Silica-Collagen Composite Ocular Device for Tissue Integration

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Solution Overview

Problem

Current artificial corneas lack mechanical strength, biocompatibility, and integration with surrounding tissues, leading to complications such as host tissue melting and intraocular infections due to their poor bio-integration and lack of epithelialization.

Innovation Solution

A silica-based composite material incorporating fibrillar proteins like collagen, which forms a hybrid matrix that enhances mechanical strength, optical transparency, and biocompatibility, allowing for tissue and cell growth, and can be used in corneal implants or contact lenses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Strength

If conventional artificial cornea materials are used, then the device can provide basic optical transparency, but the mechanical strength and biocompatibility are insufficient leading to host tissue melting and intraocular infections

Engineering Contradiction:
Improvemechanical strengthVSAvoidbiocompatibility
Core Design Contradiction:
StrengthVSReliability

Solution Approach 1:

The patent employs a composite material system consisting of a biocompatible polymer matrix (such as silicone or polyacrylate) reinforced with inorganic filler particles (such as silica, glass ions, or hydroxyapatite). This composite structure provides both the mechanical strength needed to prevent host tissue melting and the biocompatibility required to prevent intraocular infections, resolving the contradiction between these two critical properties.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent modifies the physical and chemical parameters of the artificial cornea material by adjusting the crosslinking density, molecular weight, and compositional ratios of the polymer matrix and inorganic fillers. These parameter changes enable the material to simultaneously achieve enhanced mechanical strength for structural integrity and improved biocompatibility for safe integration with host tissue, eliminating the trade-off between these properties.

Inventive Principle:
Principle #35Parameter changes

2Adaptability or versatility

If conventional artificial cornea materials are used, then the device can be implanted, but poor bio-integration and lack of epithelialization occur leading to complications

Engineering Contradiction:
Improvebio-integrationVSAvoidepithelialization
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The patent introduces surface modifications with specific local properties, such as hydrophilic coatings, RGD peptide grafts, or endothelial cell layer coatings on specific regions of the artificial cornea. These localized quality enhancements promote epithelialization at the tissue interface while maintaining the overall structural integrity and optical properties of the implant, resolving the contradiction between bio-integration and epithelialization.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent employs intermediary substances such as growth factors (e.g., EGF, bFGF), extracellular matrix components (e.g., fibronectin, laminin), or bioactive glass particles that mediate between the artificial cornea material and host tissue. These intermediaries facilitate epithelialization and bio-integration by providing biochemical signals and adhesion sites, enabling reliable tissue integration without compromising the implant's structural function.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Reliability

If the ocular device promotes tissue growth and epithelialization, then biocompatibility improves, but the complexity of the material structure increases

Engineering Contradiction:
ImprovebiocompatibilityVSAvoidmaterial structure
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent divides the artificial cornea into functionally segmented layers: an optical zone for light transmission, a structural zone for mechanical support, and a bioactive zone for tissue integration and epithelialization. Each layer has optimized composition and thickness, allowing the device to promote biocompatibility through targeted tissue interaction while maintaining manageable overall structural complexity through modular design.

Inventive Principle:
Principle #1Segmentation

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 silica-collagen composite material provides a strong, transparent, and biocompatible ocular device that promotes epithelialization and integration with the host tissue, reducing complications and improving the efficacy of corneal implants and contact lenses.

Implementation Method 1

A silica-based composite material incorporating fibrillar proteins like collagen, which forms a hybrid matrix

Methodology Applied
Scientific EffectChemical bonding: Chemical Bonding

Implementation Method 2

incorporating fibrillar proteins like collagen, which forms a hybrid matrix

Methodology Applied
Scientific EffectPhysical entanglement:

Implementation Method 3

enhances mechanical strength, optical transparency

Methodology Applied
Scientific EffectLight transmission: Light

Implementation Method 4

allowing for tissue and cell growth, promotes epithelialization and integration with the host tissue

Methodology Applied
Scientific EffectCell adhesion: Adhesive

Data Source

PatentUS9492271B2Silica-based composite ocular device and methods
Publication Date: 2016.11.15 REGENTS OF THE UNIVERSITY OF MINNESOTA
  • US9492271B2 patent drawing
  • US9492271B2 patent drawing
  • US9492271B2 patent drawing

AI summary

Disclosed herein are synthetic silica-based ocular devices fabricated from a composite material comprising silica and a fibrillar protein, together with methods of making and using the ocular devices.