Relevant bibliographies by topics / Phosphate ceramics

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Phosphate ceramics'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "Phosphate ceramics"

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Kazakova, G. K., T. V. Safronova, and T. B. Shatalova. "Ceramics based on powders synthesized from ammonium hydrophosphate and acetates of calcium and magnesium." Materials Science, no. 4 (April 20, 2021): 33–40. http://dx.doi.org/10.31044/1684-579x-2021-0-04-33-40.

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Ceramics the phase composition of which included tricalcium phosphate, calcium magnesium ortophosphate and magnesium pyrophosphate has been produced from nanosized powders synthesized by chemical deposition from 1M aqueous solutions of ammonium hydrogen phosphate and calcium and / or magnesium acetates. According to XRD analysis the phase composition of the powder synthesized from calcium acetate included calcium hydroxyapatite Ca5(PO4)3(OH), octacalcium phosphate Ca8H2(PO4)6·5H2O and brushite CaHPO4·2H2O. The phase composition of the powder synthesized from magnesium acetate included struvite MgNH4PO4·6H2O. And the phase composition of the powder synthesized from solution containing calcium and magnesium acetates at the cation ratio Са: Mg = 9: 1 included hydroxyapatite Ca5(PO4)3(OH), whitlockite Ca18Mg2H2(PO4)14, and struvite MgNH4PO4·6H2O. Ceramic materials containing the bioresorbable and biocompatible phases of calcium and / or magnesium phosphates can be used to make bone implants for treatment of bone tissue defects. Keywords: tricalcium phosphate, calcium magnesium orthophosphate, magnesium pyrophosphate, whitlockite, octacalcium phosphate, hydroxyapatite, brushite, struvite, ceramics.
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Sogo, Yu, Atsuo Ito, Koshiro Fukasawa, Tokoha Sakurai, Noboru Ichinose, and Racquel Z. LeGeros. "Zinc-Containing Calcium Phosphate Ceramics with a (Ca+Zn)/P Molar Ratio of 1.67." Key Engineering Materials 284-286 (April 2005): 31–34. http://dx.doi.org/10.4028/www.scientific.net/kem.284-286.31.

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Zinc-containing calcium phosphate ceramics with a (Ca+Zn)/P molar ratio of 1.67 (ZnHAP ceramics) were synthesized to clarify the main phase for zinc release. ZnHAP ceramics with a zinc content at or more than 0.20 wt% contained zinc-containing tricalcium phosphate. The ion activity product of monophasic ZnHAP ceramic containing at or less than 0.13 wt% of zinc corresponded to that of pure HAP ceramic. The presence of tricalcium phosphate (TCP) phases was necessary condition for ZnHAP ceramics to release zinc. The coexistence of TCP phases in the ZnHAP ceramics meant that a phase with a (Ca+Zn)/P molar ratio higher than 1.67 also coexisted. Although the phase was assumed to be zinc oxide, zinc was not concentrated anywhere in the ZnHAP ceramics including grain boundaries.
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Tamai, Masato, Ryusuke Nakaoka, and Toshie Tsuchiya. "Cytotoxicity of Various Calcium Phosphate Ceramics." Key Engineering Materials 309-311 (May 2006): 263–66. http://dx.doi.org/10.4028/www.scientific.net/kem.309-311.263.

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The cytotoxicity of five calcium phosphate ceramics, hydroxyapatite (HAp), flouroapatite (FAp), α-tricalcium phosphate (α-TCP), β-tricalcium phosphate (β-TCP) and tetracalcium phosphate (TTCP), was investigated. Based on the guidelines of biological test for medical devices in Japan, a cytotoxicity test of these calcium phosphates was carried out using Chinese hamster V79 lung fibroblasts. The cytotoxic study revealed that FAp and α-TCP showed high cytotoxicities. From various analyses, it was considered that the cytotoxicity of the FAp was due to fluorine ions extracted in a culture medium and the cytotoxicity of α-TCP resulted from a decrease in pH of the medium by the phosphoric acid, which produced by hydrolysis of( the α-TCP.
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Tanaka, R., A. Fujishima, Y. Shibata, A. Manabe, and T. Miyazaki. "Cooperation of Phosphate Monomer and Silica Modification on Zirconia." Journal of Dental Research 87, no. 7 (July 2008): 666–70. http://dx.doi.org/10.1177/154405910808700705.

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Ceramic restorations with resin-based adhesive systems have been the focus of recent attention in clinical dentistry. Yttrium-oxide-partially-stabilized zirconia (YPSZ) ceramics have optimized physical properties and exhibit favorable fracture toughness, though their bonding properties are problematic. Although functional phosphate monomers and silica-coating by tribochemical modification were expected to improve the bonding properties between YPSZ ceramics and resin-based adhesives, these two methods remain controversial. This study evaluated the efficiency of silica-coating by tribochemical modification of YPSZ ceramics. The application of phosphate monomer and a silane coupling agent on silica-coated YPSZ was also investigated. The silica-coating of YPSZ ceramics by tribochemical modification was not efficient, given the higher mechanical toughness of the densely sintered ceramics. Stable shear bond strength was achieved on silica-coated YPSZ ceramics with the cooperative interaction of phosphate monomer and silane coupling.
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Mardziah, C. M., Mohamad Firdaus Abdul Wahid, Koay Mei Hyie, Nik Rozlin Nik Masdek, and Z. Salleh. "Effect of Sintering Temperature on Zinc Substituted Calcium Phosphate Ceramics." Materials Science Forum 890 (March 2017): 209–12. http://dx.doi.org/10.4028/www.scientific.net/msf.890.209.

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Calcium phosphate ceramics were substituted with several concentrations of zinc ions (0, 5, 10 and 15 mol%) using precipitation method. The effect of sintering temperature at 900 and 1000°C on zinc substituted calcium phosphate ceramics were observed. By increasing the sintering temperature, XRD peaks for zinc substituted calcium phosphate ceramics changed significantly. At sintering temperature of 900°C, hydroxyapatite phase was the major phase in the calcium phosphates containing 0 and 5 mol% zinc. However, at the sintering temperature of 1000°C, hydroxyapatite phase was partly transformed to another phase which was tricalcium phosphate. FESEM observations at sintering temperature of 1000°C exhibit that the particle size of the samples increased with addition of more zinc ions.
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Mayr, Helmar, Susanne Schlüfter, Rainer Detsch, and Günter Ziegler. "Influence of Phase Composition on Degradation and Resorption of Biphasic Calcium Phosphate Ceramics." Key Engineering Materials 361-363 (November 2007): 1043–46. http://dx.doi.org/10.4028/www.scientific.net/kem.361-363.1043.

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In this study the degradation behaviour of pure hydroxyapatite (HA), pure tricalcium phosphate (β-TCP) and four biphasic calcium phosphate ceramics was studied to gain information about the influence of the phase composition on this property with the aim to tailor individually adapted bone substitute materials. The chemical dissolution of each ceramic composition was measured by its release of calcium ions into a buffered solution. With decreasing HA content in the ceramics the degradation rate increased. Cell experiments were carried out with stimulated osteoclast-like RAW 264.7 cells. Using biochemical, genetic and microscopic analysis, the differentiation of the cells on the ceramic samples was studied. The monocytic precursor cells differentiated into osteoclast-like cells on all ceramics. The strongest cell differentiation into osteoclast-like cells was found on ceramics with HA/β-TCP ratios of 80/20, 60/40 and 40/60. Cells on these ceramics had many nuclei and the largest cell size. As a result of resorption, lacunas were found on all ceramics except β-TCP. All these experimental results proved the influence of the phase composition on degradation and resorption of calcium phosphate ceramics. Biphasic calcium phosphate ceramics with HA/β-TCP ratios of 80/20 and 60/40 exhibited the most promising properties to serve as synthetic bone substitute materials because for integration in the physiological bone remodeling process the implanted bone substitute materials should have optimized dissolution and resorption properties.
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Ota, Toshitaka, Takahiro Eitsuka, Haruki Yoshida, and Nobuyasu Adachi. "Porous Apatite Ceramics Derived from Woods." Advanced Materials Research 11-12 (February 2006): 247–50. http://dx.doi.org/10.4028/www.scientific.net/amr.11-12.247.

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Porous calcium phosphate ceramics (apatite and TCP) with wood-like microstructures, analogous to that of silicified wood, were prepared from natural woods as templates. The production of these ceramic woods was performed by the following process: (1) infiltration with an ethanol solution containing tri-ethyl phosphate and calcium nitrate tetra-hydrate into wood specimens, (2) drying to form a calcium phosphate gel in the cell structure, (3) firing in air to form apatite and TCP. The microstructure of the obtained ceramic woods retained the same structure as that of the raw woods: with the pore sizes corresponding to those of the original wood, and the major pores being unidirectionally connected.
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Lazar, Dolores Ribeiro Ricci, Sandra Maria Cunha, Valter Ussui, E. Fancio, Nelson Batista de Lima, and Ana Helena A. Bressiani. "Effect of Calcination Conditions on Phase Formation of Calcium Phosphates Ceramics Synthesized by Homogeneous Precipitation." Materials Science Forum 530-531 (November 2006): 612–17. http://dx.doi.org/10.4028/www.scientific.net/msf.530-531.612.

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Phase composition of calcium phosphate ceramics is a characteristic directly related to the biological response of implants due to the differences in mechanical and biochemical properties of these compounds. In this sense, it was evaluated in this work the crystalline phase evolution of calcium phosphates samples synthesized by wet precipitation route. Fixing Ca/P atomic ratio as 1.67, precipitation was carried out from heated aqueous solutions of calcium chloride and ammonium hydrogen phosphate, in ammonium medium (pH = 10). After washing and drying steps, calcination was performed at 600 to 1100 oC for 1 and 3 hours. Milled and pressed powders were sintered at 1250 oC for 1 hour. Samples were characterized by X-ray diffraction, chemical analysis, scanning electron microscopy, gaseous adsorption, laser diffraction and apparent density measurements. Results indicate the formation of a biphasic calcium phosphate ceramic containing hydroxyapatite as a major phase and β - tricalcium phosphate, the later obtained by heat treatment above 600 oC.
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Moguš-Milanković, Andrea, Ana Šantić, Luka Pavić, and Kristina Sklepić. "Iron Phosphate Glass-ceramics." Croatica Chemica Acta 88, no. 4 (2015): 553–60. http://dx.doi.org/10.5562/cca2759.

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KASUGA, TOSHIHIRO, and MASAYUKI NOGAMI. "MACHINABLE CALCIUM PHOSPHATE CERAMICS." Phosphorus Research Bulletin 13 (2002): 153–58. http://dx.doi.org/10.3363/prb1992.13.0_153.

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Dissertations / Theses on the topic "Phosphate ceramics"

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Sreeram, Attiganal Narayanaswamy. "Topological disorder in phosphate and other ceramics." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/32679.

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Thesis (Sc. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 1995.
Includes bibliographical references (leaves 146-157).
by Attiganal Narayanaswamy Sreeram.
Sc.D.
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Jensen, Amy S. "Phosphate bonding of ceramic hollow sphere foams." Thesis, Georgia Institute of Technology, 1992. http://hdl.handle.net/1853/19444.

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Langstaff, Sarah Dorthea. "Calcium phosphate ceramics capable of supporting osteoclastic resorption." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape11/PQDD_0005/NQ42953.pdf.

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Walsh, Pamela Judith. "Natural calcium phosphate ceramics for tissue engineering application." Thesis, Queen's University Belfast, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.486236.

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There is a great need for new bone graft materials. Bone related problems have increased considerably over the last few decades, owing to an ageing populate and the associated prevalence of bone disease. The traditional method of grafting to bridge bone defects are still widely used, despite a wide selection of new synthetic alternatives materials becoming available. These tend to lack the physical properties, such as porosity, interconnective and mechanical strength required for bone repair. Coral derived CaP ceramics have shown good potential, as substitute materials, offering the desirable physiochemical characteristics required for bone repair. This study investigated the development of a bioceramic from marine origins for use in bone tissue applications. Algae species were specifically selected to take account of their fast growth rate and aquaculture potential, which would minimise the environmental impact of harvesting. The conversion of alga was achieved through a novel technique, involving well controlled thermal processing followed by low pressure temperature hydrothermal synthesis technique. Using this technique, the original skeletal morphology of the alga was retained throughout processing. The resultant material was found to be a tri-phasic ceramic, with a > 90% composition of HA. Calcite and 13-TCP were the other two phases identified in the material. Cell studies confirmed the material to have good biocompatibility. A preliminary scaffold fabrication study incorporated the CaP material into a polymeric scaffold. The study found that the CaP material was robust and capable of withstanding rigorous processing. The work presented in this thesis indicates that this novel process is capable of synthesising a reproducible CaP material, which possesses suitable physiochemical properties for use in bone tissue engineering applications.
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De, Mestral François. "Calcium phosphate glasses and glass-ceramics for medical applications." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=65405.

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Qadri, Syed Jalaluddin. "Phosphate and vanadate ceramics with xenotime and monazite structures." Thesis, University of Warwick, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.406808.

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Lloyd, Michael Charles. "The dissolution of soluble phosphate glasses." Thesis, University of Leeds, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293799.

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Shaw, Lindsey Ann. "The development of chemical bonding systems for refractories/ceramics." Thesis, Keele University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341290.

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Berg, Camilla. "Influence of Magnesium in theFormation of Phosphate Spheres : A simple method for the fabrication of sphericalparticles of calcium and magnesium phosphate." Thesis, Uppsala universitet, Oorganisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-326255.

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Calcium phosphates and recently also magnesium phosphates, are used for medical applications, due to their biocompatibility and bioactivity. These properites makes spherical particles of calcium and magnesium phosphate suitable for carrier materials for drug delivery applications. By creating porous and/or hollow particles itis possible to load the particles with a drug and control therelease of the active substance. In this work, an ion-induced method for the synthesis of spherical calcium and magnesium phosphates was developed. A simple precipitation reaction was used, where substituting magnesium ions could replace the function of templates, such as surfactants or micelles, to induce the formation of spheres of a certain size and morphology. Experimental results showed that magnesium had an inhibitory effect on the nucleation and crystal growth of calcium phosphates. By using substituting ions as a structural regulator, it was possible to alter the size, morphology and phase composition of the spheres. At low magnesium concentrations, the spheres had a smooth surface andwere between 200 nanometer to 1 micrometer in diameter and composed of hydroxyapatite and/or magnesium-substituted beta-TCP. At higher magnesium concentrations, the spheres were about 10-50 micrometer with a rough, flaky surface. Results also proved that calcium ionshave the same effect on the crystallisation and self-assembly of magnesium phosphates. Apart from the magnesium concentration, reaction temperature proved to have a high influence on the sphereformation, whereas Ca/P ratio and reaction times above three hours did not affect the sphere formation to the same extent.
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Gallinetti, Sara. "New approaches in calcium phosphate cements and ceramics for bone regeneration." Doctoral thesis, Universitat Politècnica de Catalunya, 2014. http://hdl.handle.net/10803/279558.

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Bone is among the most frequently transplanted tissues in the body. In Europe, about one million patients encounter a surgical bone reconstruction annually. The worldwide market of bone replacement materials is currently estimated at 5 billion Euros, with a 10% growth due to the ageing of the population. Natural grafts present several drawbacks which pushed scientists to investigate synthetic biomaterials. Although most synthetic bone substitutes available possess some of the positive properties of autografts, none yet have all the benefits of one's own bone. Among the available biomaterials, Calcium Phosphates (CaPs) are of great interest. Nonetheless, these materials can still be improved in several respects. The main aim of this PhD Thesis is to contribute to the improvement of the properties of CaPs for bone regeneration with primary regard to Calcium Phosphate Cements (CPCs). The Thesis is divided in three main parts: i) Biphasic Calcium Phosphate Cements (BCPCs) with modified solubility and ion release; ii) Fibre Reinforced Calcium Phosphate cements (FRCPCs) with improved mechanical properties; iii) Macroporous CaP scaffolds for simvastatin acid release. In the first part novel biphasic CDHA/ß-TCP cements were obtained by mixing two Tricalcium Phosphate (TCP) polymorphs with different solubility (a-TCP and ß-TCP) at different a-TCP/ß-TCP ratios, and characterised in terms of setting properties, mechanical properties, and degradation. In the second part of this manuscript, new FRCPCs were fabricated with a focus on improving the adhesion fibres/matrix, in order to enhance the load transfer and, thus, the toughness of the material and their physico-chemical properties were investigated. Different approaches were studied. The first approach was to increase the chemical affinity of the fibres towards the matrix, adding an element in the matrix with high affinity to the fibres. In the first approach, TryMethyl Chitosan (TMC) was introduced in the liquid phase of a matrix reinforced with chitosan fibres. In the same line, lactic acid (LA) was added in the liquid phase of cements reinforced with Poly-L-lactic acid (PLLA) yarns. The biological characterisation of FRCPCs was explored using human osteoblastic-like cells MG63 . Another approach was to investigate the potential of low temperature plasma surface modification of PLLA yarns for reinforcement of CPCs. Oxygen low pressure plasma was employed at different treatment times and the surface properties of the untreated and plasma-treated PLLA were evaluated. The third part of this Thesis consisted in producing low temperature (CDHA) or high temperature (ß-TCP) macroporous scaffolds as carriers for Simvastatin acid (SVA), an osteogenic and angiogenic promoter. In order to modulate the drug release beyond the intrinsic capacity of the material, plasma polymerisation with PCL:PEG copolymers was used to dry-coat the CaP scaffolds. The material properties, the plasma polymer layer and the drug release from the scaffold were characterised.
El hueso es uno de los tejidos más trasplantados del cuerpo. Sólo en Europa, se cuentan alrededor de un millón de cirugías de reconstrucción ósea anualmente. La estimación del mercado global de los sustitutos óseos es aproximadamente de cinco billones de Euros por año, con un 10% de crecimiento anual debido al envejecimiento de la población. Debido a los problemas asociados a los injertos biológicos, la investigación y el desarrollo de materiales sintéticos y biocompatibles (Biomateriales) ha experimentado un gran auge. Aunque la mayoría de sustitutos sintéticos disponibles poseen algunas de las características de los autoinjertos, hasta el momento ninguno reúne todos los beneficios del hueso del propio individuo. Dentro de los biomateriales para regeneración ósea, los fosfatos de calcio han sido de gran interés debido a su composición química similar a la del hueso. Sin embargo, aún se requieren mejoras en distintos aspectos de estos materiales. El objetivo principal de esta Tesis Doctoral es contribuir a la mejora de las propiedades de los fosfatos de calcio para la regeneración ósea, con un interés especial en los cementos de fosfato de calcio. La Tesis investiga diferentes estrategias para el desarrollo de materiales para la sustitución ósea, novedosos y con propiedades mejoradas respecto a los actuales. La Tesis comprende tres partes principales: i) Cementos bifásicos de fosfato de calcio (BCPCs), constituidos por materiales con diferente solubilidad; ii) Fosfatos de calcio reforzados con fibras (FRCPCs), para la mejora de las propiedades mecánicas; iii) Andamios macroporosos para la liberación de una sal de simvastatina. En la primera parte de la Tesis, se describe el desarrollo de BCPCs compuestos por hidroxiapatita deficiente en calcio (CDHA) y fosfato tricálcico ß (ß-TCP). Estos materiales derivan de la reacción de las mezclas de dos polimorfos de fosfato tricalcico (TCP) con diferente solubilidad (a-TCP y ß-TCP) y, en esta tesis, se caracterizan su fraguado, sus propiedades mecánicas y degradación. En la segunda parte, se han desarrollado nuevos FRCPCs con especial atención hacia la mejora de la adhesión entre fibras y matriz, con el objetivo de mejorar la transferencia de carga entre ellos y por tanto, las propiedades mecánicas del compuesto. Se han investigado distintas estrategias. La primera de ellas basada en la investigación de materiales con una fase común (o con alta afinidad química) entre las fibras y la fase liquida del cemento; de esta manera se pretende crear un enlace más fuerte entre las fibras y la matriz. En un primer material se incorporó un 1 w/v% de Trimetilo de quitosán (TMC) en la fase líquida del cemento que a su vez se reforzó con fibras de quitosán. En un segundo grupo de materiales, se añadió un 10 v/v% de ácido láctico (LA) a la matriz del cemento junto con hilos discontinuos de ácido poliláctico (PLLA). Estos cementos también se caracterizaron biológicamente por medio de células osteoblásticas MG63. La segunda estrategia investigada en los FRCPCs se basa en la modificación superficial de las fibras de PLLA con plasma de baja temperatura con el fin de mejorar sus propiedades de mojado. Las fibras se trataron con plasma de oxigeno de baja presión a distintos tiempos y se incorporaron a la matriz de cemento, y se caracterizaron tanto las modificaciones superficiales de las fibras como las propiedades del cemento. La tercera parte ha consistido en el desarrollo de andamios macroporosos obtenidos a baja (CDHA) o alta (ß-TCP) temperatura para ser utilizados como formas de liberación de una sal de simvastatina (SVA), con propiedades osteogénicas y angiogénicas. Para conseguir modular la liberación del fármaco se recubrieron los andamios cargados con SVA con un copolímero de PCL:PEG mediante polimerización por plasma. Se caracterizaron las propiedades tanto del material como del recubrimiento y se evaluó la liberación del fármaco.
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Books on the topic "Phosphate ceramics"

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Komlev, V. S. (Vladimir Sergeevich), ed. Biokeramika na osnove fosfatov kalʹt︠s︡ii︠a︡: Calcium phosphate based bioceramics. Moskva: Nauka, 2005.

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S, Komlev V., ed. Calcium phosphate based bioceramics for bone tissue engineering. Stafa-Zuerich, Switzerland: Trans Tech Publications, 2008.

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Sharpe, Justin Robert. The effect of phase variation on the biological response to calcium phosphate ceramics. Birmingham: University of Birmingham, 1998.

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Deckman, Douglas E. Vaporphase deposition studies of phosphate esters on metal and ceramic surfaces. Washington, D.C: National Institute of Standards and Technology, 1988.

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Deckman, Douglas E. Vapor phase deposition studies of phosphate esters on metal and ceramic surfaces. Gaithersburg, MD: U.S. Dept. of Commerce, National Institute of Standards and Technology, 1988.

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Chapman, Chris. Development of process to manufacture glass/glass-ceramic products from phosphogypsum: Final report. Bartow, Fla: The Institute, 2006.

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Chemically Bonded Phosphate Ceramics. Elsevier, 2016. http://dx.doi.org/10.1016/c2014-0-02562-2.

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Chemically Bonded Phosphate Ceramics. Elsevier, 2004. http://dx.doi.org/10.1016/b978-0-08-044505-2.x5000-5.

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Wagh, Arun S. Chemically Bonded Phosphate Ceramics: Twenty-First Century Materials with Diverse Applications. Elsevier, 2016.

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Wagh, Arun S. Chemically Bonded Phosphate Ceramics: Twenty-First Century Materials with Diverse Applications. Elsevier Science & Technology Books, 2016.

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Book chapters on the topic "Phosphate ceramics"

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Arcos, Daniel. "Calcium Phosphate Bioceramics." In Bio-Ceramics with Clinical Applications, 23–71. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118406748.ch3.

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Singh, Dileep, Roopa Ganga, Jose Gaviria, and Yusuf Yusufoglu. "Chemically Bonded Phosphate Ceramics: Stabilization of Secondary Wastes Streams." In Engineered Ceramics, 445–56. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119100430.ch22.

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Li, Yan Bao, Dong Xu Li, and Wen Jian Weng. "In Vitro Dissolution Behavior of Biphasic Tricalcium Phosphate Composite Powders Composed of α-Tricalcium Phosphate and β-Tricalcium Phosphate." In High-Performance Ceramics V, 1206–8. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/0-87849-473-1.1206.

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Tamai, Masato, Ryusuke Nakaoka, and Toshie Tsuchiya. "Cytotoxicity of Various Calcium Phosphate Ceramics." In Bioceramics 18, 263–66. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-992-x.263.

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Li, Tong Wei, Zheng Xin Tang, Wei Wei Ju, and Xiao Yang Gong. "Electrical Conductivity in Alkali Iron Phosphate Glasses." In High-Performance Ceramics V, 1446–48. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/0-87849-473-1.1446.

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Yang, De An, Zi Yang, Weijie Hu, Yuan Yuan Li, and Huan Wang. "Synthesis of Calcium Phosphate/Gypsum Composite Powders." In High-Performance Ceramics III, 1559–62. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-959-8.1559.

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Baccour, Hajer, Hela Koubaa, and Samir Baklouti. "Phosphate Sludge from Tunisian Phosphate Mines: Valorisation as Ceramics Products." In Recent Advances in Environmental Science from the Euro-Mediterranean and Surrounding Regions, 1479–80. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-70548-4_431.

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Ji, Jin Gou, Yi Xu, Song Chen, Wei Qi Liu, and Jun Guo Ran. "Dense Calcium Phosphate Bioceramics Sintered by Microwave Plasma." In High-Performance Ceramics V, 1181–83. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/0-87849-473-1.1181.

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SanSoucie, Michael, and Robert W. Hyers. "Calcium Phosphate Based Ceramics Via Spinodal Decmoposition." In Ceramic Transactions Series, 111–17. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118408414.ch13.

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Lv, Qing, Kevin W. H. Lo, Lakshmi S. Nair, and Cato T. Laurencin. "Calcium-Phosphate-Based Ceramics for Biomedical Applications." In Biodegradable Polymers in Clinical Use and Clinical Development, 495–517. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118015810.ch14.

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Conference papers on the topic "Phosphate ceramics"

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Sakamoto, K., Y. Tsunawaki, J. Takahashi, T. Matsumoto, A. Nakahira, S. Yamaguchi, M. Inoue, and M. Okazaki. "BIOACTIVE BONE CEMENTS OF CALCIUM PHOSPHATE - MONO(METHACRYLOYLOXYETHYL) ACID PHOSPHATE COMPOSITE." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0130.

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Ito, A., K. Ojima, K. Kawamura, N. Ichinose, P. Layrolle, K. Hayashi, and T. Tateishi. "ZINC-RELEASING CALCIUM PHOSPHATE CERAMICS STIMULATING BONE FORMATION." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0136.

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Terebilenko, Kateryna, Oleksandr Alekseev, Maksym Lazarenko, Sergii G. Nedilko, Mykola Slobodyanik, Volodymyr Boyko, and Vitalii Chornii. "Luminescent Bi-containing Phosphate-Molybdate Glass-Ceramics." In 2020 IEEE 10th International Conference Nanomaterials: Applications & Properties (NAP). IEEE, 2020. http://dx.doi.org/10.1109/nap51477.2020.9309625.

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Gross, U., C. Voigt, A. Hering, R. Rahmanzadeh, and C. Müller-Mai. "RESORPTION OF CALCIUM PHOSPHATE CERAMICS OF DIFFERENT CRYSTAL SIZE." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0067.

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Petit, L., H. Nguyen, M. Hongisto, T. Salminen, T. Hakkarainen, P. Lopez-Iscoa, D. Pugliese, N. G. Boetti, and D. Milanese. "Novel Er3+ doped phosphate glass-ceramics for photonics." In 2017 19th International Conference on Transparent Optical Networks (ICTON). IEEE, 2017. http://dx.doi.org/10.1109/icton.2017.8024877.

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Kikuchi, Masanori, Yasushi Suetsugu, Yoshihisa Koyama, Shinichi Sotome, Soichiro Itoh, Kazuo Takakuda, Kenichi Shinomiya, Kazuya Edamura, Katsuyoshi Nagaoka, and Shigeo Tanaka. "Bone Regeneration Materials Based on Calcium Phosphate Ceramics." In In Commemoration of the 1st Asian Biomaterials Congress. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812835758_0021.

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Yokogawa, Y., K. Nishizawa, F. Nagata, and T. Kameyama. "FORMATION OF CALCIUM PHOSPHATE OVER POROUS PHOSPHORYLATED CHITOSAN SPONGES." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0031.

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Suzuki, Katsuji, Mitsuko Yamada, and Tsuneyo Matsubayashi. "HYDROXYAPATITE TRICALCIUM PHOSPHATE AS A FILLER FOR INFECTED BONE DEFECTS." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0002.

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You, Changkook, Kyoungmin Kim, Joon Hee Lee, and Sukyoung Kim. "BIODEGRADABLE CALCIUM PHOSPHATE COATING ON Ti6A14V BY SOL-GEL PROCESS." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0121.

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Asaoka, Nobuyuki, Motohiko Misago, Masahiro Hirano, and Hiroyasu Takeuchi. "MECHANICAL AND CHEMICAL PROPERTIES OF THE INJECTABLE CALCIUM PHOSPHATE CEMENT." In Proceedings of the 12th International Symposium on Ceramics in Medicine. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814291064_0126.

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Reports on the topic "Phosphate ceramics"

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Singh, D., R. Ganga, J. Gaviria, and Y. Yusufoglu. Secondary waste form testing : ceramicrete phosphate bonded ceramics. Office of Scientific and Technical Information (OSTI), June 2011. http://dx.doi.org/10.2172/1020703.

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Singh, D., A. S. Wagh, J. C. Cunnane, and J. L. Mayberry. Chemically bonded phosphate ceramics for low-level mixed waste stabilization. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/10114142.

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Author, Not Given. Stabilization Using Phosphate Bonded Ceramics. Salt Containing Mixed Waste Treatment. Mixed Waste Focus Area. OST Reference No. 117. Office of Scientific and Technical Information (OSTI), September 1999. http://dx.doi.org/10.2172/1248378.

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Anderson, M. A., W. A. Zeltner, and C. G. Jr Hill. Development of phosphate-based ceramic membranes. Office of Scientific and Technical Information (OSTI), November 1992. http://dx.doi.org/10.2172/7164518.

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Anderson, M. A., W. A. Zeltner, and C. G. Jr Hill. Development of phosphate-based ceramic membranes. Final report. Office of Scientific and Technical Information (OSTI), November 1992. http://dx.doi.org/10.2172/10186324.

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Shirish Patil, Godwin A. Chukwu, Gang Chen, and Santanu Khataniar. Novel Chemically-Bonded Phosphate Ceramic Borehole Sealants (Ceramicretes) for Arctic Environments. Office of Scientific and Technical Information (OSTI), December 2008. http://dx.doi.org/10.2172/963362.

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Deckman, Douglas E., Douglas E. Deckman, Stephen M. Hsu, and E. Erwin Klaus. Vapor phase deposition studies of phosphate esters on metal and ceramic surfaces. Gaithersburg, MD: National Institute of Standards and Technology, 1988. http://dx.doi.org/10.6028/nist.sp.754.

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Wagh, A. S., D. Singh, and S. Y. Jeong. Stabilization of hazardous ash waste with newberyite-rich chemically bonded magnesium phosphate ceramic. Office of Scientific and Technical Information (OSTI), November 1995. http://dx.doi.org/10.2172/510298.

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Sugama, T., and N. R. Carciello. Advanced zinc phosphate conversion and pre-ceramic polymetallosiloxane coatings for corrosion protection of steel and aluminum, and characteristics of polyphenyletheretherketone-based materials. Final report. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/10135338.

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