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Improved LFIAs for highly sensitive detection of BNP at point-of-care

Heart failure (HF) has become a major cause of morbidity and mortality with a significant global economic burden. Although well-established clinical tests could provide early diagnosis, access to these tests is limited in developing countries, where a relatively higher incidence of HF is present. Th...

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Autores principales: Gong, Yan, Hu, Jie, Choi, Jane Ru, You, Minli, Zheng, Yamin, Xu, Bo, Wen, Ting, Xu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479264/
https://www.ncbi.nlm.nih.gov/pubmed/28670119
http://dx.doi.org/10.2147/IJN.S135735
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author Gong, Yan
Hu, Jie
Choi, Jane Ru
You, Minli
Zheng, Yamin
Xu, Bo
Wen, Ting
Xu, Feng
author_facet Gong, Yan
Hu, Jie
Choi, Jane Ru
You, Minli
Zheng, Yamin
Xu, Bo
Wen, Ting
Xu, Feng
author_sort Gong, Yan
collection PubMed
description Heart failure (HF) has become a major cause of morbidity and mortality with a significant global economic burden. Although well-established clinical tests could provide early diagnosis, access to these tests is limited in developing countries, where a relatively higher incidence of HF is present. This has prompted an urgent need for developing a cost-effective, rapid and robust diagnostic tool for point-of-care (POC) detection of HF. Lateral flow immunoassay (LFIA) has found widespread applications in POC diagnostics. However, the low sensitivity of LFIA limits its ability to detect important HF biomarkers (e.g., brain natriuretic peptide [BNP]) that are normally present in low concentration in blood. To address this issue, we developed an improved LFIA by optimizing the gold nanoparticle (GNP)–antibody conjugate conditions (e.g., the conjugate pH and the amount of added antibody), the diameter of GNP and the concentration of antibody embedded on the test line and modifying the structure of test strip. Through these improvements, the proposed test strip enabled the detection of BNP down to 0.1 ng/mL within 10–15 min, presenting ~15-fold sensitivity enhancement over conventional lateral flow assay. We also successfully applied our LFIA in the analysis of BNP in human serum samples, highlighting its potential use for clinical assessment of HF. The developed LFIA for BNP could rapidly rule out HF with the naked eye, offering tremendous potential for POC test and personalized medicine.
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spelling pubmed-54792642017-06-30 Improved LFIAs for highly sensitive detection of BNP at point-of-care Gong, Yan Hu, Jie Choi, Jane Ru You, Minli Zheng, Yamin Xu, Bo Wen, Ting Xu, Feng Int J Nanomedicine Original Research Heart failure (HF) has become a major cause of morbidity and mortality with a significant global economic burden. Although well-established clinical tests could provide early diagnosis, access to these tests is limited in developing countries, where a relatively higher incidence of HF is present. This has prompted an urgent need for developing a cost-effective, rapid and robust diagnostic tool for point-of-care (POC) detection of HF. Lateral flow immunoassay (LFIA) has found widespread applications in POC diagnostics. However, the low sensitivity of LFIA limits its ability to detect important HF biomarkers (e.g., brain natriuretic peptide [BNP]) that are normally present in low concentration in blood. To address this issue, we developed an improved LFIA by optimizing the gold nanoparticle (GNP)–antibody conjugate conditions (e.g., the conjugate pH and the amount of added antibody), the diameter of GNP and the concentration of antibody embedded on the test line and modifying the structure of test strip. Through these improvements, the proposed test strip enabled the detection of BNP down to 0.1 ng/mL within 10–15 min, presenting ~15-fold sensitivity enhancement over conventional lateral flow assay. We also successfully applied our LFIA in the analysis of BNP in human serum samples, highlighting its potential use for clinical assessment of HF. The developed LFIA for BNP could rapidly rule out HF with the naked eye, offering tremendous potential for POC test and personalized medicine. Dove Medical Press 2017-06-15 /pmc/articles/PMC5479264/ /pubmed/28670119 http://dx.doi.org/10.2147/IJN.S135735 Text en © 2017 Gong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Gong, Yan
Hu, Jie
Choi, Jane Ru
You, Minli
Zheng, Yamin
Xu, Bo
Wen, Ting
Xu, Feng
Improved LFIAs for highly sensitive detection of BNP at point-of-care
title Improved LFIAs for highly sensitive detection of BNP at point-of-care
title_full Improved LFIAs for highly sensitive detection of BNP at point-of-care
title_fullStr Improved LFIAs for highly sensitive detection of BNP at point-of-care
title_full_unstemmed Improved LFIAs for highly sensitive detection of BNP at point-of-care
title_short Improved LFIAs for highly sensitive detection of BNP at point-of-care
title_sort improved lfias for highly sensitive detection of bnp at point-of-care
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5479264/
https://www.ncbi.nlm.nih.gov/pubmed/28670119
http://dx.doi.org/10.2147/IJN.S135735
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