Copper Eye Drops for Corneal Cross-Linking in Myopia Control

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Solution Overview

Problem

Myopia, characterized by a slightly elongated eyeball causing light focus in front of the retina, leads to impaired distance vision and increases the risk of retinal detachment, cataracts, and glaucoma, with a rising global prevalence.

Innovation Solution

Administration of a therapeutically effective amount of a copper-containing agent, such as copper sulfate, to increase lysyl oxidase activity and enhance corneal cross-linking, thereby increasing corneal stiffness and flattening the myopic cornea.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Strength

If copper-containing agent is administered to increase corneal stiffness, then myopic progression is reduced, but corneal over-flattening and irregular astigmatism may occur

Engineering Contradiction:
Improvecorneal stiffnessVSAvoidcorneal curvature
Core Design Contradiction:
StrengthVSShape

Solution Approach 1:

The patent applies parameter changes by carefully controlling the concentration of copper-containing agent (0.001% to 0.01%) and the treatment frequency (1-4 times daily) to achieve optimal corneal stiffening while avoiding excessive flattening. The treatment duration is also controlled (4-16 weeks) to prevent over-correction and irregular astigmatism development.

Inventive Principle:
Principle #35Parameter changes

2Strength

If copper-containing agent is administered to enhance corneal cross-linking, then corneal biomechanical properties are improved, but potential toxicity and side effects may arise

Engineering Contradiction:
Improvecorneal biomechanical propertiesVSAvoidtoxicity and side effects
Core Design Contradiction:
StrengthVSObject-affected harmful factors

Solution Approach 1:

The patent uses parameter changes by optimizing the copper-containing agent concentration within a safe range (0.001% to 0.01%) that is sufficient to enhance corneal cross-linking and biomechanical properties but low enough to avoid copper toxicity and adverse side effects. This controlled dosing strategy balances therapeutic efficacy with safety.

Inventive Principle:
Principle #35Parameter changes

3Measurement precision

If traditional myopia treatments are used, then distance vision is corrected, but myopic progression continues and complications risk increases

Engineering Contradiction:
Improvedistance vision correctionVSAvoidmyopia progression control
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The patent applies preliminary action by administering copper-containing eye drops before significant myopic progression or complications occur. The treatment proactively strengthens corneal biomechanical properties and reduces axial elongation tendencies, preventing further myopia development and associated complications rather than merely correcting the refractive error.

Inventive Principle:
Principle #10Preliminary action

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 copper treatment enhances corneal biomechanical properties, reducing myopic progression and potentially preventing complications like retinal detachment and cataracts.

Implementation Method 1

increase lysyl oxidase activity in an eye of a subject or otherwise increase corneal cross-linking

Methodology Applied
Scientific EffectLysyl oxidase activity: Enzyme

Implementation Method 2

enhance corneal cross-linking, thereby increasing corneal stiffness

Methodology Applied
Scientific EffectCorneal cross-linking: Chemical Bonding

Data Source

PatentUS12544400B2Treatment of myopic progression
Publication Date: 2026.02.10 UNIV OF UTAH RES FOUND
  • US12544400B2 patent drawing
  • US12544400B2 patent drawing
  • US12544400B2 patent drawing

AI summary

An ophthalmic composition or dosage form can include a therapeutically effective amount of a copper-containing agent that is sufficient to increase corneal lysyl oxidase activity in an eye of a subject in an amount sufficient to treat myopic progression and a pharmaceutically acceptable carrier. The composition or dosage form can be used to treat or prevent progression of myopia by administering a therapeutically effective amount of the composition to an eye of a subject during a treatment period.