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Cytocompatibility of Ti–xZr alloys as dental implant materials


Ti–xZr (x = 5, 15, 25, 35, 45% wt%) alloys with low elastic modulus and high mechanical strength were fabricated as a novel implant material. The biocompatibility of the Ti–xZr alloys was evaluated by osteoblast-like cell line (MG63) in terms of cytotoxicity, proliferation, adhesion, and osteogenic induction using CCK-8 and live/dead cell assays, electron microscopy, and real-time PCR. The Ti–xZr alloys were non-toxic and showed superior biomechanics compared to commercially pure titanium (cpTi). Ti–45Zr had the optimum strength/elastic modulus ratio and osteogenic activity, thus is a promising to used as dental implants.


Tooth loss is a common problem that can weaken chewing function, and even lead to more serious complications such as alveolar bone atrophy, masticatory muscle atrophy, facial collapse, etc. Dental implants are routinely used in oral rehabilitation to replace lost teeth (unitary or total), and have improved patient quality of life [1]. Pure titanium (Ti) is a standard dental implant material owing to its excellent mechanical properties and good biocompatibility [2, 3]. However, the tensile strength of commercially pure titanium (cpTi) is low, which can result in implant fractures, especially in individuals that exhibit bruxism [4]. In addition, Wachi et al. reported that the Ti ions released from these implants can trigger peri-implant mucositis, which eventually progress to peri-implantitis accompanied by alveolar bone resorption [5]. Therefore, different metal alloys are being considered due to their enhanced mechano-physical properties, which can potentially improve the clinical performance of the implants [6]. For instance, the Ti–6Al–4V alloy is increasingly replacing cpTi on account of its greater strength [7] and enhanced mechanical performance [8]. However, it is biomechanically incompatible to the human bone due to threefold higher Young’s elastic modulus (~110 GPa compared to human bones), which results in the “stress shielding effect” on the supporting tissues [9]. Furthermore, the vanadium (V) ions released into the blood and urine [10] can initiate an inflammatory cascade leading to osteolysis [11, 12], and aluminum (Al) ions are frequently present in the brain tissues of Alzheimer’s disease patients, which indicates a neurodegenerative effect [13]. Therefore, there is an urgent need to synthesize novel alloys with high mechanical strength and biocompatibility, and low elastic modulus.

Zirconium (Zr), a transient element belonging to Group 4 (according to new IUPAC name) in the periodic table, is chemically similar to Ti and does not display any local or systemic toxic effects [14]. The elastic modulus of Zr is 88 GPa, which is closer to that of the bone. Abdullah et al. compared Ti and Zr implants in a rabbit model, and observed similar bone contact with both, although Zr had superior biomechanics due to lower elasticity. In addition, the Zr ions released from the implant further increased the bone response [15]. Kobayashi et al. first proposed the biomedical application of Ti–Zr alloys in 1995 based on their superior mechanical and tensile strength [16]. Furthermore, binary Ti–Zr alloys with Ti as the primary component have shown encouraging results as dental implants [17, 18], in terms of both biomechanics [19, 20] and bioactivity [21]. The binary Ti–Zr alloy with 13~17% Zr is currently marketed as an implant material under the trade name Roxolid. In addition, equiatomic Ti–Zr alloys have also demonstrated excellent mechanical properties and good corrosion resistance [22, 23]. Kobayashi et al. found that Ti–Zr binary alloys with 30–60% Zr have higher Vickers hardness and superior tensile strength [24], which was confirmed by another study that observed higher micro-hardness and bending strength of Ti–Zr alloy with 40% Zr (Ti–40Zr) [25, 26]. Teisuke et al. found that Ti–30Zr or alloys with >50% Zr were ideal for clinical applications in terms of corrosion resistance [27]. Taken together, Ti–Zr alloys are a mechanically improved alternative to cpTi with similar biocompatibility, and can reduce the risk of implant fracture.

However, the optimal proportion of Zr and Ti for dental applications has not been established. We recently prepared Ti–xZr alloys with varying amounts of Zr (x = 5, 15, 25, 35, 45% wt%) by combining powder metallurgy with heat treatment. The Ti–xZr alloys exhibited maximum bending strength of 867.1 MPa and maximum compressive strength of 1599.8 MPa, which are superior to that of cpTi. Furthermore, all Ti–Zr alloys showed a lower elastic modulus (53.5–59.3 GPa) compared to cpTi (103 GPa) [28]. However, the biocompatibility of these binary alloys also need to be determined for any future clinical applications. To this end, we analyzed the cytocompatibility and osteogenic activity of Ti–xZr alloys in vitro to ascertain the optimal Zr concentration for dental implants.

Materials and methods

Preparation of Ti–Zr alloys

The Ti–Zr alloys comprising of 5–45% Zr by weight were prepared by powder metallurgy as described previously [28]. Pure Ti and Zr were supplied by Zhongzhou Alloy Material Co. Ltd. The chemical composition is presented in Table 1.

Table 1 The impurities of in Ti and Zr powder

Preparation of alloy specimens

Ti and Zr discs measuring 10 mm in diameter and 1 mm in thickness were polished using silicon carbide papers up to 1200 grit. After sequential cleansing with acetone, ethanol and deionized water under sonication for 15 min each, the specimens were sterilized in an autoclave.

Ion release test

The alloy discs (three samples per group) were immersed statically in 6 ml modified SBF solution (pH 7.4) at 37 °C for 30 days. The specimens were removed, and the concentration of metal ions in the SBF solution was measured by Inductively Coupled Plasma-Atomic Emission Spectrometer (PROFILE SPEC, Leeman). The experiment was repeated three times.

Cell culture

The MG63 human osteoblast cell line was provided by The Center for Advanced Research of Central South University, China. The cells were cultured in DMEM supplemented with 10% FBS and 1% penicillin-streptomycin at 37 °C, 5% CO2 and 95% humidity. The medium was replaced every 48 h, and the cells were passaged at 80% confluency following trypsin (0.25%) digestion, and re-seeded at the appropriate density for in vitro assays.

Preparation of alloy extraction medium

The alloy specimens were immersed in complete DMEM and incubated at 37 °C, 5% CO2 and 95% humidity for 72 h. The ratio of the disc surface area to the extraction medium volume ratio was 3:1 in accordance with EN ISO standard 10993:12 [29]. The resulting 100% extraction medium was used for testing cell viability.

Live/dead cell assay

MG63 cells were seeded in a 24-well plate at the density of 2 × 104 cells per well and incubated for 24 h to facilitate attachment. After replacing the media with 1 ml 100% extraction medium, the cells were cultured for another 24 h, washed twice with PBS, and stained with 50 μl Hoechst 33342 (0.25%) and 50 μl PI (0.5%) at 4 °C for 20 min. The cells were then rinsed with PBS, and observed under a fluorescence microscope at the excitation wavelengths of 346 and 488 nm. The number of live and dead cells were counted in three random fields per well at ×10 magnification using the Image Proplus6 (ipp6) software.

Cell Counting Kit-8 assay

The MG63 cells were seeded in a 96-well plate at the density of 1 × 104 cells per well, and allowed to adhere for 24 h. The medium was replaced with 1 ml 100% extraction medium, and the cells were cultured for 1, 3, and 5 days, with fresh medium replenished every 2 days. To determine the viability of the cells, 20 μl of CCK-8 test solution (Cell Counting Kit-8; Dojindo, Japan) was added to each well, and the cells were incubated for another 1.5 h. The absorbance at 450 nm was measured using an ELISA microplate reader (Molecular Devices, USA). Sterile culture media was used as the negative control, and cells incubated in 100% cpTi extraction medium as the positive control. Each sample was measured four times.

Acridine orange (AO) staining

MG63 cells were seeded on alloy surfaces at the density of 1 × 104 cell per well in complete DMEM, and cultured for 6, 24, and 48 h. After washing twice with PBS, the cells were fixed with 95% alcohol for 10 min, air dried, and stained with 300 μl acridine orange (0.01%) per well for 5 min. The stained cells were rinsed with PBS for 1 min, cleared with 0.1 mM calcium chloride for 1 min, and rinsed again. The cells were observed under a fluorescence microscope at an excitation wavelength of 518 nm. The number of stained cells were counted in five random fields at ×10 magnification, using the Image Proplus6 (ipp6) software. The experiment was repeated thrice.

Scanning electron microscopy (SEM)

MG63 cells were seeded on the alloy surfaces at the density of 1 × 104 cells per well, and cultured in complete DMEM for 6 h, 48 h, and 9 days. The cells were fixed with 2.5% glutaraldehyde for 40 min, rinsed with PBS, and dehydrated through an ethanol gradient (25, 50, 75, 90, 95, 100%) for 15 min. After vacuum drying for 12 h, the specimens were sputter coated with 10 nm gold and observed under the Hitachi S-4800N field emission SEM.

Real-time polymerase chain reaction (RT-PCR)

The MG63 cells were seeded on the different alloy surfaces at the density of 10,000 cells per well, and cultured for 3, 6, 9, and 12 days in complete DMEM. Total RNA was extracted from the cells using Omega R6934-01 Total RNA Kit II (BioTek, USA) and reversed transcribed to cDNA with the PrimeScript RT Master Mix (Takara) according to the manufacturers’ instructions. RT-PCR was performed using SYBR Premix Ex Taq II (Takara) on the CFX96 PCR System (Bio-Rad). Relative expression levels of Ki67, COLI-α1, ALP, OC, integrinβ1, and Cbfα-1 were calculated in terms of the comparative cycle threshold (Ct) as 2(−ΔΔCt), with GAPDH as the internal control. The primer sequences are shown in Table 2.

Table 2 Primers used for RT-PCR analysis

Statistical analysis

The experimental data were expressed as the mean ± standard deviation of three replicates, and compared by two-way analysis of variance followed by Tukey’s multiple comparison test. p < 0.05 with a 95% confidence interval was considered statistical significance. GraphPad Prism 6 software (GraphPad Software Inc. La Jolla, CA, USA) was used for statistical analysis.


Ti–xZr alloys are mechanically superior to cpTi

The mechanical properties of Ti–xZr alloys are summarized in Table 3, and indicate that the bending strength and compressive strength of the alloys increased with Zr content. Ti–45Zr exhibited the maximum bending and compressive strength values of 867.1 and 1599.8 MPa respectively, which are significantly higher compared to that of cpTi. The elastic modulus of the alloys ranged from 53.5 GPa for Ti–35Zr to 59.3 GPa for Ti–xZr, and were markedly lower than that of cpTi (103 GPa).

Table 3 Mechanical properties of cpTi and the Ti–xZr alloys (x = 5, 15, 25, 35, 45 wt%)

Ti–xZr alloys are stable in vitro

The stability of the different alloys was evaluated by measuring the amount of ions released into the SBF. As shown in Table 4, less Ti or Zr ions were released from the Ti–xZr alloys compared to cpTi, which can be attributed to the formation of stable corrosion resistant films on the alloys.

Table 4 Ti and Zr ions in SBF

Ti–xZr alloys are biocompatible

The biocompatibility of the Ti–xZr alloys was determined by analyzing the viability and proliferation of the MG63 cells grown in the alloy extraction media or on the different alloy surfaces. As shown in Fig. 1, very few dead cells were detected following 24 h incubation with the different 100% extraction media, and ~97% cells were viable. In addition, the viability was slightly higher in the Ti–xZr alloys compared to the cpTi group.

Fig. 1

Representative fluorescence microscopy images showing Hoechst 3342 and PI-stained live (blue) and dead (red) cells after 24 h of incubation with different 100% extraction media

The proliferation rates of the MG63 cells cultured in the different 100% extraction media were also measured over a period of 5 days. As shown in Fig. 2, the number of cells increased steadily in a time-dependent manner in all groups, and the proliferation rate was ∼80% on day 5 as compared to day 1 (p < 0.001). Furthermore, the viability and proliferation rates of cells cultured in the 100% extraction media of all but the Ti–15Zr and Ti–35Zr alloys were comparable to that of cells grown in cpTi extraction medium (p < 0.05).

Fig. 2

CCK-8 assays of the proliferation of cells cultured in 100% extraction medium of Ti–xZr alloys (5, 15, 25, 35, and 45% Zr) and cpTi on days 1, 3, and 5, with cpTi as control. Data are expressed as mean ± SD (n = 3). *p < 0.05, ***p < 0.001

Consistent with the above, the MG63 grown on the surface of the different alloys were also viable over a period of 48 h. As shown in Fig. 3a, the cells were able to attach to the metal surface within 6 h, and proliferated rapidly for 48 h. Furthermore, the total number of cells at 6 and 24 h were significantly higher on Ti–5Zr samples compared to the others at each time point (**p < 0.01). The cell count increased significantly in all groups by 48 h, and was highest on Ti–45Zr (***p < 0.001), and least on the Ti–25Zr alloys (***p < 0.001) (Fig. 3b). Taken together, the Ti–xZr alloys are non-toxic and can support the growth of osteoblasts, and Ti–45Zr shows greater biocompatibility compared to cpTi.

Fig. 3

a Representative fluorescence microscopy images showing acridine orange-stained MG63 cells cultured for 6, 24, and 48 h on (i) Ti, (ii) Ti–5Zr, (iii) Ti–15Zr, (iv) Ti–25Zr, (v) Ti–35Zr, and (vi) Ti–45Zr. Scale is 50 μm. b The number of viable cells at the different time points in the indicated groups. Data are expressed as mean ± SD (n = 3). *p < 0.05; **p < 0.01; ***p < 0.001

The Ti–xZr alloys supported cellular adhesion and spread

The adhesion, differentiation, and migration of the MG63 cells on the cpTi and different alloy surfaces were analyzed by SEM. As shown in Fig. 4, the cells adhered to all surfaces within 6 h, and exhibited typical ellipse-like morphology while covering ~40–50% of the area. By 48 h, the cells had acquired a spindle-like morphology with uniform spread and prominent filopodia extending in all directions. In addition, ~70% of the surface area of all specimens except that of Ti–35Zr was occupied with the growing cells, which also showed considerable overlap indicating healthy growth. After 9 days, the surfaces of all specimens were completely covered by a highly dense cellular monolayer with multiple filopodia-like intercellular connections protruding from the edges of cells. The filopodia were particularly extensive along the leading edges of the cells. Thus, the Ti–xZr alloys allow osteoblast adhesion and growth comparable to that on cpTi.

Fig. 4

Representative SEM images showing the morphology of cells frown on different surfaces for 6 h, 48 h, and 9 days

Ti–xZr alloys induced osteogenic differentiation

The osteogenic capacity of the different alloys was determined by analyzing the expression levels of osteogenesis-related genes in MG63 cells cultured for 3, 6, 9, and 12 days on cpTi and Ti–xZr alloys. As shown in Fig. 5c, COLI-α1 levels peaked on the 3rd day of culture and declined thereafter in all groups, and was similar between cpTi and the Ti–xZr alloys except Ti–35Zr, which showed lower expression compared to cpTi. In contrast, ALP (Fig. 5d), Cbf α-1 (Fig. 5e), and OC (Fig. 5f) were significantly downregulated in the cells grown on Ti–5Zr, Ti–15Zr, and Ti–25Zr on days 9 and 12 compared to that in the cpTi group (p < 0.001). Interestingly, Ki67 levels were lower in the Ti–5Zr and Ti–15Zr groups compared to that in cpTi on day 9 (p < 0.01), but significantly higher in Ti–35Zr and Ti–45Z groups (p < 0.001) (Fig. 5a). Furthermore, integrin β1 levels in Ti–5Zr, Ti–15Zr, and Ti–25Zr were significantly lower relative to the cpTi group on day 3 (p < 0.05) (Fig. 5b). To summarize, Ti–45Zr showed the maximum osteogenic activity compared to the other alloys, almost comparable to that of cpTi.

Fig. 5

The induction of osteoblast differentiation-related genes in MG63 cells cultured on the different surfaces. Relative expression levels of (a) Ki67, (b) Integrin β1, (c) COLI-α1, (d) ALP, (e) Cbf α1, and (f) OC in the indicated groups. Data are expressed as mean ± SD (n = 3). *p < 0.05; **p < 0.01; ***p < 0.001


The primary reason for dental implant failure is “stress shielding” due to the dissimilar elastic modulus of the implant material and bone tissue. To maximize longevity of the implants and avoid the stress shielding effect, it is essential to fabricate materials with high tensile strength as well as a low elastic modulus comparable to that of the surrounding bone tissue. Studies have shown that Ti–Zr alloys can achieve good osseointegration and survival of the osteoblasts [30,31,32,33]. However, casting these alloys into dental molds is technically demanding and economically inefficient. Therefore, powder metallurgy is increasingly being used to produce dental alloys [34,35,36] of Ti and Zr in a cost-effective manner [37]. We used powder metallurgy to prepare Ti–Zr alloys across a range of Zr concentrations that showed good mechanical properties, excellent corrosion resistance and low elastic modulus [28]. In the present study, we evaluated the biocompatibility and osteogenic capacity of these alloys to determine their potential as dental implants.

Biocompatibility is an essential criterion for a medical implant, which should not cause any thrombogenic, toxic, allergic, or inflammatory responses in vivo. Ti dental implants usually fail due to the allergic reaction to Ti ions that leach from the alloys, eventually leading to inflammation in the surrounding tissues [38, 39]. Wachi et al. reported that Ti ions are the causative factor of peri-implant mucositis, which can progress to peri-implantitis accompanied by alveolar bone resorption [5]. Therefore, dental implant materials with high corrosion resistance are urgently needed. We tested the corrosion of the Ti–Zr alloys in SBF, and detected only miniscule amounts of Ti and Zr ions in the solution after 30 days of incubation. The higher stability of Ti–Zr alloys compared to cpTi can be attributed to the formation of corrosion resistant oxide films on the alloy surface. Consistent with our results, Akimoto et al. found that 90% less Ti ions were released from Ti–30Zr compared to pure Ti after 1 week of immersion in physiological fluid. This indicates that the ZrO2 film is more stable and resilient to dissolution compared to the oxide of Ti, and addition of Zr can significantly reduce Ti ion dissolution [27]. Therefore, binary Ti–Zr alloys have gained considerable attention in biomedical applications on account of their higher mechanical strength [40, 41], corrosion resistance [42], and biocompatibility compared to cpTi [31, 43].

The cytocompatibility of the Ti–Zr alloys was evaluated in the MG63 osteoblast cell line. This line was originally isolated from human osteosarcoma, and retains the osteogenic characteristics along with the advantage of unlimited growth [44]. In recent years, they have completely replaced osteoblasts for analyzing the cytotoxicity of biomaterials in vitro [45]. However, in the study of cell morphology and osteogenic differentiation, MSCs cells with differentiation potential have more advantages [46]. The alloys were highly conducive to the survival and proliferation of MG63 cells, which is consistent with the general biosafety of Zr [47]. Cell adhesion to the implant surface is crucial for the subsequent growth, differentiation, and migration [48]. We found that the MG63 cells adhered to, spread and rapidly proliferated on the alloy surfaces. Consistent with our results, Saldana et al. also showed [49] that osteoblasts can attach to coarse-grain or fine-grain Zr surfaces, and subsequently spread, proliferate, differentiate, and mature to a similar extent as on the Ti6Al4V alloy. Furthermore, the ZnO2 film can also promote cellular adhesion, proliferation, and differentiation [50], thus underscoring the suitability of Ti–Zr alloys as surfaces for osteoblast growth [51]. The differentiation of osteoblasts into mature osteocytes involves proliferation, extracellular matrix maturation, and matrix mineralization. Integrin β1 and COL1 α-1 levels were similar across all groups during osteoblastic adhesion and early proliferation. In contrast, the osteogenic markers (Ki67, ALP, Cbf α1, and OC) were significantly upregulated in the late proliferation and maturation stages of osteoblast differentiation on cpTi and Ti–45Zr, whereas the alloys with higher Zr content showed stronger osteogenic activity, which could be attributed to the superior osteo-inductivity of Zr. A recent study showed that ZrO2 and Zr ions promoted the proliferation and differentiation of human osteoblasts in vitro [52, 53].

To summarize, Ti–xZr alloys have superior biomechanics compared to cpTi with high tensile strength and low elastic modulus, along with similar biocompatibility, which can reduce implant stress shielding and improve longevity. Ti–45Zr in particular showed the optimum strength/elastic modulus ratio and osteogenic activity, and is therefore a promising alternative to cpTi as a dental implant.


The Ti–xZr (x = 5, 15, 25, 35, 45 wt%) alloys are stable and do not adversely affect osteoblast adhesion and proliferation in vitro. Ti–45Zr showed excellent cytocompatibility and osteogenic activity comparable to that of pure Ti. indicating its potential as a dental implant material.


  1. 1.

    Fernandez-Estevan L, Selva-Otaolaurruchi EJ, Montero J, Sola-Ruiz F. Oral health-related quality of life of implant-supported overdentures versus conventional complete prostheses: retrospective study of a cohort of edentulous patients. Med Oral Patol Oral Cir Bucal. 2015;20:450–8.

    Google Scholar 

  2. 2.

    Geetha M, Singh AK, Asokamani R, Gogia AK. Ti based biomaterials, the ultimate choice for orthopedic implants-a review. Prog Mater Sci. 2009;54:259–64.

    Google Scholar 

  3. 3.

    Chen Q, Thouas GA. Metallic implant biomaterials. Mater Sci Eng R. 2015;87:1–57.

    Google Scholar 

  4. 4.

    Gealh WC, Mazzo V, Barbi F, Camarini ET. Osseointegrated implant fracture: causes and treatment. J Oral Implantol. 2011;37:499–503.

    Google Scholar 

  5. 5.

    Wachi T, Shuto T, Shinohara Y, Matono Y, Makihira S. Release of titanium ions from an implant surface and their effect on cytokine production related to alveolar bone resorption. Toxicology. 2015;327:1–9.

    CAS  Google Scholar 

  6. 6.

    Cordeiro JM, Barão VAR. Is there scientific evidence favoring the substitution of commercially pure titanium with titanium alloys for the manufacture of dental implants? Mater Sci Eng C. 2017;71:1201–15.

    CAS  Google Scholar 

  7. 7.

    Hacisalihoglu I, Samancioglu A, Yildiz F, Purcek G, Alsaran A. Tribocorrosion properties of different type titanium alloys in simulated body fluid. Wear. 2015;332–333:679–86.

    Google Scholar 

  8. 8.

    Mishnaevsky L, Levashov E, Valiev RZ, Segurado J, Sabirov I, Enikeev N, et al. Nanostructured titanium-based materials for medical implants: modeling and development. Mater Sci Eng R Rep. 2014;81:1–19.

    Google Scholar 

  9. 9.

    Miura K, Yamada N, Hanada S, Jung T, Itoi KE. The bone tissue compatibility of a new Ti-Nb-Sn alloy with a low Young’s modulus. Acta Biomater. 2011;7:2320–6.

    CAS  Google Scholar 

  10. 10.

    Catalani S, Stea S, Beraudi A, Gilberti ME, Bordini B, Toni A. Vanadium release in whole blood, serum and urine of patients implanted with a titanium alloy hip prosthesis. Clin Toxicol. 2013;51:550–6.

    CAS  Google Scholar 

  11. 11.

    Kaufman AM, Alabre CI, Rubash HE, Shanbhag AS. Human macrophage response to UHMWPE, TiAlV, CoCr, and alumina particles: analysis of multiple cytokines using protein arrays. J Biomed Mater Res A. 2008;84:464–74.

    Google Scholar 

  12. 12.

    Liu N, Meng J, Wang Z, Zhou G, Shi T, Zhao J. Autophagy mediated TiAl(6)V(4) particle-induced peri-implant osteolysis by promoting expression of TNF-alpha. Biochem Biophys Res Commun. 2016;473:133–9.

    CAS  Google Scholar 

  13. 13.

    Mirza A, King A, Troakes C, Exley C. Aluminium in brain tissue in familial Alzheimer’s disease. J Trace Elem Med Biol. 2017;40:30–6.

    CAS  Google Scholar 

  14. 14.

    Okamoto H. Sn-Zr (Tin-Zirconium). J Phase Equilib Diff. 2010;31:411–2.

    CAS  Google Scholar 

  15. 15.

    AlFarraj AA, Sukumaran A, Al Amri MD, Van Oirschot AB, Jansen JA. A comparative study of the bone contact to zirconium and titanium implants after 8 weeks of implantation in rabbit femoral condyles. Odontology. 2018;106:37–44.

    CAS  Google Scholar 

  16. 16.

    Wen B, Zhu F, Li Z, Zhang P, Lin X, Dard M. The osseointegration behavior of titanium- zirconium implants in ovariectomized rabbits. Clin Oral Implants Res. 2014;25:819–25.

    Google Scholar 

  17. 17.

    Grandin HM, Berner S, Dard M. A review of titanium zirconium (TiZr) alloys for use in endosseous dental implants. Materials. 2012;5:1348–60.

    CAS  Google Scholar 

  18. 18.

    Liu X, Chen S, Tsoi JKH, Martinlinna JP. Binary titanium alloys as dental implant materials—a review, regenerative. Biomaterials. 2017;5:315–23.

    Google Scholar 

  19. 19.

    Wen CE, Yamada Y, Hodgson PD. Fabrication of novel TiZr alloy foams for biomedical applications. Mater Sci Eng C. 2006;26:1439–44.

    CAS  Google Scholar 

  20. 20.

    Ho WF, Cheng CH, Pan CH, Wu SC, Hsu HC. Structure, mechanical properties and grindability of dental Ti-10Zr-X alloys. Mater Sci Eng C. 2009;29:36–43.

    CAS  Google Scholar 

  21. 21.

    Sista S, Nouri A, Li Y, Wen C, Hodgson PD, Pande G. Cell biological responses of osteoblasts on anodized nanotubular surface of a titanium-zirconium alloy. J Biomed Mater Res A. 2013;101:3416–30.

    Google Scholar 

  22. 22.

    Oliveira NTC, Ferreira EA, Duarte LT, Biaggio SR, Rocha-Filho RC, Bocchi N. Corrosion resistance of anodic oxides on the Ti–50Zr and Ti-13Nb–13Zr alloys. Electrochim Acta. 2006;51:2068–75.

    CAS  Google Scholar 

  23. 23.

    Oliveira NT, Biaggio SR, Rocha-Filho RC, Bocchi N. Electrochemical studies on zirconium and its biocompatible alloys Ti-50Zr at.% and Zr-2.5Nb wt.% in simulated physiologic media. J Biomed Mater Res A. 2005;74:397–407.

    Google Scholar 

  24. 24.

    Kobayashi E, Matsumoto S, Doi H, Yoneyama T, Hamanaka H. Mechanical-properties of the binary titanium-zirconium alloys and their potential for biomedical materials. J Biomed Mater Res. 1995;29:943–50.

    CAS  Google Scholar 

  25. 25.

    Ho WF, Chen WK, Wu SC, Hsu HC. Structure, mechanical properties, and grindability of dental Ti-Zr alloys. J Mater Sci Mater Med. 2008;19:3179–86.

    CAS  Google Scholar 

  26. 26.

    Hsu HC, Wu SC, Sung YC, Ho WF. The structure and mechanical properties of as-cast Zr-Ti alloys. J Alloy Compd. 2009;488:279–83.

    CAS  Google Scholar 

  27. 27.

    Teisuke A, Takeshi U, Yusuke T, Hisashi D, Takao H, Noriyuki W. Evaluation of corrosion resistance of implant-use Ti-Zr binary alloys with a range of composition. J Biomed Mater Res B: Appl Biomater. 2018;106:73–9.

    Google Scholar 

  28. 28.

    Baoqi W, Wei R, Jue L, Taomei ZH, Hailin Y, Jianming R. Microstructure, mechanical properties, and preliminary biocompatibility evaluation of binary Ti–Zr alloys for dental application. J Biomater Appl. 2019;33:766–75.

    Google Scholar 

  29. 29.

    International Organization for Standardization. ISO-10993-12: biological evaluation of medical devices part 12: sample preparation and reference materials. Arlington, VA: ANSI/AAMI; 2007.

    Google Scholar 

  30. 30.

    Wen B, Zhu F, Li Z, Zhang P. The osseointegration behavior of titanium-zirconium implants in ovariectomized rabbits. Clin Oral Implants Res. 2014;25:819–25.

    Google Scholar 

  31. 31.

    Sista S, Wen CE, Hodgson PD, Pande G. The influence of surface energy of titanium-zirconium alloy on osteoblast cell functions in vitro. J Biomed Mater Res A. 2011;97:27–36.

    Google Scholar 

  32. 32.

    Saulacic N, Bosshardt D, Bornstein M, Berner S, Buser D. Bone apposition to a titanium-zirconium alloy implant, as compared to two other titanium-containing implants. Eur Cell Mater. 2012;23:273–86.

    CAS  Google Scholar 

  33. 33.

    Bolat G, Izquierdo J, Santana JJ, Mareci D, Souto RM. Electrochemical characterization of ZrTi alloys for biomedical applications. Electrochim Acta. 2013;88:447–56.

    CAS  Google Scholar 

  34. 34.

    Arifin A, Sulong AB, Muhamad N, Syarifa J, Ramli MI. Material processing of hydroxyapatite and titanium alloy (HA/Ti) composite as implant materials using powder metallurgy: a review. Mater Des. 2014;55:165–75.

    CAS  Google Scholar 

  35. 35.

    Froes FH. Titanium powder metallurgy: a review—part 1. Advanced Materials & Processes; Asm INT, Subscriptions Specialist Customer Service, Materials Park, OH 44073-0002 USA, 2012. pp. 16–22.

  36. 36.

    Wang H, Fang ZZ, Sun PA. Critical review of mechanical properties of powder metallurgy titanium. Int J Powder Metall. 2010;46:545–57.

    CAS  Google Scholar 

  37. 37.

    Ljerka S, Anita S, Zoran G. Synthesis of Ti-Zr alloy by powder metallurgy. Eng Rev. 2019;39:115–23.

    Google Scholar 

  38. 38.

    Fretwurst T, Nelson K, Tarnow DP, Wang HL, Giannobile WV. Is metal particle release associated with Peri-implant bone destruction? An emerging concept. J Dent Res. 2018;97:259–65.

    CAS  Google Scholar 

  39. 39.

    Noronha OM, Schunemann WVH, Mathew MT. Can degradation products released from dental implants affect peri-implant tissues? J Periodontal Res. 2018;53:1–11.

    Google Scholar 

  40. 40.

    Grandin HM, Berner S, Dard M. A review of titanium zirconium (TiZr) alloys for use in endosseous dental implants. Materials (Basel). 2012;5:1348–60.

    CAS  Google Scholar 

  41. 41.

    Correa DRN, Vicente FB, Donato TAG, Arana-Chavez VE, Buzalaf MAR, Grandini CR. The effect of the solute on the structure, selected mechanical properties, and biocompatibility of Ti-Zr system alloys for dental applications. Mater Sci Eng C. 2014;34:354–9.

    CAS  Google Scholar 

  42. 42.

    Akimoto T, Ueno T, Tsutsumi Y, Doi H, Hanawa T, Wakabayashi N. Evaluation of corrosion resistance of implant-use Ti-Zr binary alloys with a range of compositions. J Biomed Mater Res B Appl Biomater. 2018;106:73–9.

    CAS  Google Scholar 

  43. 43.

    Ikarashi Y, Toyoda K, Kobayashi E, Doi H, Yoneyama T, Hamanaka H, et al. Improved biocompatibility of titanium-zirconium (Ti-Zr) alloy: tissue reaction and sensitization to Ti-Zr alloy compared with pure Ti and Zr in rat implantation study. J Jpn Inst Met. 2007;71:395–401.

    CAS  Google Scholar 

  44. 44.

    Johnson WL. Bulk glass-forming metallic alloys: Science and technology. MRS Bull. 1999;24:42–56.

    CAS  Google Scholar 

  45. 45.

    Lin HT, Cheng HY. Study on cell behavior on surfaces with various nanostructured modifications. J Biomater Tiss Eng. 2019;9:1021–6.

    Google Scholar 

  46. 46.

    Sun XY, Su W, Ma XM, Zhang HY, Sun Z, Li XD. Comparison of osteogenic capability of rat bone mesenchymal stem cells on collagen, collagen/hydroxyapatite, hydroxyapatite and biphasic calcium phosphate. Regenerative Biomater. 2018;5:93–103.

    CAS  Google Scholar 

  47. 47.

    Dongmei ZH, Cynthia SW, Cuie W, Yuncang L. Cellular responses of osteoblast-like cells to 17 elemental metals. J Biomed Mater Res Part A. 2017;105:148–58.

    Google Scholar 

  48. 48.

    Dai Y, Liu H, Liu B, Wang Z, Li Y, Zhou G. Porous β-Ca2SiO4ceramic scaffolds for bone tissue engineering: in vitro and in vivo characterization. Ceram Int. 2015;41:5894–902.

    CAS  Google Scholar 

  49. 49.

    Saldaña L, Mendéz-Vilas A, Jiang L, Multigner M, González-Carrasco JL, Pérez-Prado MT, et al. In vitro biocompatibility of an ultrafine grained zirconium. Biomaterials. 2007;28:4343–54.

    Google Scholar 

  50. 50.

    Josset Y, Oum’Hamed Z, Zarrinpour A, Lorenzato M, Adnet JJ, Laurent-Maquin D. In vitro reactions of human osteoblasts in culture with zirconia and alumina ceramics. J Biomed Mater Res. 1999;47:481–93.

    CAS  Google Scholar 

  51. 51.

    Sista S, Nouri A, Li Y. Cell biological responses of osteoblasts on anodized nanotubular surface of a titanium-zirconium alloy. J Biomed Mater Res A. 2013;101:3416–30.

    Google Scholar 

  52. 52.

    Chen Y, Roohani-Esfahani SI, Lu Z, Zreiquat H, Dunstan CR. Zirconium ions up-regulate the BMP/SMAD signaling pathway and promote the proliferation and differentiation of human osteoblasts. PLoS ONE. 2015;10:1–17.

    Google Scholar 

  53. 53.

    Lee BA, Kim HJ, Park YJ, Chung HJ, Kim YJ. Osteoblastic behavior to zirconium coating on Ti-6Al-4V alloy. J Adv Prosthodont. 2014;5:512–20.

    Google Scholar 

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This work was partly supported by the National Natural Science Foundation of China (No. 51904357) and the Natural Science Foundation of Hunan Province (Nos. 2020JJ5862 and 2020JJ5985).

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Ou, P., Hao, C., Liu, J. et al. Cytocompatibility of Ti–xZr alloys as dental implant materials. J Mater Sci: Mater Med 32, 50 (2021).

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