Dual-Mode Analyte Detection Device for Simultaneous Semi-Quantification

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Solution Overview

Problem

Existing devices and methods for detecting analytes in samples are limited in their ability to simultaneously and semi-quantitatively detect multiple analytes using a single device.

Innovation Solution

A device comprising a first test portion with a test membrane for chemical assays and a second test portion with a conjugate pad and immunoreaction membrane for immunoassays, allowing for the detection of two analytes of interest in a single sample through vertical and lateral flow assays.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If a single device is used to detect multiple analytes, then detection efficiency is improved, but device complexity increases

Engineering Contradiction:
Improvedetection efficiencyVSAvoiddevice complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent combines a chemical assay test portion and an immunoassay test portion into a single device, allowing simultaneous detection of multiple analytes (e.g., glucose and hCG) in one sample application, thereby improving detection efficiency while integrating multiple functions into one unified device structure

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The device is designed with multi-functional test portions that can detect different types of analytes using different assay methods (chemical and immunoassay) within a single device, enabling universal detection capabilities across multiple analyte types without requiring separate devices

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

2Measurement precision

If semi-quantitative detection is implemented, then measurement capability is improved, but device complexity increases

Engineering Contradiction:
Improvemeasurement capabilityVSAvoiddevice complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent employs color intensity changes in test signals that are directly proportional to analyte concentrations, with color indicators provided for comparison to enable semi-quantitative measurement. This allows measurement capability improvement through visual colorimetric analysis without requiring complex electronic sensors or instrumentation

Inventive Principle:
Principle #32Color changes

Solution Approach 2:

The device enables self-service semi-quantitative measurement through built-in color indicators and test signals that automatically provide concentration information through color intensity comparison, eliminating the need for external measurement equipment or complex data processing systems

Inventive Principle:
Principle #25Self-service

3Adaptability or versatility

If multiple test portions are integrated in one device, then detection versatility is improved, but manufacturing complexity increases

Engineering Contradiction:
Improvedetection versatilityVSAvoidmanufacturing complexity
Core Design Contradiction:
Adaptability or versatilityVSEase of manufacture

Solution Approach 1:

The device is divided into separate functional test portions (chemical assay portion and immunoassay portion) that can be independently designed and manufactured, then assembled into a complete device. This segmentation allows each portion to be optimized for its specific assay type while simplifying the overall manufacturing process through modular assembly

Inventive Principle:
Principle #1Segmentation

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

Enables simultaneous detection and semi-quantification of multiple analytes in a single sample, improving efficiency and accuracy in analyte detection.

Implementation Method 1

causing the sample to flow vertically onto a test membrane

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Implementation Method 2

causing the sample to flow laterally from the test membrane onto a conjugate pad

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Implementation Method 3

The second analyte of interest, if present in the sample, may be caused to bind to the detection particles at the conjugate pad, thereby forming a complex

Methodology Applied
Scientific EffectImmunological binding: Adsorption

Implementation Method 4

The complex if formed may be caused to bind to the one or more test antibodies to produce a test signal at the test zone

Methodology Applied
Scientific EffectImmunological binding: Adsorption

Implementation Method 5

The sample may be caused to chemically react with a reaction mixture blotted on the test membrane to produce a test signal at a chemical test signal zone

Methodology Applied
Scientific EffectChemical reaction: Chemical Bonding

Data Source

PatentUS20250130228A1Devices and methods for detecting analytes
Publication Date: 2025.04.24 UNIQ BIOTECH LTD
  • US20250130228A1 patent drawing
  • US20250130228A1 patent drawing
  • US20250130228A1 patent drawing

AI summary

A device and method for detecting a plurality of analytes of interest in a sample are disclosed. The device has a first portion for detection of a first analyte of interest, and a second test portion for detection of a second analyte of interest. The first test portion has a test membrane with a chemical reaction side having a reaction mixture blotted thereon. The second test portion has a conjugate pad having detector particles bound thereon and an immunoreaction membrane having a test zone comprising a test antibody bound thereon, and a control zone comprising a control antibody bound thereon. The first test portion is in fluid-flow contact with the second test portion, arranged for transporting the sample away from the first test portion towards the second test portion.