Microfluidic Device with Top Access Port for 3D Cell Culture

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Solution Overview

Problem

Current microfluidic devices for in vitro 3D cell culture experimentation have limited accessibility and difficulty in manipulating and analyzing cells, especially in complex geometries, which hinders high spatial and temporal resolution monitoring and individual cell retrieval.

Innovation Solution

A microfluidic device with a culture chamber that opens into an access port on its outer top surface, allowing direct access and manipulation of the scaffolding substance, and featuring fluid flow barriers to mimic interstitial fluid forces, enabling precise control of fluid flow and nutrient supply, and facilitating high-resolution monitoring.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If a closed microfluidic system is used to control fluid flow and culture conditions, then precise control of cell culture environment is achieved, but accessibility for cell manipulation and analysis is limited

Engineering Contradiction:
Improvecontrol precision of culture conditionsVSAvoidaccessibility for cell manipulation
Core Design Contradiction:
Manufacturing precisionVSEase of operation

Solution Approach 1:

The microfluidic device is divided into distinct functional modules: a culture chamber for cell cultivation, an access port for manipulation, and fluidic pathways for controlled delivery. This segmentation allows each component to perform its specific function optimally while maintaining overall system control.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The access port serves as an intermediary structure that bridges the closed culture chamber and the external environment. It enables introduction of cells, materials, and instruments into the culture chamber without compromising the controlled microfluidic environment, thus resolving the contradiction between closure for control and openness for accessibility.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Ease of operation

If conventional 2D cell culture methods are used, then ease of operation and simplicity are maintained, but physiological relevance and predictive value are lost

Engineering Contradiction:
Improvesimplicity of culture methodVSAvoidpredictive value for clinical efficacy
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The invention transitions from conventional two-dimensional planar culture to three-dimensional microfluidic culture. The culture chamber provides a 3D environment that better mimics in vivo tissue architecture, while the microfluidic pathways deliver nutrients and remove waste in a physiologically relevant manner, thereby improving predictive value while maintaining operational simplicity.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

3Reliability

If 3D scaffolding systems are used to achieve tissue-like connectivity, then physiological context is improved, but control over cell culture conditions and nutrient supply is limited

Engineering Contradiction:
Improvephysiological context of cell cultureVSAvoidcontrol precision of culture conditions
Core Design Contradiction:
ReliabilityVSManufacturing precision

Solution Approach 1:

The invention employs microfluidic hydraulic control to deliver nutrients, growth factors, and drugs through defined pathways to the 3D scaffolding. The fluid flow rates, pressures, and timing are precisely controlled, enabling accurate delivery of culture conditions while maintaining the physiological benefits of 3D tissue-like structures.

Inventive Principle:
Principle #29Pneumatics and hydraulics

Solution Approach 2:

The system enables dynamic adjustment of culture parameters including fluid flow rate, nutrient concentration, oxygen levels, and mechanical stress on the 3D scaffolding. These parameters can be changed in real-time to optimize cell culture conditions while maintaining the physiological relevance of the 3D environment.

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

This design enhances the ability to mimic in vivo tissue environments, allowing for precise control of cell culture conditions, improved accessibility for cell manipulation, and high-resolution monitoring, thereby improving the accuracy and reproducibility of cell culture experiments.

Implementation Method 1

the scaffolding substance which forms a fluid flow barrier separating the fluid path from the access port

Methodology Applied
Scientific EffectFluid flow barrier:

Implementation Method 2

Because of the micro geometrical dimensions, the flow of fluids is laminar

Methodology Applied
Scientific EffectLaminar flow: Laminar Flow

Implementation Method 3

the culture chamber above the scaffolding substance opens into an access port provided at an outer top surface of the body for direct access to the scaffolding substance

Methodology Applied
Scientific EffectDirect access:

Data Source

PatentUS10744505B2Microfluidic device for in vitro 3D cell culture experimentation
Publication Date: 2020.08.18 INTECRYPT BV
  • US10744505B2 patent drawing
  • US10744505B2 patent drawing
  • US10744505B2 patent drawing

AI summary

A microfluidic device for in vitro 3D cell culture experimentation comprises a body in which is provided a cell culture chamber that is at least partly filled with a scaffolding substance for maintaining a cell culture. In the body a fluid path is provided that communicates with the cell culture chamber for directing a fluid stream along the scaffolding substance. The culture chamber above the scaffolding substance opens into an access port which is provided at an outer top surface of the body to provide direct access to the scaffolding substance. The scaffolding substance forms a fluid flow barrier which separates the fluid path from the access port.