Acellular Dermal Matrix Cryoprotectant Optimization

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Solution Overview

Problem

Conventional methods for preparing acellular dermal matrices face issues with tissue stability and biological property changes due to inadequate penetration of cryoprotectants and ice crystal formation, leading to rapid degradation and weakened tissue structure.

Innovation Solution

A method involving the removal of epidermis and cells from allograft skin, followed by the preparation of a cryoprotectant solution with glycerol, propylene glycol, and sucrose, which is then penetrating into the skin and freeze-dried to create a stable acellular dermal matrix, optimizing the mixing ratio of sucrose, glycerol, and propylene glycol to prevent ice crystal formation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If conventional cryoprotectant methods are used, then the preparation process is simple, but the cryoprotectant does not sufficiently penetrate into collagen tissues and ice crystals form during freezing

Engineering Contradiction:
Improvepreparation process simplicityVSAvoidtissue stability
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent modifies the chemical composition parameters of the cryoprotectant by adding sucrose to the basic glycerol-propylene glycol solution. This parameter change enables sufficient penetration into collagen tissues while preventing ice crystal formation during freezing, thereby maintaining tissue stability without complicating the preparation process

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite cryoprotectant system by combining multiple substances (glycerol, propylene glycol, and sucrose) with complementary properties. This composite approach allows the cryoprotectant to simultaneously achieve deep tissue penetration and effective ice crystal prevention, resolving the contradiction between manufacturing simplicity and tissue stability

Inventive Principle:
Principle #40Composite materials

2Ease of manufacture

If low concentration of sugar is used in cryoprotectant, then the preparation is easier, but moisture cannot be sufficiently excluded from collagen tissues leading to ice crystal formation

Engineering Contradiction:
Improvecryoprotectant preparation easeVSAvoidice crystal formation
Core Design Contradiction:
Ease of manufactureVSObject-affected harmful factors

Solution Approach 1:

The patent optimizes the sugar concentration parameter to a specific range (20-40% sucrose) in the cryoprotectant solution. This parameter optimization achieves sufficient moisture exclusion from collagen tissues to prevent ice crystal formation while maintaining reasonable ease of preparation through a controlled but not excessive concentration level

Inventive Principle:
Principle #35Parameter changes

3Temperature

If ice crystals form during freezing, then the freezing process is simpler, but many pores are created in tissues during drying and collagen tissues are destroyed

Engineering Contradiction:
Improvefreezing process simplicityVSAvoidcollagen tissue structure
Core Design Contradiction:
TemperatureVSStrength

Solution Approach 1:

The patent applies preliminary anti-action by incorporating sucrose into the cryoprotectant before freezing. This pre-prepared composition actively prevents ice crystal formation during the freezing process, thereby avoiding the subsequent harmful effects of pore creation and collagen tissue destruction during drying

Inventive Principle:
Principle #9Preliminary anti-action

4Productivity

If conventional cryoprotectant penetration is used, then the process is faster, but tissue stability is not sufficiently increased and biological properties change

Engineering Contradiction:
Improvepreparation speedVSAvoidtissue stability
Core Design Contradiction:
ProductivityVSStability of the object's composition

Solution Approach 1:

The patent modifies the cryoprotectant composition parameters by adding sucrose, which enhances penetration capability and tissue stabilization. This parameter modification allows for relatively fast preparation while simultaneously achieving sufficient tissue stability and minimizing biological property changes

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

The method significantly enhances tissue stability, maintains the extracellular matrix and basement membrane integrity, and minimizes biological property changes, resulting in improved grafting success rates and reduced treatment duration.

Implementation Method 1

penetrating the cryoprotectant into the skin from which epidermis and cells in dermis are removed

Methodology Applied
Scientific EffectDiffusion: Diffusion

Implementation Method 2

low concentration of sugar cannot sufficiently exclude moisture from collagen tissues

Methodology Applied
Scientific EffectOsmotic pressure: Osmotic Pressure

Implementation Method 3

many ice crystals are formed at the time of freezing. Such ice crystals make many pores in tissues in the course of drying and destroy collagen tissues

Methodology Applied
Scientific EffectFreezing point depression: Freezing

Data Source

PatentUS9623149B2Method for producing an acellular dermal matrix, and acellular dermal matrix produced by same
Publication Date: 2017.04.18 CG BIO CO LTD
  • US9623149B2 patent drawing
  • US9623149B2 patent drawing
  • US9623149B2 patent drawing

AI summary

The present invention relates to a method for producing an acellular dermal matrix, and to an acellular dermal matrix produced by same, and more particularly, to a method for producing an acellular dermal matrix, in which sucrose is added to base ingredients consisting of glycerol, propylene glycol, and a base solvent or solution so as to produce a cryoprotectant, the solution is injected into the skin below the epidermis and dermis from which cells have been removed, and freeze-drying is then performed.