Dense Collagen–Hydroxyapatite Compositions for Injectable Bone Repair
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Solution Overview
Problem
Existing injectable and implantable compositions for mineralized tissue repair and regeneration, such as bone, lack biomimetic properties, mechanical strength, and are not easily injectable, often requiring chemical crosslinking that can cause inflammation and poor biological response.
Innovation Solution
A composition comprising dense collagen microparticles (>90% collagen) combined with biomimetic hydroxyapatite or its precursors and a physiologically compatible aqueous solvent, allowing for injectable and implantable mineralized tissue substitutes that mimic bone ultrastructure and promote host cell colonization without inflammation.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Ease of operation
If low concentrated collagen is used to form injectable microspheres, then injectability is improved, but mechanical strength and structural stability deteriorate due to fragility requiring chemical crosslinking
Solution Approach 1:
The patent combines high concentrated collagen with hydroxyapatite to form a composite material that achieves both injectability and mechanical strength. The hydroxyapatite particles act as a reinforcing phase that provides structural stability to the collagen matrix, eliminating the need for chemical crosslinking while maintaining structural integrity during injection and implantation.
Solution Approach 2:
The patent changes the concentration parameter of collagen from low (in existing microspheres) to high (in the new composition), enabling the formation of a structurally stable matrix that can be injected and implanted without chemical crosslinking. The high collagen concentration allows the material to maintain its shape and mechanical properties while remaining injectable.
2Stability of the object's composition
If chemical crosslinking is applied to stabilize low concentrated collagen microspheres, then structural stability is improved, but biological response deteriorates due to inflammation from residual crosslinking agents
Solution Approach 1:
The patent extracts and eliminates the need for chemical crosslinking agents by using high concentrated collagen combined with hydroxyapatite. The high collagen concentration and hydroxyapatite reinforcement provide structural stability through physical rather than chemical means, removing the source of inflammation and improving biocompatibility.
3Ease of operation
If low concentrated collagen is used for injectability, then ease of injection is improved, but ability to form bone-like 3D architecture deteriorates because collagen self-assembly threshold is not reached
Solution Approach 1:
The patent changes the collagen concentration parameter from low to high, exceeding the self-assembly threshold required for forming bone-like 3D architecture. The high concentrated collagen naturally assembles into fibrillar structures that mimic native bone extracellular matrix, while the material remains injectable due to its formulation and the reinforcing effect of hydroxyapatite.
4Shape
If high concentrated collagen is used to form bone-like ultrastructure, then biomimetic properties are improved, but injectability deteriorates due to high viscosity
Solution Approach 1:
The patent creates a composite material combining high concentrated collagen with hydroxyapatite particles. The hydroxyapatite acts as a space-filling reinforcement that allows the high concentrated collagen to maintain its bone-like ultrastructure while reducing the overall viscosity and improving injectability of the composition.
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 biocompatible, biomimetic mineralized tissue substitutes with improved mechanical properties and adhesion, facilitating rapid tissue regeneration and bone repair without the need for chemical crosslinking.
Implementation Method 1
the 3D organization of highly concentrated collagen materials appears as a sine qua non condition to mimic the ultrastructure of biological tissues
Implementation Method 2
the mineralization of highly concentrated collagen matrices promotes both the formation of biomimetic hydroxyapatite nanoplatelets and their co-alignment with collagen fibrils
Data Source
AI summary
The present disclosure relates to injectable or implantable compositions that are able to mimic different types of mineralized biological tissues and their uses in mineralized tissues repair and regeneration.


