Mesenchymal Stem Cell Preservation in Human Plasma

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Solution Overview

Problem

Current methods for preserving mesenchymal stem cells (MSC) for cell therapy are cumbersome due to the need for cryogenic storage, which requires specialized equipment and can reduce cell viability and increase contamination risks during transportation and handling.

Innovation Solution

Non-cryogenic suspension storage of MSC in a composition comprising at least 20% v/v human plasma or human serum at temperatures between 0.1°C and 25°C, maintaining the cells in a liquid state for extended periods.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If cryopreservation at -196°C is used to preserve cell viability, then cell viability is maintained, but transportation becomes logistically burdensome and requires specialised equipment

Engineering Contradiction:
Improvecell viabilityVSAvoidtransportation logistics
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The invention changes the temperature parameter from cryogenic (-196°C) to refrigerated (2-8°C), allowing cells to be preserved without freezing while maintaining viability. This parameter change eliminates the need for liquid nitrogen tanks and specialized cryogenic equipment during transportation.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention introduces plasma or serum as an intermediary substance in the storage composition, which protects cells during refrigerated storage and prevents damage that would normally occur at higher temperatures. This intermediary enables the temperature parameter change while maintaining cell viability.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Duration of action of stationary object

If cryopreservation is used for cell storage, then cells can be stored indefinitely, but additional handling steps (thawing, washing, resuspension) reduce cell viability and increase contamination risk

Engineering Contradiction:
Improvestorage durationVSAvoidcell viability
Core Design Contradiction:
Duration of action of stationary objectVSReliability

Solution Approach 1:

The invention maintains cells in a continuous viable state through refrigerated storage in plasma/serum composition, eliminating the discontinuous handling steps (freezing, thawing, washing) required by cryopreservation. Cells remain ready for use without interruption, maintaining viability throughout extended storage periods.

Inventive Principle:
Principle #20Continuity of useful action

Solution Approach 2:

The invention performs preliminary preparation by suspending cells in plasma or serum composition before storage, which pre-conditions the cells for long-term stability at refrigerated temperatures. This preliminary action eliminates the need for subsequent processing steps like thawing and washing that could compromise viability.

Inventive Principle:
Principle #10Preliminary action

3Duration of action of stationary object

If cryopreservation is used for cell storage, then cells can be stored long-term, but the risk of contamination increases during handling

Engineering Contradiction:
Improvestorage durationVSAvoidcontamination risk
Core Design Contradiction:
Duration of action of stationary objectVSObject-affected harmful factors

Solution Approach 1:

By maintaining cells in a continuous refrigerated storage state without freezing/thawing cycles, the invention eliminates multiple handling steps that expose cells to contamination risks. The continuous viable state reduces opportunities for contaminant introduction while maintaining long-term storage capability.

Inventive Principle:
Principle #20Continuity of useful action

4Ease of operation

If aqueous storage liquids based on culture media are used for non-cryogenic storage, then transportation is simplified, but cell viability and stability deteriorate during extended storage

Engineering Contradiction:
Improvetransportation logisticsVSAvoidcell viability
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The invention copies the protective properties of plasma/serum (which naturally protect blood cellular components) and applies them to therapeutic cells through plasma/serum-based storage composition. This copying of natural protective mechanisms enables simplified transportation while maintaining cell viability.

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The invention changes the composition parameter from standard culture media to plasma/serum-based composition, which provides superior protection for cells during refrigerated storage. This compositional change enables both simplified logistics and maintained viability simultaneously.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentEP3285575B1In vitro preservation of therapeutic cells
Publication Date: 2019.08.14 BONE THRAPEUTICS SA
  • EP3285575B1 patent drawingFigure 1
  • EP3285575B1 patent drawingFigure 2
  • EP3285575B1 patent drawingFigure 3

AI summary

The invention concerns in vitro preservation of living animal cells. In particular, the invention provides a method for in vitro preservation of cells comprising maintaining adherent mesenchymal stem cells (MSC) or adherent MSC-derived cells in suspension in a composition comprising at least 20% v/v human plasma or human serum or a mixture thereof.