Multiplex Assay Separation Structures for Cross-Contamination Control

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Solution Overview

Problem

Existing multiplex assays face challenges in efficiently separating and analyzing multiple liquid samples without cross-contamination and optimizing sample distribution in a single device.

Innovation Solution

A multiplex assay device with a separating structure, such as a trench or hydrophilic strip, and a well structure, where at least a portion of the separating structure is not covered by the sample contact area, allowing for precise separation and analysis of liquid samples into distinct areas.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If a multiplex assay device uses a separating structure (trench or hydrophilic strip) that is not covered by the sample contact area, then liquid samples can be separated into distinct areas with minimal cross-contamination, but the device complexity increases due to the additional separating structure

Engineering Contradiction:
Improvesample separation accuracyVSAvoiddevice structure complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The device divides the sample contact area into multiple distinct regions using separating structures (trenches or hydrophilic strips). Each region can independently receive and contain specific liquid samples, preventing cross-contamination between different assay locations. This segmentation approach directly addresses the reliability requirement for accurate sample separation.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The separating structure acts as an intermediary element between different sample contact areas. It physically or chemically mediates the interaction between samples, blocking lateral flow and preventing mixing between adjacent regions. This intermediary structure enables reliable sample separation while maintaining a relatively simple overall device architecture.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If the separating structure is not covered by the sample contact area, then sample distribution into distinct areas is optimized, but the manufacturing precision requirements increase

Engineering Contradiction:
Improvesample analysis efficiencyVSAvoidseparating structure positioning accuracy
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The separating structure is strategically positioned in specific locations where sample separation is most needed, rather than uniformly across the entire device. This localized approach optimizes sample distribution efficiency while reducing the overall manufacturing precision requirements, as only specific regions require high-precision separation features.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The separating structures (trenches or hydrophilic strips) are pre-formed during device fabrication before sample loading. This preliminary creation of separation pathways ensures that samples are automatically directed into correct regions during the assay process, reducing the need for high-precision positioning during sample application and improving overall manufacturing feasibility.

Inventive Principle:
Principle #10Preliminary action

3Productivity

If multiple liquid samples are analyzed simultaneously in separate areas, then the productivity of multiplex assays increases, but the device complexity increases

Engineering Contradiction:
Improvemultiplex assay throughputVSAvoiddevice structure complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The device uses a universal separating structure design (trenches or hydrophilic strips) that can accommodate multiple different sample types and assay configurations within the same basic framework. This multi-functional design enables simultaneous analysis of multiple liquid samples without requiring completely different device architectures for each assay type, thereby increasing productivity while controlling device complexity.

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

Solution Approach 2:

Multiple sample contact areas with separating structures are merged into a single integrated device platform. This consolidation allows simultaneous processing of multiple samples in parallel, significantly improving productivity. The merged design shares common components such as the base plate, cover plate, and separation structures, preventing device complexity from scaling linearly with the number of samples analyzed.

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

The device effectively separates and analyzes multiple liquid samples with minimal cross-contamination, enabling simultaneous detection of different analytes in separate areas, enhancing the efficiency and accuracy of multiplex assays.

Implementation Method 1

a separating structure selected from, for example, a trench or a hydrophilic strip on a plate

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Implementation Method 2

at least a portion of the separating structure is not covered by the sample contact area

Methodology Applied
Scientific EffectSurface tension: Surface Tension

Implementation Method 3

a cover plate that opposes the base plate, the cover plate covers at least a portion of the well area

Methodology Applied
Scientific EffectPhysical containment: Physical Containment

Data Source

PatentUS20250269374A1Multiplex Assays Using Separation Structure and Well Structure
Publication Date: 2025.08.28 ESSENLIX CORP
  • US20250269374A1 patent drawing
  • US20250269374A1 patent drawing
  • US20250269374A1 patent drawing

AI summary

A multiplex assay device including: a separation structure on a first plate; and a sample contact area on the surface of the first plate. Also disclosed is a method for fabricating a multiplex assay, including: making a reagent into a non-liquid reagent particle; creating a well on a sample contact area of a plate of a Q-card two plate sample card; and dropping one or more of the non-liquid reagent particles into at least one well.