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Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker

The research and the individuation of tumour markers in biological fluids are currently one of the main tools to support diagnosis, prognosis, and monitoring of the therapeutic response in oncology. Although the identification of tumour markers in asymptomatic patients is crucial for early diagnosis...

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Autores principales: Gallo, Valentina, Lai, Antonia, Pasquo, Alessandra, Almaviva, Salvatore, Iacobelli, Stefano, Persichetti, Luca, Capellini, Giovanni, Antonini, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533257/
https://www.ncbi.nlm.nih.gov/pubmed/32875368
http://dx.doi.org/10.1007/s00216-020-02903-2
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author Gallo, Valentina
Lai, Antonia
Pasquo, Alessandra
Almaviva, Salvatore
Iacobelli, Stefano
Persichetti, Luca
Capellini, Giovanni
Antonini, Giovanni
author_facet Gallo, Valentina
Lai, Antonia
Pasquo, Alessandra
Almaviva, Salvatore
Iacobelli, Stefano
Persichetti, Luca
Capellini, Giovanni
Antonini, Giovanni
author_sort Gallo, Valentina
collection PubMed
description The research and the individuation of tumour markers in biological fluids are currently one of the main tools to support diagnosis, prognosis, and monitoring of the therapeutic response in oncology. Although the identification of tumour markers in asymptomatic patients is crucial for early diagnosis, its application is still limited by the relatively low sensitivity and the complexity of existing methods (i.e. ELISA, mass spectrometry). We developed an easy, fast, and ultrasensitive surface-enhanced Raman scattering (SERS)–based system, for the detection and quantitation of the LGALS3BP (90K) biomarker that was used as a model, based on the development of antibody-functionalized nanostructured gold surfaces. The detection system was effective for the ultrasensitive detection and characterization of samples of different biochemical compositions. In conclusion, this work could provide the foundation for the development of a medical diagnostic device with the highest predictive power when compared with the methods currently used in cancer diagnostics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02903-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-75332572020-10-19 Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker Gallo, Valentina Lai, Antonia Pasquo, Alessandra Almaviva, Salvatore Iacobelli, Stefano Persichetti, Luca Capellini, Giovanni Antonini, Giovanni Anal Bioanal Chem Research Paper The research and the individuation of tumour markers in biological fluids are currently one of the main tools to support diagnosis, prognosis, and monitoring of the therapeutic response in oncology. Although the identification of tumour markers in asymptomatic patients is crucial for early diagnosis, its application is still limited by the relatively low sensitivity and the complexity of existing methods (i.e. ELISA, mass spectrometry). We developed an easy, fast, and ultrasensitive surface-enhanced Raman scattering (SERS)–based system, for the detection and quantitation of the LGALS3BP (90K) biomarker that was used as a model, based on the development of antibody-functionalized nanostructured gold surfaces. The detection system was effective for the ultrasensitive detection and characterization of samples of different biochemical compositions. In conclusion, this work could provide the foundation for the development of a medical diagnostic device with the highest predictive power when compared with the methods currently used in cancer diagnostics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02903-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-09-02 2020 /pmc/articles/PMC7533257/ /pubmed/32875368 http://dx.doi.org/10.1007/s00216-020-02903-2 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Paper
Gallo, Valentina
Lai, Antonia
Pasquo, Alessandra
Almaviva, Salvatore
Iacobelli, Stefano
Persichetti, Luca
Capellini, Giovanni
Antonini, Giovanni
Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker
title Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker
title_full Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker
title_fullStr Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker
title_full_unstemmed Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker
title_short Surface-enhanced Raman scattering (SERS)–based immunosystem for ultrasensitive detection of the 90K biomarker
title_sort surface-enhanced raman scattering (sers)–based immunosystem for ultrasensitive detection of the 90k biomarker
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533257/
https://www.ncbi.nlm.nih.gov/pubmed/32875368
http://dx.doi.org/10.1007/s00216-020-02903-2
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