PEEK/Zeolite/Ion Implants for Small Joint and Bony Defects

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Solution Overview

Problem

Current joint and bony segment replacements, including small and large joints, face challenges in customization, biologic microenvironment manipulation, and structural integrity, particularly in cases of bone loss or complex reconstructive scenarios.

Innovation Solution

Utilizing additive manufacturing with PEEK/zeolite/ion (PZI) material, where different heavy metal ions are used to provide varying properties to different implant surfaces, enhancing biologic activity and structural support, such as encouraging soft tissue or bony tissue formation, and providing antimicrobial environments.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional joint replacement materials (cadaveric sections, homologous anatomy, or 3D-printed titanium) are used, then structural strength is provided, but biologic compatibility and localized biologic activity are insufficient

Engineering Contradiction:
Improvebiologic compatibilityVSAvoidlocalized biologic activity
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent applies local quality by incorporating different heavy metal ions (copper, zinc, silver, strontium, sodium) at different locations within the PZI material structure. Each ion provides specific localized functions: copper for soft tissue formation, zinc for bony tissue formation, silver for antimicrobial activity, strontium for bone regeneration, and sodium for ion exchange with the surrounding environment. This spatial differentiation of ionic components enables the implant to perform multiple localized biologic activities simultaneously.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent employs composite materials by combining PEEK polymer with zeolite and multiple heavy metal ions to create the PZI material system. This composite structure integrates the structural properties of PEEK, the ion-exchange capabilities of zeolite, and the specific biologic activities of different metal ions, achieving both structural strength and enhanced biologic compatibility with localized functionality.

Inventive Principle:
Principle #40Composite materials

2Strength

If 3D-printed titanium is used for bony segment replacements, then structural integrity is maintained, but customization and biologic microenvironment manipulation are limited

Engineering Contradiction:
Improvestructural integrityVSAvoidbiologic microenvironment manipulation
Core Design Contradiction:
StrengthVSAdaptability or versatility

Solution Approach 1:

The patent applies parameter changes by modifying the chemical composition of the implant material from pure titanium to PZI material containing multiple heavy metal ions. This compositional parameter change enables the material to actively manipulate the biologic microenvironment through ion release, influencing processes such as bone formation, soft tissue regeneration, and microbial inhibition, while maintaining structural integrity through the additive manufacturing process.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent transitions from homogeneous titanium to composite PZI material, combining PEEK polymer, zeolite framework, and multiple heavy metal ions. This composite structure provides both the structural integrity needed for load-bearing applications and the chemical versatility to manipulate the biologic microenvironment through controlled ion release.

Inventive Principle:
Principle #40Composite materials

3Ease of manufacture

If homogeneous implant materials are used, then manufacturing simplicity is maintained, but surface-specific biologic functions cannot be provided

Engineering Contradiction:
Improvemanufacturing simplicityVSAvoidsurface-specific biologic functions
Core Design Contradiction:
Ease of manufactureVSAdaptability or versatility

Solution Approach 1:

The patent implements local quality by distributing different heavy metal ions to different surfaces or regions of the implant corresponding to different biologic requirements. For example, copper may be concentrated at articular surfaces for soft tissue formation, zinc at bony attachment sites for osteogenesis, and silver in regions prone to infection for antimicrobial protection. The additive manufacturing process enables this spatial distribution while maintaining a single integrated manufacturing step.

Inventive Principle:
Principle #3Local quality

4Strength

If current joint replacement options are used, then immediate structural support is provided, but long-term biologic integration and customization for complex reconstructive challenges are insufficient

Engineering Contradiction:
Improvestructural supportVSAvoidbiologic integration
Core Design Contradiction:
StrengthVSReliability

Solution Approach 1:

The patent uses composite PZI material that combines the structural properties of PEEK and titanium-like strength with the biologic activity of multiple metal ions. This composite enables both immediate structural support upon implantation and long-term biologic integration through controlled ion release that promotes osseointegration, soft tissue attachment, and resistance to infection over time.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent applies self-service by enabling the implant material to actively participate in its own integration with surrounding tissues. The heavy metal ions in the PZI material autonomously perform functions such as stimulating bone formation, promoting soft tissue regeneration, and inhibiting microbial growth without requiring additional surgical interventions or external treatments, thereby enhancing long-term biologic integration.

Inventive Principle:
Principle #25Self-service

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

Customizable implants with PZI material offer improved biologic compatibility, structural strength, and localized biologic activity, addressing the limitations of existing technologies in joint and bony segment replacements.

Implementation Method 1

The ion in the at least one PZI material may be sodium, and an ion exchange may result with a surrounding environment to provide uniform properties at all surfaces where the at least one PZI material is introduced

Methodology Applied
Scientific EffectIon exchange: Ion Exchange

Implementation Method 2

The ion in the at least one PZI material may be copper which encourages soft tissue formation when at the at least one PZI material is applied to cartilaginous surfaces

Methodology Applied
Scientific EffectBiologic tissue formation:

Implementation Method 3

The ion in the at least one PZI material may be zinc, strontium, or a combination of the same which encourages bony tissue formation

Methodology Applied
Scientific EffectBiologic tissue formation:

Implementation Method 4

The ion in the at least one PZI material may be silver which provides an antimicrobial environment

Methodology Applied
Scientific EffectAntimicrobial effect:

Implementation Method 5

utilizing additive manufacturing (e.g., 3D printing) of various anatomic constructs with PEEK/zeolite/ion (PZI) material

Methodology Applied
Scientific EffectAdditive manufacturing: 3D Printing

Data Source

PatentUS20250312160A1Apparatus and Methods for Small Joint and Bony Defect Replacement
Publication Date: 2025.10.09 KRAEMER PAUL E

AI summary

Apparatus and methods for joint and bony segment replacement may utilize additive manufacturing (e.g., 3D printing) of various anatomic constructs with PEEK/zeolite/ion (PZI) material. Heavy metal ion loading options may be utilized which may provide differing properties to different surfaces of the resultant apparatus. Moreover, using the PZI material, the apparatus being implanted in joint and bony segment replacement may favorably manipulate the biologic microenvironment in which it may be implanted. Further, through use of PZI material, current large joint replacement options also may be disrupted including, but not limited to, modifications of the joint replacement itself, and the augments and supporting joint reconstruction devices used in bone loss situations. Methods for joint and bony segment replacement may provide mixing two or more types of PZI material together through an additive manufacturing process; and introducing the mixture as part of an implantable apparatus.