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PII: S1010-5182(15)00418-7
DOI: 10.1016/j.jcms.2015.12.004
Reference: YJCMS 2257
Please cite this article as: Bral A, Mommaerts MY, In vivo biofunctionalization of titanium patient-specific
implants with nano hydroxyapatite and other nano calcium phosphate coatings: A systematic review,
Journal of Cranio-Maxillofacial Surgery (2016), doi: 10.1016/j.jcms.2015.12.004.
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Alexander Bral*
Maurice Y. Mommaerts *
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* European Face Centre, University Hospital Brussels, Belgium.
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Corresponding Author: Maurice Y. Mommaerts
Laarbeeklaan 101
B-1090 Brussels
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Email: Maurice.Mommaerts@uzbrussel.be
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surgery using nano-sized calcium phosphate coatings on titanium patient specific implants.
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Materials and methods: A multi-database single-reviewer systematic literature review was conducted.
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Results: Twenty-eight papers consisting of twenty-five animal studies and three human studies met the
selection criteria. The results of existing literature suggest that titanium implants coated with nano
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calcium phosphate and hydroxyapatite improves osseointegration and implant fixation. However, not
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coating thickness, calcium phosphate solubility, and nanotopography contribute significantly to
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biofunctionalization. Nonetheless, additional data derived from clinical studies are needed to support
Summary
INTRODUCTION
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Calcium phosphate (CaP) coatings on titanium implants have been shown to improve biofunctionalization, because they facilitate
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osseointegration and functional longevity (Le Guehennec et al., 2007). Furthermore, failure to achieve osseointegration results from
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insufficient bone formation on the implant surface, which can lead to incomplete fixation of the implant (Mendonca et al., 2008).
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Hence, the philosophy behind the use of nano CaP and hydroxyapatite (HA) coatings is that the chance of biological integration is
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higher when the structure mimics human bone more closely (Alberts et al., 2002).
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The nanoscale ranges from 0.1 nm to 100 nm. However, if the dimensions of the particles range from 100 nm to 1 µm, they are called
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submicron particles (Ehrenfest et al., 2004). Important inorganic components of bone are nanoscale CaP particles within the 20- to 40-
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nm size range. Further, nanoparticles smaller than 100 nm have the highest reported efficacy regarding cellular integration, and it has
been suggested that these particles induce responses different from submicron structures, which could imply that nano HA and
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possibly other CaP coatings could create biocompatible surfaces that unite with bone tissue (Webster et al., 2004, Basu et al., 2009).
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HA is a calcium orthophosphate that is composed of calcium, phosphorus, and hydroxide and has a chemical formula of
Ca10(PO4)6(OH)2. Furthermore, HA has a CaP ratio of 1.67, and is the least soluble and most stable calcium orthophosphate. The
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various forms of CaP differ in solubility and stability, which are both characteristics that alter biocompatibility. As well, the coating
technique is another important factor that can alter the solubility and the stability of the coating (Sergey 2007).
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The investigation and characterization of nanostructures on implant surfaces is challenging. At present, no quantitative technique is
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available to accurately assess the nanotopography on a micro-texturized surface due to an interference between both components.
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Consequently, only field emission scanning electron microscopy (FE-SEM) enables the accurate examination of micro-texturized
surfaces (Ehrenfest et al., 2004). The majority of the publications included in the current review involved the use of scanning electron
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microscopy (SEM) to investigate the coating on implant surfaces. However, atomic force microscopy (AFM) and optical
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interferometry (OI) were also used to examine the coating roughness.
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Various techniques exist to create nano CaP coatings, such as the dip coating process (Guo et al., 2004), the sol-gel method (Ben-
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Nissan et al,. 2006), the electrochemical method, the electrophoretic deposition process, the biomimetic deposition process, the
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hydrothermal treatment method, and ion beam-assisted deposition (IBAD). In addition, each technique has different advantages and
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disadvantages in terms of processing and outcome (Li et al., 2003, Narayanan et al., 2008, Chae et al., 2008, Hu et al., 2010, Lobo et
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al., 2011).
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The effectiveness of nano-CaP coatings can be compared in a hierarchical order on the basis of in vitro and in vivo studies and clinical
studies. In vitro research of surface coatings primarily focuses on evaluating biocompatibility and assessing cytotoxicity, whereas in
vivo studies principally involve histomorphometrical analysis and removal torque (RTQ) testing (Coelho et al., 2009b). The
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histomorphometrical measurements are capable of showing biocompatibility, osseoconductivity, and the general tissue response of
implants, and the biomechanical tests measure the force or torque that is required to induce failure in the bond between the bone and
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implant surface (Recker, 1983). The objective of this paper is to provide a structural review of the techniques that can produce a CaP
coating that yields good in vivo results, and to compare these results to micro CaP–coated and uncoated titanium implants.
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Furthermore, this paper includes a systematic review of CaP coatings on titanium implants using histomorphometrical analysis and
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RTQ testing.
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MATERIAL AND METHODS
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To compare coatings with nano CaP particles with uncoated titanium implants, studies involving animal models as well as human
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subjects were included; however, studies that investigated implants with submicron coatings were excluded. Coatings were compared
based on the use of histomorphometrical analysis to obtain the percentage of bone-to-implant contact (BIC) and the use of RTQ values
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Six search engines were used, including PubMed, Web of Science, Directory of Open Access Journals, SAGE journals, the Wiley
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Online Library, and the Cochrane Library. A search of PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) using the MeSH terms “nano
hydroxyapatite” OR “nano calcium phosphate,” yielded 974 articles. A Web of Science (https://webofknowledge.com/) search with
TOPIC: (nano hydroxyapatite titanium), OR TOPIC: (nano hydroxyapatite coating), OR TOPIC: (nano calcium phosphate coating),
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OR TOPIC: (nano calcium phosphate titanium) yielded 1431 articles. In the Directory of Open Access Journals, a search using the
MeSH terms “nano hydroxyapatite” OR “nano calcium phosphate” generated 19 articles, whereas a search of SAGE premier 2011
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(http://online.sagepub.com/) using the search terms “nano hydroxyapatite” OR “nano calcium phosphate” returned 93 articles. A
search of the Wiley Online Library (http://onlinelibrary.wiley.com/) using the MeSH terms “nano hydroxyapatite titanium,” OR “nano
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hydroxyapatite coating,” OR “nano calcium phosphate coating,” OR “nano calcium phosphate titanium” in Full Text provided a total
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of 4389 articles. Finally, the Cochrane Library (http://www.cochranelibrary.com/) was searched using the MeSH terms “nano calcium
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phosphate” OR “nano hydroxyapatite,” which yielded 18 articles.
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After the completion of the database searches, the resulting abstracts were screened using the following inclusion criteria: animal or
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human studies containing data on BIC or RTQ testing for nano-coated cpTi (commercially pure titanium) or Ti6Al4V (titanium alloy)
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implants. If the abstract met the inclusion criteria, the full article was checked for compliance with the inclusion criteria. Additional
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articles identified in the reference lists of the articles meeting the inclusion criteria were likewise searched. Only articles written in
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English, German, French, or Dutch were included, and the article publication dates were restricted to before September 1, 2014.
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After verifying that the articles met the inclusion criteria, PubMed yielded 12 articles, Web of Science database returned 9 articles,
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SAGE premier produced 1 article, and the Wiley Online Library yielded 11 articles. No articles from Open Access Journals or the
Cochrane Database met the required inclusion criteria. After removal of duplicate articles, 18 articles remained. Another 6 articles
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were identified by manually searching the reference lists of the 18 articles that met the study inclusion criteria, which yielded a total of
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RESULTS
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NanoTite™
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Method
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The NanoTite™ coating technique is a colloidal sol-gel process. The procedure starts with the dipping of the samples in an alcohol-
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based solution containing CaP nanoparticles. After withdrawal of the substrate, the sample is dried at 100°C. The procedure is able to
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generate a discrete crystalline deposition (DCD) composed of nano-structured CaP particles that cover 50% of the surface with CaP
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nanocrystals, with the remaining surface covered by a TiO2 layer. The CaP particles have a nominal size of 20–100 nm and a
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A study compared titanium implants implanted in the posterior maxilla for an average of 8 weeks. (Orsini et al., 2007) Average BIC
values of nano HA coated implants was significantly higher than the BIC values of the control groups (Table 1). The results suggested
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that the coating of implants could shorten implant osseointegration time, which could be clinically advantageous for minimizing
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In another experiment involving human subjects, DAE implants were compared in the posterior maxillary bone with NanoTite™
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implants (Goene et al., 2007). The implants were harvested at 4 and 8 weeks after healing. Histomorphometrical analysis showed
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enhanced BIC at 4 and 8 weeks for NanoTite™ compared to OSSEOTITE®, which supported increased early osseointegration for
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Another group investigated the histomorphometrical healing properties of dual acid-etched mini-implant surfaces and implants coated
with nHA particles (Telleman et al., 2010). The study design entailed the fixation of iliac crest bone grafts onto maxillary bone with
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coated or uncoated DAE implants. Harvesting and analysis occurred after 3 months. Histomorphometrical measurements revealed
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higher BIC and bone area values for coated implants compared to uncoated DAE implants in the maxillary bone. The authors
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concluded that implants coated with nano HA particles improved the osseointegration in the maxillary bone only in comparison to
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DAE treated titanium implants. NanoTite™ did not improve healing properties at the graft area, which might be due to reduced
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The interfacial bonding strength of NanoTite™ coated cpTi and Ti6Al4V implants were compared with uncoated cpTi and Ti6Al4V
implants (Mendes et al., 2007). The mean RTQ indicated that uncoated cpTi and Ti6Al4V implants had significantly lower RTQ
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values than coated implants (Table 2). As well, the values of these 2 coatings was significantly higher for the Ti6Al4V coated
implants. The authors concluded that nHA deposits are able to promote bone bonding on cpTi and Ti6Al4V surfaces. They
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hypothesized that the increased nanosurface complexity induced the bone bonding process, and not so the CaP chemistry.
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The same group tested bone growth following the implantation of “ingrowth chambers” in the same animal model (Mendes et al.
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2009). Miniature bone ingrowth chambers were made of commercially pure titanium or titanium alloy that were dual acid etched
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(DAE) and coated by the NanoTite™ method, or only acid etched by a DAE method. Nine days after implantation, a statistically
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significant difference was detected between NanoTite™ coated implants, which had higher BIC values, compared to implants that
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were only acid-etched. No statistically significant difference was found between DCD CpTi and DCD titanium alloy Ti6Al4V implant
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chambers. The authors concluded that deposition of discrete CaP nanocrystals on a complex microtopography significantly enhanced
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osseointegration.
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In a separate study, dual acid-etched implants and implants coated by DCD nanoparticles were compared following insertion in fresh
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extraction sockets of beagle dogs. Harvesting was performed after 2, 4, and 8 weeks (Vignoletti et al., 2009). Higher numerical BIC
percentages were apparent at the early healing phases (2 and 4 weeks); however, no statistically significant differences were detected.
Further, because each group was composed of only 3 dogs, the sample size might have been too low to show any significant
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difference. Another study compared the BIC values of grit-blasted and acid-etched implants with grit-blasted, acid-etched, and
nanoscale HA surface-modified implants in canine premolar sockets (Al-Hamdan et al., 2011). Implantation was in perfectly sized
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implant beds, and in a non-submerged position. The authors observed increased BIC values for both implant groups during the
implantation time between 2 and 8 weeks. As well, the authors confirmed that both implant surfaces were able to induce
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osseointegration and to stimulate crestal bone formation. However, the authors were not able to determine whether nanoscale CaP
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coatings resulted in an increased bone response at 2, 4, and 8 weeks.
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Osseointegration was also evaluated in a canine mandibular model by histomorphometrical analysis of NanoTite™ implants versus
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DAE implants (de Barros et al., 2012). Insertion was performed in a no-gap model, as well as in a 1-mm, 1.5-mm, and a 2-mm gap
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model. After 8 weeks of healing, BIC values were not significantly higher for NanoTite™ coated implants, although the
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microroughened implants exhibited higher numerical values. The authors could not show any benefit of the DCD CaP coating.
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Additionally, a separate study examined bone healing to dual acid-etched implants with and without a nano CaP coating (Abrahamson
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et al., 2013). The BIC was significantly higher for the uncoated implants compared to nano CaP–coated implants at 2 and 4 weeks
after implantation. Hence, the authors theorized that the additional coating of dual acid-etched implants does not improve the early
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Method
The nHA promimic method is a technique that involves an aqueous solution composed of calcium, phosphor, and a surfactant. The
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solution is placed in an ammonia atmosphere to induce the formation of nano-sized crystals, after which the treated liquid is diluted
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with a hydrophobic organic solvent to obtain a solvent of nano-sized crystals in water. An oxide coated substrate is then immersed in
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the nanocrystal solvent. After removal from the solvent, the organic solvent and surfactant are removed from the surface coating
(Kjellin et Andersson. 2005). This technique has the capacity to produce a nano HA particle coating with dimensions ranging in width
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from 10 to 15 nm and in length from 100 to 200 nm (Jimbo et al., 2011b, Jimbo et al., 2012).
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In vivo animal experiments
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A comparison of the osseointegration of electropolished titanium implants and electropolished titanium implants modified using the
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nHA promimic method was conducted in an animal model (Meirelles et al., 2008b). Implants were fixed and stabilized by 2
corticomedullary screws. The results of the experiment indicated that nHA implants had significantly higher BIC values after 4 weeks
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compared to the uncoated implants. Surface roughness parameters revealed similar summit densities, whereas AFM showed increased
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average height deviation at the nanomolar level for the nHA coated implants. However, the difference measured by AFM might have
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been due to increased surface porosity (percentage) and the number of pores in nHA-coated implants. Implant surface modification
was also conducted to remove microstructures and prevent their interaction. Based on the information obtained, the authors concluded
that differences in osseointegration are only explained by differences in nanotopography and surface chemical composition.
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Another study employed a similar rabbit model as well as electropolished titanium implants and nHA coated titanium implants, but
involved implantation sites that were increased by a 0.35-mm radius to induce a gap healing model (Meirelles et al., 2008a).
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Electropolished implants showed higher values, but the differences were not statistically significant. These data did not support the
observations of the previous study. The authors hypothesized that the 0.35-mm gap design might have disrupted osseointegration, and
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that a more precise surgical fit was needed.
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In another experiment, the enhancement of osseointegration was evaluated using nHA coatings compared to a nano-titanium–covered
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surface (Meirelles et al., 2008d). The nano-titanium implants were coated with the MetAlvive method, which is a dip-coating
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technique that produces a coating layer composed of titanium particles that are 30 nm in diameter. The results indicated that nano-
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titanium–coated implants had a higher feature density and percentage of implant coverage (45%) compared to nHA, which covered
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only 23% of the implant surface. In addition, AFM images revealed that the nano-titanium particles had a higher average diameter
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compared to the nHA particles. The histomorphometrical analysis showed BIC values of 17% for nHA and 21% for nano-titanium–
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coated implants measured on the lateral wall, but the difference was not significant. At the apical region, BIC values were 19% for
nano-titanium–coated implants compared to 7% for nHA, which indicated a significant increase in osseointegration. However, the
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results in the nano-titanium implants might have been influenced by increased developed surface ratio (Sdr) values at the apical
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region. Similar differences were not detected at the lateral wall, and the values for bone area measurements were similar for both
coatings (48%). Hence, these results did not support the enhancement of bone formation by bioactive HA. The authors concluded that
the bone healing events in the study were dependent only on the nano feature size and distribution after a 4-week healing period.
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The results of a different study suggested that implants chemically modified with nHA would show enhanced osseointegration
compared to uncoated implants with similar microtopography (Meirelles et al., 2008c). The authors evaluated osseointegration in the
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proximal rabbit tibia after 4 weeks. OI microscopy revealed similar average height deviations for blasted implants (1.42 µm) and
nHA-coated implants (1.36 µm). At 4 weeks, a significantly higher BIC was observed for the nHA-coated implants compared to
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blasted implants. In addition, RTQ testing revealed similar values for nHA compared to titanium dioxide.
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A separate study involving a rabbit model evaluated bone apposition onto coated and uncoated heat treated pure titanium implants
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(Jimbo et al., 2011b). After 2 weeks of healing, the mean percentage of newly formed bone for the nHA coated implants was
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significantly higher. However, after 2 weeks of healing, the BIC values from uncoated implants seemed to reach a plateau. Therefore,
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the mean BIC value after 4 weeks of healing was in the uncoated implants, which was significantly lower than the BIC observed for
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nHa-coated implants. No significant differences in average height deviation or surface roughness were observed on the OI images.
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Early osseointegration in the rabbit tibia was likewise investigated using nHA-coated implants and sand-blasted, acid-etched, and
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heat-treated Ti6Al4V implants (Jimbo et al., 2012). The animals were euthanized after 3 weeks. No significant differences in BIC
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values were observed for the nHA-coated implants compared to the uncoated implants. However, nano-indentation testing revealed a
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significant difference between the uncoated and nHA implants. Consequently, the authors concluded that bone quality around the nHA
Another study compared implants in rabbit femurs at 12 weeks that were sand blasted and acid etched followed by either heat
treatment or coating with nHA particles using the nanoHA promimic method (Bryingtong et al., 2013). Interferometer characterization
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revealed significant differences in the arithmetic average height deviation from a mean plane with a smoother surface for the nHA-
coated implants (0.93 µm) relative to the controls (1.026 µm). All implants were stable at the time of implant retrieval. However, the
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heat treated implants exhibited improved BIC values compared to nHA-coated implants. Furthermore, the data indicated that after a
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healing period of 12 weeks, noncoated surfaces with increased microroughness had improved osseointegration compared to nHA
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coated surfaces. Hence, the authors concluded that nanocrystals deposited onto blasted and acid-etched titanium implants did not
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enhance the osseointegration after 12 weeks compared to the control implants. This could suggest that the microtopography is more
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important after longer healing periods, whereas the nHA coating has an higher impact on the early bone-healing period.
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Sol-gel method
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The methods used in these experiments were very similar to those used with NanoTite™. In the first experiment presented, the coating
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comprised nanoparticles between 25 and 35 nm, whereas the second experiment involved particles that were approximately 25 nm in
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One study compared bioresorbable screws, uncoated Ti6Al4V screws, and Ti6Al4V screws coated with nano HA or micro HA
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(Aksakal et al., 2014). The bioresorbable screws were composed of lactic acid and trimethylene carbonate. The screws were implanted
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in the tibial bone of sheep, and harvested after 8 weeks by axial pull-out testing. The highest fixation strength was achieved using
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nanoscale HA-coated screws, which was higher than microscale-coated implants and the uncoated implants. The authors concluded
that nHA coated screws provide good and stable retention during the bone healing process without inducing any adverse effects.
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Another experiment compared intramedullary nails that were uncoated or coated with nHA or microscale HA (mHA).(Varis et al.,
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2013). The titanium implants were placed endomedullary in a rabbit model for 45 days. The affiliated analyses revealed that the nHA
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and mHA group had a statistically higher tensile strength than implants in the control group. As well, the results of axial pull-out tests
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demonstrated statistically significant increases in tensile resistance in the mHA and nHA groups compared to the control group.
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Biomimetically deposited calcium phosphate coating (BCaP) and electrochemical deposited hydroxyapatite (EDHA) coatings were
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investigated and compared by a single experimental group, which explains the grouping of these 2 different coatings.
Method
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The biomimetically deposited CaP coating is produced in 2 steps. The implants are first soaked in a supersaturated calcium and
phosphate solution at a high salt concentration. Inhibitors of crystal growth are then added to aid heterogeneous nucleation. Implants
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are soaked for 24 hours and afterward soaked in another solution of supersaturated CaP solution with another composition of salts.
This technique yields a sharp crystal flake approximately 6 to 8 µm long and 100 nm thick composed of octacalcium phosphate, which
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covers the entire surface of the implant (Figure 2B).
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The electrochemical deposition of hydroxyapatite uses the implant as a working electrode, and a platinum plate as the counter
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electrode. The electrolyte solution contains calcium nitrate (Ca(NO3)2) and ammonium phosphate (NH4H2PO4) with a CaP ratio of
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1.67. A direct current induces the deposition of CaP nanocrystals onto the implant surface, and the process is completed within 2
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hours. The coating homogenously covers the entire surface with oriented and dense rod-like crystals 70–80 nm in diameter (Figure
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2C) (Guo-Li et al., 2009, Guo-Li et al., 2010)
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The interfacial biomechanical properties of biomimetically deposited CaP and electrochemically deposited nano HA coatings were
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compared with roughened implants (Figure 2A) (Guo-Li et al., 2009). IThe mean RTQ of the EDHA coated implants exhibited
significantly greater values at all healing periods compared with the roughened and biomimetically deposited calcium phosphate
coatings. The biomimetic deposition did not increase implant fixation compared to roughened implants. The authors concluded that
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EDHA coatings improve fixation between implant and bone compared to the roughened surface; however, biomimetic CaP coatings
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To assess osseous healing of biomimetically and electrochemically deposited nHA coatings, the same research group examined
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intracortical implants in the tibial bone of rabbits (Guo-Li et al., 2010). The animals were divided into 2 groups, the first of which was
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sacrificed at 6 weeks and the second at 12 weeks. Histomorphometrical measurements for electrochemically deposited nano HA
coatings showed significantly greater values at both healing periods compared to the BDCaP implants. No significant differences were
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found between BDCaP and roughened implants. At 6 weeks, EDHA implants showed significantly higher BIC values compared to
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roughened implants, but no changes were noted after a 12-week healing period. The results of the study indicated that the thinner
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EDHA coating is more favorable for bone integration, which could ensure long-term stable bony fixation of a porous implant.
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A separate study tested electrochemically deposited nano HA-coated implants in ovariectomized rats to assess osseointegration
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(Zhipeng et a., 2012). The animals were sacrificed after 12 weeks, and RTQ testing and histomorphometrical analysis were conducted.
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Mean surface roughness of the roughened titanium implants (control group) and of the HA-coated implants (experimental group) were
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1.185 and 1.167, respectively; however, no significant difference in mean surface roughness was found between the groups. The
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histomorphometrical results revealed significantly greater BIC and bone area percentages for nano HA–coated implants compared to
roughened implants by large corundum grit blasting. The authors also found significantly greater RTQ values for the nano HA–coated
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implants. Hence, the authors demonstrated that a thin nano HA coating is able to increase bone bonding strength and to improve
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Ion beam–assisted deposition
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In vivo animal experiments
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The performance of a nano-thick ion beam–assisted deposition (IBAD) coating was evaluated after 3 and 5 weeks in a canine model.
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Four different groups of alumina-blasted/acid-etched Ti6Al4V implants were compared, as well as uncoated implants (control group),
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and implants coated by either 1 of 2 IBAD setups or plasma sprayed HA (PSHA) (Coelho et al., 2009c). The difference between the 2
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IBAD coating techniques was the duration of coating procedure, which yielded a thickness of 30–50 nm for IBAD II and a submicron
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coating of 300–500 nm for IBAD I. As well, in vivo testing showed significantly higher torque-to-interface fracture values for PSHA
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and IBAD II. Higher BIC values were also found for the PSHA, IBAD I , and IBAD II coatings compared to the control group.
Therefore, the nanocoating yielded inferior results for bone anchorage compared to the micron and submicron coatings.
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The same group compared BIC percentages and bone anchorage of the proximal tibia in dogs using a rotational torque test (Coelho et
al., 2009a). The implant surfaces consisted of alumina-blasted and acid-etched Ti6Al4V implants, as well as the same implants
modified with an IBAD coating. The control group had higher RTQ values at 2 weeks and 4 weeks compared to the nano group. The
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resulting BIC values were similar at 2 weeks and 4 weeks for control and nano-coated implants. The results of the study indicated that
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Other techniques
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In the proximal tibial metaphysis and femur of rabbits, the BIC percentage and bone anchorage for CaP-coated implants and porous
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oxide surface coated implants were compared (Fontana et al., 2011). The coating procedure comprised of dip coating the implant in a
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solution of water, surfactant, and nano CaP particles. Afterward, the implants were dried and heat treated. The coating was comprised
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of nano CaP particles with a nominal size of 10 nm and a thickness of 200 nm, and both implant surfaces had a surface roughness of
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1.3 µm. After healing periods of 2, 4, and 9 weeks, no significant differences were found in BIC or RTQ values. Furthermore, the
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authors did not detect an improvement in interfacial strength or bone apposition with nano CaP coated implants, and even noted
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decreases during the 2- to 9-week healing period. In a separate study, grit-blasted/acid-etched surface Ti-implants were compared with
hydrothermally treated implants in the femoral condyles of rats (mJin-Woo et al., 2009). The CaP coating consisted of a 100 nm thick
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CaP layer, with the surface containing micron, submicron, and nano features. After 6 weeks, the harvested implants demonstrated
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significantly greater osseointegration with the CaP-coated implants compared to grit-blasted/acid-etched implants.
DISCUSSION
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It is known that microcoatings improve early fixation, increase BIC, and aid in the distribution of forces on the implant surface
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(Stellino et al., 2002). Clinical studies have established high implant survival rates; however, controversy exists regarding the clinical
benefit of PSHA-coated implants (McGlumphy et al., 2003). This is partly due to the coating adhesion strength, which is poor and may
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separate after long implantation periods. The loosened fragments subsequently dissolve in the surrounding tissue fluids and contribute
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to the breakdown of bone around the implant. Furthermore, there is a risk that coating mechanical properties diminish and result in
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fractures in the coating surface (Lacefield et al., 1998, Yang et al., 2005). For nanocoatings, the problem of a secondary interface can
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be avoided with total dissolution, which has been verified in multiple studies (Guo-Li et al. 2009, Guo-Li et al., 2010). Furthermore,
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the dissolution of nanocoatings occurs gradually due to contact with tissue fluids and osteoclastic breakdown. An added benefit is that
the nHA promimic and NanoTite™ coatings do not fully cover the surface. The NanoTite™ coatings are composed of small islands
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that prevent the occurrence of fractures, which is a great advantage compared to coatings with a microthickness, because coating
It has already been determined that nHA particles enhance osteoblast proliferation, adhesion, and calcium deposition (Guo et al.,
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2007). Additionally, previous studies have established that nano CaP coatings improve osseointegration in vivo. However, whether
this can be attributed to the chemical alteration or the nanotopography, or whether they act synergistically to improve biofunctionality,
is not known. Two studies investigated the importance of both factors. One study compared the nHA promimic method with nano-
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titanium. One group investigated chemically different coatings, but there were also dissimilarities in surface coverage and particle
size. (Mereilles et al., 2008c) Considering the smaller surface coverage of the nHA coating compared to nano-titanium coating, these
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findings could be biased. However, these data support the theory that the nano feature size and distribution improves tissue response.
The other study showed that CaP coatings improve osteogenic gene expression and enhance distinct biochemical responses in vivo,
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but there was a difference in chemical alteration as well as nanotopography (Jimbo et al., 2011a). It can be concluded that the
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nanotopography improves biofunctionality; however, it has not been established whether chemical alteration has a significant effect in
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vivo.
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Roughened implants improve biofunctionality and ensure higher bone anchorage as opposed to smooth implants. As well, roughened
implants have shown a higher success rate compared to smooth implants (Cochran, 1999). The optimal roughness parameters have
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been investigated in numerous studies, and they can be defined as an Sa of approximately 1.5 µm with an Sdr of 50%. The ideal
nanotopography has not yet been established in vivo, although it has been studied thoroughly in vitro, and has been shown to improve
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adhesion (Curtis and Wilkinson, 1997) The implant coatings used in prior research have different nanotopography and particle size,
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which is a likely explanation for the apparent dissimilarities in the reported results. Thus, future research should be performed in vivo
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Seven studies were identified that utilized the nHA promimic technique, all of which compared titanium implants with or without
nano HA modification. No clinical studies were identified. One study demonstrated that the nHA coating could improve
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osseointegration on smooth implants (Meirelles et al., 2008b). However, the improved biofunctionality did not correlate with a gap
model, which would suggest that the nHA coating is not capable of enhancing osseointegration in the absence of a tight fit (Meirelles
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et al., 2008a). Another study with similar microroughness reported no significant differences in BIC values; however, at 4 weeks, the
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BIC values were numerically higher than corresponding values in the control group (Jimbo et al., 2012). Additionally, the study
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demonstrated improved bone strength quality with a nano-indenter. A different study reported improved RTQ, whereas another
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showed similar results as well as improved BIC values (Meirelles et al., 2008c, Jimbo et al., 2011b). Moreover, these studies
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demonstrated improved osseointegration and higher fixation strength for nHA-coated implants on a smooth surface and on a
microroughened surface.
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One study comparing uncoated implants with a higher microroughness during a 12-week healing span showed lower BIC values for
the nano HA promimic–coated implants compared to sand-blasted and acid-etched implants (Bryingtong et al., 2013). The results
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indicate that microroughness has a higher impact on short-term periods compared to nanotopography, which has already been shown
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to be of great importance. The early enhancement of osseointegration is hypothesized to be due to dissolution of nano HA particles
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from the surface coating. Hence, the nano HA particles accounted for improved bone formation and supported the differentiation and
proliferation of osteoblast cells (Guo-Li et al., 2010). The microroughness has an important effect early and following longer healing
periods, when dissolution of nHA particles no longer occurs. These findings suggest that the nHA promimic coating technique is
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capable of improving osseointegration by altering the surface nanotopography and chemical composition. Therefore, this coating
assists in improving the micro-roughened implant fixation and shortens the required healing period. No long-term survival rates were
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reported, which indicates the need for testing in long-term clinical studies.
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Six animal and 3 human studies involving NanoTite™ implants were included. Two animal studies reported an increase in
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osseointegration and bone anchorage over a short-term healing period of 9 days (Mendes et al., 2007, Mendes et al., 2009). As well,
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numerically higher BIC values were noted in 1 animal study; however, it should be noted that the relatively small sample size might
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have negatively influenced the significance of this difference (Vignoletti et al., 2009). Two studies reported no improved
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osseointegration after a long-term healing period, 1 of which did not establish any enhancement of BIC at early implantation.
Furthermore, 1 study reported poor results for nHA-coated dual acid-etched implants, which exhibited significantly lower
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histomorphometrical results for the test implants. All 3 human studies demonstrated increased BIC values after 4 to 8 weeks of
implantation (Goene et al., 2007, Orsini et al., 2007, Telleman et al., 2010). These findings suggest improved osseointegration and
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bone anchorage for NanoTite™ implants compared to DAE implants. Furthermotr, 2 clinical studies published by the same group
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evaluated immediate loading implants coated with the NanoTite™ coating, and both studies demonstrated high survival rates within a
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1-year follow-up period. Moreover, they established that NanoTite™ implants are viable if the implants have an adequate primary
stability (Ostman et al., 2010, Ostman et al., 2013). Nonetheless, further research involving a longer implantation time is warranted to
Two animal studies involving different sol-gel coating techniques showed promising results, which is in accordance with the sol-gel
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method used for NanoTite™ implants but has yet to be confirmed in long-term clinical studies (Varis et al., 2013, Aksakal et al.,
2014). However, the histomorphometrical measurements of nHA IBAD coatings revealed inferior osseointegration results when
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compared to PSHA coated and submicron IBAD coated implants (Coelho et al., 2009c, Coelho et al., 2009a). We can conclude that
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the results of this type of nanocoating are inferior to those of submicron IBAD and PSHA coatings, and that the nHA IBAD coating
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does not improve osseointegration or fixation over short-term healing periods.
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Both studies involving BDCaP coatings failed to show an improvement in porous titanium implants with regard to osseointegration
and bone anchorage. (Guo-Li et al., 2009, Guo-Li et al., 2010). Moreover, the authors reported that the EDHA coating is a better
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coating in the short-term healing period. Consequently, these findings demonstrate the superiority of the EDHA coating compared to
the BDCaP coating for short-term healing periods. The findings can be attributed to the composition of the BDCaP coating, which is
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composed of octacalciumphosphate, which renders it more prone to dissolve in vivo compared to the HA in the EDHA coating
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(Kamakura et al., 2002). This difference in solubility is presumed to be partially responsible for the resulting variable bone formation.
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The dissolution of CaP is essential for ideal bone growth and strong anchorage during early implantation (Barrere et al., 2003). In
fact, it has been suggested that the ideal outcome is for dissolution to occur gradually and completely. This would imply that the
dissolution rate of the coating is similar to the formation of new bone, and that total resorption does not occur before completion of
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new bone formation. In addition, the total resorption ensures that no possible fractures can occur after long-term healing periods at the
interfacial bonding (Barrere et al., 2003). The dissolution rate of the BDCaP coating was higher than the corresponding rate for the
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EDHA coating, and total dissolution occurred before 2 weeks. Furthermore, improved osseointegration could also be attributed to the
surface chemistry or nanotopography of the HA coating compared to the CaP coating. It has already been established that nHA
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particles improve osteoblast proliferation, adhesion, and calcium deposition (Lacefield 1998, Wennerberg 1998). In fact, 1 of the
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studies demonstrated that bone failure appeared in the bone trabeculae for the EDHA-coated implants, whereas bone failure occurred
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at the interface between the implant and bone in the BDCaP-coated implants (Guo-Li et al., 2009). Based on all of these findings, we
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can conclude that BDCaP-coated implants produce inferior bone anchorage and integration compared to the EDHA-coated implants.
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These results are in accordance with the findings of a different study that evaluated titanium implants dip coated with nHA, and
reported no difference in implant fixation or osseointegration within a short healing period. Likewise, the lack of biofunctionality can
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be attributed to the faster dissolution of the CaP produced by this coating technique (Fontana et al., 2011).
The limitations of the current study are that the majority of the prior studies that were included investigated implants over a short
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healing period (i.e., between 2 and 12 weeks), and involved relatively small sample sizes, which might have introduced a bias. As
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well, because the 24 studies that were included consisted of different animal models and different implant designs, the data cannot be
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compared. We can only report the coatings that improved biofunctionality, and the evidence on which our findings are based. It should
be noted that the results of numerous studies were not significant, which could be due to the small sample sizes. It is likewise
important to note that the animal studies were based on study models for dental or orthopedic implants. Furthermore, although the
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human and clinical studies involved the maxillary and mandibular alveolar bone, it is not definite that the findings correlate with
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CONCLUSION
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Many prior studies have demonstrated that nano-CaP coatings improve biocompatibility and implant fixation; however, not all nano-
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CaP coatings yield the same results. It has been established that the IBAD technique, dip-coating, and BDCaP coatings revealed no
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enhancement on roughened implants. However, the nHA promimic coating has exhibited good results in vivo and in human studies
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involving early and intermediate healing periods. As well, the NanoTite™ coating demonstrated good results in vivo, as well as in
clinical studies within a 1-year follow-up period. Two different sol-gel methods and a hydrothermal treatment have shown favorable
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results in early healing periods. These coatings do not appear to exhibit the problems encountered with conventional mHA coatings,
and seem to improve the biofunctionality of the implant. The effect of these added coatings is the ability to minimize the problems of
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slow osseointegration and implantation failure. The different techniques produce coatings with varying thickness, nanotopography,
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particle size, and solubility, which all influence the reaction of bone. At present, the best coating surface is not known. Based on the
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current data, the NanoTite™ and nHA promimic coatings yield the most promising results. However, future research should involve a
randomized controlled clinical trial to investigate the coating that yields the best results.
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Conflict of interest
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The authors have no financial interest regarding the content of this article.
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Zhipeng C, Caihong G, Wenjing D, Fu-ming H, Shi-fang H, Gui-Li H: Effect of thin nano-hydroxyapatite coating on implant
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Figure 1. PRISMA diagram: selection procedure of the articles included in the review.
Figure 2. (A) Roughened group; (B) BDCaP-coated surface; (C) EDHA coated surface (Guo-Li
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et al., 2009).
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Number G
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Anatomical Implantation of si
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Orsini et Posterior
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al., 2007 maxilla Ti6Al4V Dual acid etched 8 wk 16 0
CaP particles
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Dual etched and DCD 20-100nm in
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coating size 8 wk 16 0
Goene et Posterior
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al., 2007 maxilla Ti6Al4V Dual acid etched 4 wk 3 0
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CaP particles
coating size 4 wk 3 0
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Posterior
CaP particles
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coating size 8 wk 5 0
Telleman Posterior
2010
CaP particles
coating size 12 wk 15 0
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Implantation period, duration between implantation and harvesting of implant; Number of
implants, number of implants in that group that were implanted; Gap size, difference in diameter
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between implant and implantation bed; BIC, bone implant contact of implant after harvesting; P
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value, P value between bone–implant contact values of implant group and implant group of the
row below. AN
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Table 2. Animal study data
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Anatomical Implantation
Aksakal et
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Al-
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Hamdan et Premolar Grit blasted and acid
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al.,2011 Beagle dogs sockets Ti6Al4V etched 2w
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coating 20-100 nm 2w
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Beagle dogs sockets Ti6Al4V etched 4w
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coating 20-100 nm 4w
coating 20-100 nm 8w
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de Barros Premolar
coating 20-100 nm 8w
Premolar
coating 20-100 nm
Premolar
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coating 20-100 nm 8w
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Premolar
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Dual etched and DCD CaP particles
coating 20-100 nm 8w
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Bryingtong Swedish lop- Sand blasted, acid etched,
particles: 10-
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Alumina blastting/acid
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Alumina blasting/acid
Alumina blasting/acid
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Alumina blasting/acid
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etched and ion beam– HA 300-500
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Alumina blasting/acid
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assisted deposition I nm thick 3w
AN Alumina blasting/acid
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etched and ion beam– HA 300-500
Aluminum blasting/acid
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Commercialy available
plasma sprayed
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Alumina blastting/acid
Plasma sprayed
hydroxyapatite coating
Aluminum blasting/acid
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assisted deposition I nm thick 5w
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Coelho et Alumina blasting/acid
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Aluminum blasting/acid
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assisted deposition I nm thick 2w
AN Aluminum blasting/acid
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Beagle dogs Tibia Ti6Al4V etched 4w
Aluminum blasting/acid
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Aluminum blasting/acid
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Aluminum blasting/acid
C
Aluminum blasting/acid
assisted deposition I
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<200 nm
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thick, HA
particles 10
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Ca-P–coated implant nm in
surface diameter 2w
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New Zealand Titanium porous oxide
thick, HA
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particles 10
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surface diameter 4w
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<200 nm
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thick, HA
particles 10
Ca-P–coated implant nm in
surface diameter 9w
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<200 nm
thick, HA
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particles 10
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Ca-P–coated implant nm in
surface diameter 2w
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New Zealand Titanium porous oxide
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<200 nm
AN thick, HA
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particles 10
Ca-P–coated implant nm in
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surface diameter 4w
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<200 nm
thick, HA
C
particles 10
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Ca-P–coated implant nm in
surface diameter 9w
<200 nm
thick, HA
particles
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Ca-P–coated implant 10nm
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surface diameter 2w
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New Zealand Titanium porous oxide
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<200 nm
AN thick, HA
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particles 10
Ca-P–coated implant nm in
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surface diameter 4w
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<200 nm
C
thick, HA
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particles 10
Ca-P–coated implant nm in
surface diameter 9w
100-nm thick
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CaP CaP 6w
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Polished, sandblasted, and
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100 nm thick
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biomimetical deposited 6-8 µm long
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Polished, sandblasted, and
deposited HA 80 nm HA 6w
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deposited HA 80 nm HA 12w
CaP
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deposited HA 80 nm HA 6w
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100-nm thick
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biomimetical deposited 6-8 µm long
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Roughened and Crystals with
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deposited HA 80 nm HA 12w
100-nm thick
CaP CaP 2w
C
CaP
100-nm thick
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Roughened and crystal flake
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biomimetical deposited 6-8 µm long
CaP CaP 8w
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Polished, sandblasted, and
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Roughened and Crystals with
AN electrochemically diameter 70-
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deposited HA 80 nm HA 2w
deposited HA 80 nm HA 4w
deposited HA 80 nm HA 8w
CaP
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electrochemically diameter 70-
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deposited HA 80 nm HA 2w
100-nm thick
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Roughened and crystal flake
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White rabbits Femur Titanium CaP CaP 4w
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electrochemically diameter 70-
deposited HA 80 nm HA 4w
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100-nm thick
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deposited HA 80 nm HA 8w
particles: 10-
15 nm wide
and 100-200
nm long
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Swedish lop-
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eared rabbits Femur cpTi No modification 4w
nHA
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particles: 10-
15 nm wide
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and 100-200
AN nHA promimic method nm long 4w
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Jimbo et Swedish lop-
nHA
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particles: 10-
treatment nm long 3w
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treatment dimensions 6w
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Meirelles
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promimic method particles 4w
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Meirelles
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2008a rabbits Tibia cpTi Electropolished 4w
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promimic method particles 4w
Meirelles
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et al., New Zealand Grit blasting and titanium 24-nm nano-
Meirelles
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nHA
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Mendes et
coating 20-100 nm
Mendes et
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coating 20-100 nm 9d
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Varis et New Zealand
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nHA
particles 25
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sol gel method nHA nm 6w
AN mHA
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New Zealand particles 25
nHA
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particles 25
Vignoletti Premolar
coating 20-100 nm 2w
Premolar
coating 20-100 nm
Premolar
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coating 20-100 nm 8w
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Zhipeng et Ovariectomized
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Rodlike
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coated not shown 12w
Ovariectomized
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rats Tibia Titanium Roughened 12w
Rodlike
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implants, number of implants in that group that were implanted; Gap size, difference in diameter
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between implant and implantation bed, given in millimeters; RTQ, removal torque values in
newton centimeters and standard deviation if known; BIC, bone implant contact of implant after
harvesting in percentage and standard deviation if known; P value, P value between bone–
implant contact or removal torque values of implant group and implant group of row below.
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*Some data are repeated due to the statistical comparison of the implant group with the implant
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