Dynamic Bioactive Bone Graft Material for Customizable Shape and Handling

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Solution Overview

Problem

Current bone graft materials lack the necessary chemical and physical properties for optimal bone grafting, including variable porosity, differential resorption capacity, and ease of handling, and often pose risks such as disease transmission and complications from natural material harvesting.

Innovation Solution

Development of dynamic bioactive synthetic bone graft materials with varying levels of porosity (nano, micro, meso, macro) and differential bioresorbability, featuring bioactive glass fibers and particulates that can be molded into clinically relevant shapes, providing antimicrobial properties and drug delivery capabilities, and are designed to facilitate tissue formation through a physiologic process.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If autograft materials are used for bone grafts, then acceptable physical and biological properties are achieved, but multiple or extended surgeries are required and considerable pain and morbidity occur at the donor site

Engineering Contradiction:
Improvephysical and biological propertiesVSAvoidpain and morbidity at donor site
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent creates synthetic bone graft materials that replicate the physical and biological properties of natural autograft bone without requiring harvesting from the patient. The synthetic materials are designed to mimic the structural characteristics, porosity, and osteoconductivity of natural bone, providing the same regenerative benefits while eliminating donor site trauma and the need for additional surgical procedures

Inventive Principle:
Principle #26Copying

2Object-affected harmful factors

If allograft devices are used for bone grafts, then risk and pain to the patient are decreased, but increased risk of disease transmission and rejection occurs

Engineering Contradiction:
Improvepain and risk to patientVSAvoidrisk of disease transmission and rejection
Core Design Contradiction:
Object-affected harmful factorsVSReliability

Solution Approach 1:

The patent employs synthetic bone graft materials that are manufactured anew for each application rather than being harvested from donors. These synthetic materials eliminate the risk of disease transmission and immune rejection associated with allografts, while providing comparable mechanical support and osteoinductive properties. The materials are designed to be resorbable, gradually replaced by native bone tissue over time

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

3Reliability

If autograft and allograft devices are used, then bone grafting can be performed, but variations on shape and size are restricted

Engineering Contradiction:
Improvebone grafting capabilityVSAvoidshape and size variations
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent describes synthetic bone graft materials with dynamic properties that allow them to be molded, shaped, and customized intraoperatively to match the specific anatomical defect. The materials can be formed into various shapes and sizes depending on the patient's needs, providing unlimited adaptability while maintaining structural integrity and promoting bone regeneration

Inventive Principle:
Principle #15Dynamics

4Reliability

If calcium phosphate materials are used for artificial bone grafts, then properties similar to natural bone are achieved, but ease of handling and flexibility are reduced

Engineering Contradiction:
Improveproperties similar to natural boneVSAvoidease of handling and flexibility
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent modifies the physical and chemical parameters of calcium phosphate materials to improve their handling characteristics while preserving their bone-like properties. This includes adjusting porosity, particle size distribution, and incorporating binding agents that allow the material to be molded and shaped easily during surgery, transforming rigid calcium phosphate into a more versatile, formable graft material

Inventive Principle:
Principle #35Parameter changes

5Strength

If calcium phosphate materials are made rigid to match natural bone, then structural strength is improved, but capacity to serve as liquid carrier/storage media is reduced

Engineering Contradiction:
Improvestructural strengthVSAvoidcapacity as liquid carrier/storage media
Core Design Contradiction:
StrengthVSAdaptability or versatility

Solution Approach 1:

The patent incorporates porous structures within the calcium phosphate bone graft material, creating interconnected void spaces that can hold and release liquid biologics, growth factors, or antibiotics. This porous architecture maintains adequate structural strength for mechanical support while providing reservoirs for controlled drug delivery and enhancing the material's versatility as a carrier system

Inventive Principle:
Principle #31Porous materials

Data Source

PatentEP2493425B1Dynamic bioactive bone graft material and methods for handling
Publication Date: 2016.10.05 PROSIDYAN INC
  • EP2493425B1 patent drawingFigure 1A~1B
  • EP2493425B1 patent drawingFigure 2A~2C
  • EP2493425B1 patent drawingFigure 3A~3B

AI summary

The present disclosure relates to a dynamic bioactive bone graft material and a method of handling the material to prepare an implant. In one embodiment, a method of preparing a dynamic bioactive bone graft implant is provided. The method includes the step of providing a porous, fibrous composition of bioactive glass fibers, wherein the fibers are characterized by fiber diameters ranging from about 5 nanometers to about 100 micrometers, and wherein the porosity of the matrix ranges from about 100 nanometers to about 1 millimeter. The porous, fibrous composition is introduced into a mold tray, and a shaped implant is created using the mold tray. The composition may be wetted with a fluid such as saline or a naturally occurring body fluid like blood prior to creating the shaped implant. In another embodiment, the porous, fibrous composition is provided with the mold tray as a kit.