Stair-Step Membrane Array for Whole Blood Analysis

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Solution Overview

Problem

Current analytical devices for detecting analytes in fluid samples, particularly whole blood, face challenges in achieving rapid and high sensitivity detection with minimal hemolysis and background interference, especially when using small sample volumes.

Innovation Solution

A membrane array comprising three or more porous membranes arranged in a stair-step configuration, where the first membrane contains a detection reagent, the second membrane has a lower porosity to further retard red blood cells, and the third membrane contains a capture reagent, facilitating capillary flow and minimizing hemolysis for efficient analyte detection.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If a single membrane or two-membrane system is used, then the device complexity is reduced, but the sensitivity and detection efficiency are insufficient

Engineering Contradiction:
Improvedetection sensitivityVSAvoidmembrane array configuration
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The device divides the detection function into three separate porous membranes with different porosity values, where each membrane performs a specific function in the detection process. This segmentation allows for optimized analyte capture and detection at each stage, improving overall sensitivity while maintaining manageable device complexity through modular design

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Each porous membrane is assigned a specific local function based on its porosity: the first membrane (higher porosity) allows sample penetration and initial analyte capture, the second membrane (intermediate porosity) provides additional capture capacity, and the third membrane (lowest porosity) enables concentrated detection. This local quality differentiation optimizes detection sensitivity across the membrane array

Inventive Principle:
Principle #3Local quality

2Speed

If the sample flow rate is increased to achieve rapid detection, then the detection speed is improved, but hemolysis and background interference increase

Engineering Contradiction:
Improvedetection speedVSAvoidhemolysis
Core Design Contradiction:
SpeedVSObject-affected harmful factors

Solution Approach 1:

The device changes the porosity parameter across the three membranes to control sample flow dynamics. The gradient in porosity (decreasing from first to third membrane) creates optimal flow resistance at each stage, allowing rapid analyte transport while preventing excessive shear forces that would cause hemolysis. This parameter variation enables fast detection without the harmful effects of high flow rates

Inventive Principle:
Principle #35Parameter changes

3Quantity of substance

If smaller sample volumes are used, then the sample volume requirement is reduced, but the detection sensitivity decreases

Engineering Contradiction:
Improvesample volumeVSAvoiddetection sensitivity
Core Design Contradiction:
Quantity of substanceVSMeasurement precision

Solution Approach 1:

The three porous membranes are arranged in a nested configuration where the sample flows sequentially through each membrane layer. This nested structure allows the analyte to be captured and concentrated across multiple stages within a compact volume, enabling high sensitivity detection from small sample volumes by progressively enriching the analyte signal at each membrane level

Inventive Principle:
Principle #7Nested doll (Nesting)

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 configuration enables rapid, highly efficient, and sensitive detection of analytes in small volumes of whole blood with minimal hemolysis, providing stable and accurate results within a short time frame.

Implementation Method 1

The presence of an analyte in the sample can be detected either visually or by using reflectance or fluorescence based detection systems and instruments. Oftentimes, the label is an enzyme label or a particulate direct label, for instance a gold sol label.

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Implementation Method 2

Immunoassay devices and procedures currently exist for detecting the presence of an analyte in a sample of biological fluid. Typically, immunochemical reactions involving antigen/antibody reactions take place on dry porous carriers such as cellular membranes

Methodology Applied
Scientific EffectImmunochemical reaction:

Implementation Method 3

The membrane array comprises a two membrane system including a first separation membrane and an analytical capture membrane

Methodology Applied
Scientific EffectAdsorption: Adsorption

Data Source

PatentEP1896851B1Membrane array and analytical device
Publication Date: 2013.08.21 ZBX CORP
  • EP1896851B1 patent drawingFigure 1
  • EP1896851B1 patent drawingFigure 2
  • EP1896851B1 patent drawingFigure 3

AI summary

A membrane array used to detect one or more analytes from a small sample of fluid with high sensitivity is provided. The membrane array can be employed in various analytical devices and is especially useful for identifying analytes from whole blood with minimal or negligible background interference.