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Direct monitoring of single-cell response to biomaterials by Raman spectroscopy
There is continued focus on the development of new biomaterials and associated biological testing methods needed to reduce the time taken for their entry to clinical use. The application of Raman spectroscopy to the study of individual cells that have been in contact with biomaterials offers enhance...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643295/ https://www.ncbi.nlm.nih.gov/pubmed/34862915 http://dx.doi.org/10.1007/s10856-021-06624-5 |
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author | McIvor, Mary Josephine Sharma, Preetam K. Birt, Catherine E. McDowell, Hayley Wilson, Shannon McKillop, Stephen Acheson, Jonathan G. Boyd, Adrian R. Meenan, Brian J. |
author_facet | McIvor, Mary Josephine Sharma, Preetam K. Birt, Catherine E. McDowell, Hayley Wilson, Shannon McKillop, Stephen Acheson, Jonathan G. Boyd, Adrian R. Meenan, Brian J. |
author_sort | McIvor, Mary Josephine |
collection | PubMed |
description | There is continued focus on the development of new biomaterials and associated biological testing methods needed to reduce the time taken for their entry to clinical use. The application of Raman spectroscopy to the study of individual cells that have been in contact with biomaterials offers enhanced in vitro information in a potentially non-destructive testing regime. The work presented here reports the Raman spectral analysis of discreet U-2 OS bone cells after exposure to hydroxyapatite (HA) coated titanium (Ti) substrates in both the as-deposited and thermally annealed states. These data show that cells that were in contact with the bioactive HA surface for 7 days had spectral markers similar to those cultured on the Ti substrate control for the same period. However, the spectral features for those cells that were in contact with the annealed HA surface had indicators of significant differentiation at day 21 while cells on the as-deposited surface did not show these Raman changes until day 28. The cells adhered to pristine Ti control surface showed no spectral changes at any of the timepoints studied. The validity of these spectroscopic results has been confirmed using data from standard in vitro cell viability, adhesion, and proliferation assays over the same 28-day culture period. In this case, cell maturation was evidenced by the formation of natural bone apatite, which precipitated intracellularly for cells exposed to both types of HA-coated Ti at 21 and 28 days, respectively. The properties of the intracellular apatite were markedly different from that of the synthetic HA used to coat the Ti substrate with an average particle size of 230 nm, a crystalline-like shape and Ca/P ratio of 1.63 ± 0.5 as determined by SEM-EDX analysis. By comparison, the synthetic HA particles used as a control had an average size of 372 nm and were more-rounded in shape with a Ca/P ratio of 0.8 by XPS analysis and 1.28 by SEM-EDX analysis. This study shows that Raman spectroscopy can be employed to monitor single U-2 OS cell response to biomaterials that promote cell maturation towards de novo bone thereby offering a label-free in vitro testing method that allows for non-destructive analyses. [Image: see text] |
format | Online Article Text |
id | pubmed-8643295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-86432952021-12-15 Direct monitoring of single-cell response to biomaterials by Raman spectroscopy McIvor, Mary Josephine Sharma, Preetam K. Birt, Catherine E. McDowell, Hayley Wilson, Shannon McKillop, Stephen Acheson, Jonathan G. Boyd, Adrian R. Meenan, Brian J. J Mater Sci Mater Med Biomaterials Synthesis and Characterization There is continued focus on the development of new biomaterials and associated biological testing methods needed to reduce the time taken for their entry to clinical use. The application of Raman spectroscopy to the study of individual cells that have been in contact with biomaterials offers enhanced in vitro information in a potentially non-destructive testing regime. The work presented here reports the Raman spectral analysis of discreet U-2 OS bone cells after exposure to hydroxyapatite (HA) coated titanium (Ti) substrates in both the as-deposited and thermally annealed states. These data show that cells that were in contact with the bioactive HA surface for 7 days had spectral markers similar to those cultured on the Ti substrate control for the same period. However, the spectral features for those cells that were in contact with the annealed HA surface had indicators of significant differentiation at day 21 while cells on the as-deposited surface did not show these Raman changes until day 28. The cells adhered to pristine Ti control surface showed no spectral changes at any of the timepoints studied. The validity of these spectroscopic results has been confirmed using data from standard in vitro cell viability, adhesion, and proliferation assays over the same 28-day culture period. In this case, cell maturation was evidenced by the formation of natural bone apatite, which precipitated intracellularly for cells exposed to both types of HA-coated Ti at 21 and 28 days, respectively. The properties of the intracellular apatite were markedly different from that of the synthetic HA used to coat the Ti substrate with an average particle size of 230 nm, a crystalline-like shape and Ca/P ratio of 1.63 ± 0.5 as determined by SEM-EDX analysis. By comparison, the synthetic HA particles used as a control had an average size of 372 nm and were more-rounded in shape with a Ca/P ratio of 0.8 by XPS analysis and 1.28 by SEM-EDX analysis. This study shows that Raman spectroscopy can be employed to monitor single U-2 OS cell response to biomaterials that promote cell maturation towards de novo bone thereby offering a label-free in vitro testing method that allows for non-destructive analyses. [Image: see text] Springer US 2021-12-04 2021 /pmc/articles/PMC8643295/ /pubmed/34862915 http://dx.doi.org/10.1007/s10856-021-06624-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biomaterials Synthesis and Characterization McIvor, Mary Josephine Sharma, Preetam K. Birt, Catherine E. McDowell, Hayley Wilson, Shannon McKillop, Stephen Acheson, Jonathan G. Boyd, Adrian R. Meenan, Brian J. Direct monitoring of single-cell response to biomaterials by Raman spectroscopy |
title | Direct monitoring of single-cell response to biomaterials by Raman spectroscopy |
title_full | Direct monitoring of single-cell response to biomaterials by Raman spectroscopy |
title_fullStr | Direct monitoring of single-cell response to biomaterials by Raman spectroscopy |
title_full_unstemmed | Direct monitoring of single-cell response to biomaterials by Raman spectroscopy |
title_short | Direct monitoring of single-cell response to biomaterials by Raman spectroscopy |
title_sort | direct monitoring of single-cell response to biomaterials by raman spectroscopy |
topic | Biomaterials Synthesis and Characterization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643295/ https://www.ncbi.nlm.nih.gov/pubmed/34862915 http://dx.doi.org/10.1007/s10856-021-06624-5 |
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