Microfluidic Particle Detection Using Conductive Nanoparticle Labeling

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Solution Overview

Problem

Existing methods for detecting specific pathogens in a mixture of bacteria using electrical impedance spectroscopy (EIS) are limited in their ability to differentiate between labeled and non-labeled microparticles, especially at low conductivity levels, leading to difficulties in accurately identifying target microparticles.

Innovation Solution

A method involving a microfluidic particle analysis device with electrodes and a system for applying an alternating current, where target microparticles are labeled with electrically conducting nanoparticles and the conductivity of the sample fluid is adjusted to 5,000 μS/cm to 50,000 μS/cm, allowing for differentiation using the phase and/or amplitude of the electrical signal.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Difficulty of detecting and measuring

If target microparticles are detected using EIS in low conductivity saline solutions, then it becomes easier to distinguish bacteria from other particles, but the ability to differentiate between labeled and non-labeled particles deteriorates

Engineering Contradiction:
Improvedifficulty to distinguish bacteria from other particlesVSAvoidprecision to differentiate labeled and non-labeled particles
Core Design Contradiction:
Difficulty of detecting and measuringVSMeasurement precision

Solution Approach 1:

The patent changes the conductivity parameter of the saline solution from low conductivity to high conductivity (5,000-50,000 μS/cm). This parameter change enables the EIS system to detect phase and amplitude differences in electrical signals between labeled and non-labeled particles, resolving the contradiction between ease of distinction and measurement precision.

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If the conductivity of the sample fluid is increased to 5,000 μS/cm to 50,000 μS/cm, then the detection sensitivity and selectivity of EIS is improved, but the complexity of the system increases

Engineering Contradiction:
Improvedetection sensitivity and selectivityVSAvoidsystem complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent adjusts the conductivity parameter of the sample fluid to an optimal range (5,000-50,000 μS/cm) to enhance EIS detection capability. This parameter optimization improves detection sensitivity and selectivity without requiring complex system modifications, as the enhancement is achieved through sample preparation rather than system complexity.

Inventive Principle:
Principle #35Parameter changes

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

This approach enables the sensitive and specific detection of target microparticles by effectively distinguishing labeled from non-labeled particles, even in the presence of measuring artifacts, enhancing the selectivity and sensitivity of EIS in microfluidic systems.

Implementation Method 1

the target microparticle is detected by electrical impedance spectroscopy (EIS) in a microfluidic device

Methodology Applied
Scientific EffectElectrical Impedance Spectroscopy: Electrical Resistance

Implementation Method 2

labelling the complex of the recognition binding partner and the identification binding partner with electrically conducting nanoparticles

Methodology Applied
Scientific EffectElectrical Conduction: Conduction (electrical)

Data Source

PatentUS20240241028A1A method of detecting a target microparticle
Publication Date: 2024.07.18 SBT INSTR AS
  • US20240241028A1 patent drawing
  • US20240241028A1 patent drawing
  • US20240241028A1 patent drawing

AI summary

The present invention relates to a method of detecting a target microparticle in a fluid in a microfluidic particle analysis device comprising a measuring channel with a first electrode and a second electrode defining an operating space between and being in electrical connection with an electric current source and a device for monitoring an electrical signal from the first and/or the second electrode. A sample fluid suspected of containing a target microparticle exposing an identification binding partner is mixed with a recognition binding partner component to provide a complex of the recognition binding partner and the identification binding partner, and the complex is labelled with electrically conducting nanoparticles; before optionally adjusting the conductivity to be in the range of 5,000 μS/cm to 50,000 μS/cm and applying a flow of the suspension to the measuring channel of the microfluidic particle analysis device; before applying a current to create an electric field in the operating space and monitoring an electrical signal between the first and the second electrode to detect target microparticles labelled with the electrically conducting nanoparticles. The method is suited to detect a pathogenic bacterium in a water or another fluid.