Abstract
Fish scales of the Arapaima gigas (pirarucu) species were heat-treated to obtain natural hydroxyapatite (HAp), and it was doped with niobium (Nb) by physical ultrasound interference to confirm an effective route to the production of Nb-doped HAp powders. The effect of ultrasound application on doping was investigated. The structure of the powders was elucidated using X-ray diffractometry (XRD), scanning electron microscopy, IR spectroscopy, and X-ray fluorescence spectroscopy (XRF). XRD results of Nb-doped HAp powders were compared with undoped natural hydroxyapatite and ICSD-26204 standard as controls. The crystallinity of Nb-doped HAp powders increased from 39% to 51% after the ultrasound application. IR spectroscopy confirmed hydroxyl, carbonate, and phosphate functional groups in the sample. Results obtained by XRF confirmed the ionic substitution of Ca for Nb with an average content of 1%. Therefore, the effectiveness of the synthesis route was confirmed to produce hydroxyapatite-niobium crystalline powder with physicochemical integrity as a potential biomaterial for bone implant application.
Keywords:
natural hydroxyapatite; niobium; powders; ultrasound
INTRODUCTION
Hydroxyapatite [Ca10(PO4)6(OH)2] is considered a healing material because its interaction with surrounding tissue provides a conductive microenvironment that enables the bone formation and growth 11 A. Moraes, A. Bierhalz, A. Pires, Quím. Nova 38, 7 (2015) 957.. There is a superficial chemical similarity between hydroxyapatite (HAp) and bone, which permits a better cell interaction with the HAp once implanted in the host 22 A. Prasad, B. Devendar, M.R. Sankar, P. Robi, Mater. Today Proc. 2, 4 (2015) 1216.), (33 M. Tang, N. Krishnamra, J. Thongbunchoo, N. Charoenphandhu, P. Suntornsaratoon, W. Pon-On, Mater. Sci. Eng. 62 (2015) 183.. The HAp presents molar ratio Ca/P equal to 1.67 44 R.F. Bonan, P.R.F. Bonan , A.U.D. Batista, J.E. Oliveira, R.R. Menezes, E.S. Medeiros, Cerâmica 60, 355 (2014) 402., and its hexagonal unit cell has a=b=9.389 Å, c=6.869 Å, α=β=90°, and γ=120° 55 T.S.A. Batista, J.B. Santos-Filho, Calcita, hidroxiapatita e β-fosfato tricálcio como absorvedores do ultravioleta, IFS, Aracaju (2016).. In recent years, there are a large number of studies involving the synthesis of natural hydroxyapatite from biogenic sources through heat treatment 66 S. Kongsri, K. Janpradit, K. Buapa, S. Techawongstien, S. Chanthai, Chem. Eng. J. 215-216 (2013) 522.)- (99 N.N. Panda, K. Pramanik, L.B Sukla, Bioproc. Biosyst. Eng. 37, 3 (2013) 433.. Besides, methods to obtain the hydroxyapatite powders can be combined with the physical interference methods. Brundavanam et al. 1010 R.K. Brundavanam, G.E.J. Poine, D. Fawce, Am. J. Mater. Sci. 3, 4 (2013) 84. proved the application of physical effects to stimulate chemical reactivity in mixtures. The recommended equipment for this procedure is an ultrasonic homogenizer because it is more efficient due to the high cavitation energy 1010 R.K. Brundavanam, G.E.J. Poine, D. Fawce, Am. J. Mater. Sci. 3, 4 (2013) 84..
The doping of a ceramic structure with metallic elements through combined synthesis routes would result in a promising product in the development of biomaterials. In this case, niobium is an example of a metal element with excellent mechanical properties, biocompatibility, and corrosion resistance 1111 N. Demirkol, N.F. Oktar, S.E. Kayali, Eng. Mater. 529-530 (2013) 29.), (1212 E. Simomukay, E.C.F. de Souza, S.R.M. Antunes, C.P.F. Borges, M.D. Michel, A.C. Antunes, Cerâmica 62, 361 (2016) 9.. The niobium oxide presents low cytotoxicity, bioactivity, and biocompatibility in a ceramic structure 1313 I.L. Denry, J.A. Holloway, R.J. Nakkula, J.D. Walters, J. Biomed. Mater. Res. B 75 (2005) 18.), (1414 M. Tamai, K. Isama, R. Nakaoka, T. Tsuchiya, J. Artif. Organs 10 (2007) 8.. Besides, niobium ions are obtained in the laboratory when the chemical species Nb (V) is introduced into an aqueous solution. The aqueous solution must be under constant agitation for ion exchange between the niobium and calcium ions. On the other hand, niobium ions can replace phosphorus ions in the ceramic structure (HAp), and they form the O-P-O-Nb-O bonds 1515 A. Obata, Y. Takahashi, T. Miyajima, K. Ueda, T. Narushima, T. Kasuga, ACS Appl. Mater. Interfaces 4, 10 (2012) 5684..
This study investigated the effects of adding niobium ions in a matrix of HAp obtained from fish scales of the Arapaima gigas species after the physical ultrasound interference application. The samples were investigated by structural, chemical, and morphological characterization tools to confirm the presence of hydroxyapatite-niobium crystalline powder with physicochemical integrity.
MATERIALS AND METHODS
Obtaining natural hydroxyapatite: the scales of Arapaima gigas (pirarucu) were purchased from Iranduba Frigorífico Pescados located in Iranduba, Brazil. The scales were separated and washed under running water at room temperature. Thereafter, the synthesis method comprised the heat treatment route at 700 °C for 2 h at a heating rate of 10 °C/min. This procedure comprised the removal of organic parts and the formation of HAp crystals induced by thermal energy 66 S. Kongsri, K. Janpradit, K. Buapa, S. Techawongstien, S. Chanthai, Chem. Eng. J. 215-216 (2013) 522.)- (99 N.N. Panda, K. Pramanik, L.B Sukla, Bioproc. Biosyst. Eng. 37, 3 (2013) 433.; then, the heat-treated material was cooled in a closed container. After that, the sample was sieved (325 mesh) to obtain a uniformly homogenized powder, and the sample was stored in Eppendorf tubes for the physical, chemical, and morphological characterizations.
Doping with niobium ions: the niobium chloride solution was prepared by the addition of 0.27 g of niobium chloride (Sigma, 99%) and 100 mL of ethanol, both placed in a container, and the mixture was stirred vigorously for 10 min. A quantity of niobium chloride to substitute 1 wt% Ca with Nb was added to the solution. The HAp powder obtained in the previous step was added to the niobium chloride solution. The synthesis was performed by mixing, always under stirring by a magnetic stirrer to provide the availability of Ca2+ and PO4 3- ions for the Nb ion replacement reaction. After that, the precursor solution was filtered. The sample was washed 3 times with deionized water (30 mL) to remove the unreacted ions. Finally, the material was dried in an electric oven at 110 °C for 24 h. Thereafter, heat treatment was performed at 900 °C in a muffle furnace for 3 h at a heating rate of 10 °C/min. The procedure was completed with a sieving step (325 mesh).
Physical ultrasound interference: a QR1000 Ultrasonic Sonicator (Eco-Sonics) was used to cause physical agitation at a frequency of 20 kHz for 30 min and 70% ultrasonic power control. After physical ultrasound interference, the sample was placed for maturation for 24 h; then, it was washed 3 times with deionized water and dried in an electric oven for 24 h at 100 °C.
Characterization techniques: the samples were analyzed by X-ray diffraction (XRD) using Panalytical Empyrean X-ray diffractometer with CuKα radiation (1.5418 Å) in a range of 10° to 100° (2θ). Fourier-transform infrared (FTIR) spectroscopy was performed with IRAffinity-1 Shimadzu spectrometer with 32 scans in the range of 4000 to 400 cm-1. Each sample was mixed with KBr at a ratio of 1:100 and vacuum-pressed. The X-ray fluorescence (XRF) spectroscopy was performed on powders by Panalytical Epsilon 3-X equipment with a voltage of 50 kV and a maximum current of 3 mA in a helium gas atmosphere (10 atm). The crystallite size was determined using the Scherrer equation, and the crystallinity was determined using the Rietveld refinement with the GSAS Crystallography Data and High Score Plus programs.
RESULTS AND DISCUSSION
Table I shows the phases obtained after the refinement of XRD data. The presence of niobium oxide in the HAp matrix allows a potential application in implants and bone restoration. Wei et al. 1616 P. Wei, J. Fang, L. Fang, K. Wang, X. Lu, F. Ren, Appl. Mater. Today 15 (2019) 531. developed HAp nanocomposites with niobium that showed improvements in biological and mechanical properties, and this could make the material composed of bioactive HAp-Nb and allows better cell interaction with bone tissue. The monolithic apatite structure is present in the XRD patterns in Fig. 1. The structural integrity was maintained, as shown by the peaks in the range of 20° to 35°. This range includes the reflection by crystalline planes with Miller indices of (200), (111), (002), (102), (210), and (300) 77 B. Mondal, S. Mondal, A. Mondal, N. Mandal, Mater. Charact. 121 (2016) 112.), (1414 M. Tamai, K. Isama, R. Nakaoka, T. Tsuchiya, J. Artif. Organs 10 (2007) 8.), (1717 D.N. Rocha, M.H.P. Silva, L.A. Gobbo, J. Mater. Res. Technol. 2, 1 (2013) 24.)- (1919 S. Paul, A. Pal, A.R. Choudhury, S. Bodhak, V.K. Balla, A. Sinha, M. Das, Ceram. Int. 43, 17 (2017) 15678.. Furthermore, a well-defined structure and peaks are shown. There were secondary phases with low-intensity peaks due to calcium and phosphorus byproducts 2020 G.A. dos Santos, A.A. Barbosa, L.M. de Oliveira, A.V. Ferraz, N.C. Olivier, W. Acchar, A.C.S. Dantas, Cerâmica 63, 368 (2017) 557.. The crystallinity of the precipitates was high due to heat treatment. The peaks of the HAp-Nb curve were composed of the phases HAp, CaNb2O6, and Nb2O5, due to the replacement of calcium ions by niobium ions at peaks at 25°, 33°, 35°, 46°, and 50° 1111 N. Demirkol, N.F. Oktar, S.E. Kayali, Eng. Mater. 529-530 (2013) 29..
Contents (±0.5%) of the main phases detected in the HAp-Nb sample after the refinement of XRD data.
XRD patterns of natural HAp and hydroxyapatite-niobium samples compared to the ICSD-26204 file.
The FTIR spectroscopy confirmed XRD results. In Fig. 2, FTIR spectra show the characteristic bands of HAp due to the presence of hydroxyl, phosphate, and carbonate functional groups. The peaks in the range of 3750 to 3500 cm-1 indicated the presence of OH- and in the range of 1500 to 1250 cm-1 and at 873 cm-1 characterized the CO3 2- ions. Also, the bands in the ranges of 1000 to 900 cm-1 and 610 to 560 cm-1 indicated the presence of the PO4 3- ions. The peaks at 3497, 631, and 456 cm-1 confirmed the crystallinity of the powders because these wavenumbers are related to the vibrational mode of OH bond (hydroxyl group) 77 B. Mondal, S. Mondal, A. Mondal, N. Mandal, Mater. Charact. 121 (2016) 112.), (1818 X. Gao, C. Dai, W. Liu, R. Shen, X. Zheng, K. Duan, J. Weng, S. Qu, J. Mater. Sci. Mater. Med. 28, 6 (2017) 83.)- (2020 G.A. dos Santos, A.A. Barbosa, L.M. de Oliveira, A.V. Ferraz, N.C. Olivier, W. Acchar, A.C.S. Dantas, Cerâmica 63, 368 (2017) 557.. The band at 1406 cm-1 indicated the presence of the CO3 2- group. Absorption in this region indicated the replacement of OH- ion (present in the chemical structure of HAp) by carbon dioxide. Also, CO3 2- ions confirmed the formation of HAp because this group is found in the inorganic phase of bone (biological hydroxyapatite phase) 2121 N. Muhammad, Y. Gao, F. Iqbal, P. Ahmad, R. Ge, U. Nishan, A. Rahim, G. Gonfa, Z. Ullah, Sep. Purif. Technol. 161 (2016) 129.. Moreover, the curve profile was maintained after the replacement of Ca2+ ions by Nb ions in the hydroxyapatite structure 2222 Y. Sogo, A. Ito, K. Fukasawa, T. Sakurai, N. Ichinose, Mater. Sci. Technol. 20, 9 (2004) 1079.)- (2424 Y. Sogo , A. Ito , K. Senda, A. Oyane, A. Yamazaki, R.Z. Legeros, J. Biomed. Mater. Res. 1, 3 (2006) 134.. Besides, the spectrum of HAp-Nb did not show a significant difference compared to the natural HAp spectrum. However, in the curve of the HAp-Nb sample, the peak of the carbonate group had a lower intensity than the same group in the curve of the natural HAp sample. This could be a consequence of the phosphate groups replaced by negatively charged niobate species. So, the decrease in the number of phosphate groups in the structure could cause a reduction of the sites for the incorporation of carbonate groups in the main phase. Besides, the vibrational contributions of niobium oxides were not observed in the spectra of Fig. 2 due to these groups being outside the detectable range 2525 N.S.V. Capanema, A.A.P. Mansur, S.M. Carvalho, A.R.P. Silva, V.S. Ciminellí, H.S. Mansur, Materials 8 (2015) 4191.. The HAp-Nb sample showed peaks of the carbonate functional group in the region between 2500 and 2250 cm-1 because this sample was more exposed to the atmospheric air. According to Capanema et al. 2525 N.S.V. Capanema, A.A.P. Mansur, S.M. Carvalho, A.R.P. Silva, V.S. Ciminellí, H.S. Mansur, Materials 8 (2015) 4191., the carbonate groups are detected by characterization due to the presence of surface ions. The carbonate ions replaced the sites of the PO4 3- and OH- ions. The result of this substitution was the formation of carbonated hydroxyapatite. Table II shows the results of IR spectroscopy for the detected functional groups.
Table III shows the results of X-ray fluorescence (XRF) analysis. Results confirmed the presence of the metallic Nb element in the sample with an average content of ~1%. According to Rocha et al. 1717 D.N. Rocha, M.H.P. Silva, L.A. Gobbo, J. Mater. Res. Technol. 2, 1 (2013) 24., the addition of metallic ion caused a decrease in the size of HAp crystals due to the ionic radius of niobium being smaller than of calcium. In high concentrations, niobium inhibits the growth of HAp crystals, and this would cause a delay in the growth of crystals in the apatite phase 1717 D.N. Rocha, M.H.P. Silva, L.A. Gobbo, J. Mater. Res. Technol. 2, 1 (2013) 24.. The percentage of Ca element had precedence in literature due to the presence of CaO. Besides, the content of Ca was higher than the content of phosphorus (P) because the doping in the ceramic structure probably did not occur at the PO4 3- site 1717 D.N. Rocha, M.H.P. Silva, L.A. Gobbo, J. Mater. Res. Technol. 2, 1 (2013) 24.. Moreover, the Ca/P molar ratio found was lower than the apatite phase found in the literature (1.58 < 1.67 44 R.F. Bonan, P.R.F. Bonan , A.U.D. Batista, J.E. Oliveira, R.R. Menezes, E.S. Medeiros, Cerâmica 60, 355 (2014) 402.) due to the doping procedure, which decreased the amount of calcium ions in the sample, while the number of the phosphate ions remained constant. The temperature of heat treatment in the first stage of the experiment was crucial to obtain a crystalline profile of the sample. Besides, the doping with niobium ions maintained the crystalline phase due to the abundance of exchangeable sites 2626 M.F. Rolland, T.J. Cole, M. Sempé, J. Tichet, C. Rossignol, A. Charraud, Eur. J. Clin. Nutr. 45 (1991) 13.. Heat treatment time favored the atomic diffusion within the particles, and it reduced the presence of the pores. This diffusion contributed to the homogenization of the niobium ions introduced in the ceramic structure 2727 K.A.S. Farias, W.J.B. Sousa, M.J.B. Cardoso, R.J.S. Lima, M.A. Rodriguez, M.V.L. Fook, Cerâmica 65, 373 (2019) 99..
Table IV summarizes the results of the crystallite size, lattice parameters, and volume of the unit cell of the synthesized powders. The heat treatment of the samples contributed to grain growth. The HAp-Nb sample prepared with ultrasound had a smaller crystallite size compared to the HAp sample without ultrasound. This fact confirmed the XRF data because the niobium ion inhibits the growth of the HAp crystals. Besides, this result confirmed the introduction of Nb ions into the sites that contained calcium in the structure. The effect of the doping with Nb in the PO4 3- sites was to the increase of lattice parameters a and c (Table IV). The chemical species with Nb (V) has an ionic radius greater than the PO4 3-, and there is an increase in the parameters of the samples with Nb 2525 N.S.V. Capanema, A.A.P. Mansur, S.M. Carvalho, A.R.P. Silva, V.S. Ciminellí, H.S. Mansur, Materials 8 (2015) 4191.. The samples submitted to the ultrasound had a smaller size of crystallites, confirming the efficiency of the physical interference procedure. The effects of the physical interference were the dissolution of particles and the precipitation of chemical species. This result showed a decrease in the size of the crystallites after the physical ultrasound interference procedure. Besides, there was an increase in the unit cell volume of the HAp-Nb sample compared to the HAp sample, both prepared with ultrasonication, due to the effective replacement of niobate species in the PO4 3- sites in the hydroxyapatite structure.
Fig. 3 shows the X-ray diffraction patterns of the HAp-Nb samples prepared with and without physical ultrasound interference. The curve of the sample with physical ultrasound interference showed more isolated peaks. This could be a consequence of using a wet route and a physical interference to present a qualitative improvement in the XRD pattern. Similar results were found in other studies 2828 M.C. Barbosa, “Síntese de hidroxiapatita por via úmida assistida por métodos físicos”, Un. Vale Paraíba, S. José Campos (2014).), (2929 A.L. Macipe, J.G. Morales, R.R. Clemente, Adv. Mater. 10 (1998) 49., which showed the use of physical interference methods for increasing the crystallinity of the samples. In HAp samples, the crystallinity increased from 34% to 48% after the ultrasound application. Besides, HAp-Nb samples showed an increase in crystallinity from 39% to 51%. The physical effects induced by the ultrasound method provided crystallites with a smaller size, and the refinement of XRD results indicated a higher crystallinity. The size of the crystallites decreased significantly after the ultrasound method. In HAp-Nb samples, the crystallite size decreased from 104 to 50 nm. According to Barbosa 2828 M.C. Barbosa, “Síntese de hidroxiapatita por via úmida assistida por métodos físicos”, Un. Vale Paraíba, S. José Campos (2014)., the crystallites with a size of less than 100 nm improve the interaction in applications of the biomaterials to implants and bone restoration. The results of the refinement of the XRD data confirmed the obtention of a material with a higher crystallinity after the application of the ultrasound method. The crystallinity is an important property for bioceramic materials because it contributes to making these materials more resistant to degradation and resorption.
X-ray diffraction patterns of the HAp-Nb samples prepared with and without physical ultrasound interference.
Fig. 4 shows the results of scanning electron microscopy of the HAp-Nb samples prepared with and without physical ultrasound interference. Both samples showed the formation of polygonal grain structures and agglomerated particles. The morphology of the sample prepared with ultrasound showed smoother particles due to the ultrasound procedure to induce the dissolution and the precipitation of solids. Meanwhile, the sample prepared without ultrasound showed a higher particle density. The doping procedure and the physical ultrasound interference were important steps in the methodology to obtain a defined morphology. The samples submitted to the physical ultrasound interference presented more isolated particles due to the dispersion and intense agitation process 2828 M.C. Barbosa, “Síntese de hidroxiapatita por via úmida assistida por métodos físicos”, Un. Vale Paraíba, S. José Campos (2014).. Besides, the HAp-Nb sample prepared with ultrasound showed particles with smaller crystallites (Table IV).
SEM micrographs of HAp-Nb samples prepared without (a) and with (b) physical ultrasound interference.
CONCLUSIONS
This study demonstrated the efficiency of the experimental process to obtain natural hydroxyapatite from fish scales as the raw material. Furthermore, the doping with niobium ions was optimized by the physical ultrasound interference, as shown by the XRD and SEM results. The refinement of XRD results showed an increase in the crystallinity from 34% to 51% and a decrease in the size of crystallites from 128 to 50 nm. The micrographs showed smoother and more isolated particles after the application of the physical ultrasound method. As such, the combination of the synthesis steps was efficient for the laboratory production of an Nb-doped HAp powder, and the results indicated excellent physicochemical characteristics of the sample. Therefore, this article confirmed a new route for the production of a ceramic material doped with metallic ions for implants and bone restoration applications.
ACKNOWLEDGMENTS
The authors are grateful to the Foundation for Research Support of the State of Amazonas (FAPEAM) for financial support and the Pro-Rectory of Research and Graduate Studies (PROPESP) of the Federal University of Amazonas for the support for the realization of this research.
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Publication Dates
-
Publication in this collection
10 Feb 2021 -
Date of issue
Jan-Mar 2021
History
-
Received
27 Oct 2019 -
Reviewed
24 Jan 2020 -
Reviewed
31 Mar 2020 -
Reviewed
22 June 2020 -
Reviewed
14 July 2020 -
Accepted
19 July 2020