journal article·2021-07-03Open access

Zn-Doped CaP-Based Coatings on Ti–6Al–4V and Ti–6Al–7Nb Alloys Prepared by Magnetron Sputtering: Controllable Biodegradation, Bacteriostatic, and Osteogenic Activities

Konstantin A. Prosolov, Dmitrii V. Mitrichenko, Aleksandr B. Prosolov, Olga O. Nikolaeva, Vladimir V. Lastovka, Olga A. Belyavskaya, Valentina A. Chebodaeva, Ivan A. Glukhov, Larisa S. Litvinova, Valeria V. Shupletsova, Olga G. Khaziakhmatova, Vladimir V. Malashchenko, Kristina A. Yurova, Egor O. Shunkin, Maxim A. Fedorov, Andrei R. Komkov, Vladimir V. Pavlenko, Ilya I. Anisenya, Yurii P. Sharkeev, Alina Vladescu, Igor A. Khlusov

Coatings· Volume 11· Issue 7

Abstract

New TiNb-based alloys, such as Ti–6Al–7Nb, are currently being studied around the world as an alternative to other Ti alloys, e.g., instead of Ti–6Al–4V. We conducted a pilot study where thin (approximately 1.2 micron) CaP coatings containing low doses of Zn2+ (0.4–0.8 wt.%) were prepared by the radio frequency magnetron sputtering (RFMS) of Zn-hydroxyapatite (HA) target on Ti–6Al–4V and Ti–6Al–7Nb substrates and investigated their physicochemical properties, in vitro solubility, cytotoxicity, and antibacterial and osteogenic activities. The thickness of the obtained coatings was approximately 1.2–1.3 microns. Zn substitution did not result in roughness or structural or surface changes in the amorphous CaP coatings. The distributions of Ca, P, and Zn were homogeneous across the film thickness as shown by the EDX mapping of these elements. Zn doping of CaP coatings on both types of Ti-based alloys statistically influenced the results of the scratch-test. However, obtained values are satisfactory to use Zn-CaP coatings on biomedical implants. Increased Zn2+ release vs. tapered output of Ca and phosphate ions occurred during 5 weeks of an in vitro immersion test in 0.9% NaCl solution. Ti–6Al–7Nb alloy, unlike Ti–6Al–4V, promoted more linear biodegradation of CaP coatings in vitro. As a result, CaP-based surfaces on Ti–6Al–7Nb, compared with on Ti–6Al–4V alloy, augmented the total areas of Alizarin red staining in a 21-day culture of human adipose-derived mesenchymal stem cells in a statistically significant manner. Moreover, Zn–CaP coatings statistically reduced leukemic Jurkat T cell survival within 48 h of in vitro culture. Along with the higher solubility of the Zn–CaP surface, a greater reduction (4- to 5.5-fold) in Staphylococcus aureus growth was observed in vitro when 7-day extracts of the coatings were added into the microbial culture. Hence, Zn–CaP-coated Ti–6Al–7Nb alloy with controllable biodegradation as prepared by RFMS is a prospective material suitable for bone applications in cases where there is a risk of bacterial contamination with severe consequences, for example, in leukemic patients. Further research is needed to closely investigate the mechanical features and pathways of their solubility and antimicrobial, antitumor, and osteogenic activities.
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Research context

OpenAlex topics: Orthopaedic implants and arthroplasty · Bone Tissue Engineering Materials · Titanium Alloys Microstructure and Properties

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

Affiliations

Laboratory of Physics of Nanostructured Biocomposites, Institute of Strength Physics and Materials Science SB RAS (ISPMS SB RAS), 634055 Tomsk, Russia

LLC “SPC SINTEL”, 634061 Tomsk, Russia

Center for Immunology and Cell Biotechnology, Immanuel Kant Baltic Federal University, 236029 Kaliningrad, Russia

Siberian Federal Scientific and Clinical Center of the Federal Medical-Biological Agency, 636070 Seversk, Russia

Division of Traumatology and Orthopedics, Regional Clinical Emergency Hospital, 650000 Kemerovo, Russia

Medical Officer for Science, Regional Clinical Emergency Hospital, 650000 Kemerovo, Russia

Department of General Oncology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, 634009 Tomsk, Russia

Research School of High-Energy Physics, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia

National Institute of Research and Development for Optoelectronics INOE2000, Magurele, 077125 Bucharest, Romania

Research School of Chemistry and Applied Biomedical Sciences, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia

Department of Morphology and General Pathology, Siberian State Medical University, 634050 Tomsk, Russia

Funding

Foundation for Assistance to Small Innovative Enter-669 prises in Science and Technology Sector, Russian Federation · CoatDegraBac – ID-31 on Program ERA.NET RUS PLUS CALL 2017

References (60)

Show source-provided references
1. A review of biomaterials in bone defect healing, remaining shortcomings and future opportunities for bone tissue engineering10.1302/2046-3758.73.BJR-2017-0270.R1 ↗
3. Vanadium ionic species from degradation of Ti-6Al-4V metallic implants: In vitro cytotoxicity and speciation evaluation10.1016/j.msec.2018.11.090 ↗
4. Wear and corrosion behaviour of Ti–13Nb–13Zr and Ti–6Al–4V alloys in simulated physiological solution10.1016/j.corsci.2010.11.014 ↗
5. Zadpoor, A.A. (2018). Current trends in metallic orthopedic biomaterials: From additive manufacturing to bio-functionalization, infection prevention, and beyond. Int. J. Mol. Sci., 19.10.3390/ijms19092684 ↗
6. Dorozhkin, S.V. (2016). Calcium phosphates. Handbook of Bioceramics and Biocomposites, Springer.10.1002/9783527699315 ↗
7. Bioactive glass thin films deposited by magnetron sputtering technique: The role of working pressure10.1016/j.apsusc.2010.05.035 ↗
8. Titanium-Nitride Coating of Orthopaedic Implants: A Review of the Literature
9. Leó, B., and Jansen, J.A. (2009). Thin Calcium Phosphate Coatings for Medical Implants, Springer.10.1007/978-0-387-77718-4 ↗
10. Implant-Associated Infections: A Review of the Safety of Cardiac Implants
11. Efficacy of antimicrobial coated orthopaedic implants on the prevention of periprosthetic infections: A systematic review and meta-analysis10.7150/jbji.44839 ↗
12. Substituted hydroxyapatites for biomedical applications: A review10.1016/j.ceramint.2015.03.316 ↗
13. Biological behavior of magnesium-substituted hydroxyapatite during bone repair10.1590/1519-6984.217769 ↗
14. TOFSIMS and XPS characterisation of strontium in amorphous calcium phosphate sputter deposited coatings10.1016/j.matchar.2020.110739 ↗
15. Incorporation of silver nanoparticles into magnetron-sputtered calcium phosphate layers on titanium as an antibacterial coating10.1016/j.colsurfb.2017.05.016 ↗
16. Influence of oblique angle deposition on Cu-substituted hydroxyapatite nano-roughness and morphology10.1016/j.surfcoat.2020.125883 ↗
17. Copper substituted hydroxyapatite and fluorapatite: Synthesis, characterization and antimicrobial properties10.1016/j.ceramint.2014.07.086 ↗
18. The deposition of strontium and zinc Co-substituted hydroxyapatite coatings10.1007/s10856-017-5846-2 ↗
19. Substituted hydroxyapatites with antibacterial properties10.1155/2014/178123 ↗
20. Graziani, G., Boi, M., and Bianchi, M.A. (2018). Review on ionic substitutions in hydroxyapatite thin films: Towards complete biomimetism. Coatings, 8.10.3390/coatings8080269 ↗
21. Prosolov, K.A., Lastovka, V.V., Belyavskaya, O.A., Lychagin, D.V., Schmidt, J., and Sharkeev, Y.P. (2020). Tailoring the Surface Morphology and the Crystallinity State of Cu- and Zn-Substituted Hy-droxyapatites on Ti and Mg-Based Alloys. Materials, 13.10.3390/ma13194449 ↗
22. Osteoblast proliferation on hydroxyapatite coated substrates prepared by right angle magnetron sputtering10.1002/jbm.a.32556 ↗
23. Preparation, solubility, and cytocompatibility of zinc-releasing calcium phosphate ceramics10.1002/(SICI)1097-4636(200005)50:2<178::AID-JBM12>3.0.CO;2-5 ↗
24. The effects of inorganic additives to calcium phosphate on in vitro behavior of osteoblasts and osteoclasts10.1016/j.biomaterials.2010.01.002 ↗
25. Calcium phosphate targets for RF magnetron sputtering of biocoatings10.1063/1.5131903 ↗
26. World Medical Association (WMA) Declaration of Helsinki (2009). Ethical principles for medical research involving human subjects. Jahrb. Wiss. Ethik, 14.10.1515/9783110208856.233 ↗
27. Avdeeva, E., Shults, E., Rybalova, T., Reshetov, Y., Porokhova, E., Sukhodolo, I., Litvinova, L., Shupletsova, V., Khaziakhmatova, O., and Khlusov, I. (2019). Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro. Biomolecules, 9.10.3390/biom9050189 ↗
28. Khlusov, I.A., Litvinova, L.S., Shupletsova, V.V., Khaziakhmatova, O.G., Malashchenko, V.V., Yurova, K.A., Shunkin, E.O., Krivosheev, V.V., Porokhova, E.D., and Sizikova, A.E. (2020). Costimulatory Effect of Rough Calcium Phosphate Coating and Blood Mononuclear Cells on Adipose-Derived Mesenchymal Stem Cells In Vitro as a Model of In Vivo Tissue Repair. Materials, 13.10.3390/ma13194398 ↗
29. In-Vitro Dissolution and Structural and Electrokinetic Characteristics of Titanium-Oxynitride Coatings Formed via Reactive Magnetron Sputtering10.1134/S1027451016020166 ↗
30. Application of High-Frequency Magnetron Sputtering to Deposit Thin Calcium-Phosphate Biocompatible Coatings on a Titanium Surface10.1134/S1027451007060109 ↗
31. Khlusov, I.A., Slepchenko, G.B., Dambaev, G.T., Zagrebin, L.V., Shestov, S.S., Antipov, S.A., Feduschak, T.A., Khlusova, M.Y., Kokorev, O.V., and Yermakov, A.Y. (2011). Trace Elements and Nanoparticles, Nova Sci. Publ. Inc.
32. Litvinova, L., Yurova, K., Shupletsova, V., Khaziakhmatova, O., Malashchenko, V., Shunkin, E., Melashchenko, E., Todosenko, N., Khlusova, M., and Sharkeev, Y. (2020). Gene Expression Regulation and Secretory Activity of Mesenchymal Stem Cells upon In Vitro Contact with Microarc Calcium Phosphate Coating. Int. J. Mol. Sci., 21.10.3390/ijms21207682 ↗
33. Komarova, E.G., Sharkeev, Y.P., Sedelnikova, M.B., Prymak, O., Epple, M., Litvinova, L.S., Shupletsova, V.V., Malashchenko, V.V., Yurova, K.A., and Dzyuman, A.N. (2020). Zn- or Cu-containing CaP-Based Coatings Formed by Micro-Arc Oxidation on Titanium and Ti-40Nb Alloy: Part II—Wettability and Biological Performance. Materials, 13.10.3390/ma13194366 ↗
34. Topography effects of pure titanium substrates on human osteoblast long-term adhesion10.1016/j.actbio.2004.11.009 ↗
35. Fabrication of hydroxyapatite thin films for biomedical applications using RF magnetron sputtering10.1016/j.nimb.2006.03.126 ↗
36. Li, G., Gan, Y., Liu, C., Shi, Y., Zhao, Y., and Kou, S. (2020). Corrosion and Wear Resistance of Fe-Based Amorphous Coatings. Coatings, 10.10.3390/coatings10010073 ↗
37. Tribological behavior of Ti-6Al-4V and Ti-6Al-7Nb Alloys for Total Hip Prosthesis10.1155/2014/451387 ↗
38. Oxide-dependent adhesion of the Jurkat line of T lymphocytes10.1021/la8040192 ↗
39. Analysis of metal ion-induced DNA damage, apoptosis, and necrosis in human (Jurkat) T-cells demonstrates Ni2+ and V3+ are more toxic than other metals: Al3+, Be2+, Co2+, Cr3+, Cu2+, Fe3+, Mo5+, Nb5+, Zr2+10.1002/jbm.a.31789 ↗
40. Khlusov, I., Litvinova, L., Shupletsova, V., Khaziakhmatova, O., Melashchenko, E., Yurova, K., Leitsin, V., Khlusova, M., Pichugin, V., and Sharkeev, Y. (2018). Rough titanium oxide coating prepared by micro-arc oxidation causes down-regulation of hTERT expression, molecular presentation, and cytokine secretion in tumor Jurkat T cells. Materials, 11.10.3390/ma11030360 ↗
41. Zn-, Cu- or Ag-incorporated micro-arc coatings on titanium alloys: Properties and behavior in synthetic biological media10.1016/j.surfcoat.2019.04.021 ↗
42. ISO 10993-5:2009 (2009). Biological Evaluation of Medical Devices—Part 5: Tests for In Vitro Cytotoxicity, International Organization for Standardization.
43. Updates on the research and development of absorbable metals for bio-medical applications10.1007/s40204-018-0091-4 ↗
44. Surface modification of valve metals using plasma electrolytic oxidation for antibacterial applications: A review10.1002/jbm.a.36259 ↗
45. Cellular response to zinc-containing organoapatite: An in vitro study of proliferation, alkaline phosphatase activity and biomineralization10.1016/j.biomaterials.2005.01.043 ↗
46. Zinc-substituted hydroxyapatite: A biomaterial with enhanced bioactivity and antibacteri-al properties10.1007/s10856-012-4817-x ↗
47. Differentiation of osteoblasts and in vitro bone formation from murine embryonic stem cells10.1089/107632700300003323 ↗
48. Pearse, A.G.E. (1960). Histochemistry: Theoretical and Applied, Little, Brown & Company. [2nd ed.].
49. Composites of gellan gum hydrogel enzymatically mineralized with calcium-zinc phosphate for bone regeneration with antibacterial activity10.1002/term.2062 ↗
50. Zinc may increase bone formation through stimulating cell proliferation, alkaline phosphatase activity and collagen synthesis in osteoblastic MC3T3-E1 cells10.4162/nrp.2010.4.5.356 ↗
51. Physiologic actions of zinc re-lated to inhibition of acid and alkali production by oral streptococci in suspensions and biofilms10.1046/j.0902-0055.2003.00109.x ↗
52. Zinc: A precious trace element for oral health care?
53. An injectable and antibacterial calcium phosphate scaffold inhibiting Staphylococcus aureus and supporting stem cells for bone regeneration10.1016/j.msec.2020.111688 ↗
54. Antoniac, I. (2015). Biofilm Formation on Implants and Prosthetic Dental Materials. Handbook of Bioceramics and Biocomposites, Springer.
55. von Recum, A.F. (1986). Implant infections. Handbook of Biomaterials Evaluation, MacMillan.
56. Adhesion of Staphylococcus aureus to implants with different physicochemical characteristics10.1023/A:1021567804286 ↗
57. Antibacterial coatings: Challenges, perspectives, and opportunities10.1016/j.tibtech.2015.09.002 ↗
58. Antimicrobial effects and human gingival biocompatibility of hydroxyapatite sol-gel coatings10.1002/jbm.b.30365 ↗
59. Ratner, B.D. (2004). Biomaterials Science: An Introduction to Materials in Medicine, Elsevier Academic Press. [2nd ed.].
60. Ion-substituted calcium phosphate coatings by physical vapor deposition magnetron sputtering for biomedical applications: A review10.1016/j.actbio.2019.03.006 ↗