In Vivo Characterization of Titanium Implants Coated with Synthetic Hydroxyapatite by Electrophoresis

HA-coated Ti implant

In Vivo Characterization of Titanium Implants Coated with Synthetic Hydroxyapatite by Electrophoresis

Cristina Costa de Almeida^I; Lídia Ágata Sena^I; Marcelo Pinto^II; Carlos Alberto Muller^II; José Henrique Cavalcanti Lima^III; Glória de Almeida Soares^I

^IDepartment of Metallurgical and Materials Engineering, COPPE/UFRJ, Rio de Janeiro, RJ, Brazil

^IIInstitute Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, RJ, Brazil

IIIBrazilian Institute of Implantology (IBI), Rio de Janeiro, RJ, Brazil

^{Correspondence}

ABSTRACT

This study compared in vivo the performances of commercially pure titanium (cp Ti) screw dental implants either uncoated or coated with synthetic hydroxyapatite (HA) by electrophoresis. The HA coating was characterized by scanning electron microscopy, energy dispersive spectroscopy (EDS) and Fourier-transform infrared (FT-IR) spectroscopy. Well-adhered carbonated-hydroxyapatite layers (4- to-8-µm-thick) were obtained. In vivo tests were carried out by insertion of both uncoated and HA-coated implants into rabbit tibiae for 8 or 12 weeks. Histomorphometric analysis was performed by scanning electron microscopy with the aid of image-processing software. Results showed significantly greater bone-implant contact for HA-coated implants (p<0.05) than cp Ti implants. Comparison of bone content inside the screw implants showed no significant differences (p>0.05) between both types of implants, although cp Ti had numerically higher percentage of bone content than HA-coated implants. In conclusion, the HA-coated implants had better performance regarding the bone-implant contact area than the uncoated implants; coating by electrophoresis proved to be a valuable process to coat metallic implants with an osteoconductive material such as hydroxyapatite.

Key Words: titanium, coating, hydroxyapatite, in vivo study.

RESUMO

Este estudo comparou in vivo a performance de implantes orais rosqueáveis fabricados em titânio comercialmente puro (Ti cp) e implantes recobertos com hidroxiapatita (HA) estequiométrica pelo processo de eletroforese. A camada recoberta foi caracterizada por microscopia eletrônica de varredura, espectroscopia de energia dispersiva e espectroscopia de infravermelho com transformada de Fourier. Foram obtidas camadas de carbonato-apatita bem aderidas ao substrato metálico, com espessura variando de 4 a 8 µm. Testes in vivo foram realizados por meio da inserção de implantes em tíbias de coelho por períodos de 8 ou 12 semanas. A análise histomorfométrica foi realizada quantificando-se imagens obtidas em microscopia eletrônica de varredura e com o auxílio de um software de processamento de imagens. Os resultados mostraram que a porcentagem de contato direto osso-implante foi significativamente maior para os implantes recobertos (p<0,05) do que para os implantes de titânio cp. A comparação da quantidade de osso no interior das roscas não mostrou diferença significativa para os dois tipos de implantes (p>0,05), embora os implantes de titânio cp tenham apresentado valores de porcentagem numericamente maiores que os implantes recobertos. Concluiu-se que os implantes recobertos com hidroxiapatita tiveram melhor performance em relação à área de contato osso-implante que os implantes de titânio cp. O processo de eletroforese parece ser uma alternativa simples e viável para se recobrir implantes de titânio com material osteocondutivo, como a hidroxiapatita.

INTRODUCTION

Due to its biocompatibility, titanium is considered the universal material for permanent implants, such as endosseous dental implants. In other applications requiring higher mechanical strength, titanium-based alloys or Co-Cr alloys are preferred.

Coating metallic implants with biologically active materials, i.e., hydroxyapatite (Ca₁₀(PO₄)₆(OH) ₂; HA) aims to accelerate bone formation on the initial stages of osseointegration, thus improving implant fixation (1,2). HA-coated dental implants are often recommended for the maxillary area where bone is less dense. HA coating is commercially produced by plasma spray techniques, which, in spite of the high productivity, demand expensive equipment and a robotic system to guarantee a uniform coating on complex shapes. In order to overcome plasma spray disadvantages, alternative processes have been developed (3-6).

Deposition by electrophoresis has some advantages over other techniques, including its short coating time (2-3 min) and high reproducibility. However, hydroxyapatite adhesion to metallic substrates can be unsatisfactory without the previous blasting of titanium surface to enhance roughness, and calcination to improve coating adhesion (6-8). During heat treatment, hydroxyapatite, especially calcium-deficient-HA, can be partially converted into tricalcium phosphates (a-TCP or b-TCP), which are more soluble than the hydroxyapatite (9). Stability and solubility of calcium phosphate materials are strongly dependent on their composition and crystallographic structure. Among the tricalcium phosphates, amorphous calcium phosphate (ACP) is the most soluble, while sintered stoichiometric HA is the least soluble. Coatings with higher ACP/HA ratios will dissolve or biodegrade to a greater extent than coatings with a low ACP/HA ratio or higher cristallinity (9).

The purpose of this study was to compare the in vivo performances of titanium implants either uncoated or coated with synthetic hydroxyapatite by electrophoresis.

MATERIAL AND METHODS

Twenty screw-shaped commercially pure titanium (cp Ti) implants with an outer diameter of 3.75 mm and 7 mm in length were used in this study. Ten implants were left "as-received" (cp Ti implants) and ten were coated with synthetic hydroxyapatite by electrophoresis (HA-coated implants).

A precipitation-wet method was used to synthesize hydroxyapatite producing a powder with 1.66 ± 0.04 Ca/P ratio. The morphology of HA powder showed acicular nanocrystals and cell parameters compatible with stoichiometric hydroxyapatite (6). The coating methodology was developed by Sena (6), following the Zhitomirsky and Gal-Or procedure (7). Titanium implants were used as cathode and platinum was used as anode in an electrophoretic cell with the electrodes positioned 40 mm apart. HA suspension in ethanol was prepared using hydrochloric acid as a dispersing agent, this process being carried out at 24 V for 3 min. After deposition, the coated specimens were calcined in a tubular furnace at 800ºC for 2 h.

The characterization of the titanium implants was carried out on 4 specimens (2 HA-coated and 2 uncoated implants) by using a scanning electron microscope (DSM 940A model; Carl Zeiss, Jena, GmbH, Germany) on secondary electron and energy dispersive spectroscopy (EDS). A Nicolet-520G spectrometer with diffuse reflectance stage (Thermo Nicolet Corp., Madison, WI, USA) was used for Fourier-transform infrared (FT-IR) analysis.

Eight adult New Zealand rabbits of both sexes, weighing between 3.2 and 4 kg, were used. Each animal received 2 implants, 1 cp Ti (uncoated) and 1 HA-coated, both inserted in the tibial metaphysis. Four animals received cp Ti implants in the proximal tibial metaphysis and HA-coated implants in the distal tibial metaphysis. After a 4-week interval, the other four animals received the remaining implants following an inverse design, i.e., the HA-coated implants were inserted in the proximal tibial metaphysis while the cp Ti implants were inserted in the distal tibial metaphysis. All implants were supposed to remain in place for 12 weeks.

The animals were fasted 12 h before surgery and no prophylactic medication was prescribed. Ketamine (Francotar, Virbac, Carros, French; 50 mg/kg body weight) and Acepromazine (Acepran, Univet, São Paulo, SP, Brazil; 2 mg/kg body weight) were administered intramuscularly. After sedation, the left tibia of each animal was shaved and thereafter washed with Extran MA02 detergent (Merck, Rio de Janeiro, RJ, Brazil)

Surgical procedures were conducted in compliance with ethical principles for animal research, as approved by institutional guidelines. With the animals placed on their backs, a 3-cm-length incision was made through the skin and the fasciae in the tibial metaphysis to expose the tibial crest. Bone was perforated using segmental drills at low-speed with profuse saline cooling and the bone holes were carefully threaded. The implants were gently screwed into place and the fascia and skin were sutured with Prolene 2-0 Ethicon (Johnson-Johnson, São José dos Campos, SP, Brazil). The animals were allowed full weight bearing without any mobility restrictions immediately postoperatively.

Regrettably, two animals that received the implants at the second moment died before completion of the study, reducing the sample size to 6 animals and 12 implants (6 cp Ti and 6 HA-coated implants). To prevent further deaths, all animals were sacrificed at that time with intravenous overdoses of Tiopenthal (Cristália, Itapira, SP, Brazil): four completed approximately twelve postoperative weeks and the two survived up to eight weeks after surgery. Sections of each implant with surrounding bone tissue were removed and fixed with glutaraldehyde (Pelco International, Redding, CA, USA) in sodium cacodylate (Pelco International) at pH 7.2, dehydrated in graded acetone and embedded in low viscosity "Spurr" kit (Pelco International). Resin polymerization was carried out at 60ºC for 24 h. The 12 sections were bisected and each surface (A side and B side) was submitted to grinding with water-cooled 1200-grit SiC paper and sputter-coating with gold. Backscattered electron (BSE) images (X100 magnification) of both sides (A and B) of each section were obtained by SEM. The digital images were processed using image-analysis software (Global Lab Image, Data Translation, Marlboro, MA, USA). The percentage of direct bone contact was calculated as being the length of the implant in contact with bone divided by the total length of the screw (Fig. 1). In addition, the bone area inside the threads, expressed as a percentage of the total area, was also determined.

For statistical analysis, the variables were considered to have normal or about normal distribution. Bone-implant contact means for the three best consecu tive threads and for all threads, as well as the means of bone area inside the HA-coated and uncoated implant threads were compared using the F test (a=0.05%). Student's t-test for two samples supposing equivalent variances or different variances was also done.

RESULTS

Coating Characterization

SEM micrographs of HA-coated implants (Fig. 2) showed homogenous layers of hydroxyapatite with a "crackled" appearance due to the volumetric contraction after calcination (Fig. 2). EDS spectra (Fig. 3) showed peaks of titanium, calcium and phosphorus. On FT-IR spectra (Fig. 3), the characteristic bands of the group PO₄^-3 (566, 570, 605, 1030 and 1100 cm^-1) of hydroxyapatite were identified. The band at 872 cm^-1 correspondent to CO₃^-2 in HA A sites and the bands at 1422 and 1449 cm^-1 related to HA A and B sites were also identified, indicating that the coatings were composed by carbonated-hydroxyapatite.

Histologic Analysis

SEM images of bone sections showed an almost continuous Ca-P-rich layer, with thickness ranging from 4 to 8 µm, well adhered to titanium implant (10). In Figure 4, a fracture line can be seen along the HA-bone interface, probably caused by the rapid polymerization of acrylic resin. Regions where the fracture gap was thicker than 10 µm were not considered as osseointegrated. For all HA-coated implants, this fracture occurred at the bone-hydroxyapatite interface, the coating layer remaining adhered to the metal.

Histomorphometric Analysis

Table 1 shows the means (±SD) of the percentage of bone-implant contact obtained after 8 and 12 weeks for the three best consecutive threads and for all threads in the cortical area. No statistically significant differences (p>0.05) were observed when the 8- and 12-week results were compared. Data were grouped, regardless of the osseointegration period, and the percentage of bone-implant contact of cp Ti and HA-coated implants was compared. Student's t-test showed significant differences (p<0.05) between uncoated and HA-coated implants for the three best consecutive threads and for all threads (Fig. 5). Means (±SD) for the bone area inside the three best titanium threads and for all threads are given in Figure 6. Student's t-test showed no statistically significant difference (p>0.05) between the results obtained for both types of surfaces.

DISCUSSION

In this study, titanium implants were satisfactorily coated with hydroxyapatite by using electrophoresis. According to Sena et al. (6) and Lacefield (11), calcination is of paramount importance to enhance adhesion and promote hydroxyapatite densification. HA deposition by electrophoresis was described by Ducheyne and Qiu (12) as the best technique to coat irregular surfaces, such as those of the screw-shaped dental implants. The "crackled" appearance of HA coatings (Fig. 2) is characteristic of metal-ceramic systems and is attributed to the development of thermal tensions due to the different expansion coefficients between the metal and ceramic layers during heating and cooling cycles (6,8).

Carbonate bands in HA A and B sites were identified in the FTIR spectra (Fig. 3), suggesting that the HA coating actually is a carbonated-apatite coating. These results are justified by hydroxyapatite trend to incorporate carbonate ions from air, during synthesis and/or coating process. Although carbonate ions act to turn hydroxyapatite more soluble, this appears to be positive for the osseointegration process. The partial dissolution of hydroxyapatite makes the surrounding fluids rich in calcium and phosphate ions, which seems to induce the precipitation of "bone-like" apatite on implant surface (12-14). The release of calcium and phosphate ions followed by precipitation of "bone-like" apatite can trigger cellular differentiation and consequent bone formation (apatite plus osteoblast cells), and would perhaps explain why HA-coated implants tend to exhibit faster osseointegration than uncoated implants.

Several authors (9,12,15) have stated that the role of coating ends after the initial stages of osseointegration. Therefore, the coating layer has not to be necessarily insoluble or thick, like plasma spray coatings usually are. Indeed, thick layers tend to exfoliate or delaminate (16) because the interfacial resistance decreases with increasing coating thickness. In a previous investigation, HA coatings deposited by plasma spray with thickness ranging from 75-150 µm showed delamination, while 25 to 50-µm-thick coatings were found to have no effect on fatigue strength (17). By adjusting the process parameters, electrophoresis can produce coating as thin as 5 µm.

Gotfredsen et al. (18) and Vidigal et al. (19) have proposed the use of SEM images obtained with backscattered electrons for histomorphometric analysis. This methodology allows for use of thick sections and acquisition of high-contrast images because BSE contrast is highly dependent on atomic number of chemical specimens. Consequently, bone and calcium phosphate appears darker than titanium.

The non-significant differences observed after 2 or 3 months of osseointegration in this study are in agreement with the findings of other investigations (18,20). The better performance of HA-coated implants regarding bone-implant contact percentage (Fig. 5) is also consistent with the results of previous reports (2,18). However, the number of implants and animals used in this study cannot unequivocally support such comparisons.

Determination of the bone area inside the threads (Fig. 6) showed that the cp Ti implants presented slightly higher numerical values than the HA-coated implants, but this difference was not statistically significant. Likewise, Gottlander et al. (20) reported higher values for bone area inside titanium implant threads (60.6%) than inside HA-coated implant threads (41.8%) placed on tibia bone for 6 months. This behavior suggests that the efficacy of the coating layer is somehow restricted to the surroundings of the implant surface, without any long-distance effects.

The discrepancies between in vivo investigations and clinical applications must be appreciated and in vivo results cannot be directly extrapolated to the clinical reality. Moreover, the major limitation of our study was the small number of animals, which was further reduced with the loss of two animals during the experimental phase. The findings of this study led to the conclusion that the HA-coated implants had better performance regarding the bone-implant contact area than the uncoated implants. Coating by electrophoresis proved to be a valuable process to coat metallic implants with an osteoconductive material such as hydroxyapatite, for small or medium scale production. Further investigations should be carried out before this process can be rendered commercial.

ACKNOWLEDGEMENTS

This research was supported by CNPq, CAPES, FAPERJ and FUJB. The authors are grateful to Neodent (Curitiba, PR, Brazil) for providing the titanium implants.

Accepted April 23, 2003

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Publication Dates

• Publication in this collection
  17 Aug 2005
• Date of issue
  Apr 2005

History

• Received
  23 Apr 2002
• Accepted
  23 Apr 2002