Cargando…
Scalable nanolaminated SERS multiwell cell culture assay
This paper presents a new cell culture platform enabling label-free surface-enhanced Raman spectroscopy (SERS) analysis of biological samples. The platform integrates a multilayered metal-insulator-metal nanolaminated SERS substrate and polydimethylsiloxane (PDMS) multiwells for the simultaneous ana...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433130/ https://www.ncbi.nlm.nih.gov/pubmed/34567659 http://dx.doi.org/10.1038/s41378-020-0145-3 |
_version_ | 1783751312602562560 |
---|---|
author | Ren, Xiang Nam, Wonil Ghassemi, Parham Strobl, Jeannine S. Kim, Inyoung Zhou, Wei Agah, Masoud |
author_facet | Ren, Xiang Nam, Wonil Ghassemi, Parham Strobl, Jeannine S. Kim, Inyoung Zhou, Wei Agah, Masoud |
author_sort | Ren, Xiang |
collection | PubMed |
description | This paper presents a new cell culture platform enabling label-free surface-enhanced Raman spectroscopy (SERS) analysis of biological samples. The platform integrates a multilayered metal-insulator-metal nanolaminated SERS substrate and polydimethylsiloxane (PDMS) multiwells for the simultaneous analysis of cultured cells. Multiple cell lines, including breast normal and cancer cells and prostate cancer cells, were used to validate the applicability of this unique platform. The cell lines were cultured in different wells. The Raman spectra of over 100 cells from each cell line were collected and analyzed after 12 h of introducing the cells to the assay. The unique Raman spectra of each cell line yielded biomarkers for identifying cancerous and normal cells. A kernel-based machine learning algorithm was used to extract the high-dimensional variables from the Raman spectra. Specifically, the nonnegative garrote on a kernel machine classifier is a hybrid approach with a mixed nonparametric model that considers the nonlinear relationships between the higher-dimension variables. The breast cancer cell lines and normal breast epithelial cells were distinguished with an accuracy close to 90%. The prediction rate between breast cancer cells and prostate cancer cells reached 94%. Four blind test groups were used to evaluate the prediction power of the SERS spectra. The peak intensities at the selected Raman shifts of the testing groups were selected and compared with the training groups used in the machine learning algorithm. The blind testing groups were correctly predicted 100% of the time, demonstrating the applicability of the multiwell SERS array for analyzing cell populations for cancer research. |
format | Online Article Text |
id | pubmed-8433130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84331302021-09-24 Scalable nanolaminated SERS multiwell cell culture assay Ren, Xiang Nam, Wonil Ghassemi, Parham Strobl, Jeannine S. Kim, Inyoung Zhou, Wei Agah, Masoud Microsyst Nanoeng Article This paper presents a new cell culture platform enabling label-free surface-enhanced Raman spectroscopy (SERS) analysis of biological samples. The platform integrates a multilayered metal-insulator-metal nanolaminated SERS substrate and polydimethylsiloxane (PDMS) multiwells for the simultaneous analysis of cultured cells. Multiple cell lines, including breast normal and cancer cells and prostate cancer cells, were used to validate the applicability of this unique platform. The cell lines were cultured in different wells. The Raman spectra of over 100 cells from each cell line were collected and analyzed after 12 h of introducing the cells to the assay. The unique Raman spectra of each cell line yielded biomarkers for identifying cancerous and normal cells. A kernel-based machine learning algorithm was used to extract the high-dimensional variables from the Raman spectra. Specifically, the nonnegative garrote on a kernel machine classifier is a hybrid approach with a mixed nonparametric model that considers the nonlinear relationships between the higher-dimension variables. The breast cancer cell lines and normal breast epithelial cells were distinguished with an accuracy close to 90%. The prediction rate between breast cancer cells and prostate cancer cells reached 94%. Four blind test groups were used to evaluate the prediction power of the SERS spectra. The peak intensities at the selected Raman shifts of the testing groups were selected and compared with the training groups used in the machine learning algorithm. The blind testing groups were correctly predicted 100% of the time, demonstrating the applicability of the multiwell SERS array for analyzing cell populations for cancer research. Nature Publishing Group UK 2020-06-01 /pmc/articles/PMC8433130/ /pubmed/34567659 http://dx.doi.org/10.1038/s41378-020-0145-3 Text en © The Author(s) 2020 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 | Article Ren, Xiang Nam, Wonil Ghassemi, Parham Strobl, Jeannine S. Kim, Inyoung Zhou, Wei Agah, Masoud Scalable nanolaminated SERS multiwell cell culture assay |
title | Scalable nanolaminated SERS multiwell cell culture assay |
title_full | Scalable nanolaminated SERS multiwell cell culture assay |
title_fullStr | Scalable nanolaminated SERS multiwell cell culture assay |
title_full_unstemmed | Scalable nanolaminated SERS multiwell cell culture assay |
title_short | Scalable nanolaminated SERS multiwell cell culture assay |
title_sort | scalable nanolaminated sers multiwell cell culture assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433130/ https://www.ncbi.nlm.nih.gov/pubmed/34567659 http://dx.doi.org/10.1038/s41378-020-0145-3 |
work_keys_str_mv | AT renxiang scalablenanolaminatedsersmultiwellcellcultureassay AT namwonil scalablenanolaminatedsersmultiwellcellcultureassay AT ghassemiparham scalablenanolaminatedsersmultiwellcellcultureassay AT strobljeannines scalablenanolaminatedsersmultiwellcellcultureassay AT kiminyoung scalablenanolaminatedsersmultiwellcellcultureassay AT zhouwei scalablenanolaminatedsersmultiwellcellcultureassay AT agahmasoud scalablenanolaminatedsersmultiwellcellcultureassay |