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Nanozymes featuring a mesoporous silica shell for rapid enrichment and ultrasensitive lateral flow immunoassay of influenza A

Respiratory illnesses stemming from influenza A viruses represent a significant worldwide health concern. There is an immediate need for a rapid and sensitive method to detect influenza A viruses early, without requiring extra equipment. Here, we established a lateral flow immunoassay (LFIA) for the...

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Published in:Analytica chimica acta 2025-01, Vol.1335, p.343474, Article 343474
Main Authors: Liang, Jing, Liu, Xiaoxian, Liu, Zhenzhen, Xu, Xuanming, Sun, Yinuo, Chen, Yuan, Xiao, Rui, Wang, Yajie
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container_title Analytica chimica acta
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Liu, Xiaoxian
Liu, Zhenzhen
Xu, Xuanming
Sun, Yinuo
Chen, Yuan
Xiao, Rui
Wang, Yajie
description Respiratory illnesses stemming from influenza A viruses represent a significant worldwide health concern. There is an immediate need for a rapid and sensitive method to detect influenza A viruses early, without requiring extra equipment. Here, we established a lateral flow immunoassay (LFIA) for the detection of influenza A (Flu A) using a "three-in-one" multifunctional mesoporous Fe3O4@SiO2@Pt nanozymes (Fe3O4@MSiO2@Pt NZs) with excellent magnetic separation properties, colorimetric, and peroxidase-like (POD-like) activities. Effective enrichment of target Flu A in complex samples as well as greater loading of Pt particles by mesoporous structures with large specific surface area to enhance POD-like activity can significantly improve the detection sensitivity of the LFIA. After colorimetric amplification by Fe3O4@MSiO2@Pt tags catalysis, the qualitative and quantitative results of detection for Flu A nucleoprotein (Flu A-NP) were 0.01 and 0.0089 ng mL−1, respectively. This indicated a sensitivity approximately 100 times greater than commercially available colloidal Au nanoparticle (AuNP)-based LFIA strips. For detection of inactivated H1N1 virus, quantification can be as low as 33 copies mL−1. Moreover, it demonstrated high accuracy in pharyngeal swab sample simulation experiments. Therefore, the proposed platform based on Fe3O4@MSiO2@Pt NZs-LFIA offered a promising approach for point-of-care testing (POCT), enabling rapid and ultrasensitive diagnosis of Flu A. [Display omitted] •Controlled-thickness mesoporous SiO2 layers provide high stability and larger surface area.•The synthesized Fe3O4@MSiO2@Pt NZs have superior magnetic, colorimetric, and POD-like activity.•Fe3O4@MSiO2@Pt NZs were used to construct LFIA with good sensitivity, specificity and accuracy.•The method's detection limit surpasses commercial colloidal AuNP-based LFIA strips by 100-times.
doi_str_mv 10.1016/j.aca.2024.343474
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There is an immediate need for a rapid and sensitive method to detect influenza A viruses early, without requiring extra equipment. Here, we established a lateral flow immunoassay (LFIA) for the detection of influenza A (Flu A) using a "three-in-one" multifunctional mesoporous Fe3O4@SiO2@Pt nanozymes (Fe3O4@MSiO2@Pt NZs) with excellent magnetic separation properties, colorimetric, and peroxidase-like (POD-like) activities. Effective enrichment of target Flu A in complex samples as well as greater loading of Pt particles by mesoporous structures with large specific surface area to enhance POD-like activity can significantly improve the detection sensitivity of the LFIA. After colorimetric amplification by Fe3O4@MSiO2@Pt tags catalysis, the qualitative and quantitative results of detection for Flu A nucleoprotein (Flu A-NP) were 0.01 and 0.0089 ng mL−1, respectively. This indicated a sensitivity approximately 100 times greater than commercially available colloidal Au nanoparticle (AuNP)-based LFIA strips. For detection of inactivated H1N1 virus, quantification can be as low as 33 copies mL−1. Moreover, it demonstrated high accuracy in pharyngeal swab sample simulation experiments. Therefore, the proposed platform based on Fe3O4@MSiO2@Pt NZs-LFIA offered a promising approach for point-of-care testing (POCT), enabling rapid and ultrasensitive diagnosis of Flu A. [Display omitted] •Controlled-thickness mesoporous SiO2 layers provide high stability and larger surface area.•The synthesized Fe3O4@MSiO2@Pt NZs have superior magnetic, colorimetric, and POD-like activity.•Fe3O4@MSiO2@Pt NZs were used to construct LFIA with good sensitivity, specificity and accuracy.•The method's detection limit surpasses commercial colloidal AuNP-based LFIA strips by 100-times.</description><identifier>ISSN: 0003-2670</identifier><identifier>ISSN: 1873-4324</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2024.343474</identifier><identifier>PMID: 39643324</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Colorimetric ; Colorimetry - methods ; Composite nanozymes ; Humans ; Immunoassay - methods ; Influenza A ; Influenza A virus - immunology ; Influenza A virus - isolation &amp; purification ; Influenza A Virus, H1N1 Subtype - immunology ; Influenza A Virus, H1N1 Subtype - isolation &amp; purification ; Influenza, Human - diagnosis ; Lateral flow immunoassay ; Limit of Detection ; Mesoporous material ; Platinum - chemistry ; Porosity ; Silicon Dioxide - chemistry</subject><ispartof>Analytica chimica acta, 2025-01, Vol.1335, p.343474, Article 343474</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. 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This indicated a sensitivity approximately 100 times greater than commercially available colloidal Au nanoparticle (AuNP)-based LFIA strips. For detection of inactivated H1N1 virus, quantification can be as low as 33 copies mL−1. Moreover, it demonstrated high accuracy in pharyngeal swab sample simulation experiments. Therefore, the proposed platform based on Fe3O4@MSiO2@Pt NZs-LFIA offered a promising approach for point-of-care testing (POCT), enabling rapid and ultrasensitive diagnosis of Flu A. 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There is an immediate need for a rapid and sensitive method to detect influenza A viruses early, without requiring extra equipment. Here, we established a lateral flow immunoassay (LFIA) for the detection of influenza A (Flu A) using a "three-in-one" multifunctional mesoporous Fe3O4@SiO2@Pt nanozymes (Fe3O4@MSiO2@Pt NZs) with excellent magnetic separation properties, colorimetric, and peroxidase-like (POD-like) activities. Effective enrichment of target Flu A in complex samples as well as greater loading of Pt particles by mesoporous structures with large specific surface area to enhance POD-like activity can significantly improve the detection sensitivity of the LFIA. After colorimetric amplification by Fe3O4@MSiO2@Pt tags catalysis, the qualitative and quantitative results of detection for Flu A nucleoprotein (Flu A-NP) were 0.01 and 0.0089 ng mL−1, respectively. This indicated a sensitivity approximately 100 times greater than commercially available colloidal Au nanoparticle (AuNP)-based LFIA strips. For detection of inactivated H1N1 virus, quantification can be as low as 33 copies mL−1. Moreover, it demonstrated high accuracy in pharyngeal swab sample simulation experiments. Therefore, the proposed platform based on Fe3O4@MSiO2@Pt NZs-LFIA offered a promising approach for point-of-care testing (POCT), enabling rapid and ultrasensitive diagnosis of Flu A. [Display omitted] •Controlled-thickness mesoporous SiO2 layers provide high stability and larger surface area.•The synthesized Fe3O4@MSiO2@Pt NZs have superior magnetic, colorimetric, and POD-like activity.•Fe3O4@MSiO2@Pt NZs were used to construct LFIA with good sensitivity, specificity and accuracy.•The method's detection limit surpasses commercial colloidal AuNP-based LFIA strips by 100-times.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39643324</pmid><doi>10.1016/j.aca.2024.343474</doi><orcidid>https://orcid.org/0000-0002-6313-4757</orcidid></addata></record>
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subjects Colorimetric
Colorimetry - methods
Composite nanozymes
Humans
Immunoassay - methods
Influenza A
Influenza A virus - immunology
Influenza A virus - isolation & purification
Influenza A Virus, H1N1 Subtype - immunology
Influenza A Virus, H1N1 Subtype - isolation & purification
Influenza, Human - diagnosis
Lateral flow immunoassay
Limit of Detection
Mesoporous material
Platinum - chemistry
Porosity
Silicon Dioxide - chemistry
title Nanozymes featuring a mesoporous silica shell for rapid enrichment and ultrasensitive lateral flow immunoassay of influenza A
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