Magnetic ECL Biomolecular Analysis for Higher Detection Sensitivity

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Solution Overview

Problem

Existing biomolecular analysis methods based on electrochemiluminescence (ECL) require enhanced detection sensitivity for clinical applications, particularly in the quantification of blood markers for early diagnosis of cancer or heart disease.

Innovation Solution

A biomolecular analysis method involving the use of magnetic microparticles labeled with a luminescent agent and a reaction aid, captured by a magnetic field, and luminescence measurement through a luminescent process utilizing both first and second neutral radicals to enhance ECL luminous efficiency.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If a conventional ECL method using a single reaction aid pathway is used, then the detection sensitivity is limited, but the luminous efficiency cannot be enhanced sufficiently

Engineering Contradiction:
Improvedetection sensitivityVSAvoidluminous efficiency
Core Design Contradiction:
Measurement precisionVSUse of energy by moving object

Solution Approach 1:

The patent segments the radical production pathway into two distinct routes: (1) oxidation of the reaction aid to form a cation radical, followed by decarboxylation to produce a first neutral radical; and (2) direct oxidation to produce a second neutral radical. This segmentation allows both types of radicals to contribute to ECL emission, thereby enhancing luminous efficiency and detection sensitivity simultaneously.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent changes the oxidation potential parameter by selecting a reaction aid with a specific oxidation potential range (0.8 V to 1.5 V vs. Ag/AgCl). This parameter optimization enables efficient generation of both cation radicals and neutral radicals, improving the overall luminous efficiency without compromising detection sensitivity.

Inventive Principle:
Principle #35Parameter changes

2Quantity of substance

If the oxidation potential of the reaction aid is increased to generate more radical species, then more radicals are produced, but the potential window for ECL measurement is reduced

Engineering Contradiction:
Improveradical species concentrationVSAvoidpotential window
Core Design Contradiction:
Quantity of substanceVSTemperature

Solution Approach 1:

The patent optimizes the oxidation potential parameter of the reaction aid to fall within 0.8 V to 1.5 V vs. Ag/AgCl. This parameter selection achieves an optimal balance: it generates sufficient radical species concentration for high detection sensitivity while maintaining an adequate potential window for ECL measurement and analysis.

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 method significantly enhances detection sensitivity by increasing the luminous efficiency of ECL, allowing for high-speed and high-sensitivity biomolecular analysis.

Implementation Method 1

a magnetic support over which is formed a complex including an antibody labeled with a luminescent agent and recognizing an analysis target, and a reaction aid for assisting reaction of the luminescent agent; wherein the luminescent process includes: luminescence resulting from action of a first neutral radical, produced from the reaction aid through a cation radical, on the luminescent agent; and luminescence resulting from action of a second neutral radical, produced not through a cation radical, on the luminescent agent

Methodology Applied
Scientific EffectMagnetic field: Magnetic Field

Implementation Method 2

The ECL method is a method of: generating a radical species of a reaction aid by putting a solution containing the reaction aid such as amine and a luminescent material such as a ruthenium complex in a flow cell having a working electrode, a counter electrode, and a reference electrode and applying a potential not lower than the oxidation potential of the reaction aid; forming an excited state of the luminescent material by reaction between the radical species and the luminescent material; and measuring the luminescence

Methodology Applied
Scientific EffectElectrochemiluminescence: Electrochemiluminescence

Implementation Method 3

generating a radical species of a reaction aid by putting a solution containing the reaction aid such as amine and a luminescent material such as a ruthenium complex in a flow cell having a working electrode, a counter electrode, and a reference electrode and applying a potential not lower than the oxidation potential of the reaction aid

Methodology Applied
Scientific EffectOxidation: Oxidation

Implementation Method 4

forming an excited state of the luminescent material by reaction between the radical species and the luminescent material; and measuring the luminescence

Methodology Applied
Scientific EffectChemiluminescence: Chemiluminescence

Data Source

PatentUS12529656B2Biomolecular analysis method and biomolecular analyzer
Publication Date: 2026.01.20 HITACHI HIGH TECH CORP
  • US12529656B2 patent drawing
  • US12529656B2 patent drawing
  • US12529656B2 patent drawing

AI summary

An analysis method includes: an inflow process of a solution containing a test object, a magnetic support on the surface of which a complex including an antibody labeled with a luminescent agent and recognizes the test object is formed, and a reaction aid to assist reaction of the luminescent agent in a flow cell; a process of capturing the magnetic support over a working electrode by a magnetic field; a process of making the luminescent agent illuminate by applying a voltage to the working electrode; and a process of measuring an amount of luminescence of the luminescent agent. The luminescent process includes: luminescence from action of a first neutral radical, produced from the reaction aid through a cation radical; and luminescence from action of a second neutral radical, produced not through a cation radical, on the luminescent agent. This increases the luminous efficiency of ECL and enhances detection sensitivity.