Bacterial identification in SERS-integrated microfluidics using CNN-driven 2D classification of 1D spectra.

Infectious Disease Pediatrics Radiology
Journal: Talanta
Published Date:

Abstract

Bacterial sensing involves complex and variable samples that require advanced handling and analytical methods. To address these challenges, machine learning-especially deep learning-and SERS-based microfluidics have shown great promise. While previous studies have majorly focused on 1D spectral classification, the use of 2D representations of SERS spectra has not yet been explored, particularly for on-chip bacterial identification. In this work, we introduce a novel framework that combines SERS-enabled microfluidics with optimized 2D convolutional neural networks (2D-CNNs) for bacterial classification. SERS integration inside microfluidic chips was achieved through direct laser writing, enabling custom active areas and efficient on-chip measurements. We systematically evaluated nine distinct 1D-to-2D spectral transformations, with spectrogram and continuous wavelet transform yielding test accuracies of 99 % and 97 %, respectively, on controlled datasets. Using transfer learning, we achieved 100 % accuracy on the on-chip dataset, demonstrating the model's adaptability to new data. In contrast, other transformations, like pairwise distance and autocorrelation, performed below 93 %, indicating their limited ability to capture subtle spectral features. This framework offers high sample control, parallelization, and the potential for expanding the bacteria database, making it ideal for low-data-volume situations such as rare infections. Further development and testing across strains, environments, and practical challenges can further improve our approach's reliability for real-world diagnostics.

Authors

  • Mehdi Feizpour
    Vrije Universiteit Brussel, Department of Applied Physics and Photonics, Brussels Photonics, Pleinlaan 2, 1050, Brussel, Belgium. Electronic address: [email protected].
  • Halewijn Van den Bosche
    Vrije Universiteit Brussel, Department of Applied Physics and Photonics, Brussels Photonics, Pleinlaan 2, 1050, Brussel, Belgium.
  • Lilit Melikyan
    Yerevan State University, Institute of Physics, PhotonicsAI Lab, 1 Alex Manoogian, 0025, Yerevan, Armenia.
  • Thomas Demuyser
    Department of Microbiology, Antwerp University Hospital (UZA), Edegem, 2610, Antwerp, Belgium; AIMS Lab, Center for Neurosciences, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel (VUB), 1090, Brussel, Belgium; Laboratory of Applied Microbiology and Biotechnology, Department of Bioscience Engineering, University of Antwerp, 2000, Antwerp, Belgium.
  • Piet Cools
    Faculty of Medicine and Health Sciences, Department of Diagnostic Sciences, Laboratory Bacteriology Research (LBR), Ghent University, 9000, Ghent, Belgium.
  • Hugo Thienpont
    Vrije Universiteit Brussel, Department of Applied Physics and Photonics, Brussels Photonics, Pleinlaan 2, 1050, Brussel, Belgium; Flanders Make@VUB - BP&M, Pleinlaan 2, 1050, Brussel, Belgium.
  • Tatevik Sarukhanyan
    Yerevan State University, Institute of Physics, PhotonicsAI Lab, 1 Alex Manoogian, 0025, Yerevan, Armenia.
  • Heidi Ottevaere
    Vrije Universiteit Brussel, Department of Applied Physics and Photonics, Brussels Photonics, Pleinlaan 2, 1050, Brussel, Belgium; Flanders Make@VUB - BP&M, Pleinlaan 2, 1050, Brussel, Belgium.