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End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines

[Image: see text] Lateral flow devices are rapid (and often low cost) point-of-care diagnostics—the classic example being the home pregnancy test. A test line (the stationary phase) is typically prepared by the physisorption of an antibody, which binds to analytes/antigens such as viruses, toxins, o...

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Autores principales: Baker, Alexander N., Congdon, Thomas R., Richards, Sarah-Jane, Georgiou, Panagiotis G., Walker, Marc, Dedola, Simone, Field, Robert A., Gibson, Matthew I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612620/
https://www.ncbi.nlm.nih.gov/pubmed/35425945
http://dx.doi.org/10.1021/acspolymersau.1c00032
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author Baker, Alexander N.
Congdon, Thomas R.
Richards, Sarah-Jane
Georgiou, Panagiotis G.
Walker, Marc
Dedola, Simone
Field, Robert A.
Gibson, Matthew I.
author_facet Baker, Alexander N.
Congdon, Thomas R.
Richards, Sarah-Jane
Georgiou, Panagiotis G.
Walker, Marc
Dedola, Simone
Field, Robert A.
Gibson, Matthew I.
author_sort Baker, Alexander N.
collection PubMed
description [Image: see text] Lateral flow devices are rapid (and often low cost) point-of-care diagnostics—the classic example being the home pregnancy test. A test line (the stationary phase) is typically prepared by the physisorption of an antibody, which binds to analytes/antigens such as viruses, toxins, or hormones. However, there is no intrinsic requirement for the detection unit to be an antibody, and incorporating other ligand classes may bring new functionalities or detection capabilities. To enable other (nonprotein) ligands to be deployed in lateral flow devices, they must be physiosorbed to the stationary phase as a conjugate, which currently would be a high-molecular-weight carrier protein, which requires (challenging) chemoselective modifications and purification. Here, we demonstrate that poly(vinylpyrrolidone), PVP, is a candidate for a polymeric, protein-free test line, owing to its unique balance of water solubility (for printing) and adhesion to the nitrocellulose stationary phase. End-functionalized PVPs were prepared by RAFT polymerization, and the model capture ligands of biotin and galactosamine were installed on PVP and subsequently immobilized on nitrocellulose. This polymeric test line was validated in both flow-through and full lateral flow formats using streptavidin and soybean agglutinin and is the first demonstration of an “all-polymer” approach for installation of capture units. This work illustrates the potential of polymeric scaffolds as anchoring agents for small-molecule capture agents in the next generation of robust and modular lateral flow devices and that macromolecular engineering may provide real benefit.
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spelling pubmed-76126202022-04-13 End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines Baker, Alexander N. Congdon, Thomas R. Richards, Sarah-Jane Georgiou, Panagiotis G. Walker, Marc Dedola, Simone Field, Robert A. Gibson, Matthew I. ACS Polym Au [Image: see text] Lateral flow devices are rapid (and often low cost) point-of-care diagnostics—the classic example being the home pregnancy test. A test line (the stationary phase) is typically prepared by the physisorption of an antibody, which binds to analytes/antigens such as viruses, toxins, or hormones. However, there is no intrinsic requirement for the detection unit to be an antibody, and incorporating other ligand classes may bring new functionalities or detection capabilities. To enable other (nonprotein) ligands to be deployed in lateral flow devices, they must be physiosorbed to the stationary phase as a conjugate, which currently would be a high-molecular-weight carrier protein, which requires (challenging) chemoselective modifications and purification. Here, we demonstrate that poly(vinylpyrrolidone), PVP, is a candidate for a polymeric, protein-free test line, owing to its unique balance of water solubility (for printing) and adhesion to the nitrocellulose stationary phase. End-functionalized PVPs were prepared by RAFT polymerization, and the model capture ligands of biotin and galactosamine were installed on PVP and subsequently immobilized on nitrocellulose. This polymeric test line was validated in both flow-through and full lateral flow formats using streptavidin and soybean agglutinin and is the first demonstration of an “all-polymer” approach for installation of capture units. This work illustrates the potential of polymeric scaffolds as anchoring agents for small-molecule capture agents in the next generation of robust and modular lateral flow devices and that macromolecular engineering may provide real benefit. American Chemical Society 2021-11-12 /pmc/articles/PMC7612620/ /pubmed/35425945 http://dx.doi.org/10.1021/acspolymersau.1c00032 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Baker, Alexander N.
Congdon, Thomas R.
Richards, Sarah-Jane
Georgiou, Panagiotis G.
Walker, Marc
Dedola, Simone
Field, Robert A.
Gibson, Matthew I.
End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines
title End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines
title_full End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines
title_fullStr End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines
title_full_unstemmed End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines
title_short End-Functionalized Poly(vinylpyrrolidone) for Ligand Display in Lateral Flow Device Test Lines
title_sort end-functionalized poly(vinylpyrrolidone) for ligand display in lateral flow device test lines
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612620/
https://www.ncbi.nlm.nih.gov/pubmed/35425945
http://dx.doi.org/10.1021/acspolymersau.1c00032
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