NIH/3T3 mouse fibroblasts cells | An increase in cell spheroid size and good viability was observed | Displayed continuous degradation in vivo, good wound closure property after 5 days | [76] |
Fluorinated methacrylamide chitosan (MACF) | Diabetic wound healing | Hydrogels | - | - | Good re-epithelialization with MACF + O2 treatment | [77] |
ADMSCs: adipose-derived mesenchymal stem cells; HDF: human dermal fibroblast; HUVECs: human umbilical vein endothelial cells; NHDF: normal human dermal fibroblasts
ASD: Writing—original draft, Writing—review & editing. NM and RM: Conceptualization, Writing—review & editing. All authors read and approved the submitted version
The authors declare that they have no conflicts of interest.
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ASD acknowledges Kerala State Council for Science, Technology and Environment (KSCSTE), Thiruvananthapuram, Kerala, India, for providing financial support through the fellowship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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