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On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity

The surface structure and hydrophilicity of synthetic nanocrystalline apatite with strongly bound citrates on their surface are here investigated at the molecular level, by combining advanced IR spectroscopy, microgravimetry and adsorption microcalorimetry. Citrate are found to form unidentate-like...

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Autores principales: Ivanchenko, Pavlo, Delgado-López, José Manuel, Iafisco, Michele, Gómez-Morales, Jaime, Tampieri, Anna, Martra, Gianmario, Sakhno, Yuriy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567200/
https://www.ncbi.nlm.nih.gov/pubmed/28827557
http://dx.doi.org/10.1038/s41598-017-09376-x
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author Ivanchenko, Pavlo
Delgado-López, José Manuel
Iafisco, Michele
Gómez-Morales, Jaime
Tampieri, Anna
Martra, Gianmario
Sakhno, Yuriy
author_facet Ivanchenko, Pavlo
Delgado-López, José Manuel
Iafisco, Michele
Gómez-Morales, Jaime
Tampieri, Anna
Martra, Gianmario
Sakhno, Yuriy
author_sort Ivanchenko, Pavlo
collection PubMed
description The surface structure and hydrophilicity of synthetic nanocrystalline apatite with strongly bound citrates on their surface are here investigated at the molecular level, by combining advanced IR spectroscopy, microgravimetry and adsorption microcalorimetry. Citrate are found to form unidentate-like and ionic-like complexes with surface Ca(2+) ions, with a surface coverage closely resembling that present in bone apatite platelets (i.e., 1 molecule/(n nm)(2), with n ranging between 1.4 and 1.6). These surface complexes are part of a hydrated non-apatitic surface layer with a sub-nanometre thickness. Noticeably, it is found that the hydrophilicity of the nanoparticles, measured in terms of adsorption of water molecules in the form of multilayers, decreases in a significant extent in relation to the presence of citrates, most likely because of the exposure toward the exterior of –CH(2) groups. Our findings provide new insights on the surface properties of bio-inspired nano-apatites, which can be of great relevance for better understanding the role of citrate in determining important interfacial properties, such as hydrophobicity, of bone apatite platelets. The evaluation and comprehension of surface composition and structure is also of paramount interest to strictly control the functions of synthetic biomaterials, since their surface chemistry strongly affects the hosting tissue response.
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spelling pubmed-55672002017-09-01 On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity Ivanchenko, Pavlo Delgado-López, José Manuel Iafisco, Michele Gómez-Morales, Jaime Tampieri, Anna Martra, Gianmario Sakhno, Yuriy Sci Rep Article The surface structure and hydrophilicity of synthetic nanocrystalline apatite with strongly bound citrates on their surface are here investigated at the molecular level, by combining advanced IR spectroscopy, microgravimetry and adsorption microcalorimetry. Citrate are found to form unidentate-like and ionic-like complexes with surface Ca(2+) ions, with a surface coverage closely resembling that present in bone apatite platelets (i.e., 1 molecule/(n nm)(2), with n ranging between 1.4 and 1.6). These surface complexes are part of a hydrated non-apatitic surface layer with a sub-nanometre thickness. Noticeably, it is found that the hydrophilicity of the nanoparticles, measured in terms of adsorption of water molecules in the form of multilayers, decreases in a significant extent in relation to the presence of citrates, most likely because of the exposure toward the exterior of –CH(2) groups. Our findings provide new insights on the surface properties of bio-inspired nano-apatites, which can be of great relevance for better understanding the role of citrate in determining important interfacial properties, such as hydrophobicity, of bone apatite platelets. The evaluation and comprehension of surface composition and structure is also of paramount interest to strictly control the functions of synthetic biomaterials, since their surface chemistry strongly affects the hosting tissue response. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5567200/ /pubmed/28827557 http://dx.doi.org/10.1038/s41598-017-09376-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ivanchenko, Pavlo
Delgado-López, José Manuel
Iafisco, Michele
Gómez-Morales, Jaime
Tampieri, Anna
Martra, Gianmario
Sakhno, Yuriy
On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
title On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
title_full On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
title_fullStr On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
title_full_unstemmed On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
title_short On the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
title_sort on the surface effects of citrates on nano-apatites: evidence of a decreased hydrophilicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567200/
https://www.ncbi.nlm.nih.gov/pubmed/28827557
http://dx.doi.org/10.1038/s41598-017-09376-x
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