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Related Experiment Video

Updated: Jun 3, 2026

Fluorescence detection methods for microfluidic droplet platforms
14:16

Fluorescence detection methods for microfluidic droplet platforms

Published on: December 10, 2011

Highly sensitive fluorescence detection system for microfluidic lab-on-a-chip.

Gihan Ryu1, Jingsong Huang, Oliver Hofmann

  • 1Molecular Vision Ltd. BioIncubator Unit, Bessemer Building, Imperial College London, London, SW7 2BP, UK.

Lab on a Chip
|March 25, 2011
PubMed
Summary
This summary is machine-generated.

We developed a low-cost fluorescence detection system for lab-on-a-chip devices. This practical system achieved a low limit of detection for cardiac markers in human plasma, showing potential for point-of-care diagnostics.

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Last Updated: Jun 3, 2026

Fluorescence detection methods for microfluidic droplet platforms
14:16

Fluorescence detection methods for microfluidic droplet platforms

Published on: December 10, 2011

Multicolor Fluorescence Detection for Droplet Microfluidics Using Optical Fibers
10:21

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08:27

Highly Sensitive and Rapid Fluorescence Detection with a Portable FRET Analyzer

Published on: October 1, 2016

Area of Science:

  • Biomedical Engineering
  • Analytical Chemistry
  • Optical Sensing

Background:

  • Lab-on-a-chip (LOC) devices require sensitive and cost-effective detection systems.
  • Existing fluorescence detection methods can be complex and expensive for widespread application.
  • Accurate and rapid detection of cardiac markers is crucial for diagnosing myocardial infarction.

Purpose of the Study:

  • To demonstrate a compact, low-cost, and practical fluorescence detection system for LOC applications.
  • To validate the system's performance using fluorescence immunoassays for cardiac markers.
  • To establish the limit of detection (LOD) for both optical measurements and human plasma samples.

Main Methods:

  • Utilized a commercially available 501 nm InGaN light-emitting diode (LED) as the light source.
  • Integrated organic or silicon photodiode detectors, dye-coated color filters, and polarizers.
  • Employed an injection-molded polystyrene microfluidic chip for fluorescence immunoassays of myoglobin and CK-MB.

Main Results:

  • Achieved an optical LOD of 5.6 × 10^4 beads/µl (∼3 nM fluorescein equivalent concentration).
  • Determined a LOD of 1.5 ng/ml for both myoglobin and CK-MB in human plasma immunoassays.
  • Demonstrated a practical and cost-effective fluorescence detection system suitable for LOC.

Conclusions:

  • The developed fluorescence detection system is compact, affordable, and practical for LOC diagnostics.
  • The system exhibits high sensitivity, capable of detecting cardiac markers at clinically relevant concentrations.
  • This technology holds promise for point-of-care testing and rapid disease diagnosis.