Paper-based Vertical Flow Immunoassay (VFI) for detection of bio-threat pathogens.


Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
01 Jan 2019
Historique:
received: 21 06 2018
revised: 13 08 2018
accepted: 14 08 2018
entrez: 29 9 2018
pubmed: 29 9 2018
medline: 6 11 2018
Statut: ppublish

Résumé

Currently, the standard method for identifying biological agents of potential threats to national security and public health, such as pathogens, virus, and toxins, mainly rely on microbiological cultivation. This method is time-consuming and it requires sophisticated equipment and well-trained personnel, which are often unavailable in remote areas or at point-of-need. Therefore, an alternative rapid, simple, and sensitive method for detecting bio-threat agents is in crucial need. We report a paper-based Vertical Flow Immunoassay (VFI) device that can overcome these limitations. The VFI device utilizes a nanoporous nitrocellulose membrane encapsulated in a stainless steel filter holder. As the sample is pushed through the membrane, which is pre-functionalized with capture antibody, a sandwich assay is formed and colorimetric signal is generated to reflect the presence of target antigens. Through theoretical analyses of antigen-antibody binding process inside a porous membrane, we identified two critical factors - membrane pore size and sample flow rate that can be optimized to improve the assay sensitivity. Then, the effects were demonstrated through experimental studies using Burkholderia pseudomallei (the causative agent of melioidosis) as a model pathogen. The B. pseudomallei VFI was based on an immunoassay targeting the B. pseudomallei surface capsular polysaccharide (CPS). The experimental results agreed well with the theory showing that increasing the flow speed (up to 1.06 mm/s) and reducing the membrane pore size (down to 0.1 µm) could improve the sensitivity by at least 5 times. The VFI's limit-of-detection for CPS spiked in buffer solution was determined to be 0.02 ng/mL. The developed VFI shows great potential as a point-of-care tool for detection of bio-threat agents in a variety of clinical and resource-restricted conditions.

Identifiants

pubmed: 30262102
pii: S0039-9140(18)30854-3
doi: 10.1016/j.talanta.2018.08.043
pii:
doi:

Substances chimiques

Biological Warfare Agents 0
Membranes, Artificial 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

81-88

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Peng Chen (P)

Center for Applied NanoBioscience & Medicine, College of Medicine - Phoenix, University of Arizona, Phoenix, AZ, USA. Electronic address: pengchen@email.arizona.edu.

Marcellene Gates-Hollingsworth (M)

Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, NV, USA.

Sujata Pandit (S)

Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, NV, USA.

Anson Park (A)

School of Computing, Informatics and Decision Systems Engineering, Arizona State University, Tempe, AZ, USA.

Douglas Montgomery (D)

School of Computing, Informatics and Decision Systems Engineering, Arizona State University, Tempe, AZ, USA.

David AuCoin (D)

Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, NV, USA.

Jian Gu (J)

Center for Applied NanoBioscience & Medicine, College of Medicine - Phoenix, University of Arizona, Phoenix, AZ, USA. Electronic address: jgu10@email.arizona.edu.

Frederic Zenhausern (F)

Center for Applied NanoBioscience & Medicine, College of Medicine - Phoenix, University of Arizona, Phoenix, AZ, USA. Electronic address: fzenhaus@email.arizona.edu.

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Classifications MeSH