Hyaluronic Acid Binding Peptide-Polymer System for Joint Lubrication

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Solution Overview

Problem

Current clinical strategies for enhancing tissue lubrication, such as HA injections, are ineffective due to rapid clearance and limited retention of lubricants in tissues like joints, leading to inadequate joint health and lubrication, particularly in osteoarthritis.

Innovation Solution

A biomaterial approach using a synthetic peptide-polymer system to non-covalently bind HA to the tissue surface, creating a self-healing coating that enhances lubrication and retains HA, mimicking the role of lubricin and providing physical and biological benefits.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If HA is injected into the joint to improve synovial lubrication, then the lubrication function is temporarily enhanced, but the HA is rapidly cleared and turnover occurs quickly, leading to short duration of action

Engineering Contradiction:
Improvelubrication functionVSAvoidHA retention time
Core Design Contradiction:
ReliabilityVSDuration of action of moving object

Solution Approach 1:

The patent introduces HA-binding peptides as intermediary molecules that mediate between the injected HA and the joint tissue surface. These peptides bind to HA and anchor it to the tissue, preventing rapid clearance and extending retention time while maintaining lubrication function.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent extracts and utilizes specific binding domains (HA-binding peptides) from larger proteins and incorporates them into a peptide-polymer system. This extracted functional element selectively binds HA and enables targeted retention at the joint surface without requiring the entire native protein structure.

Inventive Principle:
Principle #2Taking out (Extraction)

2Reliability

If HA is injected to enhance lubrication, then the lubrication effect is achieved, but the injection requires precise targeting of areas needing lubrication which is difficult to accomplish

Engineering Contradiction:
Improvelubrication effectVSAvoidtargeting precision
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The HA-binding peptides act as intermediaries that passively target the joint tissue surface through their natural affinity for the extracellular matrix components at the cartilage surface. This eliminates the need for active targeting mechanisms or precise injection positioning, as the peptides automatically guide HA to the appropriate location.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The peptide-polymer system performs self-targeting by utilizing the inherent binding properties of the HA-binding peptides for extracellular matrix components at the joint surface. The system automatically localizes to the tissue surface without requiring external guidance or precise surgical intervention.

Inventive Principle:
Principle #25Self-service

3Reliability

If therapeutic strategies focus only on replacing or enhancing the lubricant in the fluid phase, then the lubrication is temporarily improved, but the tissue surface remains unprotected and the effect is short-lived

Engineering Contradiction:
Improvelubrication improvementVSAvoidtissue surface protection
Core Design Contradiction:
ReliabilityVSDuration of action of stationary object

Solution Approach 1:

The patent applies HA-binding peptides to the tissue surface in advance to create a binding layer before HA injection. This preliminary action prepares the surface to immediately capture and retain HA, extending the duration of both lubrication and surface protection effects.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The HA-binding peptides serve as intermediaries that bridge the lubricant (HA) and the tissue surface, creating a stable interface that simultaneously provides lubrication enhancement and surface protection. This intermediary layer prevents direct contact between HA and the surface while maintaining the lubrication effect.

Inventive Principle:
Principle #24Intermediary (Mediator)

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 HA-binding peptide-polymer system effectively improves boundary lubrication, reduces friction, and prolongs the retention of HA, offering a stable and sustained lubrication solution for joint health, even in diseased states like osteoarthritis, and can be applied to various tissues including the eyes and pleural cavity.

Implementation Method 1

A biomaterial approach using a synthetic peptide-polymer system to non-covalently bind HA to the tissue surface

Methodology Applied
Scientific EffectNon-covalent binding: Adsorption

Implementation Method 2

improves boundary lubrication, reduces friction

Methodology Applied
Scientific EffectBoundary lubrication: Lubrication

Data Source

PatentUS11944637B2Biomaterials comprising hyaluronic acid binding peptides and extracellular matrix binding peptides for hyaluronic acid retention and tissue engineering applications
Publication Date: 2024.04.02 JOHNS HOPKINS UNIVERSITY
  • US11944637B2 patent drawing
  • US11944637B2 patent drawing
  • US11944637B2 patent drawing

AI summary

The present invention provides novel biomaterial compositions and methods having a technology to improve retention of hyaluronic acid (HA). The biomaterial compositions utilize small HA binding peptides and extracellular matrix binding (ECM) peptides that are tethered to synthetic biocompatible polymers. When tethered to the polymers, the peptide region allows the polymers to bind to HA and to tissues such as cartilage. The novel biomaterial compositions can be used to coat or chemically modify cartilage or tissues with a biologically compatible polymer having HA binding peptides, which allow HA to bind to the surface of the cartilage or tissues. Methods of using same are also provided.