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Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays

Urine is an attractive biospecimen for in vitro diagnostics, and urine-based lateral flow assays are low-cost devices suitable for point-of-care testing, particularly in low-resource settings. However, some of the lateral flow assays exhibit limited diagnostic utility because the urinary biomarker c...

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Autores principales: Chen, Sheng-You, Wu, Abe Y., Lunde, Ruby, Lai, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199386/
https://www.ncbi.nlm.nih.gov/pubmed/35721843
http://dx.doi.org/10.3389/fbioe.2022.884271
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author Chen, Sheng-You
Wu, Abe Y.
Lunde, Ruby
Lai, James J.
author_facet Chen, Sheng-You
Wu, Abe Y.
Lunde, Ruby
Lai, James J.
author_sort Chen, Sheng-You
collection PubMed
description Urine is an attractive biospecimen for in vitro diagnostics, and urine-based lateral flow assays are low-cost devices suitable for point-of-care testing, particularly in low-resource settings. However, some of the lateral flow assays exhibit limited diagnostic utility because the urinary biomarker concentration is significantly lower than the assay detection limit, which compromises the sensitivity. To address the challenge, we developed an osmotic processor that statically and spontaneously concentrated biomarkers. The specimen in the device interfaces with the aqueous polymer solution via a dialysis membrane. The polymer solution induces an osmotic pressure difference that extracts water from the specimen, while the membrane retains the biomarkers. The evaluation demonstrated that osmosis induced by various water-soluble polymers efficiently extracted water from the specimens, ca. 5–15 ml/h. The osmotic processor concentrated the specimens to improve the lateral flow assays’ detection limits for the model analytes—human chorionic gonadotropin and SARS-CoV-2 nucleocapsid protein. After the treatment via the osmotic processor, the lateral flow assays detected the corresponding biomarkers in the concentrated specimens. The test band intensities of the assays with the concentrated specimens were very similar to the reference assays with 100-fold concentrations. The mass spectrometry analysis estimated the SARS-CoV-2 nucleocapsid protein concentration increased ca. 200-fold after the osmosis. With its simplicity and flexibility, this device demonstrates a great potential to be utilized in conjunction with the existing lateral flow assays for enabling highly sensitive detection of dilute target analytes in urine.
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spelling pubmed-91993862022-06-16 Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays Chen, Sheng-You Wu, Abe Y. Lunde, Ruby Lai, James J. Front Bioeng Biotechnol Bioengineering and Biotechnology Urine is an attractive biospecimen for in vitro diagnostics, and urine-based lateral flow assays are low-cost devices suitable for point-of-care testing, particularly in low-resource settings. However, some of the lateral flow assays exhibit limited diagnostic utility because the urinary biomarker concentration is significantly lower than the assay detection limit, which compromises the sensitivity. To address the challenge, we developed an osmotic processor that statically and spontaneously concentrated biomarkers. The specimen in the device interfaces with the aqueous polymer solution via a dialysis membrane. The polymer solution induces an osmotic pressure difference that extracts water from the specimen, while the membrane retains the biomarkers. The evaluation demonstrated that osmosis induced by various water-soluble polymers efficiently extracted water from the specimens, ca. 5–15 ml/h. The osmotic processor concentrated the specimens to improve the lateral flow assays’ detection limits for the model analytes—human chorionic gonadotropin and SARS-CoV-2 nucleocapsid protein. After the treatment via the osmotic processor, the lateral flow assays detected the corresponding biomarkers in the concentrated specimens. The test band intensities of the assays with the concentrated specimens were very similar to the reference assays with 100-fold concentrations. The mass spectrometry analysis estimated the SARS-CoV-2 nucleocapsid protein concentration increased ca. 200-fold after the osmosis. With its simplicity and flexibility, this device demonstrates a great potential to be utilized in conjunction with the existing lateral flow assays for enabling highly sensitive detection of dilute target analytes in urine. Frontiers Media S.A. 2022-06-01 /pmc/articles/PMC9199386/ /pubmed/35721843 http://dx.doi.org/10.3389/fbioe.2022.884271 Text en Copyright © 2022 Chen, Wu, Lunde and Lai. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Chen, Sheng-You
Wu, Abe Y.
Lunde, Ruby
Lai, James J.
Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays
title Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays
title_full Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays
title_fullStr Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays
title_full_unstemmed Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays
title_short Osmotic Processor for Enabling Sensitive and Rapid Biomarker Detection via Lateral Flow Assays
title_sort osmotic processor for enabling sensitive and rapid biomarker detection via lateral flow assays
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199386/
https://www.ncbi.nlm.nih.gov/pubmed/35721843
http://dx.doi.org/10.3389/fbioe.2022.884271
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