Issue 39, 2024

Deep learning assisted quantitative detection of cardiac troponin I in hierarchical dendritic copper–nickel nanostructure lateral flow immunoassay

Abstract

The rising demand for point-of-care testing (POCT) in disease diagnosis has made LFIA sensors based on dendritic metal thin film (HD-nanometal) and background fluorescence technology essential for rapid and accurate disease marker detection, thanks to their integrated design, high sensitivity, and cost-effectiveness. However, their unique 3D nanostructures cause significant fluorescence variation, challenging traditional image processing methods in segmenting weak fluorescence regions. This paper develops a deep learning method to efficiently segment target regions in HD-nanometal LFIA sensor images, improving quantitative detection accuracy. We propose an improved UNet++ network with attention and residual modules, accurately segmenting varying fluorescence intensities, especially weak ones. We evaluated the method using IoU and Dice coefficients, comparing it with UNet, Deeplabv3, and UNet++. We used an HD-nanoCu-Ni LFIA sensor for cardiac troponin I (cTnI) as a case study to validate the method's practicality. The proposed method achieved a 96.3% IoU, outperforming other networks. The R2 between characteristic quantity and cTnI concentration reached 0.994, confirming the method's accuracy and reliability. This enhances POCT accuracy and provides a reference for future fluorescence immunochromatography expansion.

Graphical abstract: Deep learning assisted quantitative detection of cardiac troponin I in hierarchical dendritic copper–nickel nanostructure lateral flow immunoassay

Supplementary files

Article information

Article type
Paper
Submitted
24 Jun 2024
Accepted
28 Aug 2024
First published
03 Sep 2024

Anal. Methods, 2024,16, 6715-6725

Deep learning assisted quantitative detection of cardiac troponin I in hierarchical dendritic copper–nickel nanostructure lateral flow immunoassay

S. Zhang, L. Chen, Y. Tan, S. Wu, P. Guo, X. Jiang and H. Pan, Anal. Methods, 2024, 16, 6715 DOI: 10.1039/D4AY01187B

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