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Single-Color Barcoding for Multiplexed Hydrogel Bead-Based Immunoassays
[Image: see text] Current developments in precision medicine require the simultaneous detection of an increasing number of biomarkers in heterogeneous, complex solutions, such as blood samples. To meet this need, immunoassays on barcoded hydrogel beads have been proposed, although the encoding and d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185679/ https://www.ncbi.nlm.nih.gov/pubmed/35617151 http://dx.doi.org/10.1021/acsami.2c04361 |
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author | Weber, Tobias A. Metzler, Lukas Fosso Tene, Patrick L. Brandstetter, Thomas Rühe, Jürgen |
author_facet | Weber, Tobias A. Metzler, Lukas Fosso Tene, Patrick L. Brandstetter, Thomas Rühe, Jürgen |
author_sort | Weber, Tobias A. |
collection | PubMed |
description | [Image: see text] Current developments in precision medicine require the simultaneous detection of an increasing number of biomarkers in heterogeneous, complex solutions, such as blood samples. To meet this need, immunoassays on barcoded hydrogel beads have been proposed, although the encoding and decoding of these barcodes is usually complex and/or resource-intensive. Herein, an efficient method for the fabrication of barcoded, functionalized hydrogel beads is presented. The hydrogel beads are generated using droplet-based microfluidics in combination with photochemically induced C–H insertion reactions, allowing photo-crosslinking, (bio-) functionalization, and barcode integration to be performed in a single step. The generated functionalized beads carry single-color barcodes consisting of green-fluorescent particles of different sizes and concentrations, allowing simple and simultaneous readout with a standard plate reader. As a test example, the performance of barcoded hydrogel beads (3 × 3 matrix) functionalized with capture molecules of interest (e.g., antigens) is investigated for the detection of Lyme-disease-specific antibodies in patient sera. The described barcoding strategy for hydrogel beads does not interfere with the bioanalytical process and captivates by its simplicity and versatility, making it an attractive candidate for multiplex bioanalytical processes. |
format | Online Article Text |
id | pubmed-9185679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91856792022-06-11 Single-Color Barcoding for Multiplexed Hydrogel Bead-Based Immunoassays Weber, Tobias A. Metzler, Lukas Fosso Tene, Patrick L. Brandstetter, Thomas Rühe, Jürgen ACS Appl Mater Interfaces [Image: see text] Current developments in precision medicine require the simultaneous detection of an increasing number of biomarkers in heterogeneous, complex solutions, such as blood samples. To meet this need, immunoassays on barcoded hydrogel beads have been proposed, although the encoding and decoding of these barcodes is usually complex and/or resource-intensive. Herein, an efficient method for the fabrication of barcoded, functionalized hydrogel beads is presented. The hydrogel beads are generated using droplet-based microfluidics in combination with photochemically induced C–H insertion reactions, allowing photo-crosslinking, (bio-) functionalization, and barcode integration to be performed in a single step. The generated functionalized beads carry single-color barcodes consisting of green-fluorescent particles of different sizes and concentrations, allowing simple and simultaneous readout with a standard plate reader. As a test example, the performance of barcoded hydrogel beads (3 × 3 matrix) functionalized with capture molecules of interest (e.g., antigens) is investigated for the detection of Lyme-disease-specific antibodies in patient sera. The described barcoding strategy for hydrogel beads does not interfere with the bioanalytical process and captivates by its simplicity and versatility, making it an attractive candidate for multiplex bioanalytical processes. American Chemical Society 2022-05-26 2022-06-08 /pmc/articles/PMC9185679/ /pubmed/35617151 http://dx.doi.org/10.1021/acsami.2c04361 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Weber, Tobias A. Metzler, Lukas Fosso Tene, Patrick L. Brandstetter, Thomas Rühe, Jürgen Single-Color Barcoding for Multiplexed Hydrogel Bead-Based Immunoassays |
title | Single-Color
Barcoding for Multiplexed Hydrogel Bead-Based
Immunoassays |
title_full | Single-Color
Barcoding for Multiplexed Hydrogel Bead-Based
Immunoassays |
title_fullStr | Single-Color
Barcoding for Multiplexed Hydrogel Bead-Based
Immunoassays |
title_full_unstemmed | Single-Color
Barcoding for Multiplexed Hydrogel Bead-Based
Immunoassays |
title_short | Single-Color
Barcoding for Multiplexed Hydrogel Bead-Based
Immunoassays |
title_sort | single-color
barcoding for multiplexed hydrogel bead-based
immunoassays |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185679/ https://www.ncbi.nlm.nih.gov/pubmed/35617151 http://dx.doi.org/10.1021/acsami.2c04361 |
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