Microfluidic Culturing Station Thermal Regulation and Media Perfusion

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Solution Overview

Problem

The culturing of biological cells in microfluidic devices is hindered by the need for large amounts of costly media and the inefficiencies of traditional tissue culture methods, which are time-consuming and resource-intensive.

Innovation Solution

A culturing station equipped with thermally conductive mounting interfaces, a media perfusion system for controlled dispensing of culturing media, and a thermal regulation system to maintain optimal conditions for microfluidic devices, allowing for precise temperature control and efficient media management.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If traditional tissue culture plates and dishes are used for cell culturing, then cell culturing can be performed, but large amounts of costly media and disposable plastic materials are required

Engineering Contradiction:
Improveamount of culturing mediaVSAvoidculturing efficiency
Core Design Contradiction:
Quantity of substanceVSProductivity

Solution Approach 1:

The invention segments the cell culturing process into micro-scale operations using microfluidic devices with multiple small chambers, each capable of independently culturing cells. This segmentation allows parallel processing of multiple cell cultures in a single device, reducing the total volume of media required while maintaining high productivity through simultaneous cultivation of numerous cell samples.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention transitions from traditional two-dimensional culture surfaces in plates to three-dimensional microfluidic chambers that enable cells to be cultured in a more physiologically relevant environment. This dimensional change increases the surface area to volume ratio, allowing more efficient use of culturing media while supporting higher cell densities and improving overall culturing capacity.

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

2Productivity

If traditional tissue culture methods are used, then cell culturing can be performed, but the process is time-consuming and resource-intensive

Engineering Contradiction:
Improveculturing speedVSAvoidtime for media changes and handling
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The invention merges multiple culturing functions into a single integrated microfluidic device, combining cell injection, media perfusion, waste removal, and observation capabilities. This integration eliminates the need for repeated handling of separate plates and dishes, reducing time losses associated with media changes and sample transfers while maintaining high culturing productivity.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The microfluidic device enables continuous perfusion of culturing media through integrated channels and pumps, maintaining constant nutrient supply and waste removal without interrupting the culturing process. This continuous action eliminates the periodic downtime required for manual media changes in traditional methods, thereby increasing overall culturing speed and reducing time losses.

Inventive Principle:
Principle #20Continuity of useful action

3Quantity of substance

If microfluidic devices are used for cell culturing, then resource consumption is reduced, but precise temperature control and media management systems are required

Engineering Contradiction:
Improvemedia consumptionVSAvoidthermal regulation and perfusion systems
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The culturing station is designed as a universal platform that can accommodate multiple different microfluidic devices with varying chamber configurations and cell types. The thermal regulation and media perfusion systems are implemented as standardized multi-functional modules that serve all mounted devices, thereby managing the complexity through standardization while enabling precise control and efficient media management across diverse culturing applications.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The culturing station acts as an intermediary system between the operator and the microfluidic devices, providing automated thermal regulation and media perfusion control. This intermediary layer manages the complexity of precise temperature and flow control, shielding users from the intricacies while enabling resource-efficient culturing through optimized media delivery and environmental management.

Inventive Principle:
Principle #24Intermediary (Mediator)

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 setup enables efficient and controlled culturing of biological cells within microfluidic devices, reducing resource consumption and time, while maintaining optimal growth conditions through precise temperature control and media management.

Implementation Method 1

one or more thermally conductive mounting interfaces, each mounting interface configured for having a microfluidic device detachably mounted thereon

Methodology Applied
Scientific EffectThermal conduction: Conduction (thermal)

Data Source

PatentEP3286298A1Culturing station for microfluidic device
Publication Date: 2018.02.28 BERKELEY LIGHTS INC

AI summary

A station for culturing biological cells in a microfluidic device is provided. The station includes one or more thermally conductive mounting interfaces, each mounting interface configured for having a microfluidic device detachably mounted thereon; a thermal regulation system configured for controlling a temperature of microfluidic devices detachably mounted on the one or more mounting interfaces; and a media perfusion system configured to controllably and selectively dispense a flowable culturing media into microfluidic devices detachably mounted on the one or mounting interfaces.