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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2018-08-01
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Online Access: | https://doi.org/10.1038/s41598-018-31058-5 |
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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 |
work_keys_str_mv |
AT patriciacomeau impactofsidechainpolarityonnonstoichiometricnanohydroxyapatitesurfacefunctionalizationwithaminoacids AT thomaswillett impactofsidechainpolarityonnonstoichiometricnanohydroxyapatitesurfacefunctionalizationwithaminoacids |
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