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The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles

A wide-field surface plasmon resonance (SPR) microscopy sensor employs the surface plasmon resonance phenomenon to detect individual biological and non-biological nanoparticles. This sensor enables the detection, sizing, and quantification of biological nanoparticles (bioNPs), such as extracellular...

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Autores principales: Sharar, Nour, Wüstefeld, Konstantin, Talukder, Rahat Morad, Skolnik, Julija, Kaufmann, Katharina, Giebel, Bernd, Börger, Verena, Nolte, Friedrich, Watzl, Carsten, Weichert, Frank, Hergenröder, Roland, Shpacovitch, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136938/
https://www.ncbi.nlm.nih.gov/pubmed/37185547
http://dx.doi.org/10.3390/bios13040472
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author Sharar, Nour
Wüstefeld, Konstantin
Talukder, Rahat Morad
Skolnik, Julija
Kaufmann, Katharina
Giebel, Bernd
Börger, Verena
Nolte, Friedrich
Watzl, Carsten
Weichert, Frank
Hergenröder, Roland
Shpacovitch, Victoria
author_facet Sharar, Nour
Wüstefeld, Konstantin
Talukder, Rahat Morad
Skolnik, Julija
Kaufmann, Katharina
Giebel, Bernd
Börger, Verena
Nolte, Friedrich
Watzl, Carsten
Weichert, Frank
Hergenröder, Roland
Shpacovitch, Victoria
author_sort Sharar, Nour
collection PubMed
description A wide-field surface plasmon resonance (SPR) microscopy sensor employs the surface plasmon resonance phenomenon to detect individual biological and non-biological nanoparticles. This sensor enables the detection, sizing, and quantification of biological nanoparticles (bioNPs), such as extracellular vesicles (EVs), viruses, and virus-like particles. The selectivity of bioNP detection does not require biological particle labeling, and it is achieved via the functionalization of the gold sensor surface by target-bioNP-specific antibodies. In the current work, we demonstrate the ability of SPR microscopy sensors to detect, simultaneously, silica NPs that differ by four times in size. Employed silica particles are close in their refractive index to bioNPs. The literature reports the ability of SPR microscopy sensors to detect the binding of lymphocytes (around 10 [Formula: see text] objects) to the sensor surface. Taken together, our findings and the results reported in the literature indicate the power of SPR microscopy sensors to detect bioNPs that differ by at least two orders in size. Modifications of the optical sensor scheme, such as mounting a concave lens, help to achieve homogeneous illumination of a gold sensor chip surface. In the current work, we also characterize the improved magnification factor of the modified SPR instrument. We evaluate the effectiveness of the modified and the primary version of the SPR microscopy sensors in detecting EVs isolated via different approaches. In addition, we demonstrate the possibility of employing translation and rotation stepper motors for precise adjustments of the positions of sensor optical elements—prism and objective—in the primary version of the SPR microscopy sensor instrument, and we present an algorithm to establish effective sensor–actuator coupling.
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spelling pubmed-101369382023-04-28 The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles Sharar, Nour Wüstefeld, Konstantin Talukder, Rahat Morad Skolnik, Julija Kaufmann, Katharina Giebel, Bernd Börger, Verena Nolte, Friedrich Watzl, Carsten Weichert, Frank Hergenröder, Roland Shpacovitch, Victoria Biosensors (Basel) Article A wide-field surface plasmon resonance (SPR) microscopy sensor employs the surface plasmon resonance phenomenon to detect individual biological and non-biological nanoparticles. This sensor enables the detection, sizing, and quantification of biological nanoparticles (bioNPs), such as extracellular vesicles (EVs), viruses, and virus-like particles. The selectivity of bioNP detection does not require biological particle labeling, and it is achieved via the functionalization of the gold sensor surface by target-bioNP-specific antibodies. In the current work, we demonstrate the ability of SPR microscopy sensors to detect, simultaneously, silica NPs that differ by four times in size. Employed silica particles are close in their refractive index to bioNPs. The literature reports the ability of SPR microscopy sensors to detect the binding of lymphocytes (around 10 [Formula: see text] objects) to the sensor surface. Taken together, our findings and the results reported in the literature indicate the power of SPR microscopy sensors to detect bioNPs that differ by at least two orders in size. Modifications of the optical sensor scheme, such as mounting a concave lens, help to achieve homogeneous illumination of a gold sensor chip surface. In the current work, we also characterize the improved magnification factor of the modified SPR instrument. We evaluate the effectiveness of the modified and the primary version of the SPR microscopy sensors in detecting EVs isolated via different approaches. In addition, we demonstrate the possibility of employing translation and rotation stepper motors for precise adjustments of the positions of sensor optical elements—prism and objective—in the primary version of the SPR microscopy sensor instrument, and we present an algorithm to establish effective sensor–actuator coupling. MDPI 2023-04-12 /pmc/articles/PMC10136938/ /pubmed/37185547 http://dx.doi.org/10.3390/bios13040472 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sharar, Nour
Wüstefeld, Konstantin
Talukder, Rahat Morad
Skolnik, Julija
Kaufmann, Katharina
Giebel, Bernd
Börger, Verena
Nolte, Friedrich
Watzl, Carsten
Weichert, Frank
Hergenröder, Roland
Shpacovitch, Victoria
The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles
title The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles
title_full The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles
title_fullStr The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles
title_full_unstemmed The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles
title_short The Employment of the Surface Plasmon Resonance (SPR) Microscopy Sensor for the Detection of Individual Extracellular Vesicles and Non-Biological Nanoparticles
title_sort employment of the surface plasmon resonance (spr) microscopy sensor for the detection of individual extracellular vesicles and non-biological nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136938/
https://www.ncbi.nlm.nih.gov/pubmed/37185547
http://dx.doi.org/10.3390/bios13040472
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