Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids

Abstract In this study the affinity of three amino acids for the surface of non-stoichiometric hydroxyapatite nanoparticles (ns-nHA) was investigated under different reaction conditions. The amino acids investigated were chosen based on their differences in side chain polarity and potential impact o...

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Main Authors: Patricia Comeau, Thomas Willett
Format: Article
Language:English
Published: Nature Publishing Group 2018-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-31058-5
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spelling doaj-95b07dcbb4174b07a3b5bbc2e5da588d2020-12-08T05:14:53ZengNature Publishing GroupScientific Reports2045-23222018-08-018111110.1038/s41598-018-31058-5Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino AcidsPatricia Comeau0Thomas Willett1Composite Biomaterial Systems Laboratory, Department of Systems Design Engineering, University of WaterlooComposite Biomaterial Systems Laboratory, Department of Systems Design Engineering, University of WaterlooAbstract In this study the affinity of three amino acids for the surface of non-stoichiometric hydroxyapatite nanoparticles (ns-nHA) was investigated under different reaction conditions. The amino acids investigated were chosen based on their differences in side chain polarity and potential impact on this surface affinity. While calcium pre-saturation of the calcium-deficient ns-nHA was not found to improve attachment of any of the amino acids studied, the polarity and fraction of ionized functional side groups was found to have a significant impact on this attachment. Overall, amino acid attachment to ns-nHA was not solely reliant on carboxyl groups. In fact, it seems that amine groups also notably interacted with the negative ns-nHA surface and increased the degree of surface binding achieved. As a result, glycine and lysine had greater attachment to ns-nHA than aspartic acid under the reaction conditions studied. Lastly, our results suggest that a layer of each amino acid forms at the surface of ns-nHA, with aspartic acid attachment the most stable and its surface coverage the least of the three amino acids studied.https://doi.org/10.1038/s41598-018-31058-5
collection DOAJ
language English
format Article
sources DOAJ
author Patricia Comeau
Thomas Willett
spellingShingle Patricia Comeau
Thomas Willett
Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids
Scientific Reports
author_facet Patricia Comeau
Thomas Willett
author_sort Patricia Comeau
title Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids
title_short Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids
title_full Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids
title_fullStr Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids
title_full_unstemmed Impact of Side Chain Polarity on Non-Stoichiometric Nano-Hydroxyapatite Surface Functionalization with Amino Acids
title_sort impact of side chain polarity on non-stoichiometric nano-hydroxyapatite surface functionalization with amino acids
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-08-01
description Abstract In this study the affinity of three amino acids for the surface of non-stoichiometric hydroxyapatite nanoparticles (ns-nHA) was investigated under different reaction conditions. The amino acids investigated were chosen based on their differences in side chain polarity and potential impact on this surface affinity. While calcium pre-saturation of the calcium-deficient ns-nHA was not found to improve attachment of any of the amino acids studied, the polarity and fraction of ionized functional side groups was found to have a significant impact on this attachment. Overall, amino acid attachment to ns-nHA was not solely reliant on carboxyl groups. In fact, it seems that amine groups also notably interacted with the negative ns-nHA surface and increased the degree of surface binding achieved. As a result, glycine and lysine had greater attachment to ns-nHA than aspartic acid under the reaction conditions studied. Lastly, our results suggest that a layer of each amino acid forms at the surface of ns-nHA, with aspartic acid attachment the most stable and its surface coverage the least of the three amino acids studied.
url https://doi.org/10.1038/s41598-018-31058-5
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AT thomaswillett impactofsidechainpolarityonnonstoichiometricnanohydroxyapatitesurfacefunctionalizationwithaminoacids
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