2018
DOI: 10.1016/j.ijbiomac.2018.08.179
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Development of nanocomposite scaffolds based on biomineralization of N,O-carboxymethyl chitosan/fucoidan conjugates for bone tissue engineering

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Cited by 54 publications
(37 citation statements)
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“…No other degradation products are observed. Such chemical structure will provide appropriate chemical conditions for bone-forming hydroxyapatite crystallization and stimulate its nucleation initiation, since polymeric layers will act as an organic template [40,41]. The incorporation of the aspartic acid also proves the increased intensity of free amino groups in the crosslinked polymer (1574 and 1148 cm −1 ), compared to pure chitosan (1593 and 1149 cm −1 ).…”
Section: Ft-ir Analysismentioning
confidence: 97%
See 1 more Smart Citation
“…No other degradation products are observed. Such chemical structure will provide appropriate chemical conditions for bone-forming hydroxyapatite crystallization and stimulate its nucleation initiation, since polymeric layers will act as an organic template [40,41]. The incorporation of the aspartic acid also proves the increased intensity of free amino groups in the crosslinked polymer (1574 and 1148 cm −1 ), compared to pure chitosan (1593 and 1149 cm −1 ).…”
Section: Ft-ir Analysismentioning
confidence: 97%
“…The composites were prepared by using polymers of known applicability in tissue engineering [36][37][38]. Ready scaffolds with tunable properties were characterized over their physicochemical properties, such as chemical structure, crystallinity, morphology, effect on biomineralization, and biocompatibility with human osteosarcoma (MG-63) cell lines [39][40][41]. Obtained results showed that proposed biomaterials display extraordinary properties and may significantly contribute to bone-tissue-engineering development.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, when the DS is less than 1, the product is C6-O-carboxymethyl, and the reaction equation of this is shown in Figure 4A. When the DS is greater than or equal to 1, carboxymethyl substitution occurs simultaneously with the C6-OH and C2-NH2 groups to form N, O-carboxymethyl chitosan [61,62], and the reaction equation of this is shown in Figure 4B. The property of carboxymethyl chitosan (CMCS) is related to the DS, where the DS depends on the amount of the carboxylating agent and the molecular weight of chitosan (CSMW).…”
Section: Carboxylated Chitosanmentioning
confidence: 99%
“…Table 2 shows the applications of common chitosan derivatives in bone tissue engineering. Increased pore size and mechanical properties promote osteoblast differentiation [61] Trimethyl chitosan N,N,N-trimethyl chitosan-heparin polyelectrolyte multilayer Bionic periosteum Good cell compatibility and support osteoblast differentiation [142] Hydroxypropyltrimethylammonium chloride chitosan Alginate/HACC/oyster shell powder Preparation bracket Improve mechanical properties and enhance stent surface area [143] CMCS is a commonly used in bone tissue engineering [137][138][139][140][141]. In addition to the applications shown in Table 2, CMCS can also be used to make nanofiber scaffolds [144].…”
Section: Bone Tissue Engineering Materialsmentioning
confidence: 99%
“…The gel proved effective in regenerating cartilage in a mouse model (H. Park, Woo, & Lee, ). The N , O ‐carboxymethyl chitosan/fucoidan conjugate formed a three‐dimensional hydrogel based on interconnected macropores, for bone tissue engineering (Lu, Lu, Chen, Lu, & Mi, ). Other crosslinking methods for GAGs, such as urea‐crosslinked HA systems (Fallacara et al, ), poly(ethylene glycol) crosslinked systems (Luo, Kirker, & Prestwich, ; Shu, Liu, Palumbo, Luo, & Prestwich, ), tyramine (TA) modified HA and ChS systems (Ni et al, ) were also developed.…”
Section: Polysaccharidesmentioning
confidence: 99%