Closed-Chamber Cell Culture Pressure and pH Feedback Control

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing in vitro cell culture methods lack the ability to control pressure and dissolved gas concentration/pH in closed chambers, compromising the simulation of in vivo microenvironments and limiting long-term cell culture viability.

Innovation Solution

A method and system for controlling pressure and dissolved gas concentration/pH in a closed chamber by injecting and extracting fluid at controlled flow rates and pressures, using sensors and a controller to maintain predetermined conditions, with a feedback loop for real-time adjustments.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional in vitro cell culture methods are used in closed chambers, then cell culture simplicity and ease of operation are maintained, but the ability to control pressure and dissolved gas concentration/pH is lost, compromising the simulation of in vivo microenvironments and limiting long-term cell culture viability

Engineering Contradiction:
Improvecell culture viabilityVSAvoidcontrol system complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The control system is segmented into independent functional modules: a fluid injection module for controlling dissolved gas concentration and pH, a pressure control module for applying mechanical stress, and a sensor module for monitoring parameters. Each module operates independently but coordinates through the central controller, allowing precise control of each parameter without requiring complete system redesign.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The system implements closed-loop feedback control where sensors continuously monitor pressure, dissolved gas concentration, and pH in the culture medium. These measurements are fed back to the controller, which automatically adjusts the fluid injection rate and pressure application to maintain predetermined target values, ensuring long-term stability and cell viability.

Inventive Principle:
Principle #23Feedback

2Adaptability or versatility

If pressure control is added to simulate in vivo conditions, then the physiological relevance of the model is improved, but the device complexity and difficulty of operation increase

Engineering Contradiction:
Improvephysiological condition simulationVSAvoidoperation difficulty
Core Design Contradiction:
Adaptability or versatilityVSEase of operation

Solution Approach 1:

The pressure control mechanism is integrated into the existing closed chamber culture system, allowing the same device to perform both standard cell culture and mechanotransduction studies. The controller can operate in multiple modes: simple incubation without pressure, constant pressure application, or dynamic pressure cycling, making the system universally applicable to various experimental needs without requiring separate dedicated equipment.

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

3Manufacturing precision

If fluid injection is used to control dissolved gas concentration and pH, then the chemical environment control is improved, but the system complexity and energy consumption increase

Engineering Contradiction:
Improvechemical parameter control precisionVSAvoidenergy consumption
Core Design Contradiction:
Manufacturing precisionVSUse of energy by moving object

Solution Approach 1:

The system applies fluid injection in a controlled, partial manner rather than continuous full-flow operation. The controller adjusts the injection rate to provide just enough fluid exchange to maintain dissolved gas concentration and pH within target ranges, avoiding excessive fluid replacement that would waste energy and reagents while still achieving precise chemical environment control.

Inventive Principle:
Principle #16Partial or excessive 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

This method allows for precise control of environmental conditions in closed chambers, mimicking in vivo microphysiological conditions and maintaining cell viability for long-term studies, enabling accurate phenotypic changes and therapeutic testing.

Implementation Method 1

the fluid moving within said volume of liquid cell culture medium resulting from the injection and/or the extraction involves a change in a local pressure of the volume of liquid cell culture medium (VL) applied to said cultured biological entity

Methodology Applied
Scientific EffectPressure variation: Pressure Increase

Implementation Method 2

measuring an internal pressure inside said at least one closed chamber, and a dissolved gas concentration and/or a pH of the volume of liquid cell culture medium by at least a pressure sensor

Methodology Applied
Scientific EffectPressure measurement: Pressure Increase

Implementation Method 3

measuring an internal pressure inside said at least one closed chamber, and a dissolved gas concentration and/or a pH of the volume of liquid cell culture medium by at least a pressure sensor, and a dissolved gas concentration sensor and/or a pH sensor

Methodology Applied
Scientific EffectDissolved gas concentration detection: Absorption Spectroscopy

Data Source

PatentEP4692305A1Method for controlling pressure and dissolved gas composition and/or ph of a volume of liquid cell culture medium contained in at least one closed chamber which comprises a cultured biological entity
Publication Date: 2026.02.11 CHERRY BIOTECH SAS
  • EP4692305A1 patent drawingFigure 1~3
  • EP4692305A1 patent drawingFigure 4~5
  • EP4692305A1 patent drawing

AI summary

The invention concerns a method for controlling pressure and dissolved gas concentration and/or pH of a volume of liquid cell culture medium (VL) contained in at least one closed chamber (1) which comprises a cultured biological entity (3) which is composed of at least one cell. The method comprises a step of determining a local pressure of the volume of liquid cell culture medium (VL) applied to said cultured biological entity (3) based on measurements of an internal pressure inside said at least closed chamber (1), a dissolved gas(es) concentration and/or pH of said volume of liquid cell culture medium (VL), and adjusting, by a controller (4), the flow rate of the moving fluid (2) within said volume of liquid cell culture medium (VL) resulting from the injection and/or the extraction to control said local pressure regarding said measurements.