Purpose: The influence of the osteotome technique on the interface reaction of cylinder implants (SLA, ITI) was compared with the interface reaction of conventional implant insertion in an animal model.
Material And Methods: A total of 64 implants were placed in the cranial and caudal tibia of 8 Göttinger minipigs. The implant site was prepared either by a conventional technique with drills (control group A) or by the osteotome technique (experimental group B). Bone tissue responses were evaluated by histomorphometry, fluorescence microscopy and scanning electron microscopy after 7 and 28 days of osseointegration.
Results: The average initial (7 days) bone-to-implant contact ratio was not statistically significantly different for the osteotome technique (35.88+/-2.94%) than for the control group (43.78+/-3.39%, P<0.095). After 28 days, the bone-to-implant contact ratio became statistically significantly higher when implants were inserted by conventional preparation (44.81+/-3.07% (group B), 63.47+/-4.87% (group A), P=0.003). Whereas fluorescence and immunhistologic examination revealed new bone formation with osteocalcin deposition directly at the implant surface in both groups, the extent of direct bone/implant contact was enhanced in conventionally prepared implant sites. SEM analysis confirmed an intimate bone to implant bond without fibrous tissue formation in places of direct contact at an ultrastructured level.
Conclusion: Implant placement in conventionally prepared implantation sites is accompanied by an improved interface formation at an early stage of implantation.
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http://dx.doi.org/10.1111/j.1600-0501.2005.01111.x | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Hydrogen Fuel Cell Laboratory, Korea Institute of Energy Research (KIER), 152 Gajeong-ro, Yuseong-gu, Daejeon 34129, Korea.
Cation interdiffusion as a result of a chemical-potential gradient occurring at heterointerfaces is often regarded as an unfavorable side reaction and is typically suppressed through the use of a diffusion barrier layer. In this study, we propose a straightforward method for suppressing interdiffusion that involves the creation of nanometer-thick diffusion barrier layers by means of dopant segregation. Using the CeO/ZrO heterointerface in this study, we demonstrate that a Sc acceptor dopant tends to accumulate at the heterointerface during the sintering process, especially at the edge of the CeO grain boundary, thereby effectively suppressing Ce-Zr interdiffusion.
View Article and Find Full Text PDFAdv Colloid Interface Sci
January 2025
Department of Biological Science and Technology, China Medical University, Taiwan. Electronic address:
Among the many types of surface modifications on porous silicon (pSi), hydrosilylation stands out to be an important approach due to the formation of highly stable surface linkage through Si-C bonding. Since its conceptualization in 1998, hydrosilylation had gradually gained popularity for pSi surface modifications and had become an important approach for stabilizing pSi surfaces especially for biological applications. Over the past decade, significant advancements have been made in the hydrosilylation process for modifying porous silicon (pSi) surfaces.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Department of Chemistry & Institute for Sustainable Energy, College of Sciences, Shanghai University, Shanghai 200444, PR China. Electronic address:
Heteroatom doping into the transition metal-based catalysts is an effective strategy to improve the oxygen reduction reaction (ORR) kinetics. Herein, we proposed a one-step, soft template assisted, and green method for the synthesis of Sulfur (S) doped single atom FeNC catalyst. XAFS demonstrated that the Fe active sites in the FeNSC were more likely to possess the Fe-N configuration.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, School of Chemistry and Materials Science, Heilongjiang University, Harbin 150080, PR China. Electronic address:
Photocatalytic reduction of CO to valuable chemicals is an effective strategy to address the environmental problems and energy crisis. Covalent organic frameworks (COFs) are emerging materials known for their excellent diverse properties, albeit limited by special synthetic methods, including high temperature (120 °C) and the necessity of inert gas atmosphere. Herein, a novel synthesis method under room temperature and air was optimized to form TpPa-COF (TP-COF) by p-phenylenediamine (Pa) and 2,4,6-triformyl phloroglucinol (Tp) through electrostatic self-assembly.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Resources and Environmental Engineering, Wuhan University of Science and Technology, Wuhan 430081 China.
Metal-organic frameworks (MOFs) derived materials are extensively utilized in wastewater treatment owing to their remarkable catalytic efficacy and durability. This study exploited iron-cerium-based bimetallic metal-organic framework (FeCe-MOF) as a sacrificial template, which was subsequently calcined at 700 °C to produce an iron-cerium-based bimetallic carbon nanospheres (FeCe@C). The FeCe@C has active sites of bimetallic Fe and Ce derivatives, demonstrating exceptional activation efficiency for persulfate, resulting in approximately 98.
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