Nanofiber Spacer for Compartmentalized Cell Culture

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Solution Overview

Problem

Current cell culture methods, such as two-dimensional and three-dimensional systems, face challenges in measuring real-time cell migration and require complex manufacturing processes for creating compartmentalized nanofiber structures that facilitate oxygen, nutrient, and cell migration, while existing techniques like scaffold cultures suffer from leakage and nanoscale gaps between cell fractions.

Innovation Solution

A nanofiber structure with a spacer that divides the culture layer into at least two regions, manufactured using electrospinning and heat-treating nanofibers, allowing for cell migration channels and real-time cell analysis, where the spacer is made of the same nanofibers as the culture layer and has a decreasing width, enabling effective mass transfer and cell migration.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If compartmentalized nanofiber structures are created to facilitate oxygen transfer, nutrient transfer, and cell migration, then cell culture functionality is improved, but manufacturing complexity increases

Engineering Contradiction:
Improvecell culture functionalityVSAvoidmanufacturing complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The nanofiber structure is segmented into multiple compartments or regions within the scaffold, creating distinct zones for different cell types or culture conditions. This segmentation is achieved through controlled electrospinning parameters or post-processing techniques that divide the continuous nanofiber matrix into functional compartments, enabling simultaneous oxygen transfer, nutrient delivery, and cell migration pathways.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent implements nested microchannels within the nanofiber scaffold structure, where smaller channels are embedded within the larger porous matrix. This nested architecture allows multiple functions (oxygen transfer, nutrient delivery, waste removal) to occur simultaneously within different hierarchical levels of the same structure, improving cell culture functionality without proportionally increasing manufacturing complexity.

Inventive Principle:
Principle #7Nested doll (Nesting)

2Manufacturing precision

If micropatterning is fabricated by applying lithography or mechanical micromachining to electro-spun nanofiber scaffold, then structural precision is improved, but manufacturing complexity and difficulty increase

Engineering Contradiction:
Improvemicropatterning precisionVSAvoidmanufacturing ease
Core Design Contradiction:
Manufacturing precisionVSEase of manufacture

Solution Approach 1:

The patent incorporates micropatterning features directly into the mold or substrate used during the electrospinning process. By pre-forming the desired micropattern geometry in the supporting structure, the nanofibers naturally follow this template during deposition, achieving precise micropatterning without requiring subsequent lithography or mechanical machining steps. This preliminary action transfers the pattern definition to the earliest stage of manufacturing.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent replaces traditional mechanical micromachining or lithography processes with an electrospinning-based self-patterning approach. Instead of using complex mechanical tools to carve or deposit patterns, the electrostatic field during electrospinning naturally guides fiber deposition along desired pathways defined by the underlying mold topology, substituting mechanical precision requirements with electrical field control.

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

3Measurement precision

If real-time cell migration measurement is implemented, then measurement capability is improved, but the number of assays and time required increase

Engineering Contradiction:
Improvecell migration measurement capabilityVSAvoidtime required for measurement
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent implements continuous real-time monitoring capabilities within the nanofiber scaffold system, allowing cell migration to be tracked continuously as it occurs rather than through discrete endpoint assays. The scaffold incorporates integrated sensors or imaging-compatible features that enable uninterrupted observation of cell movement, maintaining measurement precision while eliminating the time loss associated with repeated sampling and analysis cycles.

Inventive Principle:
Principle #20Continuity of useful action

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 nanofiber structure allows for real-time measurement of cell migration and simultaneous culturing of multiple cell types, overcoming the limitations of existing methods by providing a stable and efficient compartmentalized culture system with reduced manufacturing complexity.

Implementation Method 1

manufactured using electrospinning and heat-treating nanofibers

Methodology Applied
Scientific EffectElectrospinning: Electrohydrodynamics

Implementation Method 2

manufactured using electrospinning and heat-treating nanofibers

Methodology Applied
Scientific EffectHeat treatment: Heat Treatment

Data Source

PatentUS11345881B2Nanofiber structure for cell culture, method for manufacturing the nanofiber structure, and cell analysis device including the nanofiber structure
Publication Date: 2022.05.31 IND ACADEMIC COOPERATION FOUND OF AJOU UNIV
  • US11345881B2 patent drawing
  • US11345881B2 patent drawing
  • US11345881B2 patent drawing

AI summary

The present disclosure relates to a nanofiber structure for cell culture, a method for manufacturing the structure, and a cell analysis device including the nanofiber structure for cell culture. The structure includes a cell culture layer made of nanofibers; and a spacer protruding upward from a surface of the cell culture layer, wherein the spacer divides a region on the cell culture layer into at least two culturing regions, wherein the spacer is made of the same nanofibers as the cell culture layer and thus has a cell migration channel defined therein.