journal article·2024-07-28

Macro-alignment responses of preosteoblast MC3T3-E1 cells on DCPD-coated β-TCP porous scaffolds: Effect of liquid volume/mass ratio and granular sizes

Ahmed Hafedh Mohammed Mohammed, Khairul Anuar Shariff, Mohamad Hafizi Abu Bakar, Hasmaliza Mohamad, Aira Matsugaki, Takayoshi Nakano, Intan Nirwana

Journal of Materials Research· Volume 39· Issue 14
Publisher page

Abstract

Extensive assessment of bone-like cell responses towards porous β-tricalcium phosphate scaffolds has shown promising osteoconductivity and biocompatibility. However, the activity of bone-like cells is inhibited due to the formation of dense granule structures and the high formation of dicalcium phosphate dihydrate (DCPD) between dense granules during the setting reaction of macroporous α-TCP or β-TCP granule cement. Hence, this study was carried out to investigate the macro-alignment responses of preosteoblast MC3T3-E1 cells on DCPD-coated β-TCP porous scaffolds by evaluating the effect of acidic volume-to-granular mass ratios (AV/GR) and β-TCP granule sizes (GS) on the scaffolds via a setting reaction. The fabricated porous scaffolds were first characterised using Scanning Electron Microscope (SEM), X-ray Diffraction (XRD), Fourier-Transform Infrared (FTIR), porosity, and compressive strength. Then, in vitro tests using preosteoblast MC3T3-E1 cells were performed to determine the macro-alignment of cell responses towards scaffolds. The results imply that the GS and pore size formation inside the DCPD-coated β-TCP porous scaffolds affected the macro-alignment of preosteoblast MC3T3-E1 surrounding the surface of the fabricated porous scaffold specimens. It was expected that the findings in this study will be a game changer that expedites cell responses in coating-on-ceramic technology.Graphical abstract
Source: expertdata · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Bone Tissue Engineering Materials · 3D Printing in Biomedical Research · Electrospun Nanofibers in Biomedical Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (50)

Show source-provided references
1. S. Liu, L. Mo, G. Bi, S. Chen, D. Yan, J. Yang, Y.G. Jia, L. Ren, DLP 3D printing porous β-tricalcium phosphate scaffold by the use of acrylate/ceramic composite slurry. Ceram. Int. 47, 21108–21116 (2021). https://doi.org/10.1016/J.CERAMINT.2021.04.11410.1016/J.CERAMINT.2021.04.114 ↗
2. N. Butler, Y. Zhao, S. Lu, S. Yin, Effects of light exposure intensity and time on printing quality and compressive strength of β-TCP scaffolds fabricated with digital light processing. J. Eur. Ceram. Soc. (2023). https://doi.org/10.1016/J.JEURCERAMSOC.2023.11.04610.1016/J.JEURCERAMSOC.2023.11.046 ↗
3. K. Ishikawa, T.S. Putri, A. Tsuchiya, K. Tanaka, K. Tsuru, Fabrication of interconnected porous β-tricalcium phosphate (β-TCP) based on a setting reaction of β-TCP granules with HNO3 followed by heat treatment. J. Biomed. Mater. Res. A 106, 797–804 (2018). https://doi.org/10.1002/JBM.A.3628510.1002/JBM.A.36285 ↗
4. T.S. Putri, K. Hayashi, K. Ishikawa, Bone regeneration using β-tricalcium phosphate (β-TCP) block with interconnected pores made by setting reaction of β-TCP granules. J. Biomed. Mater. Res. A 108, 625–632 (2020). https://doi.org/10.1002/jbm.a.3684210.1002/jbm.a.36842 ↗
5. J.E. Won, Y.S. Lee, J.H. Park, J.H. Lee, Y.S. Shin, C.H. Kim, J.C. Knowles, H.W. Kim, Hierarchical microchanneled scaffolds modulate multiple tissue-regenerative processes of immune-responses, angiogenesis, and stem cell homing. Biomaterials 227, 119548 (2020). https://doi.org/10.1016/J.BIOMATERIALS.2019.11954810.1016/J.BIOMATERIALS.2019.119548 ↗
6. K. Hayashi, A. Tsuchiya, M. Shimabukuro, K. Ishikawa, Multiscale porous scaffolds constructed of carbonate apatite honeycomb granules for bone regeneration. Mater. Des. 215, 110468 (2022). https://doi.org/10.1016/J.MATDES.2022.11046810.1016/J.MATDES.2022.110468 ↗
7. A.H.M. Mohammed, K.A. Shariff, D.A. Wahjuningrum, M.H.A. Bakar, H. Mohamad, A comprehensive review of the effects of porosity and macro- and micropore formations in porous β-TCP scaffolds on cell responses. J. Aust. Ceram. Soc. 2023, 1–15 (2023). https://doi.org/10.1007/S41779-023-00880-010.1007/S41779-023-00880-0 ↗
8. M. Mohammadi Zerankeshi, S. Mofakhami, E. Salahinejad, 3D porous HA/TCP composite scaffolds for bone tissue engineering. Ceram. Int. 48, 22647–22663 (2022). https://doi.org/10.1016/J.CERAMINT.2022.05.10310.1016/J.CERAMINT.2022.05.103 ↗
9. V. Mandić, F. Radovanović-Perić, I. Panžić, D. Vrsaljko, Addressing of different synthetic and shaping approaches for β-tri calcium phosphate macro-microporous scaffold fabrication. Ceram. Int. (2022). https://doi.org/10.1016/J.CERAMINT.2022.10.01010.1016/J.CERAMINT.2022.10.010 ↗
10. A. Díaz-Arca, P. Velasquez, P. Mazón, P.N. De Aza, Mechanism of in vitro reaction of a new scaffold ceramic similar to porous bone. J. Eur. Ceram. Soc. 40, 2200–2206 (2020). https://doi.org/10.1016/J.JEURCERAMSOC.2020.01.04510.1016/J.JEURCERAMSOC.2020.01.045 ↗
11. M. Sari, P. Hening, Chotimah, I.D. Ana, Y. Yusuf, Porous structure of bioceramics carbonated hydroxyapatite-based honeycomb scaffold for bone tissue engineering. Mater Today Commun 26, 102135 (2021). https://doi.org/10.1016/J.MTCOMM.2021.10213510.1016/J.MTCOMM.2021.102135 ↗
12. K.A. Shariff, M.H. AbuBakar, A. Cahyanto, Behavior of osteoclast cells response on dicalcium phosphate dihydrate layer-coated β-tricalcium phosphate granular. Mater. Sci. Forum 1010, 549–554 (2020). https://doi.org/10.4028/www.scientific.net/MSF.1010.54910.4028/www.scientific.net/MSF.1010.549 ↗
13. A.H.M. Mohammed, K.A. Shariff, M.H.A. Bakar, H. Mohamad, A review on the behavioral responses of osteoclast and osteoblast cells on the near-surface of the bioceramic coating: roles of ions released, solubility, and pH. J. Aust. Ceram. Soc. 58, 1–13 (2022). https://doi.org/10.1007/S41779-022-00806-210.1007/S41779-022-00806-2 ↗
14. F. Zhang, J. Yang, Y. Zuo, K. Li, Z. Mao, X. Jin, S. Zhang, H. Gao, Y. Cui, Digital light processing of β-tricalcium phosphate bioceramic scaffolds with controllable porous structures for patient specific craniomaxillofacial bone reconstruction. Mater. Des. 216, 110558 (2022). https://doi.org/10.1016/J.MATDES.2022.11055810.1016/J.MATDES.2022.110558 ↗
15. S. Tarafder, V.K. Balla, N.M. Davies, A. Bandyopadhyay, S. Bose, Microwave-sintered 3D printed tricalcium phosphate scaffolds for bone tissue engineering. J. Tissue Eng. Regen. Med. 7, 631–641 (2013). https://doi.org/10.1002/TERM.55510.1002/TERM.555 ↗
16. N.A.S. Zairani, M. Jaafar, N. Ahmad, K. Abdul Razak, Fabrication and characterization of porous β-tricalcium phosphate scaffolds coated with alginate. Ceram. Int. 42, 5141–5147 (2016). https://doi.org/10.1016/J.CERAMINT.2015.12.03410.1016/J.CERAMINT.2015.12.034 ↗
17. Y.Z. Shi, J. Liu, L. Yu, L.Z. Zhong, H.B. Jiang, β-TCP scaffold coated with PCL as biodegradable materials for dental applications. Ceram. Int. 44, 15086–15091 (2018). https://doi.org/10.1016/J.CERAMINT.2018.05.14210.1016/J.CERAMINT.2018.05.142 ↗
18. J. Duan, H. Shao, H. Liu, J. Xu, M. Cong, K. Zhao, T. Lin, 3D gel-printing of hierarchically porous BCP scaffolds for bone tissue engineering. J. Eur. Ceram. Soc. 43, 2646–2653 (2023). https://doi.org/10.1016/J.JEURCERAMSOC.2023.01.01010.1016/J.JEURCERAMSOC.2023.01.010 ↗
19. N.Z. Mohamad Zaidi, A.H.M. Mohammed, M.K. Sujon, K.A. Shariff, M.H.A. Bakar, Behavioural responses of bone-like cells on dense and porous dicalcium phosphate dihydrate-coated β-tricalcium phosphate granules. J. Aust. Ceram. Soc. 2023, 1–9 (2023). https://doi.org/10.1007/S41779-023-00925-410.1007/S41779-023-00925-4 ↗
20. A.H.M. Mohammed, K.A. Shariff, M. Hafizi, A. Bakar, H. Mohamad, B. My, Fabrication of macro-and micropore forming DCPD/β-TCP porous scaffolds: effect of setting-time reaction and acidic calcium phosphate solution. Iran. J. Mater. Sci. Eng. (2023). https://doi.org/10.22068/ijmse.340210.22068/ijmse.3402 ↗
21. K.A. Shariff, K. Tsuru, K. Ishikawa, Fabrication of dicalcium phosphate dihydrate-coated β-TCP granules and evaluation of their osteoconductivity using experimental rats. Mater. Sci. Eng. C 75, 1411–1419 (2017). https://doi.org/10.1016/j.msec.2017.03.00410.1016/j.msec.2017.03.004 ↗
22. A.H.M. Mohammed, K.A. Shariff, M.H. Abu Bakar, H. Mohamad, Recent methods in fabricating porous β-tricalcium phosphate scaffolds: a mini review. Mater Today Proc (2022). https://doi.org/10.1016/J.MATPR.2022.06.49810.1016/J.MATPR.2022.06.498 ↗
23. N. Fukuda, K. Tsuru, Y. Mori, K. Ishikawa, Fabrication of self-setting β-tricalcium phosphate granular cement. J. Biomed. Mater. Res. B Appl. Biomater. 106, 800–807 (2018). https://doi.org/10.1002/JBM.B.3389110.1002/JBM.B.33891 ↗
24. N. Fukuda, K. Ishikawa, K. Akita, K. Kamada, N. Kurio, Y. Mori, Y. Miyamoto, Effects of acidic calcium phosphate concentration on setting reaction and tissue response to β-tricalcium phosphate granular cement. J. Biomed. Mater. Res. B Appl. Biomater. 108, 22–29 (2020). https://doi.org/10.1002/JBM.B.3436110.1002/JBM.B.34361 ↗
25. K.A. Shariff, K. Tsuru, K. Ishikawa, Fabrication of interconnected pore forming α-tricalcium phosphate foam granules cement. J. Biomater. Appl. 30, 838–845 (2016). https://doi.org/10.1177/088532821560193910.1177/0885328215601939 ↗
26. P.T. Kien, K. Ishikawa, K. Tsuru, Setting reaction of α-TCP spheres and an acidic calcium phosphate solution for the fabrication of fully interconnected macroporous calcium phosphate. Ceram. Int. 41, 13525–13531 (2015). https://doi.org/10.1016/J.CERAMINT.2015.07.14610.1016/J.CERAMINT.2015.07.146 ↗
27. K.A. Shariff, K. Tsuru, K. Ishikawa, Regulation of DCPD formation on β-TCP granular surface by exposing different concentration of acidic calcium phosphate solution. Key Eng. Mater. 696, 27–31 (2016). https://doi.org/10.4028/WWW.SCIENTIFIC.NET/KEM.696.2710.4028/WWW.SCIENTIFIC.NET/KEM.696.27 ↗
28. N. Fukuda, K. Tsuru, Y. Mori, K. Ishikawa, Effect of citric acid on setting reaction and tissue response to β-TCP granular cement. Biomed. Mater. 12, 015027 (2017). https://doi.org/10.1088/1748-605X/AA5AEA10.1088/1748-605X/AA5AEA ↗
29. L. Siqueira, F.R. Passador, M.M. Costa, A.O. Lobo, E. Sousa, Influence of the addition of β-TCP on the morphology, thermal properties and cell viability of poly (lactic acid) fibers obtained by electrospinning. Mater. Sci. Eng. C 52, 135–143 (2015). https://doi.org/10.1016/J.MSEC.2015.03.05510.1016/J.MSEC.2015.03.055 ↗
30. S. Zeng, L. Liu, Y. Shi, J. Qiu, W. Fang, M. Rong, Z. Guo, W. Gao, Characterization of silk fibroin/chitosan 3D porous scaffold and in vitro cytology. PLoS ONE 10, e0128658 (2015). https://doi.org/10.1371/JOURNAL.PONE.012865810.1371/JOURNAL.PONE.0128658 ↗
31. A.L. Torres, V.M. Gaspar, I.R. Serra, G.S. Diogo, R. Fradique, A.P. Silva, I.J. Correia, Bioactive polymeric-ceramic hybrid 3D scaffold for application in bone tissue regeneration. Mater. Sci. Eng. C 33, 4460–4469 (2013). https://doi.org/10.1016/J.MSEC.2013.07.00310.1016/J.MSEC.2013.07.003 ↗
32. I.R. Serra, R. Fradique, M.C.S. Vallejo, T.R. Correia, S.P. Miguel, I.J. Correia, Production and characterization of chitosan/gelatin/β-TCP scaffolds for improved bone tissue regeneration. Mater. Sci. Eng. C 55, 592–604 (2015). https://doi.org/10.1016/J.MSEC.2015.05.07210.1016/J.MSEC.2015.05.072 ↗
33. A. Ślósarczyk, C. Paluszkiewicz, M. Gawlicki, Z. Paszkiewicz, The FTIR spectroscopy and QXRD studies of calcium phosphate based materials produced from the powder precursors with different CaP ratios. Ceram. Int. 23, 297–304 (1997). https://doi.org/10.1016/S0272-8842(96)00016-810.1016/S0272-8842(96)00016-8 ↗
34. X. Ye, Y. Zhang, T. Liu, Z. Chen, W. Chen, Z. Wu, Y. Wang, J. Li, C. Li, T. Jiang, Y. Zhang, H. Wu, X. Xu, Beta-tricalcium phosphate enhanced mechanical and biological properties of 3D-printed polyhydroxyalkanoates scaffold for bone tissue engineering. Int. J. Biol. Macromol. 209, 1553–1561 (2022). https://doi.org/10.1016/J.IJBIOMAC.2022.04.05610.1016/J.IJBIOMAC.2022.04.056 ↗
35. J.N. Li, P. Cao, X.N. Zhang, S.X. Zhang, Y.H. He, In vitro degradation and cell attachment of a PLGA coated biodegradable Mg-6Zn based alloy. J. Mater. Sci. 45, 6038–6045 (2010). https://doi.org/10.1007/s10853-010-4688-910.1007/s10853-010-4688-9 ↗
36. X. Ye, G. Xu, S. Cai, Y. Dou, Y. Zhu, H. Hu, Preparation, surface properties, and MC3T3-E1 cell response of mesoporous hydroxyapatite thin films. J. Mater. Sci. 47, 3763–3769 (2012). https://doi.org/10.1007/s10853-011-6227-810.1007/s10853-011-6227-8 ↗
37. H.A.M. Zaki, K.A. Shariff, M.H.A. Bakar, M.N. Azmi, Effect of different granular size on the properties of porous β-tricalcium phosphate foam granular cements. Key Eng. Mater. 829, 23–27 (2020). https://doi.org/10.4028/WWW.SCIENTIFIC.NET/KEM.829.2310.4028/WWW.SCIENTIFIC.NET/KEM.829.23 ↗
38. L.J. Wei, K.A. Shariff, S.A. Momin, M.H.A. Bakar, A. Cahyanto, Self-setting β-tricalcium phosphate granular cement at physiological body condition: effect of citric acid concentration as an inhibitor. J. Aust. Ceram. Soc. 57, 687–696 (2021). https://doi.org/10.1007/S41779-021-00575-410.1007/S41779-021-00575-4 ↗
39. K. Ishikawa, K. Tsuru, T.K. Pham, M. Maruta, S. Matsuya, Fully-interconnected pore forming calcium phosphate cement. Key Eng. Mater. 493–494, 832–835 (2012). https://doi.org/10.4028/www.scientific.net/KEM.493-494.83210.4028/www.scientific.net/KEM.493-494.832 ↗
40. A.M. Maadani, E. Salahinejad, Performance comparison of PLA- and PLGA-coated porous bioceramic scaffolds: mechanical, biodegradability, bioactivity, delivery and biocompatibility assessments. J. Control. Release 351, 1–7 (2022). https://doi.org/10.1016/J.JCONREL.2022.09.02210.1016/J.JCONREL.2022.09.022 ↗
41. S. Flauder, U. Gbureck, F.A. Müller, Structure and mechanical properties of β-TCP scaffolds prepared by ice-templating with preset ice front velocities. Acta Biomater. 10, 5148–5155 (2014). https://doi.org/10.1016/J.ACTBIO.2014.08.02010.1016/J.ACTBIO.2014.08.020 ↗
42. E. Ryan, S. Yin, Compressive strength of β-TCP scaffolds fabricated via lithography-based manufacturing for bone tissue engineering. Ceram. Int. 48, 15516–15524 (2022). https://doi.org/10.1016/J.CERAMINT.2022.02.08510.1016/J.CERAMINT.2022.02.085 ↗
43. J. Wieding, A. Fritsche, P. Heinl, C. Körner, M. Cornelsen, H. Seitz, W. Mittelmeier, R. Bader, Biomechanical behavior of bone scaffolds made of additive manufactured tricalciumphosphate and titanium alloy under different loading conditions. J Appl Biomater Funct Mater 11, 159–166 (2013). https://doi.org/10.5301/JABFM.2013.1083210.5301/JABFM.2013.10832 ↗
44. A. Reizabal, R. Brito-Pereira, M.M. Fernandes, N. Castro, V. Correia, C. Ribeiro, C.M. Costa, L. Perez, J.L. Vilas, S. Lanceros-Méndez, Silk fibroin magnetoactive nanocomposite films and membranes for dynamic bone tissue engineering strategies. Materialia 12, 100709 (2020). https://doi.org/10.1016/j.mtla.2020.10070910.1016/j.mtla.2020.100709 ↗
45. Z. Montaseri, S.S. Abolmaali, A.M. Tamaddon, F. Farvadi, Composite silk fibroin hydrogel scaffolds for cartilage tissue regeneration. J Drug Deliv Sci Technol 79, 104018 (2022). https://doi.org/10.1016/J.JDDST.2022.10401810.1016/J.JDDST.2022.104018 ↗
46. H. Zhang, J. Han, Y. Sun, Y. Huang, M. Zhou, MC3T3-E1 cell response to stainless steel 316L with different surface treatments. Mater. Sci. Eng. C 56, 22–29 (2015). https://doi.org/10.1016/j.msec.2015.06.01710.1016/j.msec.2015.06.017 ↗
47. A. Tevlek, S. Odabas, E. Çelik, H.M. Aydin, Preparation of MC3T3-E1 cell sheets through short-term osteogenic medium application. Artif Cells Nanomed Biotechnol 46, 1145–1153 (2018). https://doi.org/10.1080/21691401.2018.148108110.1080/21691401.2018.1481081 ↗
48. W.B. Swanson, M. Omi, Z. Zhang, H.K. Nam, Y. Jung, G. Wang, P.X. Ma, N.E. Hatch, Y. Mishina, Macropore design of tissue engineering scaffolds regulates mesenchymal stem cell differentiation fate. Biomaterials 272, 120769 (2021). https://doi.org/10.1016/J.BIOMATERIALS.2021.12076910.1016/J.BIOMATERIALS.2021.120769 ↗
49. S. Sprio, S. Panseri, M. Montesi, M. Dapporto, A. Ruffini, S.M. Dozio, R. Cavuoto, D. Misseroni, M. Paggi, D. Bigoni, A. Tampieri, Hierarchical porosity inherited by natural sources affects the mechanical and biological behaviour of bone scaffolds. J. Eur. Ceram. Soc. 40, 1717–1727 (2020). https://doi.org/10.1016/J.JEURCERAMSOC.2019.11.01510.1016/J.JEURCERAMSOC.2019.11.015 ↗
50. P. Das, S. Ganguly, P.K. Marvi, M. Sherazee, S.R. Ahmed, X. Tang, S. Srinivasan, A.R. Rajabzadeh, Borophene based 3D extrusion printed nanocomposite hydrogel for antibacterial and controlled release application. Adv. Funct. Mater. (2024). https://doi.org/10.1002/ADFM.20231452010.1002/ADFM.202314520 ↗