Polydopamine Nanoparticles-Based Three-Line Lateral Flow Immunoassay for COVID-19 Detection

Zhe Liu1,2,3, Chaoyu Cao2,3, Haoyang Tong3,4

  • 1Department of Rehabilitation Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.

Biosensors
|March 29, 2023
PubMed

Insights

A new polydopamine nanoparticle-based assay offers sensitive and quantitative detection of COVID-19 antibodies. This advanced lateral flow immunoassay improves accuracy for self-screening, aiding in early infection detection and control.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Immunodiagnostics

Background:

  • COVID-19 remains a significant global health concern, necessitating reliable self-screening tools.
  • Current serological antibody detection methods, like colorimetric lateral flow immunoassays (LFIA), often lack sensitivity and quantification capabilities, impacting early diagnosis accuracy.
  • There is a critical need for sensitive and accurate autonomous antibody detection techniques to mitigate COVID-19 spread.

Purpose of the Study:

  • To develop a novel three-line LFIA utilizing polydopamine (PDA) nanoparticles for the sensitive and quantitative detection of COVID-19 IgG and IgM antibodies.
  • To assess the performance of the PDA-based LFIA in terms of detection limits, linearity, and quantitative accuracy compared to traditional gold nanoparticle (AuNP)-based LFIAs.
  • To establish an effective tool for large-scale self-screening and determining the degree of COVID-19 infection.

Main Methods:

  • Development of a three-line lateral flow immunoassay (LFIA) incorporating polydopamine (PDA) nanoparticles.
  • Utilized the PDA-based LFIA for the detection and quantification of COVID-19 specific IgM and IgG antibodies.
  • Compared the quantitative performance of the PDA-based LFIA with a commercial gold nanoparticle (AuNP)-based LFIA using low-concentration antibody samples.

Main Results:

  • The PDA-based three-line LFIA demonstrated low detection limits: 1.51 ng/mL for IgM and 2.34 ng/mL for IgG.
  • The assay exhibited good linearity for both IgM and IgG detection, enabling quantitative measurements via optical density.
  • The developed PDA-based LFIA provided superior quantification compared to AuNP-based LFIA, especially for low-concentration samples, improving differentiation between negative and positive results.

Conclusions:

  • The developed polydopamine nanoparticle-based LFIA platform offers high sensitivity and accurate quantitative detection capabilities for COVID-19 antibodies.
  • This advanced assay can overcome the limitations of traditional methods, providing a powerful tool for large-scale, accurate self-screening.
  • The enhanced diagnostic performance holds potential for effective reduction of COVID-19 infection rates through improved early detection.

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