Compressed Bone Graft Composition for Faster Implant Integration

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Solution Overview

Problem

Current bone graft materials face challenges such as difficulty in retaining shape, poor blood vessel ingrowth, and undesirable reactions due to the use of bonding substances like glycerol, and require time to heal before tooth implant placement.

Innovation Solution

A bone graft composition is developed using decalcified cortical bone particles that are freeze-dried or hypothermically dehydrated under pressure to form a solid construct without bonding compounds, allowing for rapid bone healing and integration with metallic implants.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If particulate bone allografts are made into paste or past-like material by mixing with bonding substances, then handling characteristics are improved, but the matrices holding the particles become dense and make blood vessel ingrowth difficult to penetrate

Engineering Contradiction:
Improvehandling characteristicsVSAvoidblood vessel ingrowth
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The patent uses a porous collagen sponge matrix instead of dense paste to hold bone particles. The porous structure allows blood vessel ingrowth while maintaining handling characteristics, directly resolving the contradiction between ease of operation and reliability for vascularization.

Inventive Principle:
Principle #31Porous materials

2Ease of operation

If bonding substances such as glycerol are used to hold bone particles, then handling characteristics are improved, but undesirable reactions are produced

Engineering Contradiction:
Improvehandling characteristicsVSAvoidundesirable reactions
Core Design Contradiction:
Ease of operationVSObject-generated harmful factors

Solution Approach 1:

The patent extracts and eliminates harmful bonding substances like glycerol from the bone graft composition. The collagen sponge matrix provides binding functionality without the harmful chemical reactions, resolving the contradiction between ease of operation and harmful factors.

Inventive Principle:
Principle #2Taking out (Extraction)

3Ease of operation

If demineralized bone particles are formed into putties, gels or pastes to improve handling characteristics, then handling is improved, but time must be given to heal before placement of tooth implants

Engineering Contradiction:
Improvehandling characteristicsVSAvoidhealing time
Core Design Contradiction:
Ease of operationVSLoss of time

Solution Approach 1:

The patent creates a composite material combining collagen sponge with bone particles (allograft, xenograft, or autograft). This composite provides immediate structural integrity and handling characteristics while supporting rapid bone healing, eliminating the need for extended healing periods before implant placement.

Inventive Principle:
Principle #40Composite materials

4Reliability

If particulate bone allograft is used, then bone grafting is achieved, but the material is difficult to retain in place

Engineering Contradiction:
Improvebone grafting functionVSAvoidretention in place
Core Design Contradiction:
ReliabilityVSStability of the object's composition

Solution Approach 1:

The patent applies preliminary action by pre-forming the bone particles into a stable collagen sponge matrix structure before implantation. This pre-structuring ensures the material retains its position during and after implantation while maintaining osteoconductive properties for bone grafting.

Inventive Principle:
Principle #10Preliminary action

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 composition provides superior osteoconduction, rapid bone healing, and stable anchorage, eliminating the need for bonding materials and reducing healing time, while promoting new bone growth and integration with dental implants.

Implementation Method 1

dried by freeze-drying or hypothermic dehydration to remove water content and bind the osseous material into a solid structure

Methodology Applied
Scientific EffectFreeze-drying: Freeze Drying

Implementation Method 2

dried by freeze-drying or hypothermic dehydration to remove water content and bind the osseous material into a solid structure

Methodology Applied
Scientific EffectHypothermic dehydration: Desiccation

Implementation Method 3

packed into a constraining device or placed under pressure between plates of various materials and then dried by freeze-drying or hypothermic dehydration to remove water content and bind the osseous material into a solid structure

Methodology Applied
Scientific EffectCompression: Compression

Data Source

PatentUS20250360247A1Treated osseous particulate fluff composition
Publication Date: 2025.11.27 MALININ THEODORE
  • US20250360247A1 patent drawing
  • US20250360247A1 patent drawing
  • US20250360247A1 patent drawing

AI summary

A method of making a bone graft composition is described wherein material including decalcified bone elongated particulate bone is dried in a constraining device or under pressure to produce a solid construct having dimensions corresponding to the constraining device or space to which the material occupied under pressure.