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Sökning: WFRF:(Wennerberg Ann 1955 )

  • Resultat 81-90 av 137
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81.
  • Meirelles, Luiz, 1974, et al. (författare)
  • A novel technique for tailored surface modification of dental implants - a step wise approach based on plasma immersion ion implantation.
  • 2013
  • Ingår i: Clinical oral implants research. - : Wiley. - 1600-0501 .- 0905-7161. ; 24:4, s. 461-467
  • Tidskriftsartikel (refereegranskat)abstract
    • OBJECTIVES: A novel technique based on plasma immersion ion implantation (PIII) is presented to modify titanium implant surfaces. MATERIALS AND METHODS: Initially, the implants are cleaned with argon to remove contaminants and the nanostructures are created by the bombardment of the surface with a mix of noble gases. Desired crystal structure of the titanium is obtained by the implantation of oxygen on the contaminant-free surface with particular nanostructures. RESULTS: In this study, turned implants modified by PIII revealed a high density of rutile-TiO(2) nanostructures. Turned implants used as control revealed mainly microstructures and amorphous crystal structure. Surface roughness values were similar at the microscale for both turned and turned + PIII implants. Bone response was evaluated by removal torque tests of implants placed in the rabbit tibia and femur. After 4 weeks of healing, turned + PIII demonstrated higher removal torque values (P = 0.001) compared to turned implants. CONCLUSIONS: The presence of rutile-TiO(2) nanostructures may explain the improved bone formation to turned + PIII implants.
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82.
  • Meirelles, Luiz, 1974, et al. (författare)
  • Bone reaction to nano hydroxyapatite modified titanium implants placed in a gap-healing model
  • 2008
  • Ingår i: Journal Biomedical MAterials Research - A. - : Wiley. - 1549-3296 .- 1552-4965. ; 87:3, s. 624-631
  • Tidskriftsartikel (refereegranskat)abstract
    • Nanohydroxyapatite materials show similar chemistry to the bone apatite and depending on the underlying topography and the method of preparation, the nanohydroxyapatite may simulate the specific arrangement of the crystals in bone. Hydroxyapatite (HA) and other CaP materials have been indicated in cases in which the optimal surgical fit is not achievable during surgery, and the HA surface properties may enhance bone filling of the defect area. In this study, very smooth electropolished titanium implants were used as substrata for nano-HA surface modification and as control. One of each implant (control and nano HA) was placed in the rabbit tibia in a surgical site 0.7 mm wider than the implant diameter, resulting in a gap of 0.35 mm on each implant side. Implant stability was ensured by a fixating plate fastened with two side screws. Topographical evaluation performed with an optical interferometer revealed the absence of microstructures on both implants and higher resolution evaluation with AFM showed similar nanoroughness parameters. Surface pores detected on the AFM measurements had similar diameter, depth, and surface porosity (%). Histological evaluation demonstrated similar bone formation for the nano HA and electropolished implants after 4 weeks of healing. These results do not support that nano-HA chemistry and nanotopography will enhance bone formation when placed in a gap-healing model. The very smooth surface may have prevented optimal activity of the material and future studies may evaluate the synergic effects of the surface chemistry, micro, and nanotopography, establishing the optimal parameters for each of them.
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83.
  • Meirelles, Luiz, 1974, et al. (författare)
  • Effect of hydroxyapatite and titania nanostructures on early in vivo bone response
  • 2008
  • Ingår i: Clinical Implant Dentistry and Related Research. - : Wiley. - 1708-8208 .- 1523-0899. ; 10:4, s. 245-254
  • Tidskriftsartikel (refereegranskat)abstract
    • Objective: Hydroxyapatite or titania nano structures were applied on smooth titanium implant cylinders. The aim was to investigate whether nano HA may result in enhanced osseointegration compared to nano titania structures. Material and Methods: Surface topography evaluation included detailed characterization of nano size structures present at the implant surface combined with surface roughness parameters at the micro- and nano- meter level of resolution. Microstructures were removed from the surface to ensure that bone response observed was dependent only on the nanotopography and/or chemistry of the surface. Early in vivo bone response (4 weeks) evaluation was investigated in a rabbit model. Results: In the present study, nano titania coated implants showed an increased coverage area and feature density, forming a homogenous layer compared to nano HA implants. Bone response observed at 4 weeks could not be explained by the surface chemistry. New formed bone connected to the original cortical bone demonstrated an increase of 24% for the nano titania compared to the nano HA implant, although the difference was not statistically significant. Conclusion: Thus, no evidence of enhanced bone formation to nano hydroxyapatite modified implants was observed compared to nano titania modified implants. The presence of specific nano structures; dependent on the surface modification exhibiting different size and distribution did modulate in vivo bone response.
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84.
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85.
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86.
  • Meirelles, Luiz, 1974, et al. (författare)
  • Increased bone formation to unstable nano rough implants
  • 2007
  • Ingår i: Clin Oral Implants Res. - : Wiley. - 0905-7161. ; 18:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Early bone response to cylindrical smooth titanium implants (S(a)=0.1 microm) inserted into the rabbit tibia was compared in a stable and nonstable regime. Surface roughness parameters were calculated from measurements obtained with optical interferometry and atomic force microscopy. Contrary to our hypothesis, the nonstable implant showed higher bone to metal contact and increased bone area in the endosteal region compared with the stable implant after 4 weeks of healing. Bone area measurements in the cortical region revealed similar values. Primitive woven bone was found in close contact with both implants, but significantly more with the nonstable implant. Finding more bone-to-implant contact (BIC) need not necessarily indicate that unstable implants were more strongly integrated. Primitive bone stage development observed indicates less strong implant anchorage than could be expected from BIC percentage alone. Stable implant design used in this study is a reliable model to evaluate submicron and nanostructures in vivo, as implant stability was achieved in the absence of microirregularaties.
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87.
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88.
  • Meirelles, Luiz, 1974, et al. (författare)
  • Nano hydroxyapatite structures influence early bone formation
  • 2008
  • Ingår i: Journal Biomedical Materials Research - A. - : Wiley. - 1549-3296 .- 1552-4965. ; 87:2, s. 299-307
  • Tidskriftsartikel (refereegranskat)abstract
    • In a study model that aims to evaluate the effect of nanotopography on bone formation, micrometer structures known to alter bone formation, should be removed. Electropolished titanium implants were prepared to obtain a surface topography in the absence of micro structures, thereafter the implants were divided in two groups. The test group was modified with nanosize hydroxyapatite particles; the other group was left uncoated and served as control for the experiment. Topographical evaluation demonstrated increased nanoroughness parameters for the nano-HA implant and higher surface porosity compared to the control implant. The detected features had increased size and diameter equivalent to the nano-HA crystals present in the solution and the relative frequency of the feature size and diameter was very similar. Furthermore, feature density per m2 showed a decrease of 13.5% on the nano-HA implant. Chemical characterization revealed calcium and phosphorous ions on the modified implants, whereas the control implants consisted of pure titanium oxide. Histological evaluation demonstrated significantly increased bone formation to the coated (p < 0.05) compared to uncoated implants after 4 weeks of healing. These findings indicate for the first time that early bone formation is dependent on the nanosize hydroxyapatite features, but we are unaware if we see an isolated effect of the chemistry or of the nanotopography or a combination of both.
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89.
  • Meirelles, Luiz, 1974, et al. (författare)
  • The effect of chemical and nano topographical modifications on early stage of osseointegration
  • 2008
  • Ingår i: The International Journal of Oral & Maxillofacial Implants. - 0882-2786. ; 23:4, s. 641-7
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose: To investigate the effect of chemically modified implants with similar micro but different nano topography on early stage of osseointegration. Materials and Methods: Screw shaped implants were placed in the flat proximal medial tibial methaphyses of 10 New Zealand white rabbits. Blasted (control); blasted-fluoride and blasted-nano HA implants were investigated. Surface evaluation included chemical analyses with x-ray photoelectron spectroscopy, morphological analyses with scanning electron microscopy and topographical analyses with interferometry. Bone response was investigated with removal torque measurements and histological analyses after a healing period of 4 weeks. Results: Chemical analyses revealed the presence of Ti, O, C and N in all implant groups. The blasted-F group revealed F and the blasted nano HA group Ca and P with simultaneous decrease of Ti and O. Surface roughness parameters showed a slight decrease of the average height deviation for the blasted nano-HA and blasted-F compared to the blasted control implants. SEM images at high magnification indicated the presence of nano structures on the chemically modified implants. Removal torque (RTQ) mean values revealed an increase of 17% to 25% for the chemically modified implants compared to the control implants and the histological analyses demonstrated a similar enhanced bone formation to the chemically modified implants with nanostructures. Conclusion: Chemical modifications used in the present study were capable of producing a unique nano topography and together with the ions present at the implant surface may explain the increased RTQ and histomorphometric values after a healing period of 4 weeks.
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90.
  • Milleret, V., et al. (författare)
  • Rational design and in vitro characterization of novel dental implant and abutment surfaces for balancing clinical and biological needs
  • 2019
  • Ingår i: Clinical Implant Dentistry and Related Research. - : Wiley. - 1523-0899 .- 1708-8208. ; 21, s. 15-24
  • Tidskriftsartikel (refereegranskat)abstract
    • Background Long-term success and patient satisfaction of dental implant systems can only be achieved by fulfilling clinical as well as biological needs related to maintenance, aesthetics, soft tissue sealing, and osseointegration, among others. Surface properties largely contribute to the biological and clinical performance of implants and abutments. Purpose To decipher the clinical and biological needs in implant dentistry. To address identified needs, next-generation dental implant and abutment surfaces are designed and characterized in vitro. Materials and Methods Novel implant and abutment surface designs were produced and characterized using surface chemical analysis, surface topography analysis, scanning electron microscopy, contact-angle measurements, and cell-culture experiments. Results The novel anodized implant surface was gradually anodized, increasing the surface roughness, surface enlargement, and oxide-layer thickness from platform to apex. The surface was phosphorus enriched, nonporous, and nanostructured at the collar, and showed micropores elsewhere. The novel anodized abutment surface was smooth, nanostructured, nonporous, and yellow. Pristine surfaces with high density of hydroxyl-groups were protected during storage using a removable cell-friendly layer that allowed dry packaging. Conclusions A novel anodized implant system was developed with surface chemistry, topography, nanostructure, color, and surface energy designed to balance the clinical and biological needs at every tissue level.
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