journal article·2026-03-01Open access

Surface structural change on pellets of calcium ethyl phosphate in biomimetic solutions: Effects of carbonate concentrations

Wanyu Dong, Yuko Matsukawa, Taishi Yokoi, Kazumasa Suzuki, Chikara Ohtsuki

Abstract

Hydroxyapatite (HAp) with similarity in natural bone mineral is called bone-like apatite (BAp), and the formation of BAp on material surfaces in the body environment substantially contributes to materials to make bonding to living bone.It is proposed that designed materials, namely salts of calcium and phosphate esters (SCPEs), possess the property of enhancing BAp formation in simulated body fluid (SBF) modified with alkaline phosphatase (ALP).Such materials are called bioresponsive ceramics.The crystalline phase of BAp is generally identified as HAp by X-ray diffraction analysis.Since several-types of SBF have been reported, in this study, HAp formation on calcium ethyl phosphate (CaEtP) pellets, which is one of SCPEs, was examined in the solutions mimicking SBF, that is, modified biomimetic solution (mBS) and evolved biomimetic solution (eBS).The critical difference between these solutions and conventional SBF is carbonic acid concentrations in the solutions.It was found that capability of HAp formation of CaEtP pellets in mBS and eBS was lower than that in mBS and eBS containing ALP.The morphology of the HAp formed on the pellets was distinctive in mBS and eBS containing ALP: i.e., formation of wool-ball-like shaped particles in mBS containing ALP, while formation of fine spherical particles in eBS containing ALP.These differences, namely nucleation, crystal growth and morphology, are likely governed by concentrations of carbonate ion species in the reaction solution.It can be concluded that controlling the concentration of carbonate ions in the biomimetic solutions enables controlling the formation behavior of HAp as well as its morphology.These findings provide basic knowledge about nucleation and crystal growth of HAp in biomimetic solutions as well as basic understanding of the reactivity on bioresponsive ceramics.
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Research context

OpenAlex topics: Calcium Carbonate Crystallization and Inhibition · Minerals Flotation and Separation Techniques · Chemical and Physical Properties in Aqueous Solutions

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

Affiliations

Graduate School of Engineering, Nagoya University

Institute of Integrated Research, Institute of Science Tokyo

References (33)

Show source-provided references
1. 1) F. Barrère, C. M. van der Valk, R. A. J. Dalmeijer, G. Meijer, C. A. van Blitterswijk, K. de Groot and P. Layrolle, J. Biomed. Mater. Res. A 66A, 779 (2003).10.1002/jbm.a.10454 ↗
2. 2) V. M. Sharon and S. Malaiappan, J. Dent. 157, 105762 (2025).10.1016/j.jdent.2025.105762 ↗
3. 3) X. Liu, Y. Miao, H. Liang, J. Diao, L. Hao, Z. Shi, N. Zhao and Y. Wang, Bioact. Mater. 12, 120 (2022).10.1016/j.bioactmat.2021.10.016 ↗
4. 4) S. Itoh, M. Kikuchi, K. Takakuda, Y. Koyama, H. N. Matsumoto, S. Ichinose, J. Tanaka, T. Kawauchi and K. Shinomiya, J. Biomed. Mater. Res. 54, 445 (2001).10.1002/1097-4636(20010305)54:3<445::AID-JBM190>3.0.CO;2-9 ↗
5. 5) E. Landi, S. Sprio, M. Sandri, G. Celotti and A. Tampieri, Acta Biomater. 4, 656 (2008).10.1016/j.actbio.2007.10.010 ↗
6. 6) E. Landi, A. Tampieri, M. Mattioli-Belmonte, G. Celotti, M. Sandri, A. Gigante, P. Fava and G. Biaginib, J. Eur. Ceram. Soc. 26, 2593 (2006).10.1016/j.jeurceramsoc.2005.06.040 ↗
7. 7) Q. Liu, H. Pan, Z. Chen and J. P. Matinlinna, BioMed Res. Int. 2015, 1 (2015).10.1155/2015/601025 ↗
8. 8) C. Rey, V. Renugopalakrishman, B. Collins and M. J. Glimcher, Calcified Tissue Int. 49, 251 (1991).10.1007/BF02556214 ↗
9. 9) C. Ohtsuki, T. Kokubo and T. Yamamuro, J. Non-Cryst. Solids 143, 84 (1992).10.1016/S0022-3093(05)80556-3 ↗
10. 10) D. Santos, D. M. Silva, P. S. Gomes, M. H. Fernandes, J. D. Santos and V. Sencadas, J. Colloid Interf. Sci. 504, 101 (2017).10.1016/j.jcis.2017.05.032 ↗
11. 11) Y. W. Gu, K. A. Khor and P. Cheang, Biomaterials 25, 4127 (2004).10.1016/j.biomaterials.2003.11.030 ↗
12. 12) S. Bhumiratana, W. L. Grayson, A. Castaneda, D. N. Rockwood, E. S. Gil, D. L. Kaplan and G. Vunjak-Novakovic, Biomaterials 32, 2812 (2011).10.1016/j.biomaterials.2010.12.058 ↗
13. 13) A. Takeuchi, C. Ohtsuki, T. Miyazaki, M. Kamitakahara, S. Ogata, M. Yamazaki, Y. Furutani, H. Kinoshita and M. Tanihara, J. R. Soc. Interface 2, 373 (2005).10.1098/rsif.2005.0052 ↗
14. 14) S. Ferraris, S. Yamaguchi, N. Barbani, M. Cazzola, C. Cristallini, M. Miola, E. Vernè and S. Spriano, Acta Biomater. 102, 468 (2020).10.1016/j.actbio.2019.11.024 ↗
15. 15) T. Kokubo, H. Kushitani, S. Sakka, T. Kitsugi and T. Yamamuro, J. Biomed. Mater. Res. 24, 721 (1990).10.1002/jbm.820240607 ↗
16. 16) W. Qiao, Q. Liu, Z. Li, H. Zhang and Z. Chen, Sci. Technol. Adv. Mat. 18, 110 (2017).
17. 17) T. Yokoi, S. Tomita, J. Nakamura, A. Sugawara-Narutaki, Y. Matsukawa, M. Kawashita and C. Ohtsuki, Biomimetics 9, 502 (2024).10.3390/biomimetics9080502 ↗
18. 18) T. Yokoi, A. Mio, J. Nakamura, A. Sugawara-Narutaki, M. Kawashita and C. Ohtsuki, Sci. Technol. Adv. Mat. 23, 341 (2022).10.1080/14686996.2022.2074801 ↗
19. 19) T. Yokoi, T. Ujiyama, J. Nakamura, M. Kawashita and C. Ohtsuki, Mater. Adv. 1, 3215 (2020).10.1039/D0MA00600A ↗
20. 20) W. Dong, Y. Matsukawa, T. Yokoi, K. Suzuki and C. Ohtsuki, ACS Omega 10, 51197 (2025).
21. 21) ISO 23317:2025 Implants for surgery - In vitro evaluation for apatite-forming ability of implant materials; Geneva (2025).
22. 22) N. W. Kucko, R. P. Herber, S. C. G. Leeuwenburgh and J. A. Jansen, in “Principles of Regenerative Medicine”, Ed. by A. Atala, R. Lanza, A. G. Mikos and R. Nerem, Academic Press, London (2019) pp. 591–611.10.1016/B978-0-12-809880-6.00034-5 ↗
23. 23) W. Dong, Y. Matsukawa, Y. Long, Y. Hayashi, J. Nakamura, K. Suzuki and C. Ohtsuki, RSC Adv. 14, 38660 (2024).10.1039/D4RA07739C ↗
24. 24) W. Anutrasakda, A. Phasuk and C. Tangku, J. Environ. Chem. Eng. 9, 104658 (2021).10.1016/j.jece.2020.104658 ↗
25. 25) H. Copete, E. López and C. Baudin, Bol. Soc. Esp. Ceram. V. 63, 255 (2024).10.1016/j.bsecv.2023.12.001 ↗
26. 26) S. Liao, F. Watari, G. Xu, M. Ngiam, S. Ramakrishna and C. K. Chan, Mater. Lett. 61, 3624 (2007).10.1016/j.matlet.2006.12.007 ↗
27. 27) S. Jalota, S. B. Bhaduri and A. C. Tas, J. Mater. Sci.-Mater. M. 17, 697 (2006).10.1007/s10856-006-9680-1 ↗
28. 28) G. Ulian, D. Moro and G. Valdrè, Micro Nano Lett. 13, 4 (2018).10.1049/mnl.2017.0058 ↗
29. 29) M. Corno, C. Busco, V. Bolis, S. Tosoni and P. Ugliengo, Langmuir 25, 2188 (2009).10.1021/la803253k ↗
30. 30) H. Madupalli, B. Pavan and M. M. J. Tecklenburg, J. Solid State Chem. 255, 27 (2017).10.1016/j.jssc.2017.07.025 ↗
31. 31) B. B. V. Salzmann, M. M. van der Sluijs, G. Soligno and D. Vanmaekelbergh, Accounts Chem. Res. 54, 787 (2021).10.1021/acs.accounts.0c00739 ↗
32. 32) M. S. Tung and D. Skrtic, in “Octacalcium Phosphate”, Ed. by L. C. Chow and E. D. Eanes, Monographs in Oral Science, Karger (2001) pp. 112–129.
33. 33) I. Sunagawa, “Crystals”, Cambridge University Press, Cambridge (2005) pp. 150–152.