Phosphate Ceramics (phosphate + ceramics)

Distribution by Scientific Domains

Kinds of Phosphate Ceramics

  • calcium phosphate ceramics


  • Selected Abstracts


    3D Powder Printing of ,-Tricalcium Phosphate Ceramics Using Different Strategies,

    ADVANCED ENGINEERING MATERIALS, Issue 12 2008
    E. Vorndran
    Custom made macroporous ,-tricalcium phosphate (,-TCP) bone substitutes were fabricated using 3D powder printing comparing three different preparation strategies. Samples fabricated using a novel hydraulic cement setting reaction showed the best printing resolution and highest mechanical performance. This method is a significant step forward in producing ,-TCP monoliths by rapid prototyping and would decrease processing time for commercial fabrication due to their rapid hardening and ease of handling. [source]


    Chemically Bonded Phosphate Ceramics: I, A Dissolution Model of Formation

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2003
    Arun S. Wagh
    This is the first of three papers in which the kinetics of formation of chemically bonded phosphate ceramics is discussed. A literature survey indicates that the formation of such ceramics is a three-step process. First, oxides dissolve in a phosphoric acid or an acid phosphate solution and metal ions are released into the solution. The aquoions formed from these cations then react with phosphate anions and form a gel of metal hydrophosphates. In the last step, the saturated gel crystallizes into a ceramic. In this paper, we have proposed that the dissolution is the controlling step and developed a general dissolution model of the kinetics of formation of these ceramics. As an example, the model is used to discuss the kinetics of formation of magnesium phosphate ceramics in detail. In the second and third papers, the model has been used to develop processes to form ceramics of alumina and iron oxides. [source]


    Chemically Bonded Phosphate Ceramics: II, Warm-Temperature Process for Alumina Ceramics

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2003
    Arun S. Wagh
    This is the second of three papers on a dissolution model that describes the formation of chemically bonded phosphate ceramics. In this paper, we discuss the kinetics of formation of aluminum phosphate ceramics between 100° and 150°C. Using basic thermodynamic formulations, we calculated the temperatures of maximum solubility of alumina and its hydrated phases and predicted the temperatures of formation of ceramics. Differential thermal and X-ray diffraction analyses on samples made in the laboratory confirm these temperatures. The resulting ceramics of alumina bonded with aluminum phosphate (berlinite) show a high compressive strength of 16 000 psi. We have concluded that rapid evaporation of excess water in the slurry generates porosity in the ceramics, and that better processing methods are needed. A consolidation model is presented that describes the microstructure of the ceramic. It predicts that a very small amount of alumina must be converted to form the bonding phase; hence, the product is mostly alumina with a thin coating of berlinite on the surface of alumina particles. [source]


    Calcium phosphate-based coatings on titanium and its alloys

    JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008
    R. Narayanan
    Abstract Use of titanium as biomaterial is possible because of its very favorable biocompatibility with living tissue. Titanium implants having calcium phosphate coatings on their surface show good fixation to the bone. This review covers briefly the requirements of typical biomaterials and narrowly focuses on the works on titanium. Calcium phosphate ceramics for use in implants are introduced and various methods of producing calcium phosphate coating on titanium substrates are elaborated. Advantages and disadvantages of each type of coating from the view point of process simplicity, cost-effectiveness, stability of the coatings, coating integration with the bone, cell behavior, and so forth are highlighted. Taking into account all these factors, the efficient method(s) of producing these coatings are indicated finally. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source]


    Chemically Bonded Phosphate Ceramics: I, A Dissolution Model of Formation

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2003
    Arun S. Wagh
    This is the first of three papers in which the kinetics of formation of chemically bonded phosphate ceramics is discussed. A literature survey indicates that the formation of such ceramics is a three-step process. First, oxides dissolve in a phosphoric acid or an acid phosphate solution and metal ions are released into the solution. The aquoions formed from these cations then react with phosphate anions and form a gel of metal hydrophosphates. In the last step, the saturated gel crystallizes into a ceramic. In this paper, we have proposed that the dissolution is the controlling step and developed a general dissolution model of the kinetics of formation of these ceramics. As an example, the model is used to discuss the kinetics of formation of magnesium phosphate ceramics in detail. In the second and third papers, the model has been used to develop processes to form ceramics of alumina and iron oxides. [source]


    Chemically Bonded Phosphate Ceramics: II, Warm-Temperature Process for Alumina Ceramics

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2003
    Arun S. Wagh
    This is the second of three papers on a dissolution model that describes the formation of chemically bonded phosphate ceramics. In this paper, we discuss the kinetics of formation of aluminum phosphate ceramics between 100° and 150°C. Using basic thermodynamic formulations, we calculated the temperatures of maximum solubility of alumina and its hydrated phases and predicted the temperatures of formation of ceramics. Differential thermal and X-ray diffraction analyses on samples made in the laboratory confirm these temperatures. The resulting ceramics of alumina bonded with aluminum phosphate (berlinite) show a high compressive strength of 16 000 psi. We have concluded that rapid evaporation of excess water in the slurry generates porosity in the ceramics, and that better processing methods are needed. A consolidation model is presented that describes the microstructure of the ceramic. It predicts that a very small amount of alumina must be converted to form the bonding phase; hence, the product is mostly alumina with a thin coating of berlinite on the surface of alumina particles. [source]


    In Vivo Osteogenic Capability of Human Mesenchymal Cells Cultured on Hydroxyapatite and on ,-Tricalcium Phosphate

    ARTIFICIAL ORGANS, Issue 6 2009
    Asako Matsushima
    Abstract The aim of the current study was to examine in vitro osteogenic capability and in vivo bone formation of mesenchymal stromal cells (MSCs) on two kinds of calcium phosphate ceramics. MSCs derived from human bone marrow were seeded on either hydroxyapatite (HA) ceramic or ,-tricalcium phosphate (,-TCP) ceramic and then cultured in a medium supplemented with a donor's serum, vitamin C, ,-glycerophosphate, and dexamethasone. The culture revealed the expression of alkaline phosphatase activity, indicating the osteogenic differentiation of the MSCs on the ceramics (fabrication of tissue-engineered construct). The constructs were then implanted subcutaneously into nude rats for 8 weeks. New bone formation was observed in both types of ceramics, and human-specific Alu sequence was detected by in situ hybridization analysis. Quantitative microcomputed tomography showed that the volume of the new bone in the HA ceramic was greater than that in the ,-TCP ceramic in six of seven cases. These results suggest that human MSCs cultured on ceramics could retain their osteogenic capability even after ectopic implantation and provide a rationale for the use of tissue-engineered constructs derived from a patient's MSCs and calcium phosphate ceramics in bone tissue regeneration. [source]


    Healing of rabbit calvarial bone defects using biphasic calcium phosphate ceramics made of submicron-sized grains with a hierarchical pore structure

    CLINICAL ORAL IMPLANTS RESEARCH, Issue 3 2010
    Jin-Woo Park
    Abstract Objectives: This study investigated the efficacy of new bone graft substitutes , biphasic calcium phosphates (BCP) made of submicron-sized grains with fully interconnected wide-range micron-scale pores in two different macrodesigns: donut shaped with a 300,400 ,m central macropore (n-BCP-1) or rod-shaped (n-BCP-2) , in the healing of rabbit calvarial defects, and compared their bone-healing properties with those of various commercial bone substitutes, which included substitutes with similar BCP composition (MBCP and Osteon), anorganic bovine bone (Bio-Oss), and ,-TCP (Cerasorb). Material and methods: The surface morphology of the bone substitutes was investigated using scanning electron microscopy (SEM). Defects 8 mm in diameter were created in the calvaria of 30 adult male New Zealand White rabbits and were filled with six types of bone substitutes. The percentage of newly formed bone (NB%) was evaluated histomorphometrically 4 and 8 weeks after implantation. Results: SEM observation showed submicron-sized grains with fully interconnected micropore structures in the n-BCP-1 and n-BCP-2 groups; these groups also showed considerable new bone formation in inner micropores as well as on the outer surfaces. The n-BCP-1 group exhibited enhanced new bone formation and direct ingrowth of bone tissue with blood vessels into central pores. Histomorphometric analysis showed significantly greater NB% in the n-BCP-1 group when compared with the other groups at 4 and 8 weeks (P<0.05). Conclusion: A new BCP ceramics made of submicron-sized grains with a hierarchical pore structure was an effective osteoconductive material for the treatment of osseous defects of rabbit calvaria. To cite this article: Park J-W, Kim E-S, Jang J-H, Suh J-Y, Park K-B, Hanawa T. Healing of rabbit calvarial bone defects using biphasic calcium phosphate ceramics made of submicron-sized grains with a hierarchical pore structure. Clin. Oral Impl. Res. 21, 2010; 268,276. doi: 10.1111/j.1600-0501.2009.01846.x [source]