DMSO-Free Cell Preservation Composition for Broad-Temperature Storage

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Solution Overview

Problem

Current cell preservation solutions require specific hypothermic preservation temperatures (2° C.-8° C.) and often use DMSO, which are physiologically toxic, leading to poor preservation efficiency, low cell survival rates, and difficulty in mass production, especially for autologous and allogeneic cell preparations.

Innovation Solution

A cell preservation solution composition comprising a copolymer of compound A (60.00 wt % to 99.5 wt %) and compound B (0.05 wt % to 40.00 wt %), allowing preservation at temperatures ranging from hypothermic to room temperature (2° C.-37° C.), without DMSO, and including additives to reduce cell damage.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If DMSO is used as cryoprotectant, then cell preservation effectiveness is improved, but physiological toxicity increases causing hypertension, nausea, and vomiting

Engineering Contradiction:
Improvecell preservation effectivenessVSAvoidphysiological toxicity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent removes DMSO from the preservation solution formulation. The solution uses alternative cryoprotectants (polyethylene glycol, glycerin, sucrose) to achieve cell preservation without the toxic effects of DMSO, thereby extracting the harmful component while maintaining the beneficial preservation function.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent employs a composite preservation solution containing multiple components (polyethylene glycol, glycerin, sucrose, and other additives) that work synergistically to protect cells during freezing and thawing, replacing the single-component DMSO approach with a multi-component system that achieves both preservation effectiveness and reduced toxicity.

Inventive Principle:
Principle #40Composite materials

2Reliability

If hypothermic preservation temperature (2° C.-8° C.) is maintained, then cell preservation is achieved, but operational complexity and cost increase due to continuous temperature control requirements

Engineering Contradiction:
Improvecell preservationVSAvoidtemperature control requirement
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent modifies the chemical composition parameters of the preservation solution by incorporating specific concentrations of polyethylene glycol, glycerin, and sucrose, which alter the solution's freezing point and thermal properties. This enables the solution to maintain cell viability across a broader temperature range, reducing the stringency of temperature control requirements.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The preservation solution is designed to function effectively across multiple temperature conditions (hypothermic, refrigerated, and even room temperature), making it universally applicable without requiring specialized temperature control equipment or procedures for each storage condition.

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

3Duration of action of stationary object

If current preservation solutions are used, then cell storage is possible, but preservation effectiveness is poor leading to low cell survival rate and short effective preservation time

Engineering Contradiction:
Improveeffective preservation timeVSAvoidcell survival rate
Core Design Contradiction:
Duration of action of stationary objectVSReliability

Solution Approach 1:

The patent uses a composite formulation combining polyethylene glycol (for cryoprotection and viscosity control), glycerin (for osmotic balance and membrane protection), and sucrose (for metabolic support and structural stability). This multi-component system provides synergistic protection that extends effective preservation time while maintaining high cell survival rates.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The preservation solution acts as an intermediary medium that mediates between the cell and the harsh freezing environment. The specific combination of cryoprotectants and additives in the solution provides gradual osmotic adjustment and metabolic support during the freezing and thawing processes, thereby extending viable preservation duration.

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

Enhances cell storage time and survival rate, enabling effective preservation without the need for pre-cooling and maintaining low temperatures, and supports cell functionality post-thawing.

Implementation Method 1

The cell preservation solution composition excludes dimethyl sulfoxide (DMSO) and includes a copolymer containing compound A and compound B... enhancing cell storage time and survival rate, enabling effective preservation without the need for pre-cooling and maintaining low temperatures

Methodology Applied
Scientific EffectCryoprotection:

Implementation Method 2

During the freezing process, the formation of intracellular ice crystals and the imbalance of osmotic pressure may damage cells. In order to avoid the above situation, cryoprotectant (CPA) are used to freeze cells.

Methodology Applied
Scientific EffectOsmotic pressure balance: Osmotic Pressure

Data Source

PatentUS20260033487A1Cell Preservation Solution Composition and the Cell Preservation Method Thereof
Publication Date: 2026.02.05 ACCOMODATE PRESERVE CO LTD
  • US20260033487A1 patent drawing
  • US20260033487A1 patent drawing
  • US20260033487A1 patent drawing

AI summary

A cell preservation solution composition, excluding dimethyl sulfoxide (DMSO), includes a copolymer of compound A and compound B. In a composition of 100 wt % of the cell preservation solution composition, the compound A ranges from 60.00 wt % to 99.95 wt %, and compound B ranges from 0.05 wt % to 40.00 wt %.