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SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up

In this study Surface Enhanced Raman Spectroscopy (SERS) data recorded from mouse mammary glands cancer cells (4T1 cell line) was used to assess information regarding differences between control, death and viable cells after Photodynamic Therapy (PDT) treatment. The treatment used nanoemulsions (NE/...

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Autores principales: Veloso, A. B., Longo, J. P. F., Muehlmann, L. A., Tollstadius, B. F., Souza, P. E. N., Azevedo, R. B., Morais, P. C., da Silva, S. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543153/
https://www.ncbi.nlm.nih.gov/pubmed/28775257
http://dx.doi.org/10.1038/s41598-017-07469-1
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author Veloso, A. B.
Longo, J. P. F.
Muehlmann, L. A.
Tollstadius, B. F.
Souza, P. E. N.
Azevedo, R. B.
Morais, P. C.
da Silva, S. W.
author_facet Veloso, A. B.
Longo, J. P. F.
Muehlmann, L. A.
Tollstadius, B. F.
Souza, P. E. N.
Azevedo, R. B.
Morais, P. C.
da Silva, S. W.
author_sort Veloso, A. B.
collection PubMed
description In this study Surface Enhanced Raman Spectroscopy (SERS) data recorded from mouse mammary glands cancer cells (4T1 cell line) was used to assess information regarding differences between control, death and viable cells after Photodynamic Therapy (PDT) treatment. The treatment used nanoemulsions (NE/PS) loaded with different chloroaluminumphthalocyanine (ClAlP) photosensitizer (PS) contents (5 and 10 µmol × L(−1)) and illumination (660 nm wavelength) at 10 J × cm(−2) (10 minutes). The SERS data revealed significant molecular alterations in proteins and lipids due to the PDT treatment. Principal Component Analysis (PCA) was applied to analyze the data recorded. Three-dimensional and well reproductive PCA scatter plots were obtained, revealing that two clusters of dead cells were well separated from one another and from control cluster. Overlap between two clusters of viable cells was observed, though well separated from control cluster. Moreover, the data analysis also pointed out necrosis as the main cell death mechanism induced by the PDT, in agreement with the literature. Finally, Raman modes peaking at 608 cm(−1) (proteins) and 1231 cm(−1) (lipids) can be selected for follow up of survival rate of neoplastic cells after PDT. We envisage that this finding is key to contribute to a quick development of quantitative infrared thermography imaging.
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spelling pubmed-55431532017-08-07 SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up Veloso, A. B. Longo, J. P. F. Muehlmann, L. A. Tollstadius, B. F. Souza, P. E. N. Azevedo, R. B. Morais, P. C. da Silva, S. W. Sci Rep Article In this study Surface Enhanced Raman Spectroscopy (SERS) data recorded from mouse mammary glands cancer cells (4T1 cell line) was used to assess information regarding differences between control, death and viable cells after Photodynamic Therapy (PDT) treatment. The treatment used nanoemulsions (NE/PS) loaded with different chloroaluminumphthalocyanine (ClAlP) photosensitizer (PS) contents (5 and 10 µmol × L(−1)) and illumination (660 nm wavelength) at 10 J × cm(−2) (10 minutes). The SERS data revealed significant molecular alterations in proteins and lipids due to the PDT treatment. Principal Component Analysis (PCA) was applied to analyze the data recorded. Three-dimensional and well reproductive PCA scatter plots were obtained, revealing that two clusters of dead cells were well separated from one another and from control cluster. Overlap between two clusters of viable cells was observed, though well separated from control cluster. Moreover, the data analysis also pointed out necrosis as the main cell death mechanism induced by the PDT, in agreement with the literature. Finally, Raman modes peaking at 608 cm(−1) (proteins) and 1231 cm(−1) (lipids) can be selected for follow up of survival rate of neoplastic cells after PDT. We envisage that this finding is key to contribute to a quick development of quantitative infrared thermography imaging. Nature Publishing Group UK 2017-08-03 /pmc/articles/PMC5543153/ /pubmed/28775257 http://dx.doi.org/10.1038/s41598-017-07469-1 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
Veloso, A. B.
Longo, J. P. F.
Muehlmann, L. A.
Tollstadius, B. F.
Souza, P. E. N.
Azevedo, R. B.
Morais, P. C.
da Silva, S. W.
SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up
title SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up
title_full SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up
title_fullStr SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up
title_full_unstemmed SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up
title_short SERS Investigation of Cancer Cells Treated with PDT: Quantification of Cell Survival and Follow-up
title_sort sers investigation of cancer cells treated with pdt: quantification of cell survival and follow-up
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543153/
https://www.ncbi.nlm.nih.gov/pubmed/28775257
http://dx.doi.org/10.1038/s41598-017-07469-1
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