



@book {2413,
	title = {Osteoblast proliferation and morphology analysis on laser modified hydroxyapatite surfaces: Preliminary results},
	series = {Key Engineering MaterialsKey Eng Mat},
	volume = {309-311 I},
	year = {2006},
	note = {Cited By (since 1996): 1Export Date: 21 November 2012Source: ScopusCODEN: KEMAELanguage of Original Document: EnglishCorrespondence Address: Teixeira, S.; INEB - Instituto de Engenharia Biom{\'e}dica, Laborat{\'o}rio de Biomaterlais, Rua do Campo Alegre 823, 4150-180, Porto, Portugal; email: smsilva@ineb.up.ptReferences: Duncan, A.C., Laser microfabricated model surfaces for controlled cell growth (2002) Biosensors and Bioelectronics, 17, pp. 413-426;Walboomers, X.F., Contact guidance of rat fibroblasts on various implant materials (1999) Journal of Biomedical Materials Research, 47, pp. 204-212; 
Queiroz, A.C., Laser surface modifications of hydroxyapatite and glass-reinforced hydroxyapatite (2004) Biomaterials, 25, pp. 4607-4614; 
Ahmad, M., McCarthy, M.B., Gronowicz, G., An in vitro model for mineralization of human osteoblasts-like cells on implant materials (1999) Biomaterials, 20, pp. 211-220
},
	month = {2006///},
	pages = {105 - 108},
	abstract = {Biocompatibility has long been associated with surface microtopography, microtexture and microchemistry. The surface topography ultimately affects the nature and the strength of the interactions that occur at biomaterial-biological environment (cell adhesion, mobility, spreading and proliferation). Thus, it is necessary to produce and work with controlled microtopographical surfaces that present reproducible microdomains of a dimension similar to that of the biological elements of interest (for instance, cells). [1] There are a number of substrates that already have been studied (such as silicone, polystyrene, poly-L-lactic acid and titanium coated polystyrene) in terms of surface topography. [2] However, few studies are related to hydroxyapatite substrates. As it is well established, hydroxyapatite is a well known ceramic that is extremely used in medical applications, namely implants and coatings. In this work, the surface topography of dense hydroxyapatite substrates was altered by using KFr excimer laser. Excimer lasers produce high-intensity, pulsed ultraviolet radiation and are especially well suited for materials processing due to their large beam cross-section area, which permits using mask projection technologies to process relatively large areas in a single step.[3].},
	keywords = {Bone, cell adhesion, Cells, Ceramic materials, Excimer laser, Excimer lasers, hydroxyapatite, Microtexture, Microtopography, morphology, Strength of materials, Surface modification, Surface topography, Surface treatment},
	isbn = {10139826 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-33645413875\&partnerID=40\&md5=0234521c5cb850a0ff51ca4c64c39074},
	author = {Teixeira, S. and Queiroz, A.C. and Monteiro, F.J. and Ferraz, M.P. and Vilar, R. and Eug{\'e}nio, S.}
}
@book {2429,
	title = {Adsorption isotherm of sodium ampicillin onto dense and porous hydroxyapatite},
	series = {Key Engineering MaterialsKey Eng Mat},
	volume = {284-286},
	year = {2005},
	note = {Export Date: 21 November 2012Source: ScopusCODEN: KEMAELanguage of Original Document: EnglishCorrespondence Address: Queiroz, A.C.; INEB - Instituto de Engenharia Biom{\'e}dica, Laborat{\'o}rio de Biomaterials, Rua do Campo Alegre, 823, 4150-160 Porto, Portugal; email: aqueiroz@ineb.up.ptReferences: Nikolakakis, I., Newton, J.M., Malamataris, S., (2002) European Journal of Pharmaceutical Sciences, 17 (4-5), pp. 229-238;Barroug, A., Glimcher, M.J., (2002) Journal of Orthopaedic Research, 20 (2), pp. 274-280; 
Queiroz, A.C., Santos, J.D., Monteiro, F.J., Gibson, I.R., Knowles, J.C., (2001) Biomaterials, 22 (11), pp. 1393-1400; 
Queiroz, A.C., Teixeira, S., Santos, J.D., Monteiro, F.J., (2004) Key Enginnering Materials, 254-256, pp. 997-1000
},
	month = {2005///},
	pages = {387 - 390},
	abstract = {The adsorption behaviour of sodium ampicillin to dense and porous hydroxyapatite as been extensively studied through the obtention of an adsorption isotherm. This isotherm was produced at body temperature, and a wide range of antibiotic solutions were used. The adsorption behaviour was measured by UV spectroscopy. The shape of the isotherm for the two forms of the material,dense and porous, indicates that the adsorption behaviour of the antibiotic seems to be different, however this is due to the adsorption taking place within the pores of the porous material, thus showing a larger amount of antibiotic adsorbed.},
	keywords = {Adsorption, Adsorption behavior, Adsorption isotherms, ampicillin, Antibiotics, hydroxyapatite, Porous hydroxyapatite, Porous materials, Sodium ampicillin, Sodium compounds, Ultraviolet spectroscopy},
	isbn = {10139826 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-34249009270\&partnerID=40\&md5=1a365e0d97db937727266c9387789cdc},
	author = {Queiroz, A.C. and Santos, J.D. and Monteiro, F.J.}
}
@article {2451,
	title = {Development of a system to adsorb drugs onto calcium phosphate materials},
	journal = {Journal of Materials Science: Materials in MedicineJ. Mater. Sci. Mater. Med.},
	volume = {16},
	year = {2005},
	note = {Cited By (since 1996): 6Export Date: 21 November 2012Source: ScopusCODEN: JSMMEdoi: 10.1007/s10856-005-2535-3PubMed ID: 15965596Language of Original Document: EnglishCorrespondence Address: Queiroz, A.C.; INEB - Instituto de Engenharia Biom{\'e}dica, Laborat{\'o}rio de Biomateriais, Rua do Campo Alegre 823, 4150-180, Porto, Portugal; email: aqueiroz@ineb.up.ptChemicals/CAS: ampicillin, 69-52-3, 69-53-4, 7177-48-2, 74083-13-9, 94586-58-0; calcium phosphate, 10103-46-5, 13767-12-9, 14358-97-5, 7758-87-4; hydroxyapatite, 1306-06-5, 51198-94-8; metronidazole, 39322-38-8, 443-48-1; Ampicillin, 69-53-4; Anti-Infective Agents; calcium phosphate, 10103-46-5; Calcium Phosphates; Coated Materials, Biocompatible; Delayed-Action Preparations; Drug Carriers; Metronidazole, 443-48-1References: Seymour, R.A., Heasman, P.A., Macgregor, I.D.M., (1992) Drugs, Diseases, and the Periodontium, 1. , edited by R. A. Seymour and P. A. Heasman Oxford University Press, Oxford;Carnevale, R.A., Greco, G.W., Bullard, C.M., Hanker, J.S., (1987) Biomedical Materials and Devices, p. 247. , edited by J. S. Hanker and B. L. Giammara Materials Research Society, Pittsburgh; 
Friedman, M., Steinberg, D., (1990) Pharm. Res., 7, p. 313; 
Hagiwara, S., Takamatsu, N., Tominaga, Y., Umeda, M., (1998) J. Period., 69, p. 62; 
Wright, T.L., Ellen, R.P., Lacroix, J.M., Sinnadurai, S., Mittelman, M.W., (1997) J. Period. Res., 32, p. 473; 
Golomb, G., Friedman, M., Soskolne, A., Stabholz, A., Sela, M.N., (1984) J. Dent. Res., 63, p. 1149; 
Goodson, J.M., Hogan, P.E., Dunham, S.L., (1984) J. Period., 55, p. 81; 
Somayaji, B.V., Jariwala, U., Jayachandran, P., Vidyalakshim, K., Dudhani, R.V., (1998) J. Period., 69, p. 409; 
Stoltze, K., (1992) J. Clin. Period., 19, p. 698; 
Goodson, J.M., Holborow, D., Dunn, R.L., Hogan, P., Dunham, S., (1983) J. Period., 54, p. 575; 
Yu, D., Wong, J., Matsuda, Y., Fox, J.L., Higuchi, W.I., Otsuka, M., (1992) J. Pharm. Sci., 81, p. 529; 
Nishihara, K., (1993) Clin. Mater., 12, p. 159; 
Ferraz, M.P., Monteiro, F.J., Santos, J.D., (1999) J. Biomed. Mat. Res., 45, p. 376; 
Ferraz, M.P., Knowles, J.C., Olsen, I., Monteiro, F.J., Santos, J.D., (1999) J. Biomed. Mat. Res., 47, p. 603; 
Lopes, M.A., Santos, J.D., Monteiro, F.J., Ohtsuki, C., Osaka, A., Kaneko, S., Inoue, H., (2001) J. Biomed. Mat. Res., 54, p. 463; 
Queiroz, A.C., Santos, J.D., Monteiro, F.J., Gibson, I.R., Knowles, J.C., (2001) Biomaterials, 22, p. 1393; 
Santos, J.D., Knowles, J.C., Reis, R.L., Monteiro, F.J., Hastings, G.W., (1994) Biomaterials, 15, p. 5; 
Knowles, J.C., Santos, J.D., Hastings, G.W., World Patent, WO0068164 (1994)Myers, H.M., Tochon-Danguy, H.J., Baud, C.A., (1983) Calcif. Tissue Int., 35, p. 745; 
Ratier, A., Gibson, I.R., Best, S.M., Freche, M., Lacout, J.L., Rodrigues, F., (2001) Biomaterials, 22, p. 897; 
Ando, D.J., (1996) Ultraviolet and Visible Spectroscopy, p. 16. , John Wiley \& Sons, West Sussex
},
	month = {2005///},
	pages = {641 - 646},
	abstract = {Several studies were carried out in order to reduce the systemic use of antibiotics due to the high concentration required to provide the minimum inhibitory concentration (MIC) at infected sites. The aim of this study was to develop a system of drug adsorption onto commercial hydroxyapatite (HA, Ca                        10(PO
                        4)
                        6(OH)
                        2) and glass reinforced hydroxyapatite (GR-HA) granules. The drug will then be released for the local treatment of periodontitis. The antibiotics used in this study were metronidazole, a specific antibiotic indicated for the systemic treatment of periodontitis, and ampicillin, a wide spectrum antibiotic. UV spectroscopy was used to measure the amount of drug adsorbed onto HA and GR-HA granules. Results showed that metronidazole was unable to adsorb on the material{\textquoteright}s surface, as opposed to ampicillin which adsorbed both onto HA and GR-HA. Preliminary release kinetics studies were carried out using a flow through dissolution system. Results are discussed in terms of the influence of the different surface characteristics of the materials on the adsorption processes. {\textcopyright} 2005 Springer Science + Business Media, Inc.
},
	keywords = {Adsorption, ampicillin, Anti-Infective Agents, Antibiotics, article, Calcium Compounds, calcium phosphate, Calcium phosphates, Coated Materials, Biocompatible, concentration response, Delayed-Action Preparations, Diffusion, Dissolution, drug absorption, drug adsorption, Drug Carriers, Drug release, drug stability, glass, Glass reinforced hydroxyapatie (GR-HA), human, Humans, hydroxyapatite, Kinetics, Material{\textquoteright}s surface, Materials science, materials testing, metronidazole, minimum inhibitory concentration, Minimum inhibitory concentration (MIC), periodontitis, priority journal, Reaction kinetics, reduction, surface property, Ultraviolet spectroscopy},
	isbn = {09574530 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-21344438213\&partnerID=40\&md5=5963a17bf67c04ab22d05ce113fa12b0},
	author = {Queiroz, A.C. and Santos, J.D. and Monteiro, F.J.}
}
@book {2424,
	title = {Porous HA scaffolds for drug releasing},
	series = {Key Engineering MaterialsKey Eng Mat},
	volume = {284-286},
	year = {2005},
	note = {Cited By (since 1996): 1Export Date: 21 November 2012Source: ScopusCODEN: KEMAELanguage of Original Document: EnglishCorrespondence Address: Queiroz, A.C.; INEB, Instituto de Engenharia Biom{\'e}dica, Laborat{\'o}rio de Biomateriais, Rua do Campo Alegre 823, 4150-180 Porto, Portugal; email: aqueiroz@ineb.up.ptReferences: Queiroz, A.C., (2001) Biomaterials, 22, p. 1393},
	month = {2005///},
	pages = {407 - 410},
	abstract = {Dense and porous hydroxyapatite materials aimed at being used in controlled drug delivery, were characterised and studied in order to evaluate their ability to adsorb and release sodium ampicillin in a controlled manner, as a model for a drug delivery system, potentially applicable associated to surgery for the treatment of bone defects. These porous materials should also have adequate mechanical strength to withstand manipulation and sculpturing in surgery room. Adsorption and release profiles were obtained for a range of porous materials, leading to higher adsorption rates and more adequate release profiles than for dense materials.},
	keywords = {Adsorption, ampicillin, Controlled drug delivery, Drug release, hydroxyapatite, orthopedics, Porous hydroxyapatite, Porous hydroxyapatites, Porous materials, Scaffolds, Sodium ampicillin, Surgery, Surgery rooms},
	isbn = {10139826 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-34248995543\&partnerID=40\&md5=db9f063f6d3b98c88a9d87c693ada572},
	author = {Queiroz, A.C. and Santos, J.D. and Monteiro, F.J.}
}
@article {2475,
	title = {Laser surface modification of hydroxyapatite and glass-reinforced hydroxyapatite},
	journal = {BiomaterialsBiomaterials},
	volume = {25},
	year = {2004},
	note = {Cited By (since 1996): 12Export Date: 21 November 2012Source: ScopusCODEN: BIMADdoi: 10.1016/j.biomaterials.2003.11.054PubMed ID: 15120506Language of Original Document: EnglishCorrespondence Address: Queiroz, A.C.; INEB-Inst. de Engenharia Biomedica, Laborat{\'o}rio de Biomateriais, Rua do Campo Alegre 823, 4150-180, Porto, Portugal; email: aqueiroz@ineb.up.ptChemicals/CAS: hydroxyapatite, 1306-06-5, 51198-94-8; Biocompatible Materials; Durapatite, 1306-06-5; Macromolecular SubstancesReferences: Krejci, C.B., Bissada, N.F., Farah, C., Greenwell, H., Clinical evaluation of porous and nonporous hydroxyapatite in the treatment of human periodontal bony defects (1987) J Periodontol, 58, pp. 521-528;Seymour, R.A., Heasman, P.A., MacGregor, I.D.M., The pathogenesis of periodontal disease (1992) Drugs, Diseases, and the Periodontium, pp. 1-10. , I.D.M. MacGregor. Oxford: Oxford University Press; 
Systemic antibiotics in periodontics (1996) J Periodontol, 67, pp. 831-838; 
Steinberg, D., Friedman, M., Soskolne, A., Sela, M.N., A new degradable controlled release device for treatment of periodontal disease: In vitro release study (1990) J Periodontol, 61, pp. 393-398; 
Soskolne, W.A., Heasman, H.A., Stabholz, A., Smart, G.J., Palmer, M., Flashner, M., Newman, H.N., Sustained local delivery of chlorhexidine in the treatment of periodontitis: A multi-center study (1997) J Periodontol, 68, pp. 32-38; 
Prado Da Silva, M.H., Lemos, A.F., Gibson, I.R., Ferreira, J.M.F., Santos, J.D., Porous glass reinforced hydroxyapatite materials produced with different organic additives (2002) J Non-Cryst Solids, 304, pp. 286-292; 
Barinov, S.M., Baschenko, Y.V., Application of ceramic composits as implants: Result and problem (1992) Bioceramics and the Human Body, pp. 206-210. , A. Krajewski. UK: Elsevier Science Publishers; 
Koshino, T., Murase, T., Takagi, T., Saito, T., New bone formation around porous hydroxyapatite wedge implanted in opening wedge high tibial osteotomy in patients with osteoarthritis (2001) Biomaterials, 22, pp. 1579-1582; 
Nishihara, K., Studies on peri-root tissue formation around new type artificial root made of dense hydroxyapatite (1993) Clin Mater, 12, pp. 159-167; 
Chang, B., Lee, C., Hong, K., Youn, H., Ryu, H., Chung, S., Park, K., Osteoconduction at porous hydroxyapatite with various pore configurations (2000) Biomaterials, 21, pp. 1291-1298; 
Lopes, M.A., Monteiro, F.J., Santos, J.D., Serro, A.P., Saramago, B., Hydrophobicity, surface tensions, and zeta potential measurements of glass-reinforced hydroxyapatite composites (1999) J Biomed Mater Res, 45, pp. 370-375; 
Santos, J.D., Silva, P.L., Knowles, J.C., Talal, S., Monteiro, F.J., Reinforcement of hydroxyapatite by adding P 2O 5-CaO glasses with Na 2O, K 2O and MgO (1996) J Mater Sci: Mater Med, 7, pp. 187-189; 
Ferraz, M.P., Knowles, J.C., Olsen, I., Monteiro, F.J., Santos, J.D., Flow cytometry analysis of effects of glass on response of osteosarcoma cells to plasma-sprayed hydroxyapatite/CaO-P 2O 5 coatings (1999) J Biomed Mater Res, 47, pp. 603-611; 
Ferraz, M.P., Monteiro, F.J., Santos, J.D., CaO-P2O5 Glass hydroxyapatite double-layer plasma-sprayed coating: In vitro bioactivity evaluation (1999) J Biomed Mater Res, 45, pp. 376-383; 
Lopes, M.A., Santos, J.D., Monteiro, F.J., Ohtsuki, C., Osaka, A., Kaneko, S., Inoue, H., Push-out testing and histological evaluation of glass reinforced hydroxyapatite composites implanted in the tibia of rabbits (2001) J Biomed Mater Res, 54, pp. 463-469; 
Lopes, M.A., Knowles, J.C., Kuru, L., Santos, J.D., Monteiro, F.J., Olsen, I., Flow cytometry for assessing biocompatibility (1998) J Biomed Mater Res, 41, pp. 649-656; 
Queiroz, A.C., Santos, J.D., Monteiro, F.J., Gibson, I.R., Knowles, J.C., Adsorption and release of sodium ampicillin from hydroxyapatite and glass-reinforced hydroxyapatite composites (2001) Biomaterials, 22, pp. 1393-1400; 
Cl{\`e}ries, L., Fern{\'a}ndez-Pradas, J.M., Morenza, J.L., Behaviour in simulated body fluid of calcium phosphate coating obtained by laser ablation (2000) Biomaterials, 21, pp. 1861-1865; 
D{\textquoteright}Alession, L., Teghil, R., Zaccardo, I., Ferro, D., Marotta, V., Pulsed laser ablation and deposition of bioactive glass as coating material for biomedical applications (1999) Appl Surf Sci, 138-139, pp. 527-532; 
Fern{\'a}ndez-Pradas, J.M., Cl{\`e}ries, L., Serra, P., Sardin, G., Morenza, J.L., Evolution of the depositon rate during pulsed laser deposition of hydroxyapatite coatings and its relation with target morphology (2001) Appl Phys a, 72, pp. 613-618; 
Zeng, H., Lacefield, W.R., XPS, EDX and FTIR analysis of pulsed laser deposited calcium phosphate bioceramic coatings: The effects of various process parameters (2000) Biomaterials, 21, pp. 23-30; 
Serra, P., Fern{\'a}ndez-Pradas, J.M., Sardin, G., Morenza, J.L., Interaction effects of an excimer laser beam with hydroxyapatite targets (1997) Appl Surf Sci, 109-110, pp. 384-388; 
Serra, P., Morenza, J.L., Fluence dependence of hydroxyapatite laser ablantion plumes (1998) Thin Solid Films, 335, pp. 43-48; 
Foltyn, S.R., Dye, R.C., Ott, K.C., Peterson, E., Hubbard, K.M., Hutchinson, W., Muenchausen, R.E., Wu, X.D., Target modification in the excimer laser deposition of YBa 2Cu 3O 7-x thin films (1991) Appl Phys Lett, 59, pp. 594-596; 
Oliveira, V., Conde, O., Vilar, R., UV laser micromachining of ceramic materials: Formation of columnar topographies (2001) Adv Eng Mater, 3, pp. 75-81; 
Ricci, J.L., Alexander, H., Laser microtexturing of implant surfaces for enhanced tissue integration (2001) Key Eng Mater, 198-199, pp. 179-202; 
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Rey, C., Shimizu, M., Collins, B., Glimcher, M.J., Resolution enhanced Fourier transform infrared spectroscopy study of the environment of phosphate ion in the early deposits of a solid phase calcium phosphate in bone and enamel and their evolution with age: Investigations in the ν 4 PO 4 3- domain (1990) Calcif Tissue Int, 46, pp. 384-394; 
Rey, C., Shimizu, M., Collins, B., Glimcher, M.J., Resolution enhanced Fourier transform infrared spectroscopy study of the environment of phosphate ion in the early deposits of a solid phase calcium phosphate in bone and enamel and their evolution with age: Investigations in the ν 3 PO 4 3- domain (1991) Calcif Tissue Int, 49, pp. 383-388; 
Elliott, J.C., Structure and chemistry of apatites and other calcium orthophosphates (1994) Inorganic Chemistry, 18, p. 50. , Elliott J.C. Amsterdam: Elsevier Science; 
Dupraz, A., Nguyen, T.P., Richard, M., Dalcusi, G., Passuti, N., Influence of a cellulosic ether carrier on the structure of biphasic calcium phosphate ceramic particles in an injectable composite material (1999) Biomaterials, 20, pp. 663-673; 
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Heitz, J., Pedarning, J.D., Bauerle, D., Petzow, G., Excimer laser ablation and micro-patterning of ceramic Si 3N 4 (1997) Appl Phys a, 65, pp. 259-261; 
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Man, H.C., Zhang, X.M., Yue, T.M., Lau, W.S., Excimer-laser surface modification of engineering ceramics for adhesive bonding (1997) J Mater Proc Techn, 66, pp. 123-129; 
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Pedraza, A., Fowlkes, J.D., Lowndes, D.H., Self organized silicon microcolumns arrays generated by pulsed laser irradiation (1999) Appl Phys a, 69, pp. 731-S734; 
Usoskin, A., Freyhardt, H.C., Krebs, H.U., Influence of light scattering on the development of laser induced ridge-cone structure on target surfaces (1999) Appl Phys a, 69, pp. 823-S826
},
	month = {2004///},
	pages = {4607 - 4614},
	abstract = {Surface treatment of materials with excimer laser radiation often results in the formation of a rough columnar or cone-shaped surface topography, which leads to a considerable increase in the surface area. As a result, the search for a non-porous bioactive material with adequate mechanical properties and a high surface to volume ratio, similar to porous materials, which could be used for drug delivery in the treatment of periodontitis, justified assessing excimer laser surface treatment to promote controlled roughning of hydroxyapatite (HA) and glass-reinforced hydroxyapatite (GR-HA). A KrF excimer laser with 248nm radiation wavelength and 30ns pulse duration was used for surface modification. The laser treatment was carried out in air, using wide ranges of radiation fluence and number of laser pulses. In order to identify the physico-chemical changes induced by the laser treatment and the column formation mechanisms in these materials, the treated surfaces were characterised by laser profilometry, scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infra-red spectroscopy (FTIR). Laser processing induced the formation of a surface topography consisting of cone-shaped features. The constitution of the surface layer was also modified, as revealed by FTIR, XPS and XRD. This work has shown that laser surface modification increases the surface area of HA and GR-HA and is a promising technique to increase the reactivity and drug delivery capability of both materials. {\textcopyright} 2003 Elsevier Ltd. All rights reserved.},
	keywords = {article, Biocompatible Materials, Biomaterials, drug delivery system, Durapatite, Excimer laser, Excimer lasers, Fourier transform infrared spectroscopy, FTIR, glass, hydroxyapatite, infrared spectroscopy, laser, Lasers, Macromolecular Substances, materials testing, Molecular Conformation, Non-porous bioactive materials, periodontitis, physical chemistry, porosity, priority journal, Profilometry, Radiation Dosage, Reinforcement, Scanning electron microscopy, Surface area, Surface modification, Surface Properties, Surface treatment, topography, X ray diffraction, X ray diffraction analysis, X ray photoelectron spectroscopy, XPS, XRD},
	isbn = {01429612 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-2342427815\&partnerID=40\&md5=24da3c08c0c7b636d9d5039812944b52},
	author = {Queiroz, A.C. and Santos, J.D. and Vilar, R. and Eug{\'e}nio, S. and Monteiro, F.J.}
}
@book {2497,
	title = {Porous Hydroxyapatite and Glass Reinforced Hydroxyapatite for Controlled Release of Sodium Ampicillin},
	series = {Key Engineering MaterialsKey Eng Mat},
	volume = {254-256},
	year = {2004},
	note = {Conference code: 62053Cited By (since 1996): 5Export Date: 21 November 2012Source: ScopusCODEN: KEMAELanguage of Original Document: EnglishCorrespondence Address: Queiroz, A.C.; Inst. de Engenharia Biom{\'e}dica, Laborat{\'o}rio de Biomateriais, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal; email: aqueiroz@ineb.up.ptReferences: Krejci, C.B., Bissada, N.F., Farah, C., Greenwell, H., (1987) J Periodontol, 58, pp. 521-528;Seymour, R.A., Heasman, P.A., MacGregor, I.D.M., The pathogenesis of periodontal disease (1992) Drugs, Diseases, and the Periodontium, pp. 1-10. , MacGregor IDM, editor. Oxford: Oxford University Press; 
Steinberg, D., Friedman, M., Soskolne, A., Sela, M.N., (1990) J Periodontol, 61, pp. 393-398; 
Santos, J.D., Silva, P.L., Knowles, J.C., Talal, S., Monteiro, F.J., (1996) J Mater Sci: Mater Med, 7, pp. 187-189; 
Ferraz, M.P., Monteiro, F.J., Santos, J.D., (1999) J Biomed Mat Res, 45, pp. 376-383; 
Queiroz, A.C., Teixeira, S., Santos, J.D., Monteiro, F.J., Key Engineering Materials, , submitted; 
Nishihara, K., (1993) Clin Materials, 12, pp. 159-167; 
Queiroz, A.C., Santos, J.D., Monteiro, F.J., Gibson, I.R., Knowles, J.C., (2001) Biomaterials, 22, pp. 1393-1400
},
	month = {2004///},
	pages = {997 - 1000},
	address = {Porto},
	abstract = {Porous hydroxyapatite (HA) and glass reinforced hydroxyapatite (GRHA) with adequate macro and microporous structure were developed, aiming at being used as drug delivery carrier of antibiotics, for the in situ treatment of periodontitis. Materials were characterised by XRD and FTIR, presenting no changes from similar dense materials. Mercury intrusion porosimetry revealed micropores of less than 1 μm, accounting for 15\% of the total porosity. Compression tests have shown close values for HA and GRHA, with the former showing slightly higher values of strength. Ampicillin adsorption was more effective on porous than on dense HA, and was similar for HA and GRHA.},
	keywords = {Adsorption, Antibiotics, Coatings, Dense materials, Diseases, Drug delivery, Drug dosage, Fourier transform infrared spectroscopy, glass, Glass reinforced hydroxyapatite, hydroxyapatite, Mercury (metal), Porous, Porous materials, Scanning electron microscopy, Sodium, Strength of materials, Ultraviolet spectroscopy, X ray diffraction analysis},
	isbn = {10139826 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0347516111\&partnerID=40\&md5=a85b6393d2a4a2d3ee4b384bf4c3de78},
	author = {Queiroz, A.C. and Teixeira, S. and Santos, J.D. and Monteiro, F.J.},
	editor = {Barbosa M.A. and Monteiro F.J. and Correia R. and Leon B.}
}
@book {2477,
	title = {Production of porous hydroxyapatite with potential for controlled drug delivery},
	series = {Materials Science ForumMater Sci Forum},
	volume = {455-456},
	year = {2004},
	note = {Conference code: 63332Cited By (since 1996): 7Export Date: 21 November 2012Source: ScopusCODEN: MSFOELanguage of Original Document: EnglishCorrespondence Address: Queiroz, A.C.; INEB, Inst. de Engenharia Biom{\'e}dica, R do Campo Alegre, 823, 4150-180 Porto, Portugal; email: aqueiroz@ineb.up.ptReferences: Krejci, C.B., Bissada, N.F., Farah, C., Greenwell, H., (1987) J. Periodontology, 58, p. 521;Seymour, R.A., Heasman, P.A., MacGregor, I.D.M., The pathogenesis of periodontal disease (1992) Drugs, Diseases, and the Periodontium, , Oxford University Press; 
(1996) Journal of Periodontology, 67, p. 831; 
Soskolne, W.A., Heasman, H.A., Stabholz, A., Smart, G.J., Palmer, M., Flashner, M., Newman, H.N., (1997) Journal of Periodontology, 68, p. 32; 
Da Silva, M.H.P., Lemos, A.F., Gibson, I.R., Ferreira, J.M.F., Santos, J.D., (2002) J. of Non-crystaline Solids, 304, p. 286; 
Chang, B., Lee, C., Hong, K., Youn, H., Ryu, H., Chung, S., Park, K., (2000) Biomat., 21, p. 1291; 
Ewers, R., Simons, B., (1992) Biomaterials - Hard Tissue Repair and Replacement, , Elsevier Sc; 
Ohgushi, H., Okumura, M., Yoshikawa, T., Inoue, K., Senpuku, N., Tamai, S., Shors, E.C., (1992) Journal of Biomedical Materials Research, 26, p. 885; 
Barinov, S.M., Baschenko, Y.V., (1992) Bioceramics and the Human Body, , Elsevier Sc; 
Hing, K.A., Best, S.M., Tanner, K.E., Bonfield, W., Revell, P.A., (1997) J. Mater. Sc.: Materials in Medicine, 8, p. 731; 
Queiroz, A.C., Teixeira, S., Santos, J.D., Monteiro, F.J., (2003) Bioceramics, , accepted for; 
Santos, J.D., Monteiro, F.J., Gibson, I.R., Knowles, J.C., (2001) Biomaterial, 22, p. 1393
},
	month = {2004///},
	pages = {358 - 360},
	address = {Caparica},
	abstract = {Porous hydroxyapatite was prepared in order to be used as a drug carrier and promote bone ingrowth. For this purpose, the microstructure should have interconnective pores and micro as well as macro porosity, for bone cell adhesion and bone ingrowth. The porous hydroxyapatite prepared by the burn-out method exhibits all these features. For measuring porosity, SEM analysis, mercury intrusion porosimetry and BET were used. FT-IR and XRD analysis revealed that only hydroxyapatite phase was present, being this result similar to the one found for dense samples. The morphology obtained appears to be well adapted to bone growth and drug adsorption.},
	keywords = {Adsorption, Antibiotics, Bioceramics, Controlled drug delivery, Drug Carriers, Drug delivery, Fourier transform infrared spectroscopy, hydroxyapatite, morphology, Polyurethanes, porosity, Porous, Porous materials, Scanning electron microscopy, X ray diffraction analysis},
	isbn = {02555476 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-17044442244\&partnerID=40\&md5=7baa6f22534360d57deb7862546fb275},
	author = {Queiroz, A.C. and Teixeira, S. and Santos, J.D. and Monteiro, F.J.},
	editor = {Martins R. and Fortunato E. and Ferreira I. and Dias C.}
}
@article {2519,
	title = {Dissolution studies of hydroxyapatite and glass-reinforced hydroxyapatite ceramics},
	journal = {Materials CharacterizationMater Charact},
	volume = {50},
	year = {2003},
	note = {Conference code: 61615Cited By (since 1996): 15Export Date: 21 November 2012Source: ScopusCODEN: MACHEdoi: 10.1016/S1044-5803(03)00092-5Language of Original Document: EnglishCorrespondence Address: Prado da Silva, M.H.; DEMP, UFC, Campus PICI, Bl. 714, Fortaleza, CE 60455-760, Brazil; email: mhprado@dem.ufc.brReferences: Barinov, S.M., Baschenko, Y.V., Application of ceramic composites as implants: Result and problem (1992) Bioceramics and the Human Body, pp. 206-210. , A. Ravaglioli, \& A. Krajewski. United Kingdom: Elsevier;Nishihara, K., Studies on peri-root tissue formation around new type artificial root made of dense hydroxyapatite (1993) Clin. Mater., 12, pp. 159-167; 
Lopes, M.A., Monteiro, F.J., Santos, J.D., Serro, A.P., Saramago, B., Hydrophobicity, surface tensions, and zeta potential measurements of glass-reinforced hydroxyapatite composites (1999) J. Biomed. Mater. Res., 45, pp. 370-375; 
Santos, J.D., Silva, P.L., Knowles, J.C., Talal, S., Monteiro, F.J., Reinforcement of hydroxyapatite by adding P 2O 5-CaO glasses with Na 2O, K 2O, MgO (1996) J. Mater. Sci. Mater. Med., 7, pp. 187-189; 
Ferraz, M.P., Knowles, J.C., Olsen, I., Monteiro, F.J., Santos, J.D., Flow cytometry analysis of effects of glass on response of osteosarcoma cells to plasma-sprayed hydroxyapatite/CaO-P 2O 5 coatings (1999) J. Biomed. Mater. Res., 47, pp. 603-611; 
Ferraz, M.P., Monteiro, F.J., Santos, J.D., CaO-P 2O 5 glass hydroxyapatite double-layer plasma-sprayed coating: In vitro bioactivity evaluation (1999) J. Biomed. Mater. Res., 45, pp. 376-383; 
Lopes, M.A., Santos, J.D., Monteiro, F.J., Ohtsuki, C., Osaka, A., Kaneko, S., Push-out testing and histological evaluation of glass reinforced hydroxyapatite composites implanted in the tibia of rabbits (2001) J. Biomed. Mater. Res., 54, pp. 463-469; 
Lopes, M.A., Knowles, J.C., Kuru, L., Santos, J.D., Monteiro, F.J., Olsen, I., Flow cytometry for assessing biocompatibility (1998) J. Biomed. Mater. Res., 41, pp. 649-656; 
Kokubo, T., Ito, S., Huang, Z.T., Hayashi, T., Sakka, S., Ca, P-rich layer formed on high-strength bioactive glass-ceramic A-W (1990) J. Biomed. Mater. Res., 24, pp. 331-343; 
Kokubo, T., Kushitani, H., Kitsugi, T., Yamamuro, T., Solution able to reproduce in vivo surface-structure changes of bioactive glass-ceramic A-W (1990) J. Biomed. Mater. Res., 24, pp. 721-734; 
Klein, C.P.A.T., Wolke, J.G.C., De Blieck-Hogervorst, J.M.A., De Groot, K., Features of calcium phosphate plasma-sprayed coatings: An in vitro study (1994) J. Biomed. Mater. Res., 28, pp. 961-967; 
Klein, C.P.A.T., Wolke, J.G.C., De Blieck-Hogervorst, J.M.A., De Groot, K., Calcium phosphate plasma-sprayed coatings and their stability: An in vivo study (1994) J. Biomed. Mater. Res., 28, pp. 909-917; 
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; 
Zhang, H., Li, S., Yan, Y., Dissolution behaviour of hydroxyapatite powder in hydrothermal solution (2001) Ceram. Int., 27, pp. 451-454; 
LeGeros, R.Z., LeGeros, J.P., Calcium phosphate biomaterials in medical applications (1996) Bioceramics, 9, pp. 7-10. , T. Kokubo, T. Nakamura, \& F. Miyaji. Otsu, Japan: Elsevier; 
Queiroz, A.C., Santos, J.D., Monteiro, F.J., Gibson, I.R., Knowles, J.C., Adsorption and release studies of sodium ampicillin from hydroxyapatite and glass-reinforced hydroxyapatite composites (2001) Biomaterials, 22, pp. 1393-1400; 
Langenbucher, F., Benz, D., K{\"u}rth, W., M{\"o}ller, H., Otz, M., Standardized flow-cell method as an alternative to existing pharmacopoeial dissolution testing (1989) Pharm. Ind., 51 (11), pp. 1276-1281; 
Kokubo, T., (1990) CRC Handbook of Bioactive Ceramics, 1, p. 41. , T. Yamamuro, L.L. Hench, \& J. Wilson. Boca Raton (FL): CRC Press; 
International Standard ISO/FDIS 10993-14, Biological evaluation of medical devices: Part 14 (2001) Identification and Quantification of Degradation Products from Ceramics
},
	month = {2003///},
	pages = {197 - 202},
	address = {Rio de Janeiro},
	abstract = {In the continuous agitation assays, glass-reinforced hydroxyapatite (GR-HA) was shown to form a calcium phosphate (CaP) layer, but hydroxyapatite (HA) only formed dispersed precipitates. The formation of this layer was first detected on the GR-HA with a 7.5\% glass addition (7.5 GR-HA) after only 3 days of immersion in simulated body fluid (SBF). The time required for layer formation decreased as the amount of glass added to the HA increased. The dissolution rate of the materials followed a similar pattern, i.e. the dissolution rate for GR-HA was higher than for HA, and increased with the addition of glass. The immersion of 7.5 GR-HA in water showed almost linear dissolution kinetics over the immersion periods (3, 7, 15, 30 and 60 days). The concentration of calcium ions in solution and the scanning electron microscopy (SEM) analysis of the 7.5 GR-HA specimens immersed in water and in SBF revealed a clear competition between the material dissolution and the precipitation of a CaP phase. Fourier transformed infrared spectroscopy with alternated total reflectance (FTIR-ATR) analysis indicated that the CaP phase that formed during longer immersion times (30 and 60 days) could be a carbonate-substituted CaP precipitate. As expected from previous work, the GR-HA behavior in terms of its in vitro bioactivity is higher than HA because a homogeneous CaP layer is formed and the precipitation occurs faster. From the dissolution test and in accordance with the chemical composition of the samples, GR-HA was more soluble than HA. {\textcopyright} 2003 Elsevier Inc. All rights reserved.},
	keywords = {Ceramic materials, Dissolution, glass, Glass-reinforced hydroxyapatite, hydroxyapatite, Immersion times, Scanning electron microscopy},
	isbn = {10445803 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0141895021\&partnerID=40\&md5=9226464f75e2ecd20d23f9d42e61d69e},
	author = {Queiroz, A.C. and Santos, J.D. and Monteiro, F.J. and Prado da Silva, M.H.},
	editor = {Solorzano G. and Freire Jr. F.L. and Soares G.A. and Souza P.L.}
}
@article {2544,
	title = {Adsorption and release studies of sodium ampicillin from hydroxyapatite and glass-reinforced hydroxyapatite composites},
	journal = {BiomaterialsBiomaterials},
	volume = {22},
	year = {2001},
	note = {Cited By (since 1996): 55Export Date: 21 November 2012Source: ScopusCODEN: BIMADdoi: 10.1016/S0142-9612(00)00296-9PubMed ID: 11336313Language of Original Document: EnglishCorrespondence Address: Knowles, J.C.; Department of Biomaterials, Eastman Dental Institute, University College London, 256 Gray{\textquoteright}s Inn Road, London WC1X 8LD, United Kingdom; email: j.knowles@eastman.ucl.ac.ukChemicals/CAS: Ampicillin, 69-53-4; Durapatite, 1306-06-5; PenicillinsManufacturers: Plasma Biotal, United KingdomReferences: Farag, S.A., Simultaneous liquid chromatographic analysis of the β-lactam antibiotics cefazolin, cefadroxil, cepalexin, ampicillin, and cephradine in solution (1998) J AOAC Int, 81, pp. 381-385;Somayaji, B.V., Jariwala, U., Jayachandran, P., Vidyalakshmi, K., Dudhani, R.V., Evaluation of antimicrobial efficacy and release pattern of tetracycline and metronidazole using a local delivery system (1998) J Periodontol, 69, pp. 409-413; 
Soskolne, W.A., Heasman, P.A., Stabholz, A., Smart, G.J., Palmer, M., Flashner, M., Newman, H.N., Sustained local delivery of chlorhexidine in the treatment of periodontitis; a multi-center study (1997) J Periodontol, 68, pp. 32-38; 
Steinberg, D., Friedman, M., Soskolne, A., Sela, M.N., A new degradable controlled release device for treatment of periodontal disease; in vitro release study (1990) J Periodontol, 61, pp. 393-398; 
Stoltze, K., Concentration of metronidazole in periodontal pockets after application of a metronidazole 25\% dental gel (1992) J Clin Periodontol, 19, pp. 698-701; 
Ramaglia, L., Sbordone, L., Lenci, F., Gulletta, E., Amato, G., Kennedy, E.B., Microbiology of porous hydroxylapatite implants in human periodontal osseous defects (1986) Biomaterials and clinical applications, 7 vol., pp. 675-680. , Pizzoferrate A., Marachetti P.G., Ravaglioli A., Lee A.J.C. (Eds.), Netherlands: Elsevier; 
Wilson, J., Low, S., Fetner, A., Hench, L.L., Bioactive materials for periodontal treatment; a comparative study (1986) Biomaterials and clinical applications, 7 vol., pp. 223-228. , Pizzoferrate A., Marachetti P.G., Ravaglioli A., Lee A.J.C. (Eds.), Netherlands: Elsevier; 
Kenney, E.B., Lekovic, V., Sa Ferreira, J.C., Han, T., Dimitrijavic, B., Carranza F.A. Jr, Bone formation within porous hydroxyapatite implants in human periodontal defects (1986) J Periodontol, 57, pp. 76-83; 
Krejei, C.B., Bissada, N.F., Farah, C., Greenwell, H., Clinical evaluation of porous and nonporous hydroxyapatite in treatment of human periodontal bony defects (1987) J Periodontol, 58, pp. 521-528; 
Lopes, M.A., Monteiro, F.J., Santos, J.D., Serro, A.P., Saramago, B., Hydrophobicity, surface tensions, and zeta potential measurements of glass-reinforced hydroxyapatite composites (1999) J Biomed Mater Res, 45, pp. 370-375; 
Santos, J.D., Silva, P.L., Knowles, J.C., Talal, S., Monteiro, F.J., Reinforcement of hydroxyapatite by adding P 2O 5-CaO glasses with Na 2O, K 2O, MgO (1996) J Mater Sci Mater Med, 7, pp. 187-189; 
Lopes, M.A., Knowles, J.C., Kuru, L., Santos, J.D., Monteiro, F.J., Olsen, I., Flow cytometry for assessing biocompatibility (1998) J Biomed Mater Res, 41, pp. 649-656; 
Lopes, M.A., Santos, J.D., Monteiro, F.J., Ohtsuki, C., Osaka, A., Kaneko, S., Inoue, H., Osteocompatibility and in vivo evaluation of glass reinforced hydroxyapatite composites (1999) Bioceramics, 12 vol., pp. 421-424. , Ohgushi H., Hastings G.W., Yoshikawa T. (Eds.), Japan: World Scientific; 
Santos, J.D., Vasconcelos, M., Reis, R.L., Afonso, A., Monteiro, F.J., Hastings, G.W., Glass reinforced hydroxyapatite composites; physical properties and preliminary histological studies in rabbits (1994) Bioceramics, 7 vol., pp. 243-248. , Andersson O.H., Yli-Urpo A. (Eds.), Finland: Pergamon Press; 
Klein, C.P.A.T., Wolke, J.G.C., de Blieck-Hogervorst, J.M.A., de Groot, K., Features of calcium phosphate plasma-sprayed coatings; an in vitro study (1994) J Biomed Mater Res, 28, pp. 961-967; 
Klein, C.P.A.T., Wolke, J.G.C., de Blieck-Hogervorst, J.M.A., de Groot, K., Calcium phosphate plasma-sprayed coatings and their stability; an in vivo study (1994) J Biomed Mater Res, 28, pp. 909-917; 
Langnbucher, F., Benz, D., K{\"u}rth, W., M{\"o}ller, H., Otz, M., Standardized Flow-cell method as an alternative to existing pharmacopoeial dissolution testing (1989) Pharm Ind, 51, pp. 1276-1281; 
Santos, J.D., Knowles, J.C., Reis, R.L., Monteiro, F.J., Hastings, G.W., Microstructural characterization of glass-reinforced hydroxyapatite composites (1994) Biomaterials, 15, pp. 5-10; 
Lopes, M.A., Santos, J.D., Monteiro, F.J., Knowles, J.C., Glass-reinforced hydroxyapatite; a comprehensive study of the effect of glass composition on crystallography of the composite (1998) J Biomed Mater Res, 39, pp. 244-251; 
Thomas M. Ultraviolet and visible spectroscopy, second edition. In: Ando DJ, editor. England: Wiley, 1996. p. 16-30Itokazu, M., Itoh, Y., Fukuta, M., Miyamato, K., Ohara, A., Oshima, K., Nishimoto, Y., Shimizu, K., Treatment of osteomyelitis by using antibiotic loaded porous ceramic (1999) Bioceramics, 12 vol., pp. 3-6. , Ohgushi H., Hastings G.W., Yoshikawa T. (Eds.), Japan: World Scientific; 
Shinto, Y., Uchida, A., Korkusuz, F., Araki, N., Ono, K., Calcium hydroxyapatite ceramic used as a delivery system for antibiotics (1992) J Bone Jt Surg, 74 B, pp. 600-604; 
Downes, S., Clifford, C.J., Scotchford, C., Klein, C.P.A.T., Comparison of the release of growth hormone from hydroxyapatite, heat-treated hydroxyapatite, and fluoroapatite coatings on titanium (1995) J Biomed Mater Res, 29, pp. 1053-1060; 
Curtis, M.A., Griffiths, G.S., Johnson, N.W., The total protein concentration of gingival crevicular fluid. Variation with sampling time and gingival inflammation (1988) J Clin Periondontol, 15, pp. 628-632; 
Stoltze K. Concentration of metronidazole in periodontal pockets after application of a metronidazole 25\% dental gel. J Clin Periondontol 1992, 689-701Jones, A.A., Koenman, K.S., Newbold, D.A., Manwell, M.A., Clinical and microbiological effects of controlled release locally delivered minocycline in periodontitis (1994) J Periodontol, 65, pp. 1058-1066
},
	month = {2001///},
	pages = {1393 - 1400},
	abstract = {As a potential therapy for periodontitis, sodium ampicillin, a broad spectrum antibiotic, was adsorbed onto hydroxyapatite (HA) and glass-reinforced hydroxyaptite (GR-HA) composites, and was subsequently released in vitro. The sodium ampicillin, was adsorbed more on HA compared to the GR-HA composites. X-ray diffraction (XRD) and Rietveld analysis were used to identify and quantify the levels of HA and β-tricalcium phosphate (β-TCP) in the microstructure of the GR-HA composites. Lattice parameters changes were observed for the β-TCP phase dependant on the amount of glass added. The release kinetics were shown to be divided into three stages, the first of which where a large amount of sodium ampicillin is released, followed by a slower release rate and then a final stage where the release amount approaches zero, until no more sodium ampicillin was present. X-ray photoeletron spectroscopy (XPS) studies were carried out in order to ensure that the entire antibiotic adsorbed onto the materials had been released. These kinetics studies have indicated the possibility of using these materials as possible carriers for drug delivery. Copyright {\textcopyright} 2001 Elsevier Science Ltd.},
	keywords = {Adsorption, ampicillin, Antibiotics, article, calcium phosphate, composite material, controlled study, drug adsorption, Drug delivery, drug delivery system, Drug release, Durapatite, glass, Glass-reinforced hydroxyapatite, hydroxyapatite, Kinetics, Microstructure, Penicillins, periodontitis, priority journal, Reinforcement, Rietveld analysis, roentgen spectroscopy, Sodium ampicillin, Sodium compounds, structure analysis, unclassified drug, X ray diffraction, X ray diffraction analysis, X ray photoelectron spectroscopy, X-Ray Diffraction},
	isbn = {01429612 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0035372020\&partnerID=40\&md5=72e1b530ae04faed9cceb376c0246aa8},
	author = {Queiroz, A.C. and Santos, J.D. and Monteiro, F.J. and Gibson, I.R. and Knowles, J.C.}
}
