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Improved sensitivity of lateral flow assay using paper-based sample concentration technique.

Ruihua Tang1, Hui Yang2, Jane Ru Choi3

  • 1School of Life Sciences, Northwestern Polytechnical University, Xi'an 710072, PR China; Key Laboratory for Space Bioscience and Biotechnology, Northwestern Polytechnical University, Xi'an 710072, PR China; The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an 710049, PR China; Bioinspired Engineering and Biomechanics Center (BEBC), Xi'an Jiaotong University, Xi'an 710049, PR China.

Talanta
|March 20, 2016
PubMed
Summary

We enhanced lateral flow assays (LFAs) sensitivity using a dialysis-based concentration method. This novel device improves detection for Human Immunodeficiency Virus (HIV) nucleic acids and myoglobin, enabling more accurate point-of-care diagnostics.

Keywords:
Dialysis-based concentrationHIVLateral flow assayMYOPaper-based device

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Area of Science:

  • Biomedical Engineering
  • Analytical Chemistry
  • Point-of-Care Diagnostics

Background:

  • Lateral flow assays (LFAs) are valuable for point-of-care testing, particularly in resource-limited areas.
  • The limited sensitivity of conventional LFAs restricts their diagnostic utility and widespread adoption.
  • Improving LFA sensitivity is crucial for accurate and reliable detection of various biomarkers.

Purpose of the Study:

  • To develop an integrated device combining dialysis-based concentration with LFAs.
  • To enhance the sensitivity and lower the detection limits of LFAs for specific analytes.
  • To assess the device's potential for medical diagnostics, food safety, and environmental monitoring.

Main Methods:

  • Integration of a dialysis-based concentration technique into the LFA platform.
  • Testing the enhanced LFA device for the detection of Human Immunodeficiency Virus (HIV) nucleic acids.
  • Evaluating the device's performance for myoglobin (MYO) detection using clinically relevant concentrations.

Main Results:

  • Achieved a 10-fold signal enhancement for HIV nucleic acid detection, with a detection limit of 0.1 nM.
  • Demonstrated a 4-fold signal enhancement for myoglobin detection, achieving a detection limit of 1.56 ng/mL.
  • The integrated LFA device provided results in under 25 minutes.

Conclusions:

  • The novel integrated device significantly enhances LFA sensitivity through a simple, low-cost concentration method.
  • This approach offers a portable and effective solution for highly sensitive detection of diverse target analytes.
  • The technology shows promise for advancing point-of-care diagnostics, food safety, and environmental monitoring applications.