Assay Device with Pressing Unit for Even Solution Distribution

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Solution Overview

Problem

Existing immunochromatography methods face challenges in achieving highly accurate and sensitive detection due to uneven distribution of solution components, such as enzyme substrate solutions and signal amplification solutions, across the stationary phase carrier, resulting in uneven reaction progress.

Innovation Solution

A method and device that involve injecting test reagent, amplification, and detection solutions into a clearance between an insoluble carrier and a facing member, utilizing capillary action to ensure even solution development and distribution, with a pressing unit creating a controlled clearance to facilitate this process.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If solutions are dropped onto the detection portion of the insoluble carrier, then the operation is simple, but the solution components are not distributed evenly across the carrier

Engineering Contradiction:
Improvesimplicity of solution applicationVSAvoiduniformity of solution distribution
Core Design Contradiction:
Ease of operationVSManufacturing precision

Solution Approach 1:

A liquid-holding member is introduced as an intermediary between the solution and the insoluble carrier. This member receives the dropped solution and transports it to the detection portion through capillary action, ensuring even distribution without requiring complex application mechanisms. The liquid-holding member acts as a mediator that converts simple dropping into uniform distribution.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

Capillary action, a hydraulic phenomenon, is utilized to transport the solution from the liquid-holding member to the detection portion. The capillary forces within the porous structure of the liquid-holding member automatically drive the solution flow without external pressure, achieving both simplicity and uniformity.

Inventive Principle:
Principle #29Pneumatics and hydraulics

2Ease of operation

If conventional immunochromatography is used, then the method is simple and quick, but detection sensitivity is insufficient for extremely small amounts of analytes

Engineering Contradiction:
Improvesimplicity and speed of detectionVSAvoiddetection sensitivity
Core Design Contradiction:
Ease of operationVSMeasurement precision

Solution Approach 1:

The detection system is segmented into multiple functional components: the insoluble carrier with detection portion, the liquid-holding member for solution management, and the pressing member for contact control. This segmentation allows each component to be optimized for its specific function while maintaining overall simplicity.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The physical state and distribution parameters of the solution are changed by introducing the liquid-holding member. The solution is transformed from a directly applied liquid into a controlled flow through capillary action, improving distribution uniformity and thereby detection sensitivity without complicating the operation.

Inventive Principle:
Principle #35Parameter changes

3Manufacturing precision

If solution components are not evenly distributed, then the reaction progress becomes uneven, but achieving even distribution requires complex solution delivery mechanisms

Engineering Contradiction:
Improveuniformity of reaction progressVSAvoidcomplexity of solution delivery system
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The liquid-holding member serves as a mediator that simplifies the solution delivery system while achieving uniform distribution. Its porous structure inherently provides capillary action, eliminating the need for complex pumps or pressure systems. The intermediary converts a complex delivery problem into a simple capillary flow process.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The liquid-holding member performs self-service by using its own capillary properties to transport the solution. No external control mechanisms are needed - the porous material itself generates the driving force through capillary action, achieving uniform distribution automatically.

Inventive Principle:
Principle #25Self-service

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 highly accurate and sensitive measurement by ensuring even distribution of solutions, enhancing the detection sensitivity and specificity of analytes, particularly for bioactive substances and environmental pollutants.

Implementation Method 1

utilizing capillary action to ensure even solution development and distribution

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Data Source

PatentUS8802426B2Method and device for assay
Publication Date: 2014.08.12 FUJIFILM CORP
  • US8802426B2 patent drawing
  • US8802426B2 patent drawing
  • US8802426B2 patent drawing

AI summary

A device for assay can evenly develop solution, and performs highly accurate and sensitive measurement. A first device part (10) maintains a second insoluble carrier (12) and a third insoluble carrier (13) in such a manner that they overlap with each other at a detection portion (14) of a first insoluble carrier (11). These three carriers (11), (12) and (13) are housed not in contact with each other. A pressing unit (18) having a pressing surface (18a) that is parallel to the detection portion (14) is provided on an inner surface of the second device part (20) facing the detection portion (14). The pressing surface (18a) is displaced by being pressed toward the detection portion (14), and presses, from the upper side of the first insoluble carrier (11), the second insoluble carrier (12) and the third insoluble carrier (13) onto the first insoluble carrier (11). The first device part (10) and the second device part (20) are joined together.