Microchannel Cell Isolation Device for Migratory Population Purity

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Solution Overview

Problem

Current methods for isolating migratory cells from mixed populations are inefficient, leading to contaminated samples and limited quantities of cells suitable for molecular analysis.

Innovation Solution

The use of microchannels with an average size less than the minimum proliferation space of migratory cells allows for the isolation of a pure population of migratory cells, enabling sufficient quantities for various molecular analyses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional cell culture dishes are used to culture cells, then cells can be easily cultured and analyzed, but the results are confounded by the mixture of proliferating/non-migrating cells and migrating cells, making it difficult to exclusively study migrating cells

Engineering Contradiction:
Improvepurity of migratory cell sampleVSAvoidcomplexity of cell isolation system
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The culture dish is segmented into multiple compartments: a first compartment for non-migrating cells and a second compartment for migrating cells separated by a microporous membrane. This physical segmentation allows exclusive study of migrating cells while maintaining culturable conditions, directly resolving the contradiction between sample purity and system complexity.

Inventive Principle:
Principle #1Segmentation

2Quantity of substance

If three-dimensional cell culture methods are used to study migration, then active migration can be examined, but the amount of harvested material is limited, restricting the scope and quantity of molecular analyses that can be conducted

Engineering Contradiction:
Improveamount of migratory cells for analysisVSAvoidquality of molecular analysis
Core Design Contradiction:
Quantity of substanceVSMeasurement precision

Solution Approach 1:

The invention merges the advantages of 3D cell culture (active migration capability) with 2D culture (abundant cell harvest) by using a microporous membrane that allows cells to migrate in three dimensions while remaining attached to a substrate that supports large-scale growth. This enables both active migration study and sufficient material harvest for comprehensive molecular analyses including DNA, RNA, lipid, and protein analysis.

Inventive Principle:
Principle #5Merging (Combining)

3Quantity of substance

If traditional cell culture methods are used, then large amounts of cells can be obtained, but the sample contains both proliferating/non-migrating cells and migrating cells, rendering the sampling impure and difficult to interpret

Engineering Contradiction:
Improvenumber of migratory cellsVSAvoidpurity of cell population
Core Design Contradiction:
Quantity of substanceVSManufacturing precision

Solution Approach 1:

The invention extracts migrating cells from the mixed population by providing a microporous membrane barrier that physically separates migrating cells (which pass through to the second compartment) from non-migrating cells (which remain in the first compartment). This extraction method yields both sufficient quantity and high purity of migrating cells for analysis.

Inventive Principle:
Principle #2Taking out (Extraction)

Data Source

PatentUS12264305B2Devices and methods for isolating a migratory cell population
Publication Date: 2025.04.01 BOARD OF RGT THE UNIV OF TEXAS SYST
  • US12264305B2 patent drawing
  • US12264305B2 patent drawing
  • US12264305B2 patent drawing

AI summary

A method and device for isolating a migratory cell population from a mixed population of migratory cells and non-migratory cells is described herein. The method comprises placing the mixed population of migratory cells and non-migratory cells in contact with a device having one or more microchannels; and isolating the migratory cell population within the microchannels following an incubation period, wherein the one or more microchannels have an average size in a proliferation direction of the migratory cells that is less than a minimum proliferation space of the migratory cells along the proliferation direction.