Related Experiment Video
Updated: Aug 5, 2025

Author Spotlight: High-Quality Quantum Dot Nanobeads for Sensitive Fluorescent Lateral Flow Immunoassays
Published on: June 28, 2024
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.
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.
Abstract:
Currently, the global trend of several hundred thousand new confirmed COVID-19 patients per day has not abated significantly. Serological antibody detection has become an important tool for the self-screening of people. While the most commonly used colorimetric lateral flow immunoassay (LFIA) methods for the detection of COVID-19 antibodies are limited by low sensitivity and a lack of quantification ability. This leads to poor accuracy in the screening of early COVID-19 patients. Therefore, it is necessary to develop an accurate and sensitive autonomous antibody detection technique that will effectively reduce the COVID-19 infection rate. Here, we developed a three-line LFIA immunoassay based on polydopamine (PDA) nanoparticles for COVID-19 IgG and IgM antibodies detection to determine the degree of infection. The PDA-based three-line LFIA has a detection limit of 1.51 and 2.34 ng/mL for IgM and IgG, respectively. This assay reveals a good linearity for both IgM and IgG antibodies detection and is also able to achieve quantitative detection by measuring the optical density of test lines. In comparison, the commercial AuNP-based LFIA showed worse quantification results than the developed PDA-based LFIA for low-concentration COVID-19 antibody samples, making it difficult to distinguish between negative and positive samples. Therefore, the developed PDA-based three-line LFIA platform has the accurate quantitative capability and high sensitivity, which could be a powerful tool for the large-scale self-screening of people.
More Related Videos
10:10Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
Published on: November 13, 2021
06:00Author Spotlight: Development of a Smartphone-Enhanced Paper-Based Device for Rapid Dengue NS1 Detection
Published on: January 26, 2024