Modified Hyaluronic Acid Joint Injection for Chronic Pain Relief

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Solution Overview

Problem

Current treatments for osteoarthritis and rheumatoid arthritis, particularly those involving injections, impose a significant physical and psychological burden on patients due to frequent administration requirements, which is burdensome for chronic symptoms lasting 12 weeks or more, and existing methods fail to provide adequate long-term pain relief.

Innovation Solution

A composition containing modified hyaluronic acid with a covalently bonded anti-inflammatory compound, administered as an injection every four weeks or more, which provides sustained pain relief and improved joint function without the need for frequent injections.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If steroids or non-steroidal anti-inflammatory compounds are administered frequently to maintain sufficient medicinal effect, then pain relief effectiveness is improved, but patient burden and compliance deteriorate

Engineering Contradiction:
Improvepain relief effectivenessVSAvoidpatient burden
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent combines hyaluronic acid (which provides long-lasting joint lubrication and structural support) with anti-inflammatory compounds (steroids or non-steroidal anti-inflammatory drugs) into a single injection formulation. This merging allows the anti-inflammatory component to provide immediate pain relief while the hyaluronic acid component ensures sustained therapeutic effect, eliminating the need for frequent separate administrations of anti-inflammatory drugs.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The formulation is designed so that the anti-inflammatory compound provides immediate preliminary action upon injection to rapidly control acute inflammation and pain, while the hyaluronic acid component establishes a long-term therapeutic foundation that maintains joint function over several weeks, reducing the need for repeated interventions.

Inventive Principle:
Principle #10Preliminary action

2Duration of action of moving object

If injections are administered frequently to treat chronic joint disease, then medicinal effect is maintained, but physical and psychological burden on patient increases

Engineering Contradiction:
Improveeffect durationVSAvoidpatient burden
Core Design Contradiction:
Duration of action of moving objectVSEase of operation

Solution Approach 1:

By merging hyaluronic acid (providing sustained structural support and lubrication for several weeks) with anti-inflammatory compounds in a single injection, the formulation achieves both immediate and long-term therapeutic effects, reducing the frequency of required administrations and thereby decreasing patient burden.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The combined formulation ensures continuous therapeutic action through the synergistic effects of both components: the anti-inflammatory compound addresses acute symptoms immediately, while the hyaluronic acid maintains joint function continuously over several weeks, providing uninterrupted therapeutic coverage without requiring frequent re-administration.

Inventive Principle:
Principle #20Continuity of useful action

Data Source

PatentEP3597198B1Composition for treating joint diseases and kit including same
Publication Date: 2024.06.12 SEIKAGAKU KOGYO CO LTD
  • EP3597198B1 patent drawing
  • EP3597198B1 patent drawing
  • EP3597198B1 patent drawing

AI summary

The present invention pertains to a composition for treating joint diseases and a kit including the same, and the purpose of the present invention is to provide a composition for treating joint diseases which can be used in patients with joint diseases, and a kit which includes the same. The present invention minimizes the burden on patients with chronic joint diseases while also achieving excellent medicinal effects by means of a composition for treating joint diseases which includes a modified hyaluronic acid having a group derived from an anti-inflammatory compound or a pharmaceutically acceptable salt of the modified hyaluronic acid, and which is used by being administered to patients with human joint diseases as a single injection per period of four or more weeks.