Bone Graft Composition with Controlled Hydroxypropyl Methylcellulose Dissolution

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Solution Overview

Problem

Existing bone graft materials face limitations in biocompatibility, mechanical properties, and toxicity, particularly in achieving optimal dissolution rates for effective bone formation and adhesion.

Innovation Solution

A bone graft composition incorporating hydroxypropyl methylcellulose with a dissolution rate of 50% or more within 48 hours, combined with a porous bone graft material, is developed. This involves preparing a bone morphogenetic protein solution, adsorbing it onto graft material powder, mixing with hydroxypropyl methylcellulose, and forming a gel structure through freeze-drying to enhance adhesion and biocompatibility.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If hydroxypropyl methylcellulose is used as a binder in bone graft material, then adhesion and biocompatibility are improved, but dissolution rate control becomes difficult leading to either premature dissolution or insufficient bone formation support

Engineering Contradiction:
Improveadhesion and biocompatibilityVSAvoiddissolution rate control
Core Design Contradiction:
ReliabilityVSDuration of action of moving object

Solution Approach 1:

The patent applies parameter changes by precisely controlling the dissolution rate of hydroxypropyl methylcellulose to be 50% or more within 48 hours, and setting the content ratio between hydroxypropyl methylcellulose and bone graft material within 0.3:1 to 3:1. This optimized parameter range ensures the binder dissolves at an appropriate rate to support bone formation while maintaining adhesion and biocompatibility.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite material system combining bone graft material with hydroxypropyl methylcellulose in specific proportions. This composite approach allows the beneficial properties of both materials to work together - the bone graft material provides structural support and osteoconductivity, while the controlled-dissolution hydroxypropyl methylcellulose provides adhesion and biocompatibility, resolving the contradiction between these properties and dissolution control.

Inventive Principle:
Principle #40Composite materials

2Productivity

If bone graft material with porous structure is used, then bone formation and cell infiltration are improved, but mechanical strength and structural stability deteriorate

Engineering Contradiction:
Improvebone formation efficiencyVSAvoidmechanical strength
Core Design Contradiction:
ProductivityVSStrength

Solution Approach 1:

The patent employs composite materials by combining porous bone graft material with hydroxypropyl methylcellulose binder in optimized ratios. The porous structure maintains its osteoconductive properties for bone formation, while the binder provides mechanical reinforcement to compensate for the strength reduction caused by porosity, achieving both high bone formation efficiency and adequate mechanical strength.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent applies local quality by having the hydroxypropyl methylcellulose binder distributed within the porous structure of the bone graft material. The binder locally reinforces the porous framework where needed, providing mechanical strength at the microstructural level while preserving the macroscopic porous architecture that enables bone formation and cell infiltration.

Inventive Principle:
Principle #3Local quality

3Reliability

If hydroxypropyl methylcellulose content is increased to improve adhesion, then biocompatibility is enhanced, but dissolution occurs too quickly reducing structural integrity

Engineering Contradiction:
ImprovebiocompatibilityVSAvoidstructural integrity
Core Design Contradiction:
ReliabilityVSStability of the object's composition

Solution Approach 1:

The patent resolves this contradiction through parameter optimization by establishing that the content ratio of hydroxypropyl methylcellulose to bone graft material should be within 0.3:1 to 3:1, with the dissolution rate controlled at 50% or more within 48 hours. This specific parameter range ensures sufficient biocompatibility and adhesion while preventing premature dissolution that would compromise structural integrity.

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 composition achieves excellent adhesion and biocompatibility, preventing detachment during mastication and ensuring effective bone formation by optimizing the hydroxypropyl methylcellulose content and dissolution rate, thereby improving the efficacy of bone grafting procedures.

Implementation Method 1

the hydroxypropyl methylcellulose reaches a dissolution rate of 50% or more within 48 hours

Methodology Applied
Scientific EffectDissolution: Solvation

Implementation Method 2

adsorbing the bone morphogenetic protein onto graft material powder by mixing the bone morphogenetic protein and the graft material powder

Methodology Applied
Scientific EffectAdsorption: Adsorption

Implementation Method 3

forming a structure containing a plurality of pores by freeze-drying the gel under vacuum

Methodology Applied
Scientific EffectFreeze-drying: Freeze Drying

Data Source

PatentUS12076459B2Bone graft composition and manufacturing method thereof
Publication Date: 2024.09.03 MEDPARK CO LTD
  • US12076459B2 patent drawing
  • US12076459B2 patent drawing
  • US12076459B2 patent drawing

AI summary

The present disclosure relates to a bone graft composition, and more particularly, to a bone graft composition containing hydroxypropyl methylcellulose and a preparation method therefor. Moreover, the present disclosure relates to a bone graft composition that has an optimal composition ratio at which the dissolution rate of hydroxypropyl methylcellulose is excellent.