Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-19T13:07:10.728Z Has data issue: false hasContentIssue false

Preparation and characterization of glass–ceramic reinforced alginate scaffolds for bone tissue engineering

Published online by Cambridge University Press:  28 November 2019

Ashley Thomas
Affiliation:
Department of Ceramic Engineering, National Institute of Technology, Rourkela, Odisha 769008, India
Eldin Johnson
Affiliation:
Department of Life Science, National Institute of Technology, Rourkela, Odisha 769008, India
Ashish K. Agrawal
Affiliation:
Technical Physics Division, Bhabha Atomic Research Center, Mumbai 400085, India
Japes Bera*
Affiliation:
Department of Ceramic Engineering, National Institute of Technology, Rourkela, Odisha 769008, India
*
a)Address all correspondence to this author. e-mail: jbera@nitrkl.ac.in
Get access

Abstract

Bioactive glass–ceramic powder reinforced alginate scaffold has been successfully prepared and characterized for bone tissue engineering application. Glass-ceramic (GC) particles were synthesized through a sol–gel process. Alginate scaffolds containing different weight percentages of GC were fabricated through a freeze-drying technique. The composite scaffolds were characterized for phase analysis through X-ray powder diffraction and microstructure analysis through field emission scanning electron microscopy. The swelling behavior, degradation behavior, bioactivity, cell adhesion, and osteogenic potential of the fabricated scaffolds were evaluated. Microstructural analysis showed a highly porous behavior of the scaffold having a macroporous pore size. The composite scaffolds showed good bioactivity where GC induces apatite formation. The compressive strength of the scaffold was enhanced with GC addition due to the reinforcement of the alginate matrix. In vitro cell studies revealed that the composite scaffolds promoted cell adhesion, proliferation, and osteogenesis. Fabricated scaffolds are a promising biomaterial candidate for bone substitution because of their attractive properties.

Type
Article
Copyright
Copyright © Materials Research Society 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Jones, J.R.: Review of bioactive glass: From hench to hybrids. Acta Biomater. 9, 4457 (2013).CrossRefGoogle ScholarPubMed
Amini, A.R., Laurencin, C.T., and Nukavarapu, S.P.: Bone tissue engineering: Recent advances and challenges. Crit. Rev. Biomed. Eng. 40, 363 (2013).CrossRefGoogle Scholar
Baroli, B.: From natural bone grafts to tissue engineering therapeutics: Brainstorming on pharmaceutical formulative requirements and challenges. J. Pharm. Sci. 98, 1317 (2009).CrossRefGoogle ScholarPubMed
Dimitriou, R., Jones, E., McGonagle, D., and Giannoudis, P.V.: Bone regeneration: Current concepts and future directions. BMC Med. 9, 1 (2011).CrossRefGoogle ScholarPubMed
Yaszemski, M.J., Payne, R.G., Hayes, W.C., Langer, R., and Mikos, A.G.: Evolution of bone transplantation: Molecular, cellular and tissue strategies to engineer human bone. Biomaterials 17, 175 (1996).CrossRefGoogle ScholarPubMed
Dusseldorp, J.R. and Mobbs, R.J.: Iliac crest reconstruction to reduce donor-site morbidity: Technical note. Eur. Spine J. 18, 1386 (2009).CrossRefGoogle ScholarPubMed
Ebraheim, N.A., Elgafy, H., and Xu, R.: Bone-graft harvesting from iliac and fibular donor sites: Techniques and complications. J. Am. Acad. Orthop. Surg. 9, 210 (2001).CrossRefGoogle ScholarPubMed
Greenwald, A.S., Phil, D., Boden, S.D., Goldberg, V.M., and Khan, Y.: Bone graft substitutes: Facts, fictions & applications. J. Bone Joint Surg. Am. Vol. 83, 98 (2001).CrossRefGoogle ScholarPubMed
O’Keefe, R.J. and Mao, J.: Bone tissue engineering and regeneration: From discovery to the clinic—An overview. Tissue Eng., Part B 17, 389 (2011).CrossRefGoogle ScholarPubMed
Rezwan, K., Chen, Q.Z., Blaker, J.J., and Boccaccini, A.R.: Biodegradable and bioactive porous polymer/inorganic composite scaffolds for bone tissue engineering. Biomaterials 27, 3413 (2006).CrossRefGoogle ScholarPubMed
Boccaccini, A.R., Fleck, C., Schubert, D.W., Roether, J.A., Philippart, A., Boccaccini, A.R., Fleck, C., Schubert, D.W., and Roether, J.A.: Toughening and functionalization of bioactive ceramic and glass bone scaffolds by biopolymer coatings and infiltration: A review of the last 5 years. Expert Rev. Med. Devices 12, 93 (2014).Google Scholar
Chen, Q.Z., Thompson, I.D., and Boccaccini, A.R.: 45S5 Bioglass®-derived glass–ceramic scaffolds for bone tissue engineering. Biomaterials 27, 2414 (2006).CrossRefGoogle Scholar
Baino, F. and Vitale-Brovarone, C.: Three-dimensional glass-derived scaffolds for bone tissue engineering: Current trends and forecasts for the future. J. Biomed. Mater. Res., Part A 97, 514 (2011).CrossRefGoogle ScholarPubMed
Shuai, C., Huang, W., Feng, P., Gao, C., Shuai, X., Xiao, T., Deng, Y., Peng, S., and Wu, P.: Tailoring properties of porous poly(vinylidene fluoride) scaffold through nano-sized 58s bioactive glass. J. Biomater. Sci., Polym. Ed. 27, 97 (2016).CrossRefGoogle ScholarPubMed
Moncal, K.K., Heo, D.N., Godzik, K.P., Sosnoski, D.M., Mrowczynski, O.D., Rizk, E., Ozbolat, V., Tucker, S.M., Gerhard, E.M., Dey, M., Lewis, G.S., Yang, J., and Ozbolat, I.T.: 3D printing of poly(ε-caprolactone)/poly(D,L-lactide-co-glycolide)/hydroxyapatite composite constructs for bone tissue engineering. J. Mater. Res. 33, 1972 (2018).CrossRefGoogle Scholar
Elsayed, H., Zocca, A., Schmidt, J., Günster, J., Colombo, P., and Bernardo, E.: Bioactive glass–ceramic scaffolds by additive manufacturing and sinter-crystallization of fine glass powders. J. Mater. Res. 33, 1960 (2018).CrossRefGoogle Scholar
Kumbar, S.G., Laurencin, C., and Deng, M.: Natural and Synthetic Biomedical Polymers (Elsevier, USA, 2014).Google Scholar
Srinivasan, S., Jayasree, R., Chennazhi, K.P.P., Nair, S.V.V., and Jayakumar, R.: Biocompatible alginate/nano bioactive glass ceramic composite scaffolds for periodontal tissue regeneration. Carbohydr. Polym. 87, 274 (2012).CrossRefGoogle Scholar
Rehm, B. H.A. and Moradali, M. Fata: Alginates and Their Biomedical Applications (Springer, Singapore, 2018).CrossRefGoogle Scholar
Zhao, F., Zhang, W., Fu, X., Xie, W., and Chen, X.: Fabrication and characterization of bioactive glass/alginate composite scaffolds by a self-crosslinking processing for bone regeneration. RSC Adv. 6, 91201 (2016).CrossRefGoogle Scholar
Lin, H.R. and Yeh, Y-J.: Porous alginate/hydroxyapatite composite scaffolds for bone tissue engineering: Preparation, characterization, and in vitro studies. J. Biomed. Mater. Res. 71B, 52 (2004).CrossRefGoogle Scholar
Gerhardt, L-C. and Boccaccini, A.R.: Bioactive glass and glass–ceramic scaffolds for bone tissue engineering. Materials 3, 3867 (2010).CrossRefGoogle ScholarPubMed
Hench, L.L., Splinter, R.J., Allen, W.C., and Greenlee, T.K.: Bonding mechanisms at the interface of ceramic prosthetic materials. J. Biomed. Mater. Res. 5, 117 (1971).CrossRefGoogle Scholar
Abdollahi, S., Chih, A., Ma, C., and Cerruti, M.: Surface transformations of bioglass 45S5 during scaffold synthesis for bone tissue engineering. Langmuir 29, 1466 (2013).CrossRefGoogle ScholarPubMed
Sepulveda, P., Jones, J.R., and Hench, L.L.: Characterization of melt-derived 45S5 and sol–gel—Derived 58S bioactive glasses. J. Biomed. Mater. Res. 58, 734 (2001).CrossRefGoogle ScholarPubMed
Sakka, S.: Handbook of Sol–Gel Science and Technology: Processing, Characterization and Applications (Kluwer Academic Publishers, USA, 2005).Google Scholar
Mouriño, V., Newby, P., Pishbin, F., Cattalini, J.P., Lucangioli, S., and Boccaccini, A.R.: Physicochemical, biological and drug-release properties of gallium crosslinked alginate/nanoparticulate bioactive glass composite films. Soft Matter 7, 6705 (2011).CrossRefGoogle Scholar
Peitl, O., Zanotto, E.D., Serbena, F.C., and Hench, L.L.: Compositional and microstructural design of highly bioactive P2O5–Na2O–CaO–SiO2 glass–ceramics. Acta Biomater. 8, 321 (2012).CrossRefGoogle ScholarPubMed
Savina, I.N., Cnudde, V., D’Hollander, S., Van Hoorebeke, L., Mattiasson, B., Galaev, I.Y., and Du Prez, F.: Cryogels from poly(2-hydroxyethyl methacrylate): Macroporous, interconnected materials with potential as cell scaffolds. Soft Matter 3, 1176 (2007).CrossRefGoogle Scholar
Peter, M., Sudheesh Kumar, P.T., Binulal, N.S., Nair, S.V., Tamura, H., and Jayakumar, R.: Development of novel α-chitin/nanobioactive glass ceramic composite scaffolds for tissue engineering applications. Carbohydr. Polym. 78, 926 (2009).CrossRefGoogle Scholar
Hannink, G. and Arts, J.J.C.: Bioresorbability, porosity and mechanical strength of bone substitutes: What is optimal for bone regeneration? Injury 42(Suppl. 2), S22 (2011).CrossRefGoogle ScholarPubMed
Shiraishi, N., Anada, T., Honda, Y., Masuda, T., Sasaki, K., and Suzuki, O.: Preparation and characterization of porous alginate scaffolds containing various amounts of octacalcium phosphate (OCP) crystals. J. Mater. Sci.: Mater. Med. 21, 907 (2010).Google ScholarPubMed
Maire, E.: X-ray tomography applied to the characterization of highly porous materials. Annu. Rev. Mater. Res. 42, 163 (2012).CrossRefGoogle Scholar
Thomas, A. and Bera, J.: Sol–gel synthesis and in vitro bioactivity of glass–ceramics in SiO2–CaO–Na2O–P2O5 system. J. Sol-Gel Sci. Technol. 80, 411 (2016).CrossRefGoogle Scholar
Kazy, S.K., Sar, P., Singh, S.P., Sen, A.K., and D’Souza, S.F.: Extracellular polysaccharides of a copper-sensitive and a copper-resistant Pseudomonas aeruginosa strain: Synthesis, chemical nature and copper binding. World J. Microbiol. Biotechnol. 18, 583 (2002).CrossRefGoogle Scholar
Mishra, R., Basu, B., and Kumar, A.: Physical and cytocompatibility properties of bioactive glass–polyvinyl alcohol–sodium alginate biocomposite foams prepared via sol–gel processing for trabecular bone regeneration. J. Mater. Sci.: Mater. Med. 20, 2493 (2009).Google ScholarPubMed
Kuo, C.K. and Ma, P.X.: Ionically crosslinked alginate hydrogels as scaffolds for tissue engineering: Part 1. Structure, gelation rate and mechanical properties. Biomaterials 22, 511 (2001).CrossRefGoogle ScholarPubMed
Kokubo, T. and Takadama, H.: How useful is SBF in predicting in vivo bone bioactivity? Biomaterials 27, 2907 (2006).CrossRefGoogle ScholarPubMed
Chan, B.P. and Leong, K.W.: Scaffolding in tissue engineering: General approaches and tissue-specific considerations. Eur. Spine J. 17(Suppl. 4), 467 (2008).CrossRefGoogle ScholarPubMed
Duan, S., Yang, X., Mei, F., Tang, Y., Li, X., Shi, Y., Mao, J., Zhang, H., and Cai, Q.: Enhanced osteogenic differentiation of mesenchymal stem cells on poly(L-lactide) nanofibrous scaffolds containing carbon nanomaterials. J. Biomed. Mater. Res., Part A 103, 1424 (2015).CrossRefGoogle ScholarPubMed
Hsu, Y.L., Liang, H.L., Hung, C.H., and Kuo, P.L.: Syringetin, a flavonoid derivative in grape and wine, induces human osteoblast differentiation through bone morphogenetic protein-2/extracellular signal-regulated kinase 1/2 pathway. Mol. Nutr. Food Res. 53, 1452 (2009).CrossRefGoogle ScholarPubMed
Andrade, Â.L., Valério, P., and Goes, A.: Influence of morphology on in vitro compatibility of bioactive glasses. J. Non-Cryst. Solids 352, 3508 (2006).CrossRefGoogle Scholar
Xynos, I.D., Edgar, A.J., Buttery, L.D.K., Hench, L.L., and Polak, J.M.: Ionic products of bioactive glass dissolution increase proliferation of human osteoblasts and induce insulin-like growth factor II mRNA expression and protein synthesis. Biochem. Biophys. Res. Commun. 276, 461 (2000).CrossRefGoogle ScholarPubMed
Gregory, C.A., Gunn, W.G., Peister, A., and Prockop, D.J.: An alizarin red-based assay of mineralization by adherent cells in culture: Comparison with cetylpyridinium chloride extraction. Anal. Biochem. 329, 77 (2004).CrossRefGoogle ScholarPubMed
Tsigkou, O., Jones, J.R., Polak, J.M., and Stevens, M.M.: Differentiation of fetal osteoblasts and formation of mineralized bone nodules by 45S5 bioglass® conditioned medium in the absence of osteogenic supplements. Biomaterials 30, 3542 (2009).CrossRefGoogle Scholar
Varanasi, V.G., Owyoung, J.B., Saiz, E., Marshall, S.J., Marshall, G.W., and Loomer, P.M.: The ionic products of bioactive glass particle dissolution enhance periodontal ligament fibroblast osteocalcin expression and enhance early mineralized tissue development. J. Biomed. Mater. Res., Part A 98, 177 (2011).CrossRefGoogle ScholarPubMed
Pirayesh, H. and Nychka, J.A.: Sol–gel synthesis of bioactive glass–ceramic 45S5 and its in vitro dissolution and mineralization behavior. J. Am. Ceram. Soc. 96, 1643 (2013).CrossRefGoogle Scholar