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Fabrication of Three-dimensional Paper-based Microfluidic Devices for Immunoassays
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Chemometric challenges in development of paper-based analytical devices: Optimization and image processing.

Vahid Hamedpour1, Paolo Oliveri2, Riccardo Leardi2

  • 1Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, 153-8505, Japan; Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, 223-8522, Japan.

Analytica Chimica Acta
|February 8, 2020
PubMed
Summary
This summary is machine-generated.

This study shows how design of experiments (DoE) and digital image processing can improve microfluidic paper-based analytical devices (μPADs). These methods aid in optimizing μPADs, potentially accelerating their commercialization.

Keywords:
D-optimal designDesign of experimentsImage processing algorithmMathematical morphology recognition (MMR)Microfluidic paper-based analytical devices (μPADs)Optimization

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Area of Science:

  • Analytical Chemistry
  • Biomedical Engineering
  • Materials Science

Background:

  • Microfluidic paper-based analytical devices (μPADs) show promise but face commercialization challenges.
  • Limited application of machine learning and chemometrics hinders μPAD design and optimization.
  • Addressing these limitations is crucial for advancing μPAD technology.

Purpose of the Study:

  • To demonstrate the utility of chemometric techniques in μPAD development.
  • To optimize experimental conditions for a colorimetric assay on μPADs.
  • To showcase the benefits of digital image processing for μPAD analysis.

Main Methods:

  • Design of Experiments (DoE), specifically D-optimal design, was employed for optimizing experimental factors.
  • A colorimetric assay for isoniazid, utilizing methyl orange, served as a model system.
  • Automated digital image processing based on morphological recognition was developed for RGB value analysis.

Main Results:

  • DoE successfully optimized experimental conditions for the μPAD assay.
  • Digital image processing significantly accelerated color value analysis and reduced manual selection errors.
  • The developed algorithm provided repeatable RGB value analysis.

Conclusions:

  • Chemometric techniques like DoE are vital for efficient μPAD optimization.
  • Digital image processing enhances the accuracy and speed of μPAD data analysis.
  • Integrating these methods can overcome key weaknesses in μPAD development, facilitating market entry.