4.7 Article

Machine Learning Approach to Enhance the Performance of MNP-Labeled Lateral Flow Immunoassay

Journal

NANO-MICRO LETTERS
Volume 11, Issue 1, Pages -

Publisher

SHANGHAI JIAO TONG UNIV PRESS
DOI: 10.1007/s40820-019-0239-3

Keywords

Point-of-care testing; Immunochromatography test strips; Magnetic nanoparticles; Machine learning; Support vector machine

Funding

  1. National Key Research and Development Program of China [2017YFA0205303, 2017FYA0205301, 2017FYA0205303]
  2. National Natural Science Foundation of China [81571835, 81672247]
  3. National Key Basic Research Program (973 Project) [2015CB931802]
  4. 13th Five-Year Plan Science and Technology Project of Jilin Province Education Department [JJKH20170410K]
  5. Shanghai Science and Technology Fund [15DZ2252000]

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HighlightsAn ultrasensitive multiplex biosensor was designed to quantify magnetic nanoparticles on immunochromatography test strips.A machine learning model was constructed and used to classify both weakly positive and negative samples, significantly enhancing specificity and sensitivity.A waveform reconstruction method was developed to appropriately restore the distorted waveform for weak magnetic signals. AbstractThe use of magnetic nanoparticle (MNP)-labeled immunochromatography test strips (ICTSs) is very important for point-of-care testing (POCT). However, common diagnostic methods cannot accurately analyze the weak magnetic signal from ICTSs, limiting the applications of POCT. In this study, an ultrasensitive multiplex biosensor was designed to overcome the limitations of capturing and normalization of the weak magnetic signal from MNPs on ICTSs. A machine learning model for sandwich assays was constructed and used to classify weakly positive and negative samples, which significantly enhanced the specificity and sensitivity. The potential clinical application was evaluated by detecting 50 human chorionic gonadotropin (HCG) samples and 59 myocardial infarction serum samples. The quantitative range for HCG was 1-1000mIUmL(-1) and the ideal detection limit was 0.014mIUmL(-1), which was well below the clinical threshold. Quantitative detection results of multiplex cardiac markers showed good linear correlations with standard values. The proposed multiplex assay can be readily adapted for identifying other biomolecules and also be used in other applications such as environmental monitoring, food analysis, and national security.

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