Microfluidic Fluorescence Detector for Real-Time Nucleotide Detection

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Solution Overview

Problem

Diagnostic analyses in medical diagnostics are bottlenecked by the need for expensive, specialized equipment that is not available on-demand and incurs shipping and processing delays, limiting accessibility and throughput.

Innovation Solution

A microfluidic system with integrated fluorescence detectors, using LEDs and photodiodes connected to pre-amplifier circuits with low time-constants, for real-time PCR and nucleotide detection in microfluidic channels, enabling high-throughput and easy-to-use diagnostics.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If specialized diagnostic equipment is used, then measurement precision is improved, but device complexity and cost increase

Engineering Contradiction:
Improvedetection sensitivityVSAvoidequipment complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent combines multiple diagnostic functions (PCR amplification, fluorescence detection, and signal processing) into a single integrated microfluidic device. The microfluidic channel integrates the reaction chamber, heating elements for thermal cycling, and optical detection components, eliminating the need for separate specialized equipment while maintaining detection sensitivity.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The patent uses fluorescence probes that emit light signals as optical copies of the presence and quantity of target nucleotides. This optical signaling approach allows detection without requiring complex mass spectrometry or other highly specialized equipment, achieving comparable measurement precision through a simpler optical detection system.

Inventive Principle:
Principle #26Copying

2Productivity

If batch processing is used, then device complexity is reduced, but productivity decreases

Engineering Contradiction:
ImprovethroughputVSAvoidprocessing time
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The microfluidic device is segmented into multiple independent microfluidic channels, each capable of performing PCR and detection simultaneously. This parallel architecture allows multiple samples to be processed at the same time within a single device, dramatically increasing throughput without requiring batch processing of multiple separate devices.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The device enables continuous real-time monitoring of fluorescence signals throughout the PCR amplification process. The photodiode continuously detects emitted light, and the pre-amplifier circuit continuously processes signals, allowing uninterrupted detection and immediate results without waiting for batch completion.

Inventive Principle:
Principle #20Continuity of useful action

3Loss of time

If real-time detection is implemented, then loss of time is reduced, but device complexity increases

Engineering Contradiction:
Improvedetection timeVSAvoiddetection system complexity
Core Design Contradiction:
Loss of timeVSDevice complexity

Solution Approach 1:

The patent employs simple, inexpensive photodiodes and LED light sources for fluorescence detection instead of complex and expensive specialized detectors. These basic optical components enable real-time detection functionality while keeping the overall device complexity low and the system easy to operate.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Solution Approach 2:

The patent introduces a pre-amplifier circuit as an intermediary component between the photodiode and the detection system. This pre-amplifier boosts the weak fluorescence signals in real-time before further processing, enabling sensitive detection without requiring complex signal processing equipment, thus reducing overall device complexity while achieving rapid detection.

Inventive Principle:
Principle #24Intermediary (Mediator)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The system allows for rapid, automated detection of nucleotides in biological samples with high sensitivity and throughput, reducing the need for specialized equipment and minimizing delays.

Implementation Method 1

a LED emitting light of a specified color that excites a probe

Methodology Applied
Scientific EffectLight Emitting Diode: Light Emitting Diode

Implementation Method 2

a photodiode configured to collect emitted light of the specified color

Methodology Applied
Scientific EffectPhotovoltaic Effect: Photovoltaic Effect

Implementation Method 3

excites a probe associated with one or more polynucleotides... photodiode configured to collect emitted light

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentUS12458972B2Fluorescence detector for microfluidic diagnostic system
Publication Date: 2025.11.04 HANDYLAB INC
  • US12458972B2 patent drawing
  • US12458972B2 patent drawing
  • US12458972B2 patent drawing

AI summary

The present technology provides for a fluorescent detector that is configured to detect light emitted for a probe characteristic of a polynucleotide. The polynucleotide is undergoing amplification in a microfluidic channel with which the detector is in optical communication. The detector is configured to detect minute quantities of polynucleotide, such as would be contained in a microfluidic volume. The detector can also be multiplexed to permit multiple concurrent measurements on multiple polynucleotides concurrently.