



@article {2269,
	title = {Heparinized hydroxyapatite/collagen three-dimensional scaffolds for tissue engineering},
	journal = {Journal of Materials Science: Materials in MedicineJ. Mater. Sci. Mater. Med.},
	volume = {21},
	year = {2010},
	note = {Cited By (since 1996): 8Export Date: 21 November 2012Source: ScopusCODEN: JSMMEdoi: 10.1007/s10856-010-4097-2PubMed ID: 20596760Language of Original Document: EnglishCorrespondence Address: Teixeira, S.; Divis{\~a}o de Biomateriais, INEB-Instituto de Engenharia Biom{\'e}dica, Rua do Campo Alegre 823, Porto 4150-180, Portugal; email: sandra_teixeira3@yahoo.comChemicals/CAS: collagen, 9007-34-5; cyanamide, 151-51-9, 420-04-2; heparin, 37187-54-5, 8057-48-5, 8065-01-8, 9005-48-5; hydroxyapatite, 1306-06-5, 51198-94-8; n hydroxysuccinimide, 6066-82-6; trinitrobenzenesulfonic acid, 16655-63-3, 2508-19-2; Biocompatible Materials; Bone Substitutes; Collagen, 9007-34-5; Cross-Linking Reagents; Durapatite, 1306-06-5; Heparin, 9005-49-6; PolymersReferences: Rose, F.R., Cyster, L.A., Grant, D.M., Scotchford, C.A., Howdle, S.M., Shakesheff, K.M., In vitro assessment of cell penetration into porous hydroxyapatite scaffolds with a central aligned channel (2004) Biomaterials, 25 (24), pp. 5507-5514. , DOI 10.1016/j.biomaterials.2004.01.012, PII S0142961204000134;Hong, Z., Zhang, P., He, C., Qiu, X., Liu, A., Chen, L., Chen, X., Jing, X., Nano-composite of poly(L-lactide) and surface grafted hydroxyapatite: Mechanical properties and biocompatibility (2005) Biomaterials, 26 (32), pp. 6296-6304. , DOI 10.1016/j.biomaterials.2005.04.018, PII S0142961205003297; 
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Wissink, M.J.B., Beernink, R., Pieper, J.S., Poot, A.A., Engbers, G.H.M., Beugeling, T., Immobilization of heparin to EDC/NHS-crosslinked collagen. Characterization and in vitro evaluation (2001) Biomaterials, 22 (2), pp. 151-163. , 10.1016/S0142-9612(00)00164-2 1:CAS:528:DC\%2BD3cXovFGnu7g\%3D 11101159; 
Wissink, M.J.B., Beernink, R., Poot, A.A., Engbers, G.H.M., Beugeling, T., Van Aken, W.G., Feijen, J., Improved endothelialization of vascular grafts by local release of growth factor from heparinized collagen matrices (2000) Journal of Controlled Release, 64 (1-3), pp. 103-114. , DOI 10.1016/S0168-3659(99)00145-5, PII S0168365999001455; 
Wissink, M.J.B., Beernink, R., Scharenborg, N.M., Poot, A.A., Engbers, G.H.M., Beugeling, T., Van Aken, W.G., Feijen, J., Endothelial cell seeding of (heparinized) collagen matrices: Effects of bFGF pre-loading on proliferation (after low density seeding) and pro-coagulant factors (2000) Journal of Controlled Release, 67 (2-3), pp. 141-155. , DOI 10.1016/S0168-3659(00)00202-9, PII S0168365900002029; 
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Teixeira, S., Oliveira, S., Ferraz, M., Monteiro, F.J., Three dimensional macroporous calcium phosphates scaffolds for bone tissue engineering (2008) Key Eng Mater Trans Tech, pp. 947-50; 
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Teixeira, S., Rodriguez, M.A., Pena, P., De Aza, A.H., De Aza, S., Ferraz, M.P., Monteiro, F.J., Physical characterization of hydroxyapatite porous scaffolds for tissue engineering (2009) Mater Sci Eng C, 29 (5), pp. 1510-1514. , 10.1016/j.msec.2008.09.052 1:CAS:528:DC\%2BD1MXmtVarurg\%3D
},
	month = {2010///},
	pages = {2385 - 2392},
	abstract = {Currently, in bone tissue engineering research, the development of appropriate biomaterials for the regeneration of bony tissues is a major concern. Bone tissue is composed of a structural protein, collagen type I, on which calcium phosphate crystals are enclosed. For tissue engineering, one of the most applied strategies consists on the development and application of three dimensional porous scaffolds with similar composition to the bone. In this way, they can provide a physical support for cell attachment, proliferation, nutrient transport and new bone tissue infiltration. Hydroxyapatite is a calcium phosphate with a similar composition of bone and widely applied in several medical/dentistry fields. Therefore, in this study, hydroxyapatite three dimensional porous scaffolds were produced using the polymer replication method. Next, the porous scaffolds were homogeneously coated with a film of collagen type I by applying vacuum force. Yet, due to collagen degradability properties, it was necessary to perform an adequate crosslinking method. As a result, N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) was employed as an efficient and non-toxic crosslinking method in this research. The composites were characterized by means of SEM, DSC and TNBS. Furthermore, heparin was incorporated in order to accomplish sustained delivery of a growth factor of interest namely, bone morphogenetic proteins (BMP-2). BMP-2 binding and release of non-heparinized and heparinized scaffolds was evaluated at specific time points. The incorporation of heparin leads to a reduced initial burst phase when compared to the non heparinized materials. The results show a beneficial effect with the incorporation of heparin and its potential as a localized drug delivery system for the sustained release of growth factors. {\textcopyright} 2010 Springer Science+Business Media, LLC.},
	keywords = {Achilles Tendon, Animals, Apatite, article, Beneficial effects, Binding and release, Biocompatible Materials, Biological materials, Biomaterials, Bone, Bone and Bones, bone morphogenetic protein 2, Bone morphogenetic proteins, Bone Substitutes, bone tissue, Bone tissue engineering, Bony tissue, Calcium, calcium phosphate, Calcium phosphate crystals, Cattle, Cell attachments, Collagen, collagen degradation, collagen type 1, Collagen type I, controlled study, cross linking, Cross-Linking Reagents, Crosslinking, cyanamide, Degradability, differential scanning calorimetry, Drug delivery, drug delivery system, Durapatite, Grafts, Growth factor, heparin, Hydrogels, hydroxyapatite, Microscopy, Electron, Scanning, n (3 dimethyllaminopropyl) n{\textquoteright} ethylcarbodiimide, n hydroxysuccinimide, N-hydroxysuccinimide, Nutrient transport, Peptides, polymer, Polymer replication, Polymers, Polysaccharides, porosity, Porous scaffold, priority journal, protein binding, Scaffolds, Scanning electron microscopy, SEM, Specific time, Structural proteins, Sustained release, Three dimensional, Three-dimensional porous scaffolds, Three-dimensional scaffolds, Tissue engineering, tissue scaffold, Tissue Scaffolds, trinitrobenzenesulfonic acid, unclassified drug, vacuum, Vacuum force},
	isbn = {09574530 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77956420058\&partnerID=40\&md5=a723fdb7ea856a5286080a1a4aab82a2},
	author = {Teixeira, S. and Yang, L. and Dijkstra, P.J. and Ferraz, M.P. and Monteiro, F.J.}
}
@article {2273,
	title = {In vitro study of the proliferation and growth of human bone marrow cells on apatite-wollastonite-2M glass ceramics},
	journal = {Acta BiomaterialiaActa Biomater.},
	volume = {6},
	year = {2010},
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},
	month = {2010///},
	pages = {2254 - 2263},
	abstract = {This study concerns the preparation and in vitro characterization of an apatite-wollastonite-2M bioactive glass ceramic which is intended to be used for the regeneration of hard tissue (i.e. in dental and craniomaxillofacial surgery). This bioglass ceramic has been obtained by appropriate thermal treatment through the devitrification (crystallization) of a glass with a stoichiometric eutectic composition within the Ca                        3(PO 
                        4)2-CaSiO
                        3 binary system. Crack-free specimens of the bioglass ceramic were immersed in human bone marrow cell cultures for 3, 7, 14 and 21 days, in order to study biocompatibility. Cell morphology, proliferation and colonization were assessed by scanning electron microscopy and confocal laser scanning microscopy. A total protein content assay was used to evaluate the viability and proliferation of cultured bone marrow cells. The results showed that the cells were able to adhere and proliferate on the designed material due to the essentiality of silicon and calcium as accessory factors for cell activity stimulation. {\textcopyright} 2009 Acta Materialia Inc. All rights reserved.
},
	keywords = {Apatite, Apatites, article, Bioceramics, Biocompatibility, bone marrow cell, bone prosthesis, Bone Substitutes, Calcium Compounds, calcium derivative, calcium phosphate, calcium silicate, cell activity, cell adhesion, Cell culture, cell differentiation, cell enlargement, cell growth, cell proliferation, cell structure, cell viability, Cells, Cultured, ceramics, chemistry, confocal laser microscopy, crystal structure, Crystallization, cytology, glass, Glass ceramics, human, human cell, Humans, in vitro study, materials testing, Mesenchymal stem cell, Mesenchymal Stem Cells, methodology, osteoblast, Osteoblasts, physiology, priority journal, protein content, Scanning electron microscopy, silicate, Silicates, Surface Properties, surface property, Tissue regeneration, Wollastonite, X ray fluorescence},
	isbn = {17427061 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77956625645\&partnerID=40\&md5=426d361faf4a2e3f988754fc5822ea56},
	author = {Magallanes-Perdomo, M. and De Aza, A.H. and Mateus, A.Y. and Teixeira, S. and Monteiro, F.J. and De Aza, S. and Pena, P.}
}
@article {2248,
	title = {Influence of crystallite size of nanophased hydroxyapatite on fibronectin and osteonectin adsorption and on MC3T3-E1 osteoblast adhesion and morphology},
	journal = {Journal of Colloid and Interface ScienceJ. Colloid Interface Sci.},
	volume = {351},
	year = {2010},
	note = {Cited By (since 1996): 12Export Date: 21 November 2012Source: ScopusCODEN: JCISAdoi: 10.1016/j.jcis.2010.08.013PubMed ID: 20810127Language of Original Document: EnglishCorrespondence Address: Ribeiro, N.; INEB - Instituto de Engenharia Biom{\'e}dica, Divis{\~a}o de Biomateriais, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal; email: nribeiro@ineb.up.ptChemicals/CAS: fibronectin, 86088-83-7; hydroxyapatite, 1306-06-5, 51198-94-8; osteonectin, 104052-78-0; protein, 67254-75-5; Ceramics; Durapatite, 1306-06-5; Fibronectins; OsteonectinReferences: Griffith, L.G., Naughton, G., (2002) Science, 295, p. 1009;Webster, T.J., Ergun, C., Doremus, R.H., Siegel, R.W., Bizios, R., (2000) J. Biomed. Mater. Res., 51, pp. 475-483; 
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},
	month = {2010///},
	pages = {398 - 406},
	abstract = {The characteristic topographical features (crystallite dimensions, surface morphology and roughness) of bioceramics may influence the adsorption of proteins relevant to bone regeneration. This work aims at analyzing the influence of two distinct nanophased hydroxyapatite (HA) ceramics, HA725 and HA1000 on fibronectin (FN) and osteonectin (ON) adsorption and MC3T3-E1 osteoblast adhesion and morphology. Both substrates were obtained using the same hydroxyapatite nanocrystals aggregates and applying the sintering temperatures of 725{\textdegree}C and 1000{\textdegree}C, respectively. The two proteins used in this work, FN as an adhesive glycoprotein and ON as a counter-adhesive protein, are known to be involved in the early stages of osteogenesis (cell adhesion, mobility and proliferation). The properties of the nanoHA substrates had an important role in the adsorption behavior of the two studied proteins and clearly affected the MC3T3-E1 morphology, distribution and metabolic activity. HA1000 surfaces presenting slightly larger grain size, higher root-mean-square roughness (Rq), lower surface area and porosity, allowed for higher amounts of both proteins adsorbed. These substrates also revealed increased number of exposed FN cell-binding domains as well as higher affinity for osteonectin. Regarding the osteoblast adhesion results, improved viability and cell number were found for HA1000 surfaces as compared to HA725 ones, independently of the presence or type of adsorbed protein. Therefore the osteoblast adhesion and metabolic activity seemed to be more sensitive to surfaces morphology and roughness than to the type of adsorbed proteins. {\textcopyright} 2010 Elsevier Inc.},
	keywords = {Adhesion, Adhesive proteins, Adsorption, Adsorption behavior, Animals, Apatite, article, Bioceramics, Biological materials, Biomaterials, bone development, Bone Regeneration, cell adhesion, Cell Count, cell metabolism, cell motility, Cell number, cell proliferation, cell strain 3T3, cell structure, Cell-binding domain, Cells, Cultured, cellular distribution, ceramics, controlled study, Crystallite dimension, Crystallite size, Crystallization, Durapatite, Fibronectin, Fibronectin adsorption, Fibronectins, glycoprotein, grain, Grain size, human, human cell, hydroxyapatite, Hydroxyapatite nanocrystals, MC3T3-E1, Metabolic activity, metabolism, Mice, morphology, Nano-HA, nanocrystal, nanoparticles, Nanophased hydroxyapatite, osteoblast, Osteoblast adhesion, Osteoblast morphology, Osteoblasts, Osteogenesis, osteonectin, Osteonectin adsorption, Particle Size, porosity, priority journal, protein, Proteins, Root mean square roughness, Sintering, Sintering temperatures, Surface area, Surface Properties, surface property, Surface roughness, temperature, Topographical features},
	isbn = {00219797 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77957328472\&partnerID=40\&md5=c4a13ccec89e04dbfe1920fd42fec3f5},
	author = {Ribeiro, N. and Sousa, S.R. and Monteiro, F.J.}
}
@article {2245,
	title = {Innovative macroporous granules of nanostructured-hydroxyapatite agglomerates: Bioactivity and osteoblast-like cell behaviour},
	journal = {Journal of Biomedical Materials Research - Part AJ. Biomed. Mater. Res. Part A},
	volume = {95},
	year = {2010},
	note = {Cited By (since 1996): 3Export Date: 21 November 2012Source: ScopusCODEN: JBMRCdoi: 10.1002/jbm.a.32916PubMed ID: 20845490Language of Original Document: EnglishCorrespondence Address: Laranjeira, M. S.; Divis{\~a}o de Biomateriais, INEB-Instituto de Engenharia Biom{\'e}dica, Universidade Do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal; email: dce06004@fe.up.ptChemicals/CAS: alkaline phosphatase, 9001-78-9; colony stimulating factor 1, 81627-83-0; hydroxyapatite, 1306-06-5, 51198-94-8; osteoprotegerin, 205944-50-9; polyurethan, 61789-63-7; Biocompatible Materials; Biological Markers; Durapatite, 1306-06-5; PolyurethanesReferences: Ferraz, M., Monteiro, F., Manuel, C., Hydroxyapatite nanoparticles: A review of preparation methodologies (2004) J Appl Biomater Biomech, 2, pp. 74-80;Murugan, R., Ramakrishna, S., Development of nanocomposites for bone grafting (2005) Compos Sci Technol, 65, pp. 2385-2406; 
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},
	month = {2010///},
	pages = {891 - 900},
	abstract = {To modulate the biological response of implantable granules, two types of bioactive porous granules composed of nanostructured-hydroxyapatite (HA) agglomerates and microstructured-HA, respectively, were prepared using a polyurethane sponge impregnation and burnout method. The resulting granules presented a highly porous structure with interconnected porosity. Both types of granules were characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and mercury intrusion porosimetry. Results showed that nanostructed-HA granules presented higher surface area and porosity than microstructured-HA granules. In vitro testing using MG63 human osteoblast-like cells showed that on both types of surfaces cells were able to adhere, proliferate, and migrate through the macropores, and a higher growth rate was achieved on nanostructured-HA granules than on microstructured-HA granules (76 and 40\%, respectively). In addition, these cells maintained similar expression levels of osteoblastic-associated markers namely collagen type I, alkaline phosphatase, bone morphogenetic protein-2, macrophage colony-stimulating factor, and osteoprotegerin. These innovative nanostructured-HA granules may be considered as promising bioceramic alternative matrixes for bone regeneration and drug release application. {\textcopyright} 2010 Wiley Periodicals, Inc.},
	keywords = {Agglomeration, alkaline phosphatase, Apatite, article, Bioceramics, Biocompatible Materials, Biological Markers, Biological materials, Biological response, Biomaterials, Bone, bone morphogenetic protein 2, Bone morphogenetic protein-2, Bone Regeneration, cell adhesion, cell function, cell granule, cell migration, cell proliferation, Cells, Cultured, collagen type 1, Collagen type I, colony stimulating factor 1, Colony-stimulating factor, drug activity, Drug release, Durapatite, Expression levels, Fourier transform infrared spectroscopy, Fourier transforms, Granulation, Granules, growth rate, human, human cell, Human osteoblast-like cells, Humans, hydroxyapatite, In-vitro, infrared spectroscopy, Interconnected porosity, Macro-porosity, Macropores, Macroporosity, Macroporous, materials testing, matrix, Mercury (metal), Mercury intrusion porosimetry, Microscopy, Electron, Scanning, Microstructured, Nano-materials, Nano-structured, nanomaterial, Nanomaterials, Nanostructured materials, Nanostructures, osteoblast, Osteoblast response, Osteoblast-like cells, Osteoblasts, Osteoprotegerin, Phosphatases, polyurethan, Polyurethane sponge, Polyurethanes, porosity, Porous structures, Reverse Transcriptase Polymerase Chain Reaction, Scanning electron microscopy, SEM, Spectroscopy, Fourier Transform Infrared, Surface area, surface property, X ray diffraction, X-Ray Diffraction},
	isbn = {15493296 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-78249252998\&partnerID=40\&md5=09d51d6c49d9f10e6c2d479b1fe4ace0},
	author = {Laranjeira, M.S. and Fernandes, M.H. and Monteiro, F.J.}
}
@article {2252,
	title = {Proliferation and mineralization of bone marrow cells cultured on macroporous hydroxyapatite scaffolds functionalized with collagen type I for bone tissue regeneration},
	journal = {Journal of Biomedical Materials Research - Part AJ. Biomed. Mater. Res. Part A},
	volume = {95},
	year = {2010},
	note = {Cited By (since 1996): 7Export Date: 21 November 2012Source: ScopusCODEN: JBMRCdoi: 10.1002/jbm.a.32600Language of Original Document: EnglishCorrespondence Address: Teixeira, S.; Divis{\~a}o de Biomateriais, INEB - Instituto de Engenharia Biom{\'e}dica, Rua do Campo Alegre 823, Porto 4150-180, Portugal; email: sandra_teixeira3@yahoo.comChemicals/CAS: 1 (3 dimethylaminopropyl) 3 ethylcarbodiimide, 1892-57-5, 25952-53-8, 7084-11-9; DNA, 9007-49-2; hydroxyapatite, 1306-06-5, 51198-94-8; methylene blue, 61-73-4; n hydroxysuccinimide, 6066-82-6; Collagen Type I; Cross-Linking Reagents; DNA, 9007-49-2; Durapatite, 1306-06-5; Methylene Blue, 61-73-4Manufacturers: SigmarecticelReferences: Nair, M.B., Suresh Babu, S., Varma, H.K., John, A., A triphasic ceramic-coated porous hydroxyapatite for tissue engineering application (2008) Acta Biomaterialia, 4 (1), pp. 173-181. , DOI 10.1016/j.actbio.2007.07.004, PII S174270610700102X;Navarro, M., Ginebra, M.P., Planell, J.A., Zeppetelli, S., Ambrosio, L., Development and cell response of a new biodegradable composite scaffold for guided bone regeneration (2004) Journal of Materials Science: Materials in Medicine, 15 (4), pp. 419-422. , DOI 10.1023/B:JMSM.0000021113.88702.9d; 
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},
	month = {2010///},
	pages = {1 - 8},
	abstract = {This study concerns the preparation and in vitro characterization of functionalized hydroxyapatite (HA) porous scaffolds, which are intended to be used as drug-delivery systems and bone-regeneration matrices. Hydroxyapatite scaffolds were prepared using the polymer replication method, and, after being submitted to a specific sintering cycle, collagen Type I was incorporated on the surface. After the coating procedure, collagen was crosslinked using the N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) conjugation method. In this study, hydroxyapatite scaffolds with uncrosslinked and cross-linked Type I collagen were evaluated. Cell morphology and deposition of extracellular matrix were assessed by scanning electron microscopy, whereas cell distribution was visualized by means of methylene blue staining. MTS and total DNA quantification assays were used to evaluate the viability and proliferation of human bone marrow cells cultured on all the materials for 28 days. Results showed that the cells were able to adhere, proliferate, and form a mineralized matrix on the surface of all the materials. Furthermore, the cells were able to spread from one pore to another and form cell clusters. The results show that these scaffolds are good candidates to serve as drug delivery vehicles and for tissue engineering purposes. {\textcopyright} 2010 Wiley Periodicals, Inc.},
	keywords = {1 (3 dimethylaminopropyl) 3 ethylcarbodiimide, adult, Animal cell culture, Apatite, article, Automobile exhibitions, Bone, bone marrow cell, Bone Marrow Cells, bone matrix, bone mineralization, Bone Regeneration, bone tissue, Bone tissue regeneration, Calcification, Physiologic, cell adhesion, Cell clusters, Cell culture, Cell distribution, Cell morphology, cell proliferation, cell structure, cell viability, Cells, Cultured, cellular distribution, Ceramic materials, chemistry, Coating procedures, Collagen, collagen type 1, Collagen type I, conjugation, controlled study, cross linking, cross linking reagent, Cross-Linking Reagents, Crosslinked, cytology, Cytotoxicity, DNA, DNA quantification, drug conjugation, Drug delivery, drug delivery system, Drug delivery vehicles, drug effect, Drug-delivery systems, Durapatite, Extracellular matrices, extracellular matrix, Functionalized, human, Human bone marrow cells, human cell, Humans, hydroxyapatite, in vitro study, In-vitro, Macroporous, Macroporous ceramics, male, matrix, metabolism, methylene blue, Methylene blue staining, Microscopy, Electron, Scanning, molecular scaffold, n hydroxysuccinimide, N-hydroxysuccinimide, polymer, Polymer replication, porosity, Porous scaffold, Scaffolds, Scanning electron microscopy, Sintering, Sintering cycles, spectrometry, Spectrometry, X-Ray Emission, Tissue engineering, tissue scaffold, Tissue Scaffolds, Type I collagen, Young Adult},
	isbn = {15493296 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77956483928\&partnerID=40\&md5=de85a8bfe5af88cbc45e80302ab4dfd4},
	author = {Teixeira, S. and Fernandes, M.H. and Ferraz, M.P. and Monteiro, F.J.}
}
@book {2320,
	title = {Morphology and mechanical properties of injectable ceramic microspheres},
	series = {Key Engineering MaterialsKey Eng Mat},
	volume = {396-398},
	year = {2009},
	note = {Cited By (since 1996): 1Export Date: 21 November 2012Source: ScopusCODEN: KEMAEdoi: 10.4028/0-87849-353-0.691Language of Original Document: EnglishCorrespondence Address: Oliveira, S. M.; ESTV, Departamento de Engenharia Mec{\^a}nica, Instituto Polit{\'e}cnico de Viseu, Viseu, PortugalReferences: Barrias, C.C., Ribeiro, C.C., Lamghari, M., Miranda, C.S., Barbosa, M.A., Proliferation, activity, and osteogenic differentiation of bone marrow stromal cells cultured on calcium titanium phosphate microspheres (2005) Journal of Biomedical Materials Research, 72 A (1), pp. 57-66;Barrias, C.C., Ribeiro, C.C., Barbosa, M.A., Adhesion and proliferation of human osteoblastic cells seeded on injectable hydroxyapatite microspheres (2004) Bioceramics, 16, pp. 254-262,877-880; 
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},
	month = {2009///},
	pages = {691 - 694},
	abstract = {The aim of this study was to analyze the effect of starting powder granulometry and sintering conditions on the morphological structure and mechanical properties of injectable hydroxyapaptite (HAp) microspheres. The mechanical properties of the microspheres were evaluated, to investigate if their integrity could be maintained during the injection process. To obtain microspheres, HAp powders were dispersed in a sodium alginate solution and spherical particles were prepared by droplet extrusion under a co-axial air stream, coupled with ionotropic gelation in the presence of Ca                        2+. This was followed by a sintering process at various temperatures and times. The morphology of microspheres was observed under SEM, diameter measurements were performed in an optical microscope and the compression strength was evaluated using a texture analyzer. Finally, microspheres prepared using lower granulometry HAp powders and sintered at 1200{\textdegree}C for 1 hour presented the best properties and were selected as the most suitable for the envisaged application.
},
	keywords = {Air streams, Apatite, Calcium, Ceramic microspheres, Co-axial, Coagulation, Compression strengths, Diameter measurements, Gelation, Granulometry, hydroxyapatite, Injectable, Injection process, Ionotropic gelations, Mechanical properties, Microspheres, Morphological structures, Morphology and mechanical properties, Optical microscopes, Powders, SEM, Sintering, Sintering conditions, Sintering process, Sodium, Sodium alginates, Spherical particles, Starting powders, Texture analyzers},
	isbn = {10139826 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-58849147162\&partnerID=40\&md5=5bf4364653a3ad10b5ab28c1a01568ab},
	author = {Oliveira, S.M. and Barrias, C.C. and Ribeiro, C.C. and Almeida, I.F. and Bahia, M.F. and Barbosa, M.A.}
}
@article {2308,
	title = {Physical characterization of hydroxyapatite porous scaffolds for tissue engineering},
	journal = {Materials Science and Engineering CMater. Sci. Eng. C},
	volume = {29},
	year = {2009},
	note = {Cited By (since 1996): 16Export Date: 21 November 2012Source: Scopusdoi: 10.1016/j.msec.2008.09.052Language of Original Document: EnglishCorrespondence Address: Teixeira, S.; INEB - Instituto de Engenharia Biom{\'e}dica, Divis{\~a}o de Biomateriais, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal; email: smsilva@ineb.up.ptReferences: Jones, A.C., Milthorpe, B., Averdunk, H., Limaye, A., Senden, T.J., Sakellariou, A., (2004) Biomaterials, 25 (20), p. 4947;Karageorgiou, V., Kaplan, D., (2005) Biomaterials, 26 (27), p. 5474; 
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},
	month = {2009///},
	pages = {1510 - 1514},
	abstract = {The present study refers to the preparation and characterization of porous hydroxyapatite scaffolds to be used as matrices for bone regeneration or as specific release vehicles. Ceramics are widely used for bone tissue engineering purposes and in this study, hydroxyapatite porous scaffolds were produced using the polymer replication method. Polyurethane sponges were used as templates and impregnated with a ceramic slurry at different ratios, and sintered at 1300~{\textdegree}C following a specific thermal cycle. The characteristics of the hydroxyapatite porous scaffolds and respective powder used as starting material, were investigated by using scanning electron microscopy, particle size distribution, X-ray diffraction, Fourier transformed infrared spectroscopy and compressive mechanical testing techniques. It was possible to produce highly porous hydroxyapatite scaffolds presenting micro and macropores and pore interconnectivity. {\textcopyright} 2008 Elsevier B.V. All rights reserved.},
	keywords = {Apatite, Bone, Bone regenerations, Bone tissue engineerings, Ceramic materials, Ceramic slurries, Fourier-transformed infrared spectroscopies, hydroxyapatite, infrared spectroscopy, Macro-pores, Mechanical testing, Physical characterizations, Polymer blends, Polymer replications, Polymers, Polyurethane sponges, Pore interconnectivity, Porous hydroxyapatites, Porous scaffolds, Scaffolds, Scanning electron microscopy, Spectroscopic analysis, Starting materials, Thermal cycles, Tissue engineering, X- ray diffractions},
	isbn = {09284931 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-67349181295\&partnerID=40\&md5=ea36fd01a8565ecbd7230948b317995d},
	author = {Teixeira, S. and Rodriguez, M.A. and Pena, P. and De Aza, A.H. and De Aza, S. and Ferraz, M.P. and Monteiro, F.J.}
}
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},
	month = {2008///},
	pages = {483 - 493},
	abstract = {This study concerns the preparation, physical, and in vitro characterization of two different types of hydroxyapatite (HA) microspheres, which are intended to be used as drug-delivery systems and bone-regeneration matrices. Hydroxyapatite nanoparticles (HA-1 and HA-2) were prepared using the chemical precipitation synthesis with H                        3PO
                        4, Ca(OH) 
                        2, and a surfactant, SDS (sodium dodecyl sulfate), as starting reagents. The HA powders were dispersed in a sodium alginate solution, and spherical particles were obtained by droplet extrusion coupled with ionotropic gelation in the presence of Ca
                        2+. These were subsequently sintered to produce HA-1 and HA-2 microspheres with a uniform size and interconnected microporosity. Both powders and microspheres were characterized using FTIR and X-ray diffraction. Moreover, SEM and mercury intrusion porosimetry were used to analyze the microspheres, and TEM was used to analyze the powders. Results showed that pure HA and mixtures of HA/β-TCP in the nanometer range and needlelike shape were obtained for HA-1 and HA-2 powders, respectively. Neutral Red, scanning electron microscopy and confocal microscopy were used to evaluate the behavior of osteoblastic-like MG-63 cells cultured on HA microspheres surfaces for 7 days. Results showed that good adhesion and proliferation of osteoblasts on the HA microspheres surface. Cells built bridges between adjacent microspheres, forming microspheres-cells clusters in both types of materials. {\textcopyright} 2007 Wiley Periodicals, Inc.
},
	keywords = {alginic acid, analytic method, Apatite, article, Biocompatible Materials, Biological materials, biomaterial, Bone Regeneration, Calcium, calcium hydroxide, calcium phosphate, cell adhesion, Cell Line, cell proliferation, Chemical precipitation, Chemotherapy, Comparative studies, comparative study, controlled study, dodecyl sulfate sodium, Drug delivery, Drug delivery system (DDS), Drug Delivery Systems, Drug dosage, Durapatite, Gelation, human, human cell, Humans, hydroxyapatite, Hydroxyapatite (HAP), Hydroxylation, In vitro characterization, in vitro study, infrared spectroscopy, materials testing, Medical applications, Mercury intrusion porosimetry, microsphere, Microspheres, Nano-hydroxyapatite (n-HA), Nanohydroxyapatite, nanoparticle, nanoparticles, neutral red, osteoblast, Osteoblasts, Particle Size, phosphoric acid, porosity, powder, Powders, precipitation, Precipitation (chemical), reagent, Regeneration (renovating), Scanning electron microscopy, surfactant, synthesis, Synthesis (chemical), X ray diffraction},
	isbn = {15493296 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-47049103112\&partnerID=40\&md5=138b3e2f3a97d8b398546d3f85567a0f},
	author = {Mateus, A.Y.P. and Barrias, C.C. and Ribeiro, C. and Ferraz, M.P. and Monteiro, F.J.}
}
@article {2336,
	title = {Injectability of a bone filler system based on hydroxyapatite microspheres and a vehicle with in situ gel-forming ability},
	journal = {Journal of Biomedical Materials Research - Part B Applied BiomaterialsJ. Biomed. Mater. Res. Part B Appl. Biomater.},
	volume = {87},
	year = {2008},
	note = {Cited By (since 1996): 9Export Date: 21 November 2012Source: ScopusCODEN: JBMRGdoi: 10.1002/jbm.b.31066PubMed ID: 18437700Language of Original Document: EnglishCorrespondence Address: Oliveira, S. M.; Escola Superior de Tecnologia de Viseu (ESTV), Dep. de Eng. Mec{\^a}nica e Gest{\~a}o Industrial, 3504-510 Viseu, Portugal; email: serafim@ineb.up.ptChemicals/CAS: alginic acid, 28961-37-7, 29894-36-8, 9005-32-7, 9005-38-3; calcium carbonate, 13397-26-7, 13701-58-1, 14791-73-2, 471-34-1; gluconolactonase, 9012-44-6, 9012-73-1; hydroxyapatite, 1306-06-5, 51198-94-8; Bone Substitutes; Durapatite, 1306-06-5; GelsTradenames: Captal S, Plasma BiotalManufacturers: Plasma BiotalReferences: Ribeiro, C.C., Barrias, C.C., Barbosa, M.A., Calcium phosphate-alginate microspheres as enzyme delivery matrices (2004) Biomaterials, 25, pp. 4363-4373;Grabowski, G.A., Leslie, N., Wenstrup, R., Enzyme therapy for Gaucher disease: The first 5 years (1998) Blood Rev, 12, pp. 115-133; 
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},
	month = {2008///},
	pages = {49 - 58},
	abstract = {The aim of this study was to test the injectability of a bone filler system based on the combination of ceramic microspheres with a gel-like vehicle, for noninvasive surgery. Porous hydroxyapatite microspheres with a uniform size and an average diameter of 535 {\textpm} 38 μm were prepared, and their compression strength and friability were tested. The sodium-alginate solution with a concentration of 7.25\% (w/v) was used as the vehicle. To promote its in situ gelation, calcium carbonate and D-gluconic-δ-lactone were added to the solution. Microspheres were mixed with the vehicle at different percentages (20-40 wt \%). Gelation times in the range of 8-20 min, were obtained, depending on the formulation. Mixtures of HAp microspheres with alginate solution at 7.25\% originating a gel in 11 min present an adequate handling time to perform an injection. Their injectability was evaluated using an injection device commonly employed in vertebroplasty surgical procedures, coupled to a texturometer in compression mode. Using an extrusion rate of 0.1 mm/s, the force required to extrude any of the mixtures tested was lower than 100 N. For an extrusion rate of 1 mm/s mixtures with 40 wt \% of microspheres were very difficult to inject. Mixtures with 35 wt \% of microspheres presented the best compromise between injectability and compression strength of the gelled system. MicroCT analysis revealed a homogeneous distribution of the microspheres inside the vehicle, as well as full interconnection of the intra-microspheres spaces. The compression strength for the gelled systems ranged from 80 kPa (gel itself) to 600 kPa (composite with 40 Wt \% of microspheres). {\textcopyright} 2008 Wiley Periodicals, Inc.},
	keywords = {Alginate, alginic acid, Apatite, article, Average diameter, bioengineering, Bone, bone filler system, Bone Substitutes, Calcium, Calcium carbonate, Ceramic, Ceramic microspheres, Coagulation, Colloids, compression, Compression mode, Compression strengths, Compressive Strength, Computerized tomography, Concentration (process), Data compression, Durapatite, Extrusion, Extrusion rates, Fillers, Forming, Gel-forming ability, Gelation, Gels, gluconolactonase, Handling time, Homogeneous distribution, hydrogel, hydroxyapatite, In situ gelation, in situ hybridization, In-situ, Injectability, injection, Injection (oil wells), Micro-CT, microsphere, Microspheres, Mixtures, non invasive procedure, Particle Size, Porous hydroxyapatite, Sodium, Surgery, Surgical procedures, Uniform size, Vehicles, Vertebroplasty},
	isbn = {15524973 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-52449123139\&partnerID=40\&md5=cc648bad01cb2c6aa01d885acac10e8a},
	author = {Oliveira, S.M. and Barrias, C.C. and Almeida, I.F. and Costa, P.C. and Pena Ferreira, M.R. and Bahia, M.F. and Barbosa, M.A.}
}
@article {2354,
	title = {PLD bioactive ceramic films: The influence of CaO-P                    2O 
                    5 glass additions to hydroxyapatite on the proliferation and morphology of osteblastic like-cells
},
	journal = {Journal of Materials Science: Materials in MedicineJ. Mater. Sci. Mater. Med.},
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Anselme, K., Linez, P., Bigerelle, M., Le Maguer, D., Le Maguer, A., Hardouin, P., Hildebrand, H.F., Leroy, J.M., (2000) Biomaterials, 21, p. 1567; 
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Kim, H.J., Kim, S.H., Kim, M.S., Lee, E.J., Oh, H.G., Oh, W.M., Park, S.W., Dean, D.D., (2005) J. Biomed. Mater. Res., 74, p. 366
},
	month = {2008///},
	pages = {1775 - 1785},
	abstract = {This work consists on the evaluation of the in vitro performance of Ti6Al4V samples PLD (pulsed laser deposition) coated with hydroxyapatite, both pure and mixed with a CaO-P                        2O
                        5 glass. Previous studies on immersion of PLD coatings in SBF, showed that the immersion apatite films did not present the usual cauliflower morphology but replicated the original columnar structure and exhibited good bioactivity. However, the influence of glass associated to hydroxyapatite concerning adhesion, proliferation and morphology of MG63 cells on the films surface was unclear. In this study, the performance of these PLD coated samples was evaluated, not only following the physical-chemical transformations resulting from the SBF immersion, but also evaluating the cytocompatibility in contact with osteoblast-like MG63 cells. SEM and AFM confirmed that the bioactive ceramic PLD films reproduce the substrate{\textquoteright}s surface topography and that the films presented good adherence and uniform surface roughness. Physical-chemical phenomena occurring during immersion in SBF did not modify the original columnar structure. In contact with MG63 cells, coated samples exhibited very good acceptance and cytocompatibility when compared to control. The glass mixed with hydroxyapatite induced higher cellular proliferation. Cells grown on these samples presented many filipodia and granular structures, typical features of osteoblasts. {\textcopyright} 2007 Springer Science+Business Media, LLC.
},
	keywords = {Apatite, Apatite films, Bioactive ceramic films, Bioactive glass, Bioactivity, Bioceramics, Biocompatible Materials, Biofilms, Brassica oleracea var. botrytis, Calcium Compounds, calcium oxide, Cauliflower morphology, cell adhesion, cell proliferation, cell structure, cell survival, ceramics, Columnar structure, conference paper, controlled study, Durapatite, glass, human, human cell, Humans, hydroxyapatite, Lasers, materials testing, Microscopy, Atomic Force, Microscopy, Electron, Scanning, morphology, osteoblast, Osteoblasts, oxide, Oxides, phosphorous pentoxide, Phosphorus Compounds, Polystyrenes, priority journal, Pulsed laser deposition, unclassified drug},
	isbn = {09574530 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-40949140642\&partnerID=40\&md5=de09d5133a0616668cb5e57135d91ae6},
	author = {Oliveira, G.M. and Ferraz, M.P. and Gonz{\'a}lez, P.G. and Serra, J. and Leon, B. and P{\`e}rez-Amor, M. and Monteiro, F.J.}
}
@article {2415,
	title = {Cultivation of human embryonic stem cells without the embryoid body step enhances osteogenesis in vitro},
	journal = {Stem CellsStem Cells},
	volume = {24},
	year = {2006},
	note = {Cited By (since 1996): 80Export Date: 21 November 2012Source: ScopusCODEN: STCEEdoi: 10.1634/stemcells.2005-0383Language of Original Document: EnglishCorrespondence Address: Langer, R.S.; Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139-4307, United States; email: rlanger@mit.eduChemicals/CAS: apatite, 64476-38-6; calcium, 7440-70-2; collagen, 9007-34-5; dexamethasone, 50-02-2; hydroxyapatite, 1306-06-5, 51198-94-8; phosphorus, 7723-14-0; alkaline phosphatase, 9001-78-9; calcium phosphate, 10103-46-5, 13767-12-9, 14358-97-5, 7758-87-4; osteocalcin, 136461-80-8; Alkaline Phosphatase, 3.1.3.1; Calcium Phosphates; Collagen, 9007-34-5; Osteocalcin, 104982-03-8; calcium phosphate, 10103-46-5References: Langer, R., Vacanti, J.P., Tissue engineering (1993) Science, 260, pp. 920-926;Alsberg, E., Anderson, K.W., Albeiruti, A., Cell-interactive alginate hydrogels for bone tissue engineering (2001) J Dent Res, 80, pp. 2025-2029; 
Bhatia, M., Derivation of the hematopoietic stem cell compartment from human embryonic stem cell lines (2005) Ann N Y Acad Sci, 1044, pp. 24-28; 
Thomson, J.A., Itskovitz-Eldor, J., Shapiro, S.S., Embryonic stem cell lines derived from human blastocysts (1998) Science, 282, pp. 1145-1147. , erratum in Science 1998 282:1827; 
Perlingeiro, R.C., Kyba, M., Daley, G.Q., Clonal analysis of differentiating embryonic stem cells reveals a hematopoietic progenitor with primitive erythroid and adult lymphoid-myeloid potential (2001) Development, 128, pp. 4597-4604; 
Zur Nieden, N.I., Kempka, G., Ahr, H.J., In vitro differentiation of embryonic stem cells into mineralized osteoblasts (2003) Differentiation, 71, pp. 18-27; 
Bourne, S., Polak, J.M., Hughes, S.P., Osteogenic differentiation of mouse embryonic stem cells: Differential gene expression analysis by cDNA microarray and purification of osteoblasts by cadherin-11 magnetically activated cell sorting (2004) Tissue Eng, 10, pp. 796-806; 
Buttery, L.D., Bourne, S., Xynos, J.D., Differentiation of osteoblasts and in vitro bone formation from murine embryonic stem cells (2001) Tissue Eng, 7, pp. 89-99; 
Shimko, D.A., Burks, C.A., Dee, K.C., Comparison of in vitro mineralization by murine embryonic and adult stem cells cultured in an osteogenic medium (2004) Tissue Eng, 10, pp. 1386-1398; 
Bronson, S.K., Bone nodule formation via in vitro differentiation of murine embryonic stem cells (2003) Methods Enzymol, 365, pp. 241-251; 
Sottile, V., Thomson, A., McWhir, J., In vitro osteogenic differentiation of human ES cells (2003) Cloning Stem Cells, 5, pp. 149-155; 
Bielby, R.C., Boccaccini, A.R., Polak, J.M., In vitro differentiation and in vivo mineralization of osteogenic cells derived from human embryonic stem cells (2004) Tissue Eng, 10, pp. 1518-1525; 
Cao, T., Heng, B.C., Ye, C.P., Osteogenic differentiation within intact human embryoid bodies result in a marked increase in osteocalcin secretion after 12 days of in vitro culture, and formation of morphologically distinct nodule-like structures (2005) Tissue Cell, 37, pp. 325-334; 
Ginis, I., Luo, Y., Miura, T., Differences between human and mouse embryonic stem cells (2004) Dev Biol, 269, pp. 360-380; 
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Amit, M., Carpenter, M.K., Inokuma, M.S., Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture (2000) Dev Biol, 227, pp. 271-278; 
Karp, J.M., Shoichet, M.S., Davies, J.E., Bone formation on two-dimensional poly(DL-lactide-co-glycolide) (PLGA) films and three-dimensional PLGA tissue engineering scaffolds in vitro (2003) J Biomed Mater Res, 64 A, pp. 388-396; 
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Draper, J.S., Pigott, C., Thomson, J.A., Surface antigens of human embryonic stem cells: Changes upon differentiation in culture (2002) J Anat, 200, pp. 249-258; 
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Schmitt, B., Ringe, J., Haupl, T., BMP2 initiates chondrogenic lineage development of adult human mesenchymal stem cells in high-density culture (2003) Differentiation, 71, pp. 567-577; 
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Wei, C.L., Miura, T., Robson, P., Transcriptome profiling of human and murine ESCs identifies divergent paths required to maintain the stem cell state (2005) Stem Cells, 23, pp. 166-185; 
Heng, B.C., Cao, T., Stanton, L.W., Strategies for directing the differentiation of stem cells into the osteogenic lineage in vitro (2004) J Bone Miner Res, 19, pp. 1379-1394
},
	month = {2006///},
	pages = {835 - 843},
	abstract = {Osteogenic cultures of embryonic stem cells (ESCs) are predominately derived from three-dimensional cell spheroids called embryoid bodies (EBs). An alternative method that has been attempted and merits further attention avoids EBs through the immediate separation of ESC colonies into single cells. However, this method has not been well characterized and the effect of omitting the EB step is unknown. Herein, we report that culturing human embryonic stem cells (hESCs) without the EB stage leads to a sevenfold greater number of osteogenic cells and to spontaneous bone nodule formation after 10-12 days. In contrast, when hESCs were differentiated as EBs for 5 days followed by plating of single cells, bone nodules formed after 4 weeks only in the presence of dexamethasone. Furthermore, regardless of the inclusion of EBs, bone matrix formed, including cement line matrix and mineralized collagen, which displayed apatitic mineral (PO                        4) with calcium-to-phosphorous ratios similar to those of hydroxyapatite and human bone. Together these results demonstrate that culturing hESCs without an EB step can be used to derive large quantities of functional osteogenic cells for bone tissue engineering. {\textcopyright}AlphaMed Press.
},
	keywords = {alkaline phosphatase, Apatite, article, bone development, bone growth, bone matrix, bone mineralization, Bone tissue engineering, Calcium, calcium phosphate, Calcium phosphates, Cell Culture Techniques, cell differentiation, cell separation, Collagen, collagen synthesis, culture technique, cytology, dexamethasone, embryo, embryo culture, Embryoid bodies, embryonic stem cell, extracellular matrix, human, human cell, human embryo, Human embryonic stem cells, Humans, hydroxyapatite, in vitro study, Matrix characterization, metabolism, methodology, ossification, osteocalcin, Osteogenesis, Osteogenic cell frequency, phosphorus, spheroid cell, Tissue engineering, totipotent stem cell, Totipotent Stem Cells},
	isbn = {10665099 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33745504422\&partnerID=40\&md5=214785ea9403886207b058cb87570338},
	author = {Karp, J.M. and Ferreira, L.S. and Khademhosseini, A. and Kwon, A.H. and Yeh, J. and Langer, R.S.}
}
@article {2438,
	title = {Chemical modification of chitosan by phosphorylation: An XPS, FT-IR and SEM study},
	journal = {Journal of Biomaterials Science, Polymer EditionJ. Biomater. Sci. Polym. Ed.},
	volume = {16},
	year = {2005},
	note = {Cited By (since 1996): 50Export Date: 21 November 2012Source: ScopusCODEN: JBSEEdoi: 10.1163/156856205774576736Language of Original Document: EnglishCorrespondence Address: Amaral, I.F.; Laborat{\'o}rio de Biomateriais, INEB - Instituto de Engenharia Biom{\'e}dica, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal; email: iamaral@ineb.up.ptChemicals/CAS: chitosan, 9012-76-4; phosphate, 14066-19-4, 14265-44-2; apatite, 64476-38-6; butanol, 35296-72-1, 71-36-3; calcium ion, 14127-61-8; Chitosan, 9012-76-4; PhosphatesReferences: Khor, E., (2001) Chitin: Fulfilling a Biomaterials Promise, , Elsevier Science, Oxford;Vande Vord, P.J., Matthew, H.W.T., DeSilva, S.P., Mayton, L., Wu, B., Wooley, P.H., (2002) J. Biomed. Mater. Res., 59, p. 585; 
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},
	month = {2005///},
	pages = {1575 - 1593},
	abstract = {In the present work, the surface of chitosan membranes was modified using a phosphorylation method carried out at room temperature. Phosphorylation may be of particular interest in materials for orthopaedic applications, due to the cation-exchange properties of phosphate functionalities. Phosphate groups chelate calcium ions, thus inducing the deposition of an apatite-like layer known to improve the osteoconduction of polymer-based implants. Additionally, the negatively charged phosphate functionalities, together with the positively charged amine groups from chitosan, are expected to provide chitosan with an amphoteric character, which may be useful as a combinatorial therapeutic strategy, by simultaneously allowing the immobilization of signalling molecules like growth factors. Phosphorylation was carried out at room temperature using the H                        3 PO
                        4/Et
                        3 PO
                        4/P
                        2O
                        5/butanol method. Surface characterization was performed by XPS, ATR-FT-IR, and SEM. Cross-sections were analyzed by SEM fitted with EDS. The phosphate content increased with the reaction time, as shown by XPS and ATR-FT-IR, a P/N atomic ratio of 0.73 being obtained after 48 h of treatment. High-resolution XPS spectra regarding C
                        1s, O
                        1s, N
                        1s and P
                        2p are discussed. The introduction of a neutralization step led to a reduction of P content, which pointed out to the presence of phosphates ionically bound to protonated amines, in addition to phosphate esters. EDS analysis of cross-sections revealed a gradual P reduction up to 50\% towards the inner part of the membrane. {\textcopyright} VSP 2005.
},
	keywords = {Acetylation, amine, animal, Animals, Apatite, article, bone conduction, butanol, calcium ion, cation exchange, cephalopod, chelate, Chemical modification, chemistry, Chitin, chitosan, comparative study, controlled study, Decapodiformes, Fourier transform infrared spectroscopy, Fourier transform infrared spectroscopy (FT-IR), Growth factor, immobilization, Implants (surgical), infrared spectroscopy, isolation and purification, Microscopy, Electron, Scanning, molecular weight, organophosphate, phosphate, Phosphate groups, Phosphates, Phosphorylation, Phosphorylation method, Plastics applications, priority journal, reflectometry, room temperature, Scanning electron microscopy, SEM-EDS, signal transduction, spectrometry, Spectrometry, X-Ray Emission, Spectroscopy, Fourier Transform Infrared, Surface chemical reaction, Surface Properties, surface property, temperature, time, Time Factors, viscosity, X ray photoelectron spectroscopy, X-rayphotoelectron spectroscopy (XPS)},
	isbn = {09205063 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33644875542\&partnerID=40\&md5=cb42a0fba6d2000d93b90af9724a5bc1},
	author = {Amaral, I.F. and Granja, P.L. and Barbosa, M.A.}
}
@article {2480,
	title = {Ultrastructural comparison of dissolution and apatite precipitation on hydroxyapatite and silicon-substituted hydroxyapatite in vitro and in vivo},
	journal = {Journal of Biomedical Materials Research - Part AJ. Biomed. Mater. Res. Part A},
	volume = {69},
	year = {2004},
	note = {Cited By (since 1996): 48Export Date: 21 November 2012Source: ScopusCODEN: JBMRCPubMed ID: 15162409Language of Original Document: EnglishCorrespondence Address: Porter, A.E.; Dept. of Mat. Science and Metallurgy, University of Cambridge, Pembroke Street, Cambridge, CB2 3QZ, United Kingdom; email: aep30@cam.ac.ukChemicals/CAS: apatite, 64476-38-6; carbonic acid, 3812-32-6, 463-79-6; hydroxyapatite, 1306-06-5, 51198-94-8; silicon, 7440-21-3; Biocompatible Materials; Durapatite, 1306-06-5; Silicon, 7440-21-3References: Porter, A.E., Best, S.M., Bonfield, W., Ultrastructural comparison of hydroxyapatite and silicon-substituted hydroxyapatite for biomedical applications (2003) J Biomed Mater Res, 68 A, pp. 133-141;Patel, N., Gibson, I.R., Hing, K.A., Best, S.M., Revell, P.A., Bonfield, W., A comparative study on the in vivo behaviour of hydroxyapatite and silicon substituted hydroxyapatite granules (2002) J Mater Sci Mater Med, 13, pp. 1199-1206; 
Porter, A.E., Patel, N., Skepper, J.N.S., Best, S.M., Bonfield, W., Comparison of in vivo dissolution processes in hydroxyapatite and silicon-hydroxyapatite bioceramics (2003) Biomaterials, 24, pp. 4609-4620; 
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Fujibayashi, S., Neo, M., Kim, H.-M., Kokubo, T., Nakamura, T., A comparative study between in vivo bone ingrowth and in vitro apatite formation on Na 2-CaO-SiO 2 glasses (2003) Biomaterials, 24, pp. 1349-1356; 
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},
	month = {2004///},
	pages = {670 - 679},
	abstract = {Recent histological studies have demonstrated that the substitution of silicate ions into hydroxyapatite (HA) significantly increases the rate of bone apposition to HA implants. The enhanced bioactivity of silicon-substituted HA (Si-HA) over pure HA has been attributed to the effect of silicate ions in accelerating dissolution. In the present study, high-resolution transmission electron microscopy (HR-TEM) was employed to compare dissolution of HA and Si-HA in an acellular simulated body fluid (SBF) to dissolution in an in vivo model. HR-TEM observations confirmed a difference in morphology of apatite precipitates in vivo and in SBF: apatite deposits were platelike in vivo and nodular in SBF. Compositional mapping suggested that preferential dissolution of silicon from the implant promotes the nucleation of carbonate apatite around the implant. The in vivo findings illustrated an absence of dissolution at the bone-HA or Si-HA interface, whereas dissolution was extensive from within the implant. The amount of dissolution in acellular SBF was similar to dissolution from within the implant, although the site at which the dissolution nucleates was different: dissolution predominates at the crystallite surfaces in SBF, whereas grain boundary dissolution predominates in vivo. These findings suggest that proteins in the in vivo milieu modify the processes of dissolution from the implant. {\textcopyright} 2004 Wiley Periodicals, Inc.},
	keywords = {Apatite, article, Bioactivity, Biocompatible Materials, body fluid, carbonic acid, comparative study, Composition, Dissolution, Durapatite, histology, hydroxyapatite, implant, Implants (surgical), in vitro study, in vivo study, Interfaces (materials), Microscopy, Electron, Microscopy, Electron, Scanning, morphology, precipitation, Precipitation (chemical), Silicon, Simulated body fluid, Simulated body fluids (SBF), simulation, transmission electron microscopy, ultrastructure},
	isbn = {00219304 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-2942558665\&partnerID=40\&md5=c262d4d218d8dba93d767c3b6f399564},
	author = {Porter, A.E. and Botelho, C.M. and Lopes, M.A. and Santos, J.D. and Best, S.M. and Bonfield, W.}
}
@article {2547,
	title = {Microstructural characterization and in vitro apatite formation in CaO-P                    2O
                    5-TiO
                    2-MgO-Na
                    2O glass-ceramics
},
	journal = {Journal of the European Ceramic SocietyJ Eur Ceram Soc},
	volume = {21},
	year = {2001},
	note = {Cited By (since 1996): 14Export Date: 21 November 2012Source: ScopusCODEN: JECSEdoi: 10.1016/S0955-2219(00)00202-8Language of Original Document: EnglishCorrespondence Address: Zhang, Yong; Inst de Engenharia Biomedica, Porto, PortugalReferences: Hench, L.L., Bioceramics: From concept to clinic (1991) J. Am. Ceram. Soc., 74, pp. 1487-1510;Hench, L.L., Anderson, {\"O}., (1993) An Introduction to Bioceramics, p. 41. , ed. L. L. Hench and J. Wilson. World Scientific, Singapore; 
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Kokubo, T., Kushitani, H., Ohtsuki, C., Sakka, S., Yamamuro, T., Chemical reaction of bioactive glass and glass-ceramics with a simulated body fluid (1992) J. Mater. Sci.: Mater. in Med., 3, pp. 79-83; 
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},
	month = {2001///},
	pages = {169 - 175},
	publisher = {Elsevier Science Ltd},
	abstract = {Bulk calcium phosphate glass and glass-ceramic with CaO/P                        2O
                        5 molar ratio = 1.25 were prepared through introducing small amounts of Na
                        2O, MgO, and TiO
                        2 into the glass. Using XRD analysis, biocompatible β-Ca
                        2P
                        2O
                        7 (β-DCP) and more soluble Ca and Na-containing phases were clearly identified in the microstructure. In vitro bioactivity was assessed by immersion testing in SBF-simulated body fluid and apatite crystals were formed after 4 and 8 weeks of soaking. Porous microstructure was produced through dissolution of soluble phases and desirable porous structure may be achieved by controlling size and distribution of these phases and the leaching process. Therefore, this glass-ceramic is expected to be used as bone repair and regeneration implants and drug delivery carrier.
},
	keywords = {Apatite, Bioactivity, Calcium phosphate glass, Ceramic materials, Crystal microstructure, Crystallization, dissociation, glass, Glass ceramics, Leaching, Lime, Magnesia, Phosphorus Compounds, Porous materials, Sodium compounds, Solubility, Titanium dioxide},
	isbn = {09552219 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0035254788\&partnerID=40\&md5=cca4a1c77dd23f60f95c77dd79908c88},
	author = {Zhang, Y. and Santos, J.D.}
}
@article {2539,
	title = {Mineralization of regenerated cellulose hydrogels},
	journal = {Journal of Materials Science: Materials in MedicineJ. Mater. Sci. Mater. Med.},
	volume = {12},
	year = {2001},
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},
	month = {2001///},
	pages = {785 - 791},
	abstract = {Due to their high water swelling, regenerated cellulose hydrogels and sponges were pre-incubated in a Ca-containing solution, and their mineralization was investigated. Results obtained demonstrate that a simple pre-incubation treatment in a Ca containing solution can induce mineralization in materials with limited or no tendency to mineralize. The minerals formed had an apatitic carbonated and poorly crystalline structure, resembling carbonated hydroxyapatite found in bone mineral. The apatitic layer formed showed a relatively accelerated growth using this technique, exhibiting nodules in their macroscopic structure, which seem to indicate lateral growth. The porous structure of regenerated cellulose sponges was also homogeneously mineralized using this technique. {\textcopyright} 2001 Kluwer Academic Publishers.},
	keywords = {Apatite, article, Bone, bone mineral, Calcification (biochemistry), Calcium, Carbon, Cellulose, crystal, hydrogel, Hydrogels, hydroxyapatite, Incubation, infrared spectroscopy, mineralization, porosity, priority journal, Scanning electron microscopy, surface property, Swelling, Water},
	isbn = {09574530 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0034771780\&partnerID=40\&md5=58fcd227f17f7da6e5e0af69c7351f0a},
	author = {Granja, P.L. and Ribeiro, C.C. and De J{\'e}so, B. and Baquey, C. and Barbosa, M.A.}
}
@article {2574,
	title = {CaO-P                    2O
                    5 glass hydroxyapatite double-layer plasma-sprayed coating: In vitro bioactivity evaluation
},
	journal = {Journal of Biomedical Materials ResearchJ. Biomed. Mater. Res.},
	volume = {45},
	year = {1999},
	note = {Cited By (since 1996): 31Export Date: 21 November 2012Source: ScopusCODEN: JBMRBdoi: 10.1002/(SICI)1097-4636(19990615)45:4<376::AID-JBM13>3.0.CO;2-SLanguage of Original Document: EnglishCorrespondence Address: Santos, J.D.; Departamento Engenharia Metalurgica, FEUP, Universidade do Porto, R. dos Bragas, 4099 Porto Codex, PortugalChemicals/CAS: Alloys; Calcium, 7440-70-2; CaO-SiO2-P2O5-CaF2 glass; Coated Materials, Biocompatible; Durapatite, 1306-06-5; Phosphates; Powders; Resin Cements; Solutions; titanium alloy (TiAl6V4), 12743-70-3; Titanium, 7440-32-6References: Denissen, H., Mangano, C., Venini, G., (1985) Hydroxylapatite Implants., , Padua: Piccin Nuova Libraria, S.P.A;Van Raemdonck, W., Ducheyne, P., De Meester, P., Calcium phosphate ceramics (1984) Metal and Ceramic Biomaterials, pp. 143-166. , Ducheyne P, Hastings GW, editors, Boca Raton, FL: CRC Press; 
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},
	month = {1999///},
	pages = {376 - 383},
	publisher = {John Wiley \& Sons Inc},
	abstract = {Double-layer composite coatings composed of a P                        2O
                        5-based glass/Ca
                        10(PO
                        4)
                        6(OH)
                        2 (HA) mixture top layer and a simple HA underlayer, on Ti-6AI-4V substrates, were prepared using a plasma-spraying technique. The in vitro bioactivity of these coatings was assessed by immersion testing in simulated body fluid. Both scanning electron microscopy (SEM) analysis and the ionic solution changes followed by atomic absorption spectroscopy and the molybdenum blue method demonstrated that these composite coatings induce a faster surface Ca-P layer formation than the simple HA coatings used as a control. X-ray photoelectron spectroscopy (XPS) analysis demonstrated that the Ca-P layer formed was apatite. The combination of SEM and XPS analyses showed that the apatite layer was a calcium-deficient hydroxyapatite with a Ca/P ranging from 1.3 to 1.4 with CO
                        3
                        2- groups contained in the structure.
Double-layer composite coatings composed of a P
                        2O
                        5-based glass/Ca
                        10(PO
                        4)
                        6(OH)
                        2 (HA) mixture top layer and a simple HA underlayer, on Ti-6AI-4V substrates, were prepared using a plasma-spraying technique. The in vitro bioactivity of these coatings was assessed by immersion testing in simulated body fluid. Both scanning electron microscopy (SEM) analysis and the ionic solution changes followed by atomic absorption spectroscopy and the molybdenum blue method demonstrated that these composite coatings induce a faster surface Ca-P layer formation than the simple HA coatings used as a control. X-ray photoelectron spectroscopy (XPS) analysis demonstrated that the Ca-P layer formed was apatite. The combination of SEM and XPS analyses showed that the apatite layer was a calcium-deficient hydroxyapatite with a Ca/P ranging from 1.3 to 1.4 with CO
                        3
                        2- groups contained in the structure.
},
	keywords = {alloy, Alloys, Apatite, article, Atomic absorption spectroscopy, Atomic spectroscopy, Bioactivity, Biocompatibility, biomaterial, Biomaterials, Biomedical engineering, Body fluids, Calcium, Calcium Compounds, CaO SiO2 P2O5 CaF2 glass, CaO-SiO2-P2O5-CaF2 glass, Chemical analysis, chemical composition, Coated Materials, Biocompatible, Double layer coatings, Double-layer coatings, Durapatite, film, glass, Glass plasma spraying, human, Humans, hydroxyapatite, immersion, implant, in vitro study, Ionic solution changes, Magnesium, materials testing, Molybdenum blue, Multilayers, Particle Size, phosphate, Phosphate minerals, Phosphates, Phosphorus Compounds, phosphorus pentoxide, Plasma spraying, potassium, powder, Powders, resin cement, Resin Cements, Scanning electron microscopy, Sodium, solution and solubility, Solutions, structure analysis, Substrates, Surface Properties, surface property, thickness, Tissue, Titanium, titanium alloy (TiAl6V4), Titanium alloys, X ray photoelectron spectroscopy},
	isbn = {00219304 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0033563315\&partnerID=40\&md5=8c0de1e25709302641b203efac50337b},
	author = {Ferraz, M.P. and Monteiro, F.J. and Santos, J.D.}
}
@article {2605,
	title = {Apatite deposition on titanium surfaces - The role of albumin adsorption},
	journal = {BiomaterialsBIOMATERIALS},
	volume = {18},
	year = {1997},
	note = {Cited By (since 1996): 72Export Date: 21 November 2012Source: ScopusCODEN: BIMADdoi: 10.1016/S0142-9612(97)00031-8PubMed ID: 9212191Language of Original Document: EnglishCorrespondence Address: Serro, A.P.; Centro de Quimica Estrutural, Complexo I, Instituto Superior Tecnico, Av. Rovisco Pais, 1096 Lisboa Codex, PortugalChemicals/CAS: alpha-tricalcium phosphate; Apatites; calcium phosphate, 10103-46-5; Calcium Phosphates; dicalcium phosphate anhydrous, 7757-93-9; Hanks Balanced Salt Solution; Isotonic Solutions; monocalcium phosphate; Serum Albumin, Bovine; tetracalcium phosphate; Titanium, 7440-32-6References: Sundgren, J.-E., Bodo, P., Lundstrom, I., Auger electron spectroscopic studies of the interface between human tissue and implants of titanium and stainless steel (1986) J. Colloid Interface Sci., 10, pp. 9-20;Hanawa, T., Ota, M., Characterization of surface film formed on titanium in electrolyte using XPS (1992) Appl. Surface Sci., 55, pp. 269-276; 
Sousa, S.R., Barbosa, M.A., Corrosion resistance of titanium cp in saline physiological solutions with calcium phosphate and proteins (1993) Clin. Mater., 14, pp. 287-294; 
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},
	month = {1997///},
	pages = {963 - 968},
	publisher = {Elsevier Science Ltd},
	abstract = {Titanium implant surfaces are known to spontaneously nucleate apatite layers when in contact with simulated body fluids. However, adsorption of proteins may influence the process of apatite layer formation. In this study the role of bovine serum albumin (BSA) adsorption in the process of apatite deposition on titanium substrates is investigated. Deposition of calcium phosphate was induced by immersing titanium substrates in a Hank{\textquoteright}s balanced salt solution (HBSS) for times ranging from 1 to 23 days. The resulting substrates were studied by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), wettability measurements and electrochemical impedance determinations. All these methods indicate the presence of a calcium phosphate layer. The same procedure was repeated substituting HBSS with a solution of BSA in HBSS. Although SEM, EDS and electrochemical impedance spectra do not reveal the presence of an apatite layer, XPS analysis strongly indicates that the inhibition of apatite formation by BSA is only partial. The competition between BSA adsorption and apatite deposition seems to lead to a mixed film where the protein co-exists with calcium phosphate. Wettability studies suggest that this surface film is heterogeneous and porous, similar to the thicker films formed in albumin-free HBSS.Titanium implant surfaces are known to spontaneously nucleate apatite layers when in contact with simulated body fluids. However, adsorption of proteins may influence the process of apatite layer formation. In this study the role of bovine serum albumin (BSA) adsorption in the process of apatite deposition on titanium substrates is investigated. Deposition of calcium phosphate was induced by immersing titanium substrates in a Hank{\textquoteright}s balanced salt solution (HBSS) for times ranging from 1 to 23 days. The resulting substrates were studied by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), wettability measurements and electrochemical impedance determinations. All these methods indicate the presence of a calcium phosphate layer. The same procedure was repeated substituting HBSS with a solution of BSA in HBSS. Although SEM, EDS and electrochemical impedance spectra do not reveal the presence of an apatite layer, XPS analysis strongly indicates that the inhibition of apatite formation by BSA is only partial. The competition between BSA adsorption and apatite deposition seems to lead to a mixed film where the protein co-exists with calcium phosphate. Wettability studies suggest that this surface film is heterogeneous and porous, similar to the thicker films formed in albumin-free HBSS.
},
	keywords = {Adsorption, Albumin, Albumin adsorption, Animals, Apatite, Apatite deposition, Apatites, article, Binding Sites, Bovinae, bovine serum albumin, Calcium Compounds, calcium phosphate, Calcium phosphates, Cattle, Deposition, Electric Impedance, Electrochemical impedance, Energy dispersive spectroscopy, impedance, implant, Isotonic Solutions, Microscopy, Electron, Scanning, priority journal, Prostheses and Implants, Proteins, Scanning electron microscopy, Serum Albumin, Bovine, Spectrometry, X-Ray Emission, Substrates, Surface Properties, surface property, Surfaces, Tissue Preservation, Titanium, wettability, X ray photoelectron spectroscopy},
	isbn = {01429612 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0031193883\&partnerID=40\&md5=b9eea9b29c987a3c928f576d0b9cdb67},
	author = {Serro, A.P. and Fernandes, A.C. and Saramago, B. and Lima, J. and Barbosa, M.A.}
}
@article {2601,
	title = {Treatments to induce the nucleation and growth of apatite-like layers on polymeric surfaces and foams},
	journal = {Journal of Materials Science: Materials in MedicineJ. Mater. Sci. Mater. Med.},
	volume = {8},
	year = {1997},
	note = {Cited By (since 1996): 51Export Date: 21 November 2012Source: ScopusCODEN: JSMMEdoi: 10.1023/A:1018514107669Language of Original Document: EnglishCorrespondence Address: Reis, R.L.; INEB-Inst. Biomedical Engineering, Praca do Coronel Pacheco 1, 4050 Porto, PortugalTradenames: Hostalen GM9255F, hoechst, Germany; SEVA-CManufacturers: hoechst, GermanyReferences: Lowenstam, H.A., Weiner, S., (1989) On Biomineralization, , Oxford University Press, Oxford;Mann, S., (1988) Nature, 332, p. 119; 
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Li, P., Othsuki, C., Kokubo, T., Nakanish, K., Soga, N., Nakamura, T., Yamamuro, T., (1992) J. Amer. Ceram. Soc., 75, p. 2094; 
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Radder, A.M., Leenders, H., Van Blitterswijk, C.A., (1994) J. Biomed. Mater. Res., 28, p. 141; 
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Reis, R.L., Cunha, A.M., Allan, P.S., Bevis, M.J., (1997) Adv. Polym. Technol., , in press; 
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Hata, K., Kokubo, T., Nakamura, T., Yamamuro, T., (1995) J. Amer. Ceram. Soc., 78, p. 1049; 
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},
	month = {1997///},
	pages = {897 - 905},
	publisher = {Chapman \& Hall Ltd},
	abstract = {In this work, a bioactive glass is used as a percusor of calcium-phosphate (Ca-P) film deposition onto several polymer-based materials. Both bioinert (high molecular weight polyethylene, HMWPE), and biodegradable (corn starch-based blends, SEVA-C) polymers, unreinforced or reinforced with hydroxylapatite (HA), were coated by the very simple proposed route. Also polyurethane (PU) foams, with an open-cell structure, were mineralized by the proposed method. In fact, it was possible to induce the growth of the Ca-P films not only at the surface, but also in the bulk of the PU foam. These cellular materials are intended for cancellous bone replacement applications. The morphology of the formed films was strongly dependent on the used substrate, its polar character, and on the presence of HA in its composition, as observed by SEM. Nevertheless, a well defined needle like structure was observed in all samples at high magnifications. The Ca:P ratios of the films were between 1.5 and 1.7, i.e. in the range of tricalcium phosphate-hydroxylapatite. Raman spectroscopy and thin-film x-ray diffraction (XRD) evidenced the formation of mostly amorphous calcium-phosphate films. After scraping the coating from the polymer surface and heat-treating the resulting powder at 1000{\textdegree}C for 1 h, HA and β-tricalcium phosphate (TCP) typical peaks were found on XRD patterns.In this work, a bioactive glass is used as a percussor of calcium-phosphate (Ca-P) film deposition onto several polymer-based materials. Both bioinert (high molecular weight polyethylene, HMWPE), and biodegradable (corn starch-based blends, SEVA-C) polymers, unreinforced or reinforced with hydroxylapatite (HA), were coated by the very simple proposed route. Also polyurethane (PU) foams, with an open-cell structure, were mineralized by the proposed method. In fact, it was possible to induce the growth of the Ca-P films not only at the surface, but also in the bulk of the PU foam. These cellular materials are intended for cancellous bone replacement applications. The morphology of the formed films was strongly dependent on the used substrate, its polar character, and on the presence of HA in its composition, as observed by SEM. Nevertheless, a well defined needle like structure was observed in all samples at high magnifications. The Ca:P ratios of the films were between 1.5 and 1.7, i.e. in the range of tricalcium phosphate-hydroxylapatite. Raman spectroscopy and thin-film x-ray diffraction (XRD) evidenced the formation of mostly amorphous calcium-phosphate films. After scraping the coating from the polymer surface and heat-treating the resulting powder at 1000 {\textdegree}C for 1 h, HA and β-tricalcium phosphate (TCP) typical peaks were found on XRD patterns.
},
	keywords = {Apatite, Bioactivity, Biomaterials, calcium phosphate, cancellous bone, conference paper, Deposition, Film growth, Foamed plastics, glass, Heat treatment, hydroxyapatite, implantation, mineralization, molecular weight, morphology, Nucleation, Phosphate coatings, Phosphate minerals, polyethylene, polymer, polyurethan foam, Polyurethanes, priority journal, Raman spectrometry, Raman spectroscopy, Scanning electron microscopy, X ray diffraction, Zea mays},
	isbn = {09574530 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0031466435\&partnerID=40\&md5=cf3826a417103c1e6bf61e37f681e8fe},
	author = {Reis, R.L. and Cunha, A.M. and Fernandes, M.H. and Correia, R.N.}
}
@article {2619,
	title = {Characterization of apatite layer formation on P                    2O
                    5-CaO, P
                    2O
                    5-CaO- Na
                    2O, and P
                    2O
                    5-CaO-Na
                    },
	journal = {Journal of Biomedical Materials ResearchJ. BIOMED. MATER. RES.},
	volume = {31},
	year = {1996},
	note = {Cited By (since 1996): 20Export Date: 21 November 2012Source: ScopusCODEN: JBMRBdoi: 10.1002/(SICI)1097-4636(199608)31:4<481::AID-JBM7>3.0.CO;2-HPubMed ID: 8836844Language of Original Document: EnglishCorrespondence Address: Jha, L.J.; IRC in Biomedical Materials, Queen Mary and Westfield College, Mile End Road, London E1 4NS, United KingdomChemicals/CAS: HydroxyapatitesReferences: Hyakuna, K., Yamamuro, T., Kotoura, Y., Oka, M., Kokubo, T., Kushitani, H., Surface reactions of calcium phosphate ceramics to various solutions (1990) J. Biomed. Mater. Res., 24, pp. 471-488;Ebisawa, Y., Kokubo, T., Ohura, K., Yamamuro, T., Bioactivity of CaO{\textperiodcentered}SiO 2-based glasses: In vitro evaluation (1990) J. Mater. Sci.: Mater. Med., 1, pp. 239-244; 
Kokubo, T., Kushitani, H., Ohtsuki, C., Sakka, S., Yamamuro, T., Chemical reaction of bioactive glass and glass ceramics with a simulated body fluid (1992) J. Mater. Sci.: Mater. Med., 3, pp. 79-83; 
Li, P., Yang, Q., Zhang, F., Kokubo, T., The effect of residual glassy phase in a bioactive glass-ceramic on the formation of its surface apatite layer in vitro (1992) J. Mater. Sci.: Mater. Med., 3, pp. 452-456; 
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},
	month = {1996///},
	pages = {481 - 486},
	publisher = {John Wiley \& Sons Inc},
	abstract = {P                        2O
                        5-based glass hydroxyapatite (HA) composites denoted HA-2 oxide, HA-3 oxide, and HA-4 oxide, were immersed in Hank{\textquoteright}s balanced salt solution for a period of 1, 2, 3, and 4 weeks at 37{\textdegree}C in nonagitated condition for in vitro evaluation. A surface layer was precipitated on the composites that was analyzed using scanning electron microscopy (SEM), X-ray photoelecton spectroscopy, and thin film X-ray diffractometry (TF-XRD). SEM micrographs showed complete coverage of the composite surface by crystallites after immersion of 1 week in the solution, which grew thicker with respect to immersion time. The binding energies measured by XPS indicated apatite formation and the presence of carbonate on the composite surface, showing the newly formed layer was a carbonated apatite. Confirmation of the formed apatite layer was obtained by TF-XRD.
                        2O
                        5-based glass hydroxyapatite (HA) composites denoted HA-2 oxide, HA-3 oxide, and HA-4 oxide, were immersed in Hank{\textquoteright}s balanced salt solution for a period of 1, 2, 3, and 4 weeks at 37{\textdegree}C in nonagitated condition for in vitro evaluation. A surface layer was precipitated on the composites that was analyzed using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy, and thin film X-ray diffractometry (TF-XRD). SEM micrographs showed complete coverage of the composite surface by crystallites after immersion of 1 week in the solution, which grew thicker with respect to immersion time. The binding energies measured by XPS indicated apatite formation and the presence of carbonate on the composite surface, showing the newly formed layer was a carbonated apatite. Confirmation of the formed apatite layer was obtained by TF-XRD.
},
	keywords = {Apatite, article, binding affinity, Biomaterials, bone strength, Calcium Compounds, Carbonates, Ceramic materials, Characterization, chemical composition, Composite materials, Crystallites, electron microscopy, glass, Glass hydroxyapatite composites, Hank balanced salt solution, hydroxyapatite, Hydroxyapatites, immersion, Microscopy, Electron, Scanning, Molecular Structure, Oxides, prosthesis material, Scanning electron microscopy, scanning tunneling microscopy, Spectrum Analysis, Thin film X ray diffractometry, Thin films, X ray diffraction, X ray diffraction analysis, X ray photoelectron spectroscopy, X-Ray Diffraction},
	isbn = {00219304 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0030222031\&partnerID=40\&md5=1cba84bf7d0e93a4e3a3808849398c78},
	author = {Jha, L.J. and Santos, J.D. and Knowles, J.C.}
}
@article {2631,
	title = {In vitro calcification of orthopaedic implant materials},
	journal = {Journal of Materials Science: Materials in MedicineJ. MATER. SCI. MATER. MED.},
	volume = {6},
	year = {1995},
	note = {Cited By (since 1996): 23Export Date: 21 November 2012Source: ScopusCODEN: JSMMEdoi: 10.1007/BF00134330Language of Original Document: EnglishCorrespondence Address: Leitao, E.; Instituto de Engenharia Biomedica, Faculdade de Engenharia, Universidade do Porto, Praca Coronel Pacheco 1, 4050 Porto, Portugal},
	month = {1995///},
	pages = {849 - 852},
	publisher = {Chapman \& Hall Ltd},
	abstract = {The formation of an apatite-like layer is achieved by immersing Ti6A14V and TiA12.5Fe substrata in Hank{\textquoteright}s Balanced Salt Solution (HBSS). The layer was characterized by several techniques, namely X-ray microanalysis, X-ray diffraction and X-ray photoelectron spectroscopy. The results suggest that the layer produced by immersion in HBSS is in the form of an amorphous apatite. The pH and the concentrations of calcium and phosphate were monitored as a function of time. In vitro tests with rat bone marrow were performed in order to mimic the bone/biomaterial interface. They were performed on both immersed and non-immersed samples. The in vitro bone marrow results suggest that the apatite-like layer formed may improve the bone bonding characteristics of the studied titanium alloys.The formation of an apatite-like layer is achieved by immersing Ti6Al4V and TiAl2.5Fe substrata in Hank{\textquoteright}s Balanced Salt Solution (HBSS). The layer was characterized by several techniques, namely X-ray microanalysis, X-ray diffraction and X-ray photoelectron spectroscopy. The results suggest that the layer produced by immersion in HBSS is in the form of an amorphous apatite. The pH and the concentrations of calcium and phosphate were monitored as a function of time. In vitro tests with rat bone marrow were performed in order to mimic the bone/biomaterial interface. They were performed on both immersed and non-immersed samples. The in vitro bone marrow results suggest that the apatite-like layer formed may improve the bone bonding characteristics of the studied titanium alloys.
},
	keywords = {Amorphous apatite, Amorphous materials, animal cell, Apatite, balanced salt solution, Bone, bone marrow, Calcification, Calcification (biochemistry), Calcium, calcium phosphate, conference paper, Hank balanced salt solution, immersion, implantation, Implants (surgical), metal implantation, Microanalysis, nonhuman, orthopedics, pH, phosphate, Phosphates, priority journal, rat, Spectroscopy, surface property, time, Titanium, Titanium alloys, X ray analysis, X ray diffraction, X ray photoelectron spectroscopy},
	isbn = {09574530 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0029558709\&partnerID=40\&md5=8ba348deca0317db2d0a3521d82f02e0},
	author = {Leitao, E. and Barbosa, M.A. and De Groot, K.}
}
@article {2635,
	title = {Surface modifications of glass-reinforced hydroxyapatite composites},
	journal = {BiomaterialsBIOMATERIALS},
	volume = {16},
	year = {1995},
	note = {Cited By (since 1996): 24Export Date: 21 November 2012Source: ScopusCODEN: BIMADdoi: 10.1016/0142-9612(95)91124-HPubMed ID: 7492715Language of Original Document: EnglishCorrespondence Address: Santos, J.D.; Dept Metallurgical Engineering, FEUP, University of Porto, Rua dos Bragas 4099-Porto Codex, PortugalChemicals/CAS: Biocompatible Materials; Calcium, 7440-70-2; Glass; Hydroxyapatites; Phosphorus, 7723-14-0; Silicon, 7440-21-3; Sodium, 7440-23-5},
	month = {1995///},
	pages = {521 - 526},
	publisher = {Butterworth-Heinemann Ltd},
	abstract = {Surface modifications of glass-reinforced hydroxyapatite composites immersed in a simulated physiological solution were studied using X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy. In the first stages of the apatite formation process, calcium and silicon ions were leached out from the surface of the composites. After 12 days of immersion, apatite crystals were detected on the surface indicating bioactive behaviour. Sodium ions attributed to sodium sulphate were also found in the apatite layer. Bound water on the surface also increased with immersion time.Surface modifications of glass-reinforced hydroxyapatite composites immersed in a simulated physiological solution were studied using X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy. In the first stages of the apatite formation process, calcium and silicon ions were leached out from the surface of the composites. After 12 days of immersion, apatite crystals were detected on the surface indicating bioactive behaviour. Sodium ions attributed to sodium sulphate were also found in the apatite layer. Bound water on the surface also increased with immersion time.
},
	keywords = {Apatite, article, Bioactive glass, Biocompatible Materials, Biomaterials, Calcium, chemical composition, Composite materials, Electron Probe Microanalysis, glass, Glass reinforced hydroxyapatite composites, Hydrogen-Ion Concentration, hydroxyapatite, Hydroxyapatites, immersion, Ions, Leaching, Microscopy, Electron, Scanning, Phosphates, phosphorus, priority journal, Scanning electron microscopy, Silicon, Sodium, sodium chloride, sodium sulfate, Spectrometry, X-Ray Emission, Spectroscopy, Surface modification, Surface Properties, surface property, Surface treatment, Water, X ray, X ray photoelectron spectroscopy, X ray spectroscopy},
	isbn = {01429612 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0029294502\&partnerID=40\&md5=2694e1944afd0945ac391ba41c4ec7b5},
	author = {Santos, J.D. and Jha, L.J. and Monteiro, F.J.}
}
