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Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples
Biomarkers detection at an ultra-low concentration in biofluids (blood, serum, saliva, etc.) is a key point for the early diagnosis success and the development of personalized therapies. However, it remains a challenge due to limiting factors like (i) the complexity of analyzed media, and (ii) the a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468818/ https://www.ncbi.nlm.nih.gov/pubmed/30832416 http://dx.doi.org/10.3390/bios9010037 |
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author | Valpapuram, Immanuel Candeloro, Patrizio Coluccio, Maria Laura Parrotta, Elvira Immacolata Giugni, Andrea Das, Gobind Cuda, Gianni Di Fabrizio, Enzo Perozziello, Gerardo |
author_facet | Valpapuram, Immanuel Candeloro, Patrizio Coluccio, Maria Laura Parrotta, Elvira Immacolata Giugni, Andrea Das, Gobind Cuda, Gianni Di Fabrizio, Enzo Perozziello, Gerardo |
author_sort | Valpapuram, Immanuel |
collection | PubMed |
description | Biomarkers detection at an ultra-low concentration in biofluids (blood, serum, saliva, etc.) is a key point for the early diagnosis success and the development of personalized therapies. However, it remains a challenge due to limiting factors like (i) the complexity of analyzed media, and (ii) the aspecificity detection and the poor sensitivity of the conventional methods. In addition, several applications require the integration of the primary sensors with other devices (microfluidic devices, capillaries, flasks, vials, etc.) where transducing the signal might be difficult, reducing performances and applicability. In the present work, we demonstrate a new class of optical biosensor we have developed integrating an optical waveguide (OWG) with specific plasmonic surfaces. Exploiting the plasmonic resonance, the devices give consistent results in surface enhanced Raman spectroscopy (SERS) for continuous and label-free detection of biological compounds. The OWG allows driving optical signals in the proximity of SERS surfaces (detection area) overcoming spatial constraints, in order to reach places previously optically inaccessible. A rutile prism couples the remote laser source to the OWG, while a Raman spectrometer collects the SERS far field scattering. The present biosensors were implemented by a simple fabrication process, which includes photolithography and nanofabrication. By using such devices, it was possible to detect cell metabolites like Phenylalanine (Phe), Adenosine 5-triphosphate sodium hydrate (ATP), Sodium Lactate, Human Interleukin 6 (IL6), and relate them to possible metabolic pathway variation. |
format | Online Article Text |
id | pubmed-6468818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64688182019-04-23 Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples Valpapuram, Immanuel Candeloro, Patrizio Coluccio, Maria Laura Parrotta, Elvira Immacolata Giugni, Andrea Das, Gobind Cuda, Gianni Di Fabrizio, Enzo Perozziello, Gerardo Biosensors (Basel) Article Biomarkers detection at an ultra-low concentration in biofluids (blood, serum, saliva, etc.) is a key point for the early diagnosis success and the development of personalized therapies. However, it remains a challenge due to limiting factors like (i) the complexity of analyzed media, and (ii) the aspecificity detection and the poor sensitivity of the conventional methods. In addition, several applications require the integration of the primary sensors with other devices (microfluidic devices, capillaries, flasks, vials, etc.) where transducing the signal might be difficult, reducing performances and applicability. In the present work, we demonstrate a new class of optical biosensor we have developed integrating an optical waveguide (OWG) with specific plasmonic surfaces. Exploiting the plasmonic resonance, the devices give consistent results in surface enhanced Raman spectroscopy (SERS) for continuous and label-free detection of biological compounds. The OWG allows driving optical signals in the proximity of SERS surfaces (detection area) overcoming spatial constraints, in order to reach places previously optically inaccessible. A rutile prism couples the remote laser source to the OWG, while a Raman spectrometer collects the SERS far field scattering. The present biosensors were implemented by a simple fabrication process, which includes photolithography and nanofabrication. By using such devices, it was possible to detect cell metabolites like Phenylalanine (Phe), Adenosine 5-triphosphate sodium hydrate (ATP), Sodium Lactate, Human Interleukin 6 (IL6), and relate them to possible metabolic pathway variation. MDPI 2019-03-03 /pmc/articles/PMC6468818/ /pubmed/30832416 http://dx.doi.org/10.3390/bios9010037 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Valpapuram, Immanuel Candeloro, Patrizio Coluccio, Maria Laura Parrotta, Elvira Immacolata Giugni, Andrea Das, Gobind Cuda, Gianni Di Fabrizio, Enzo Perozziello, Gerardo Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples |
title | Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples |
title_full | Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples |
title_fullStr | Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples |
title_full_unstemmed | Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples |
title_short | Waveguiding and SERS Simplified Raman Spectroscopy on Biological Samples |
title_sort | waveguiding and sers simplified raman spectroscopy on biological samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468818/ https://www.ncbi.nlm.nih.gov/pubmed/30832416 http://dx.doi.org/10.3390/bios9010037 |
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