Plasmonic Microfluidic Chip for Rapid Colorimetric Pathogen Sensing

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Solution Overview

Problem

Existing colorimetric assays for pathogen detection are time-consuming and require expensive equipment, hindering rapid and sensitive testing in low-resource settings.

Innovation Solution

A microfluidic chip with a plasmonic nanosurface and nanostructures smaller than the diffraction limit is used to sense analytes through colorimetric changes, integrated with a filter barrier and sensing chamber, allowing for rapid and sensitive detection of pathogens and antibiotic resistance without the need for expensive instrumentation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional colorimetric assays are used for pathogen detection, then sensitivity can be achieved, but assay time becomes excessively long (24-48 hours)

Engineering Contradiction:
Improvedetection sensitivityVSAvoidassay time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The assay process is segmented into distinct functional zones within the microfluidic chip: an incubation chamber for sample preparation and a sensing chamber for detection. This spatial segmentation allows parallel processing of different assay stages, reducing total assay time while maintaining sensitivity through optimized conditions in each zone.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent replaces conventional mechanical mixing and manual observation methods with a plasmonic sensing system that optically detects colorimetric changes. The plasmonic nanosurface enhances optical sensitivity, enabling rapid detection without extensive mechanical processing time, thus reducing assay time while preserving detection precision.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

2Measurement precision

If conventional clinical approaches are used for pathogen detection, then comprehensive characterization can be achieved, but equipment requirements become expensive and complex

Engineering Contradiction:
Improvedetection accuracyVSAvoidequipment requirements
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent extracts the essential detection function from complex conventional equipment and concentrates it into a simplified microfluidic chip with integrated plasmonic sensing. By removing unnecessary components and retaining only the critical sensing capability, the system achieves comparable detection accuracy with significantly reduced equipment complexity and cost.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The microfluidic chip is designed as a universal platform that can detect multiple analytes including pathogens, antibiotic resistance markers, and other clinical markers through the same plasmonic sensing mechanism. This multi-functionality eliminates the need for separate specialized equipment for different detection tasks, reducing overall equipment requirements while maintaining comprehensive detection capability.

Inventive Principle:
Principle #6Universality (Multi-functionality)

3Productivity

If rapid colorimetric detection is implemented, then assay time is reduced, but measurement sensitivity may be compromised

Engineering Contradiction:
Improveassay throughputVSAvoiddetection sensitivity
Core Design Contradiction:
ProductivityVSMeasurement precision

Solution Approach 1:

The patent employs plasmonic nanosurfaces that change their optical properties (resonance frequency, extinction coefficient) in response to analyte presence. By tuning the plasmonic parameters (nanoparticle size, shape, material composition) to match the detection wavelength, the system achieves enhanced sensitivity even with rapid, single-shot readings, thus maintaining measurement precision while improving productivity.

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

The microfluidic chip enables rapid, sensitive, and cost-effective detection of antibiotic-resistant bacteria and other analytes, reducing assay time and reagent use while maintaining high sensitivity and specificity.

Implementation Method 1

a sensing chamber fluidly connected to the incubation chamber, downstream of the filter barrier, the sensing chamber having a plasmonic nanosurface, the plasmonic nanosurface including nanostructures protruding from the plasmonic nanosurface, the nanostructures having a size that is smaller than that of the diffraction limit of light

Methodology Applied
Scientific EffectPlasmon resonance:

Implementation Method 2

Microfluidic plasmonic color reading chips and methods

Methodology Applied
Scientific EffectColorimetry:

Data Source

PatentUS12590340B2Microfluidic plasmonic color reading chips and methods
Publication Date: 2026.03.31 MCGILL UNIV
  • US12590340B2 patent drawing
  • US12590340B2 patent drawing
  • US12590340B2 patent drawing

AI summary

There is provided a microfluidic chip for sensing an analyte in a sample by colorimetry. The microfluidic chip comprises: an inlet adapted to receive the sample; an incubation chamber having an incubation chamber inlet fluidly connected to the inlet downstream thereof, to incubate the analyte in the sample; a filter barrier fluidly connected to the incubation chamber, downstream of the incubation chamber inlet; a sensing chamber fluidly connected to the incubation chamber, downstream of the filter barrier, the sensing chamber having a plasmonic nanosurface, the plasmonic nanosurface including nanostructures protruding from the plasmonic nanosurface, the nanostructures having a size that is smaller than that of the diffraction limit of light, the nanostructures having a metallic layer that is plasmon-supported on top of a back reflector layer; and an outlet fluidly connected to the sensing chamber downstream thereof.