Matrix Biomolecule Filter with Micro-Hole Window Cells

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing technologies for separating biomolecules, such as exosomes, from body fluids are inefficient, often damaging the biomolecules and requiring costly equipment and lengthy processes. Additionally, existing porous membranes are not durable and can be easily blocked by non-biomolecule substances, leading to reduced filtering efficiency.

Innovation Solution

A membrane structure with a matrix shape, featuring a filtering part with window cells arranged in a matrix pattern and a support part for durability. The window cells have micro-holes that allow biomolecules of a predetermined size or less to pass through, preventing damage and blockage by other substances.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If a simple film type porous membrane is used for biomolecule separation, then the filtering process is simple, but the membrane has poor durability and is difficult to handle and install

Engineering Contradiction:
Improvefiltering process simplicityVSAvoidmembrane durability
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The membrane structure is divided into a filtering part containing window cells with micro-holes and a support part providing mechanical strength. This segmentation allows the filtering function and structural support to be separated, achieving both easy filtering operation and high durability

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The membrane structure combines a filtering part made of porous material with a support part made of rigid material to create a composite structure. This composite design integrates the advantages of both materials: the porous structure enables filtration while the rigid support provides durability and ease of handling

Inventive Principle:
Principle #40Composite materials

2Device complexity

If a porous membrane is used in a static state for filtering, then the setup is simple, but the membrane is rapidly blocked by non-biomolecule substances, deteriorating filtering efficiency

Engineering Contradiction:
Improvefiltering setup simplicityVSAvoidfiltering efficiency
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

The membrane structure enables dynamic filtering by allowing the sample to flow along the window region rather than being filtered in a completely static state. The flow dynamics prevent substance accumulation and blockage while maintaining filtration effectiveness

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The window cells contain micro-holes with controlled pore sizes that allow selective passage of biomolecules. The porous structure is designed to prevent blockage by non-biomolecule substances while maintaining high filtering efficiency for target biomolecules

Inventive Principle:
Principle #31Porous materials

3Measurement precision

If antibodies are fixed to microchip for vesicle separation, then specific biomolecules can be separated, but expensive equipment is required and the process takes much time

Engineering Contradiction:
Improvebiomolecule separation specificityVSAvoidseparation process time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent replaces the complex biochemical antibody-fixation system with a simpler physical filtration system using micro-hole structures. This substitution eliminates the need for expensive equipment and lengthy antibody incubation processes while maintaining separation capability through size-based filtration

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

4Quantity of substance

If centrifugation is performed as pretreatment for biomolecule separation, then vesicles can be concentrated, but biomolecules may be damaged and the process requires much time

Engineering Contradiction:
Improvebiomolecule concentrationVSAvoidbiomolecule damage
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The patent changes the separation parameter from centrifugal force to size-based filtration. By using micro-holes with specific pore sizes in the window cells, the system achieves biomolecule concentration and separation without the mechanical stress of centrifugation that can damage delicate biomolecules

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 membrane structure effectively filters biomolecules while preventing damage and improving durability, reducing the time and cost of separation processes and maintaining filtering efficiency by preventing blockage by non-biomolecule substances.

Implementation Method 1

each of the window cells formed in the window region of the filtering part is configured to have micro-holes allowing the biomolecules having a predetermined size or less to pass therethrough

Methodology Applied
Scientific EffectPhysical filtration: Filter (physical)

Data Source

PatentUS12274983B2Membrane structure body having matrix structure and biomolecule filter using same
Publication Date: 2025.04.15 METAPORE CO LTD
  • US12274983B2 patent drawing
  • US12274983B2 patent drawing
  • US12274983B2 patent drawing

AI summary

A membrane structure body having a matrix structure and a biomolecule filter using the same are disclosed. The membrane structure body having a matrix structure, according to one embodiment of the present disclosure, comprises: a filtering part which includes a window region in which a plurality of window cells are formed in a matrix shape and a blocking region in which the window cells are not formed, and which filters biomolecules from a sample moving along the window region; and a support part extending from the filtering part so as to support the filtering part, wherein each of the window cells formed in the window region of the filtering part has have micro-holes allowing the biomolecules having a predetermined size or less to pass therethrough.