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Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor
Multiplex lateral flow immunoassay (LFIA) is largely used for point-of-care testing to detect different pathogens or biomarkers in a single device. The increasing demand for multitargeting diagnostics requires multi-informative single tests. In this study, we demonstrated three strategies to upgrade...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698945/ https://www.ncbi.nlm.nih.gov/pubmed/33218125 http://dx.doi.org/10.3390/s20226609 |
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author | Cavalera, Simone Di Nardo, Fabio Forte, Luca Marinoni, Francesca Chiarello, Matteo Baggiani, Claudio Anfossi, Laura |
author_facet | Cavalera, Simone Di Nardo, Fabio Forte, Luca Marinoni, Francesca Chiarello, Matteo Baggiani, Claudio Anfossi, Laura |
author_sort | Cavalera, Simone |
collection | PubMed |
description | Multiplex lateral flow immunoassay (LFIA) is largely used for point-of-care testing to detect different pathogens or biomarkers in a single device. The increasing demand for multitargeting diagnostics requires multi-informative single tests. In this study, we demonstrated three strategies to upgrade standard multiplex LFIA to multimodal capacity. As a proof-of-concept, we applied the strategies to the differential diagnosis of Human Immunodeficiency Virus (HIV) infection, a widespread pathogen, for which conventional multiplex LFIA testing is well-established. In the new two-parameter LFIA (x(2)LFIA), we exploited color encoding, in which the binding of multiple targets occurs in one reactive band and the color of the probe reveals which one is present in the sample. By combining the sequential alignment of several reactive zones along the membrane of the LFIA strip and gold nanoparticles and gold nanostars for the differential visualization, in this demonstration, the x(2)LFIA can furnish information on HIV serotype and stage of infection in a single device. Three immunosensors were designed. The use of bioreagents as the capturing ligand anchored onto the membrane or as the detection ligand labelled with gold nanomaterials affected the performance of the x(2)LFIA. Higher detectability was achieved by the format involving the HIV-specific antigens as capturing agent and labelled secondary bioligands (anti-human immunoglobulins M and protein G) as the probes. |
format | Online Article Text |
id | pubmed-7698945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76989452020-11-29 Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor Cavalera, Simone Di Nardo, Fabio Forte, Luca Marinoni, Francesca Chiarello, Matteo Baggiani, Claudio Anfossi, Laura Sensors (Basel) Article Multiplex lateral flow immunoassay (LFIA) is largely used for point-of-care testing to detect different pathogens or biomarkers in a single device. The increasing demand for multitargeting diagnostics requires multi-informative single tests. In this study, we demonstrated three strategies to upgrade standard multiplex LFIA to multimodal capacity. As a proof-of-concept, we applied the strategies to the differential diagnosis of Human Immunodeficiency Virus (HIV) infection, a widespread pathogen, for which conventional multiplex LFIA testing is well-established. In the new two-parameter LFIA (x(2)LFIA), we exploited color encoding, in which the binding of multiple targets occurs in one reactive band and the color of the probe reveals which one is present in the sample. By combining the sequential alignment of several reactive zones along the membrane of the LFIA strip and gold nanoparticles and gold nanostars for the differential visualization, in this demonstration, the x(2)LFIA can furnish information on HIV serotype and stage of infection in a single device. Three immunosensors were designed. The use of bioreagents as the capturing ligand anchored onto the membrane or as the detection ligand labelled with gold nanomaterials affected the performance of the x(2)LFIA. Higher detectability was achieved by the format involving the HIV-specific antigens as capturing agent and labelled secondary bioligands (anti-human immunoglobulins M and protein G) as the probes. MDPI 2020-11-18 /pmc/articles/PMC7698945/ /pubmed/33218125 http://dx.doi.org/10.3390/s20226609 Text en © 2020 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 Cavalera, Simone Di Nardo, Fabio Forte, Luca Marinoni, Francesca Chiarello, Matteo Baggiani, Claudio Anfossi, Laura Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor |
title | Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor |
title_full | Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor |
title_fullStr | Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor |
title_full_unstemmed | Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor |
title_short | Switching from Multiplex to Multimodal Colorimetric Lateral Flow Immunosensor |
title_sort | switching from multiplex to multimodal colorimetric lateral flow immunosensor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698945/ https://www.ncbi.nlm.nih.gov/pubmed/33218125 http://dx.doi.org/10.3390/s20226609 |
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