Author |
Silva, Flavia R. O.
![]() Lima, Nelson B. ![]() Guilhen, Sabine N. ![]() Courrol, Lilia Coronato ![]() ![]() Bressiani, Ana Helena A. ![]() |
Abstract | Europium-doped hydroxyapatite (HA), beta-tricalcium phosphate (beta-TCP) and biphasic phosphate nanopowders were synthesized by co-precipitation method and their crystal structures and fluorescence properties were investigated depending on the pH of the starting solution. In the range of pH 6-10, HA and beta-TCP phases coexist The beta-TCP proportion increased as the pH of the solution decreased, while HA yields decreased. At pH below 6, monophasic beta-TCP powder was obtained after thermal treatment. In particular, HA and beta-TCP can be used as luminescent materials when activated by Eu3+ ions in substitution of Ca2+ ions. Herein, the Eu3+ ions doped HA and beta-TCP phase composition were analyzed in order to investigate the fluorescence emission of the HA, beta-TCP and biphasic compounds. Eu-doped HA exhibited a red-orange emission at 575 nm with several minor peaks at 610-640 nm, while Eu-doped beta-TCP had an unexpected strong red emission at 610-620 nm and a secondary band at 590-600 nm. In fact, the Eu:beta-TCP integrated emission area is almost 20-fold higher than Eu:HA for the same europium ion concentration. These results demonstrate the potential of Eu:beta-TCP as biomarker for medical applications, as drug release and targeting based on their luminescent properties. (C) 2016 Elsevier B.V. All rights reserved. |
Keywords |
Hydroxyapatite
Beta tricalcium phosphate Biphasic phosphate Europium Fluorescence pH synthesis |
xmlui.dri2xhtml.METS-1.0.item-coverage | Amsterdam |
Language | English |
Sponsor | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) |
Grant number |
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Date | 2016 |
Published in | Journal Of Luminescence. Amsterdam, v. 180, p. 177-182, 2016. |
ISSN | 0022-2313 (Sherpa/Romeo, impact factor) |
Publisher | Elsevier Science Bv |
Extent | 177-182 |
Origin |
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Access rights | Closed access |
Type | Article |
Web of Science ID | WOS:000386314300027 |
URI | https://repositorio.unifesp.br/handle/11600/56691 |
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