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Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy
To treat impairments in hard tissues or overcome pathological calcification in soft tissues, a detailed understanding of mineralization pathways of calcium phosphate materials is needed. Here, we report a detailed mechanistic study of hydroxyapatite (HA) mineralization pathways in an artificial sali...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673812/ https://www.ncbi.nlm.nih.gov/pubmed/33208378 http://dx.doi.org/10.1126/sciadv.aaz7524 |
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author | He, Kun Sawczyk, Michal Liu, Cong Yuan, Yifei Song, Boao Deivanayagam, Ram Nie, Anmin Hu, Xiaobing Dravid, Vinayak P. Lu, Jun Sukotjo, Cortino Lu, Yu-peng Král, Petr Shokuhfar, Tolou Shahbazian-Yassar, Reza |
author_facet | He, Kun Sawczyk, Michal Liu, Cong Yuan, Yifei Song, Boao Deivanayagam, Ram Nie, Anmin Hu, Xiaobing Dravid, Vinayak P. Lu, Jun Sukotjo, Cortino Lu, Yu-peng Král, Petr Shokuhfar, Tolou Shahbazian-Yassar, Reza |
author_sort | He, Kun |
collection | PubMed |
description | To treat impairments in hard tissues or overcome pathological calcification in soft tissues, a detailed understanding of mineralization pathways of calcium phosphate materials is needed. Here, we report a detailed mechanistic study of hydroxyapatite (HA) mineralization pathways in an artificial saliva solution via in situ liquid cell transmission electron microscopy (TEM). It is found that the mineralization of HA starts by forming ion-rich and ion-poor solutions in the saliva solution, followed by coexistence of the classical and nonclassical nucleation processes. For the nonclassical path, amorphous calcium phosphate (ACP) functions as the substrate for HA nucleation on the ACP surface, while the classical path features direct HA nucleation from the solution. The growth of HA crystals on the surface of ACP is accompanied by the ACP dissolution process. The discoveries reported in this work are important to understand the physiological and pathological formation of HA minerals, as well as to engineer the biomineralization process for bone healing and hard tissue repairs. |
format | Online Article Text |
id | pubmed-7673812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76738122020-11-24 Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy He, Kun Sawczyk, Michal Liu, Cong Yuan, Yifei Song, Boao Deivanayagam, Ram Nie, Anmin Hu, Xiaobing Dravid, Vinayak P. Lu, Jun Sukotjo, Cortino Lu, Yu-peng Král, Petr Shokuhfar, Tolou Shahbazian-Yassar, Reza Sci Adv Research Articles To treat impairments in hard tissues or overcome pathological calcification in soft tissues, a detailed understanding of mineralization pathways of calcium phosphate materials is needed. Here, we report a detailed mechanistic study of hydroxyapatite (HA) mineralization pathways in an artificial saliva solution via in situ liquid cell transmission electron microscopy (TEM). It is found that the mineralization of HA starts by forming ion-rich and ion-poor solutions in the saliva solution, followed by coexistence of the classical and nonclassical nucleation processes. For the nonclassical path, amorphous calcium phosphate (ACP) functions as the substrate for HA nucleation on the ACP surface, while the classical path features direct HA nucleation from the solution. The growth of HA crystals on the surface of ACP is accompanied by the ACP dissolution process. The discoveries reported in this work are important to understand the physiological and pathological formation of HA minerals, as well as to engineer the biomineralization process for bone healing and hard tissue repairs. American Association for the Advancement of Science 2020-11-18 /pmc/articles/PMC7673812/ /pubmed/33208378 http://dx.doi.org/10.1126/sciadv.aaz7524 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles He, Kun Sawczyk, Michal Liu, Cong Yuan, Yifei Song, Boao Deivanayagam, Ram Nie, Anmin Hu, Xiaobing Dravid, Vinayak P. Lu, Jun Sukotjo, Cortino Lu, Yu-peng Král, Petr Shokuhfar, Tolou Shahbazian-Yassar, Reza Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
title | Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
title_full | Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
title_fullStr | Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
title_full_unstemmed | Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
title_short | Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
title_sort | revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673812/ https://www.ncbi.nlm.nih.gov/pubmed/33208378 http://dx.doi.org/10.1126/sciadv.aaz7524 |
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