Daniel Arcos

Prof. Dr. Daniel Arcos

Departamento de Química en Ciencias Farmacéuticas, Universidad Complutense de Madrid, Av. Séneca, 2, 28040 Madrid, Spain
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Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 September 2007 in Angewandte Chemie International Edition
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María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí
FBFrancisco Balas
Francisco Balas
Daniel ArcosDaniel Arcos
Daniel Arcos

1 August 2010 in Acta Biomaterialia
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Daniel ArcosDaniel Arcos
Daniel Arcos
María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí

5 February 2020 in Journal of Materials Chemistry B
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Daniel ArcosDaniel Arcos
Daniel Arcos
María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí
Surface modification of orthopedic and dental implants has been demonstrated to be an effective strategy to accelerate bone healing at early implantation times. Among the different alternatives, coating implants with a layer of hydroxyapatite (HAp) is one of the most used techniques, due to its excellent biocompatibility and osteoconductive behavior. The composition and crystalline structure of HAp allow for numerous ionic substitutions that provide added value, such as antibiotic properties or osteoinduction. In this article, we will review and critically analyze the most important advances in the field of substituted hydroxyapatite coatings. In recent years substituted HAp coatings have been deposited not only on orthopedic prostheses and dental implants, but also on macroporous scaffolds, thus expanding their applications towards bone regeneration therapies. Besides, the capability of substituted HAps to immobilize proteins and growth factors by non-covalent interactions has opened new possibilities for preparing hybrid coatings that foster bone healing processes. Finally, the most important in vivo outcomes will be discussed to understand the prospects of substituted HAp coatings from a clinical point of view.

28 May 2006 in Chemistry of Materials
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ALA. López-Noriega
A. López-Noriega
Daniel ArcosDaniel Arcos
Daniel Arcos
Isabel Izquierdo-BarbaIsabel Izquierdo-Barba
Isabel Izquierdo-Barba
YSY. Sakamoto
Y. Sakamoto
OTO. Terasaki
O. Terasaki
María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí

11 February 2015 in Journal of Materials Science: Materials in Medicine
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AMAnthony L. B. Maçon
Anthony L. B. Maçon
TKTaek B. Kim
Taek B. Kim
EVEsther M. Valliant
Esther M. Valliant
KGKathryn Goetschius
Kathryn Goetschius
RBRichard K. Brow
Richard K. Brow
JJJulian Jones
Julian Jones
The aim of this study was to propose and validate a new unified method for testing dissolution rates of bioactive glasses and their variants, and the formation of calcium phosphate layer formation on their surface, which is an indicator of bioactivity. At present, comparison in the literature is difficult as many groups use different testing protocols. An ISO standard covers the use of simulated body fluid on standard shape materials but it does not take into account that bioactive glasses can have very different specific surface areas, as for glass powders. Validation of the proposed modified test was through round robin testing and comparison to the ISO standard where appropriate. The proposed test uses fixed mass per solution volume ratio and agitated solution. The round robin study showed differences in hydroxyapatite nucleation on glasses of different composition and between glasses of the same composition but different particle size. The results were reproducible between research facilities. Researchers should use this method when testing new glasses, or their variants, to enable comparison between the literature in the future.

1 February 2013 in Acta Materialia
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Daniel ArcosDaniel Arcos
Daniel Arcos
María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí