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Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection
Optical forces are used to aggregate plasmonic nanoparticles and create SERS–active hot spots in liquid. When biomolecules are added to the nanoparticles, high sensitivity SERS detection can be accomplished. Here, we pursue studies on Bovine Serum Albumin (BSA) detection, investigating the BSA–nanor...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873019/ https://www.ncbi.nlm.nih.gov/pubmed/29562606 http://dx.doi.org/10.3390/ma11030440 |
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author | Foti, Antonino D’Andrea, Cristiano Villari, Valentina Micali, Norberto Donato, Maria Grazia Fazio, Barbara Maragò, Onofrio M. Gillibert, Raymond Lamy de la Chapelle, Marc Gucciardi, Pietro G. |
author_facet | Foti, Antonino D’Andrea, Cristiano Villari, Valentina Micali, Norberto Donato, Maria Grazia Fazio, Barbara Maragò, Onofrio M. Gillibert, Raymond Lamy de la Chapelle, Marc Gucciardi, Pietro G. |
author_sort | Foti, Antonino |
collection | PubMed |
description | Optical forces are used to aggregate plasmonic nanoparticles and create SERS–active hot spots in liquid. When biomolecules are added to the nanoparticles, high sensitivity SERS detection can be accomplished. Here, we pursue studies on Bovine Serum Albumin (BSA) detection, investigating the BSA–nanorod aggregations in a range from 100 µM to 50 nM by combining light scattering, plasmon resonance and SERS, and correlating the SERS signal with the concentration. Experimental data are fitted with a simple model describing the optical aggregation process. We show that BSA–nanorod complexes can be optically printed on non-functionalized glass surfaces, designing custom patterns stable with time. Furthermore, we demonstrate that this methodology can be used to detect catalase and hemoglobin, two Raman resonant biomolecules, at concentrations of 10 nM and 1 pM, respectively, i.e., well beyond the limit of detection of BSA. Finally, we show that nanorods functionalized with specific aptamers can be used to capture and detect Ochratoxin A, a fungal toxin found in food commodities and wine. This experiment represents the first step towards the addition of molecular specificity to this novel biosensor strategy. |
format | Online Article Text |
id | pubmed-5873019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58730192018-03-30 Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection Foti, Antonino D’Andrea, Cristiano Villari, Valentina Micali, Norberto Donato, Maria Grazia Fazio, Barbara Maragò, Onofrio M. Gillibert, Raymond Lamy de la Chapelle, Marc Gucciardi, Pietro G. Materials (Basel) Article Optical forces are used to aggregate plasmonic nanoparticles and create SERS–active hot spots in liquid. When biomolecules are added to the nanoparticles, high sensitivity SERS detection can be accomplished. Here, we pursue studies on Bovine Serum Albumin (BSA) detection, investigating the BSA–nanorod aggregations in a range from 100 µM to 50 nM by combining light scattering, plasmon resonance and SERS, and correlating the SERS signal with the concentration. Experimental data are fitted with a simple model describing the optical aggregation process. We show that BSA–nanorod complexes can be optically printed on non-functionalized glass surfaces, designing custom patterns stable with time. Furthermore, we demonstrate that this methodology can be used to detect catalase and hemoglobin, two Raman resonant biomolecules, at concentrations of 10 nM and 1 pM, respectively, i.e., well beyond the limit of detection of BSA. Finally, we show that nanorods functionalized with specific aptamers can be used to capture and detect Ochratoxin A, a fungal toxin found in food commodities and wine. This experiment represents the first step towards the addition of molecular specificity to this novel biosensor strategy. MDPI 2018-03-17 /pmc/articles/PMC5873019/ /pubmed/29562606 http://dx.doi.org/10.3390/ma11030440 Text en © 2018 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 Foti, Antonino D’Andrea, Cristiano Villari, Valentina Micali, Norberto Donato, Maria Grazia Fazio, Barbara Maragò, Onofrio M. Gillibert, Raymond Lamy de la Chapelle, Marc Gucciardi, Pietro G. Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection |
title | Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection |
title_full | Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection |
title_fullStr | Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection |
title_full_unstemmed | Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection |
title_short | Optical Aggregation of Gold Nanoparticles for SERS Detection of Proteins and Toxins in Liquid Environment: Towards Ultrasensitive and Selective Detection |
title_sort | optical aggregation of gold nanoparticles for sers detection of proteins and toxins in liquid environment: towards ultrasensitive and selective detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873019/ https://www.ncbi.nlm.nih.gov/pubmed/29562606 http://dx.doi.org/10.3390/ma11030440 |
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