Elastase-Treated Arterial Tissue Hydrogel for Biocompatibility

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Solution Overview

Problem

Existing hydrogels made from synthetic and biological materials have poor biocompatibility due to extensive chemical modification, hindering tissue treatment and regeneration.

Innovation Solution

A tissue-derived hydrogel is created by treating an acellular arterial tissue matrix with elastase, which increases biocompatibility and reduces immunogenicity, allowing the hydrogel to swell and become more malleable while retaining structural integrity and promoting native tissue re-growth.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If synthetic materials and extensive chemical modification are used to produce hydrogels, then hydrogel production is achieved, but biocompatibility deteriorates

Engineering Contradiction:
Improvehydrogel productionVSAvoidbiocompatibility
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent extracts and removes cells from arterial tissue to create an acellular matrix, eliminating immunogenic cellular components while retaining the beneficial extracellular matrix structure. This extraction process resolves the contradiction by removing harmful elements (cells that cause immune rejection) while preserving the useful framework for tissue regeneration

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent applies elastase enzyme treatment to modify the physical and chemical parameters of the arterial tissue matrix. This enzymatic treatment alters the tissue's mechanical properties, increasing swelling and softening the matrix, thereby transforming it into a hydrogel state with improved biocompatibility and reduced immunogenicity

Inventive Principle:
Principle #35Parameter changes

2Reliability

If arterial tissue is treated with elastase, then biocompatibility improves and immunogenicity reduces, but tissue structural integrity may compromise

Engineering Contradiction:
ImprovebiocompatibilityVSAvoidtissue structural integrity
Core Design Contradiction:
ReliabilityVSStrength

Solution Approach 1:

The patent uses elastase enzyme as an intermediary agent to selectively degrade specific components of the tissue matrix. The enzyme acts as a mediator that transforms the rigid arterial tissue into a softer hydrogel state while maintaining the overall structural framework necessary for tissue support and regeneration

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

Controlled enzymatic treatment with elastase modifies the physical parameters of the tissue matrix, inducing swelling and softening transitions. These parameter changes transform the tissue from a rigid state to a more compliant hydrogel state, improving biocompatibility while preserving essential structural integrity through controlled modification

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 elastase-treated arterial tissue hydrogel exhibits higher biocompatibility and reduced immunogenicity compared to synthetic hydrogels, supporting tissue regeneration and providing a flexible, moldable scaffold for tissue repair and pharmaceutical delivery.

Implementation Method 1

The hydrogel comprises an acellular arterial tissue matrix that has been treated with an elastase to form a hydrogel

Methodology Applied
Scientific EffectEnzyme: Enzyme

Implementation Method 2

treating the arterial tissue with an elastase, thereby causing the tissue matrix to substantially swell and soften

Methodology Applied
Scientific EffectHydrogel formation: Hydrogel

Data Source

PatentUS10092602B2Elastic tissue matrix derived hydrogel
Publication Date: 2018.10.09 LIFECELL CORP
  • US10092602B2 patent drawing
  • US10092602B2 patent drawing
  • US10092602B2 patent drawing

AI summary

A tissue-derived hydrogel, as well as methods of making and using such hydrogels, are provided.