An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens

We report a new competitive lateral flow immunoassay (LFIA) for hapten detection, which uses antibodies to bind antigens from a sample and form a coloured immune complex due to artificial antigens conjugated with gold nanoparticles; these were intercepted with SPA. Here, 2,4-dichlorophenoxyacetic ac...

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Autores principales: Yaning Sun, Suzhen Yang, Jifei Yang, Xiaofei Hu, Qiang Wei, Yao Wang, Yunrui Xing, Linlin Chen, Xinxin Chen, Ruiguang Deng, Gaiping Zhang
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Publicado: Taylor & Francis Group 2021
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Acceso en línea:https://doaj.org/article/1891fa5f185c473bbd31d6e682332152
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spelling oai:doaj.org-article:1891fa5f185c473bbd31d6e6823321522021-11-04T15:00:41ZAn accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens0954-01051465-344310.1080/09540105.2021.1989382https://doaj.org/article/1891fa5f185c473bbd31d6e6823321522021-01-01T00:00:00Zhttp://dx.doi.org/10.1080/09540105.2021.1989382https://doaj.org/toc/0954-0105https://doaj.org/toc/1465-3443We report a new competitive lateral flow immunoassay (LFIA) for hapten detection, which uses antibodies to bind antigens from a sample and form a coloured immune complex due to artificial antigens conjugated with gold nanoparticles; these were intercepted with SPA. Here, 2,4-dichlorophenoxyacetic acid (2,4-D) and gentamicin (GM) were selected as model analytes. The visual limit of detection of the 2,4-D strip was 25 ng/mL in tap water; the GM strip was 3.13 ng/mL in milk. This approach exhibits more than a 40-fold lower detection limit for 2,4-D and 3.2-fold lower for GM, which is compared to traditional LFIA using the same reagents. This approach can accurately control the amount of antibody, protect the activity of antibody and enhance the detection signal, thus improving the sensitivity of the LFIA and providing more and more sensitive methods for the development of LFIAs. Highlights This study developed a new method of LFIA that could improve the sensitivity of LFIA without adding any reagent. The antibodies are unlabelled; thus, the immunological properties of the antibodies are not destroyed by antibody folding during the labelling process. Sufficient gold-labelled antigens ensure that each antibody bound to the test line can combine two gold nanoparticles, thereby amplifying the overall signal.Yaning SunSuzhen YangJifei YangXiaofei HuQiang WeiYao WangYunrui XingLinlin ChenXinxin ChenRuiguang DengGaiping ZhangTaylor & Francis Grouparticlesensitive enhancementcompetitive lateral flow immunoassaytest stripgm2,4-dAgriculture (General)S1-972Immunologic diseases. AllergyRC581-607ENFood and Agricultural Immunology, Vol 32, Iss 1, Pp 766-777 (2021)
institution DOAJ
collection DOAJ
language EN
topic sensitive enhancement
competitive lateral flow immunoassay
test strip
gm
2,4-d
Agriculture (General)
S1-972
Immunologic diseases. Allergy
RC581-607
spellingShingle sensitive enhancement
competitive lateral flow immunoassay
test strip
gm
2,4-d
Agriculture (General)
S1-972
Immunologic diseases. Allergy
RC581-607
Yaning Sun
Suzhen Yang
Jifei Yang
Xiaofei Hu
Qiang Wei
Yao Wang
Yunrui Xing
Linlin Chen
Xinxin Chen
Ruiguang Deng
Gaiping Zhang
An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
description We report a new competitive lateral flow immunoassay (LFIA) for hapten detection, which uses antibodies to bind antigens from a sample and form a coloured immune complex due to artificial antigens conjugated with gold nanoparticles; these were intercepted with SPA. Here, 2,4-dichlorophenoxyacetic acid (2,4-D) and gentamicin (GM) were selected as model analytes. The visual limit of detection of the 2,4-D strip was 25 ng/mL in tap water; the GM strip was 3.13 ng/mL in milk. This approach exhibits more than a 40-fold lower detection limit for 2,4-D and 3.2-fold lower for GM, which is compared to traditional LFIA using the same reagents. This approach can accurately control the amount of antibody, protect the activity of antibody and enhance the detection signal, thus improving the sensitivity of the LFIA and providing more and more sensitive methods for the development of LFIAs. Highlights This study developed a new method of LFIA that could improve the sensitivity of LFIA without adding any reagent. The antibodies are unlabelled; thus, the immunological properties of the antibodies are not destroyed by antibody folding during the labelling process. Sufficient gold-labelled antigens ensure that each antibody bound to the test line can combine two gold nanoparticles, thereby amplifying the overall signal.
format article
author Yaning Sun
Suzhen Yang
Jifei Yang
Xiaofei Hu
Qiang Wei
Yao Wang
Yunrui Xing
Linlin Chen
Xinxin Chen
Ruiguang Deng
Gaiping Zhang
author_facet Yaning Sun
Suzhen Yang
Jifei Yang
Xiaofei Hu
Qiang Wei
Yao Wang
Yunrui Xing
Linlin Chen
Xinxin Chen
Ruiguang Deng
Gaiping Zhang
author_sort Yaning Sun
title An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
title_short An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
title_full An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
title_fullStr An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
title_full_unstemmed An accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
title_sort accurate and amplifying competitive lateral flow immunoassay for the sensitive detection of haptens
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/1891fa5f185c473bbd31d6e682332152
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