

Globally, people suffering from bone disorders are steadily increasing and bone tissue engineering is an advanced approach to treating fractured and defected bone tissues. In this study, we have prepared polymeric nanocomposite by free-radical polymerization from sodium alginate, hydroxyapatite, and silica with different GO amounts. The porous scaffolds were fabricated using the freeze drying technique. The structural, morphological, mechanical, and wetting investigation was conducted by Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscope, universal tensile machine, and water contact angle characterization techniques. The swelling, biodegradation, and water retention were also studied. The biological studies were performed (cell viability, cell adherence, proliferation, and mineralization) against osteoblast cell lines. Scaffolds have exhibited different pore morphology SAG-1 (pore size = 414.61 ± 56 μm and porosity = 81.45 ± 2.17 %) and SAG-4 (pore size = 195.97 ± 82 μm and porosity = 53.82 ± 2.45 %). They have different mechanical behavior as SAG-1 has the least compression strength and compression modulus 2.14 ± 2.35 and 16.51 ± 1.27 MPa. However, SAG-4 has maximum compression strength and compression modulus 13.67 ± 2.63 and 96.16 ± 1.97 MPa with wetting behavior 80.70° and 58.70°, respectively. Similarly, SAG-1 exhibited the least and SAG-4 presented maximum apatite mineral formation, cell adherence, cell viability, and cell proliferation against mouse pre-osteoblast cell lines. The increased GO amount provides different multifunctional materials with different characteristics. Hence, the fabricated scaffolds could be potential scaffold materials to treat and regenerate fracture bone tissues in bone tissue engineering. © 2022
| EMTREE drug terms: | acrylic acidalginic acidbiopolymergraphene oxidehydroxyapatitenanocompositenanohydroxyapatitepenicillin derivativeperoxydisulfate potassiumstreptomycinalginic acidbiomaterialhydroxyapatitesilicon dioxidewater |
|---|---|
| EMTREE medical terms: | Articleatomic emission spectrometrybiodegradationbiomineralizationbone diseasebone regenerationbone tissuecell adhesioncell culturecell proliferationcell structurecell viabilitycontact angleFourier transform infrared spectroscopyfracturefreeze dryinghydrophilicityhydrophobicityload bearingMC3T3-E1 cell linemechanical testmineralizationnonhumanoptical densityosteoblastpolymerizationscanning electron microscopyswellingsynergistic effecttissue engineeringwater retentionX ray diffractionanimalbonechemistrymouseporosityprocedurestissue scaffold |
| MeSH: | AlginatesAnimalsBiocompatible MaterialsBone and BonesDurapatiteMicePorositySilicon DioxideTissue EngineeringTissue ScaffoldsWater |
acrylic acid, 10344-93-1, 79-10-7; alginic acid, 28961-37-7, 29894-36-8, 9005-32-7, 9005-38-3; hydroxyapatite, 1306-06-5, 51198-94-8; peroxydisulfate potassium, 106015-10-5, 7727-21-1; streptomycin, 57-92-1; silicon dioxide, 10279-57-9, 14464-46-1, 14808-60-7, 15468-32-3, 60676-86-0, 7631-86-9; water, 7732-18-5;
Alginates; Biocompatible Materials; Durapatite; Silicon Dioxide; Water
Drug manufacturer:
Sigma Aldrich;
Thermo
Device manufacturer:
Bruker;
Lyovac, France;
Biotek, United States;
Olympus
| Funding sponsor | Funding number | Acronym |
|---|---|---|
| Horizon 2020 | ||
| 951747 |
We are grateful to the European Union's Horizon to support the research project. This project has received funding from the European Union's Horizon 2020 research and innovation program under grant agreement No. 951747.
Khan, M.U.A.; Biomedical Research Center, Qatar University, Doha, Qatar;
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