Immunoassay Binding Strength Detection via Displacement Kinetics

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Solution Overview

Problem

Existing methods for detecting analytes and determining their binding strength are often hindered by complex matrices like serum, leading to non-reproducible results and increased costs due to the need for additional avidity determination tests.

Innovation Solution

A procedure that involves immobilizing target molecules and reference analytes on a fixed surface, using detection fluorescence markers to measure binding, and then dissociating the analytes to determine their avidity, allowing for simultaneous detection and characterization of analytes.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Loss of time

If existing methods are used for detecting analytes and determining binding strength separately, then detection accuracy is maintained, but analysis time increases and material consumption increases

Engineering Contradiction:
Improveanalysis timeVSAvoiddetection accuracy
Core Design Contradiction:
Loss of timeVSMeasurement precision

Solution Approach 1:

The patent combines analyte detection and avidity determination into a single integrated assay. The method uses a displacement step where a second analyte competes with the first analyte for binding to the target molecule, allowing both detection and binding strength characterization to occur simultaneously in one experiment rather than requiring separate tests.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The assay system is designed to perform multiple functions: it detects the presence of analytes, quantifies their concentration, and determines their binding strength (avidity) all within the same experimental setup. The displacement-based methodology enables the system to extract multiple parameters from a single assay, making it a multi-functional analytical tool.

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

2Device complexity

If separate tests are performed for detection and avidity determination, then measurement reliability is maintained, but device complexity and cost increase

Engineering Contradiction:
Improveassay complexityVSAvoidresult reproducibility
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

The patent integrates two separate analytical processes (detection and avidity determination) into a unified displacement assay. By performing both measurements in the same system with the same reagents and under the same conditions, the method reduces device complexity and eliminates the need for multiple separate instruments or assay setups.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The assay performs detection first, and only for samples that test positive does it proceed to the displacement step for avidity determination. This preliminary action approach ensures that the more complex displacement measurements are only performed when necessary, maintaining reliability while reducing overall complexity for negative samples.

Inventive Principle:
Principle #10Preliminary action

3Loss of substance

If complex matrices like serum are used in separate detection and avidity tests, then comprehensive analysis is achieved, but result reproducibility decreases

Engineering Contradiction:
Improvematerial consumptionVSAvoidresult reproducibility
Core Design Contradiction:
Loss of substanceVSReliability

Solution Approach 1:

The patent uses the same sample material (e.g., serum) for both detection and avidity determination within a single assay. This approach conserves material by not requiring separate samples for each test and ensures reproducibility by maintaining consistent sample conditions throughout the entire experimental process, eliminating variability introduced by sample handling between separate tests.

Inventive Principle:
Principle #5Merging (Combining)

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 reduces analysis time, saves material, and enables the recording of dissociation kinetics, while also allowing for the use of existing automated systems for nucleic acid and immunoassay processing.

Implementation Method 1

using detection fluorescence markers to measure binding

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentEP4553500A1Method for detecting and determining the binding strength of at least one analyte in a sample
Publication Date: 2025.05.14 ATTOMOL MOLEULARE DIAGNOSTIKA
  • EP4553500A1 patent drawingFigure 1~2
  • EP4553500A1 patent drawingFigure 3~4B
  • EP4553500A1 patent drawing

AI summary

The present invention relates to a method for detecting and determining the binding strength of at least one analyte in a sample, based on the principle of an immunoassay. The method enables the detection and subsequent characterization of the binding properties of analytes in a single test. Furthermore, a kit for carrying out the method according to the invention is provided.