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A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices
BACKGROUND: The prevalence and death rate arising from malaria infection, and emergence of other diseases showing similar symptoms to malaria require the development of malaria-specific and sensitive devices for its diagnosis. To address this, the design and fabrication of low-cost, rapid, paper-bas...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172074/ https://www.ncbi.nlm.nih.gov/pubmed/35672848 http://dx.doi.org/10.1186/s12936-022-04187-6 |
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author | Ogunmolasuyi, Adewoyin Martin Fogel, Ronen Hoppe, Heinrich Goldring, Dean Limson, Janice |
author_facet | Ogunmolasuyi, Adewoyin Martin Fogel, Ronen Hoppe, Heinrich Goldring, Dean Limson, Janice |
author_sort | Ogunmolasuyi, Adewoyin Martin |
collection | PubMed |
description | BACKGROUND: The prevalence and death rate arising from malaria infection, and emergence of other diseases showing similar symptoms to malaria require the development of malaria-specific and sensitive devices for its diagnosis. To address this, the design and fabrication of low-cost, rapid, paper-based analytical devices (µPAD) using surface-immobilized aptamers to detect the presence of a recombinant malarial biomarker—Plasmodium falciparum lactate dehydrogenase (rPfLDH)—is reported in this study. METHODS: Test zones on paper surfaces were created by covalently immobilizing streptavidin to the paper, subsequently attaching biotinylated aptamers to streptavidin. Aptamers selectively bound rPfLDH. The measurement of captured rPfLDH enzyme activity served as the means of detecting this biomarker. Enzyme activity across three replicate sensors was digitally quantified using the colorimetric Malstat assay. RESULTS: Screening of several different aptamers reported in the literature showed that aptamers rLDH7 and 2008s immobilized in this manner specifically recognised and captured PfLDH. Using rLDH7, the sensitivity of the µPAD sensor was evaluated and the µPAD sensor was applied for preferential detection of rPfLDH, both in buffered solutions of the protein and in spiked serum and red blood cell lysate samples. In buffered solutions, the test zone of the µPAD sensor exhibited a K(D) of 24 ± 11 nM and an empirical limit of detection of 17 nM, respectively, a limit similar to commercial antibody-based sensors exposed to rPfLDH. The specific recognition of 133 nM rPfLDH in undiluted serum and blood samples was demonstrated by the µPAD. CONCLUSION: The reported µPAD demonstrates the potential of integrating aptamers into paper-based malarial rapid diagnostic tests. GRAPHICAL ABSTRACT: [Figure: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04187-6. |
format | Online Article Text |
id | pubmed-9172074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91720742022-06-08 A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices Ogunmolasuyi, Adewoyin Martin Fogel, Ronen Hoppe, Heinrich Goldring, Dean Limson, Janice Malar J Research BACKGROUND: The prevalence and death rate arising from malaria infection, and emergence of other diseases showing similar symptoms to malaria require the development of malaria-specific and sensitive devices for its diagnosis. To address this, the design and fabrication of low-cost, rapid, paper-based analytical devices (µPAD) using surface-immobilized aptamers to detect the presence of a recombinant malarial biomarker—Plasmodium falciparum lactate dehydrogenase (rPfLDH)—is reported in this study. METHODS: Test zones on paper surfaces were created by covalently immobilizing streptavidin to the paper, subsequently attaching biotinylated aptamers to streptavidin. Aptamers selectively bound rPfLDH. The measurement of captured rPfLDH enzyme activity served as the means of detecting this biomarker. Enzyme activity across three replicate sensors was digitally quantified using the colorimetric Malstat assay. RESULTS: Screening of several different aptamers reported in the literature showed that aptamers rLDH7 and 2008s immobilized in this manner specifically recognised and captured PfLDH. Using rLDH7, the sensitivity of the µPAD sensor was evaluated and the µPAD sensor was applied for preferential detection of rPfLDH, both in buffered solutions of the protein and in spiked serum and red blood cell lysate samples. In buffered solutions, the test zone of the µPAD sensor exhibited a K(D) of 24 ± 11 nM and an empirical limit of detection of 17 nM, respectively, a limit similar to commercial antibody-based sensors exposed to rPfLDH. The specific recognition of 133 nM rPfLDH in undiluted serum and blood samples was demonstrated by the µPAD. CONCLUSION: The reported µPAD demonstrates the potential of integrating aptamers into paper-based malarial rapid diagnostic tests. GRAPHICAL ABSTRACT: [Figure: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04187-6. BioMed Central 2022-06-07 /pmc/articles/PMC9172074/ /pubmed/35672848 http://dx.doi.org/10.1186/s12936-022-04187-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ogunmolasuyi, Adewoyin Martin Fogel, Ronen Hoppe, Heinrich Goldring, Dean Limson, Janice A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices |
title | A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices |
title_full | A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices |
title_fullStr | A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices |
title_full_unstemmed | A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices |
title_short | A microfluidic paper analytical device using capture aptamers for the detection of PfLDH in blood matrices |
title_sort | microfluidic paper analytical device using capture aptamers for the detection of pfldh in blood matrices |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172074/ https://www.ncbi.nlm.nih.gov/pubmed/35672848 http://dx.doi.org/10.1186/s12936-022-04187-6 |
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