Ophthalmic Microneedle Patch With PVA for Corneal Drug Retention

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Commercial sodium hyaluronate eye drops with a concentration of 0.1% have poor therapeutic effects on severe corneal wounds due to short ocular surface retention time, poor corneal barrier penetration, and poor patient compliance, leading to inflammation and potential blindness.

Innovation Solution

A sodium hyaluronate-containing ophthalmic microneedle patch is prepared by mixing sodium hyaluronate with polyvinyl alcohol (PVA) to enhance mechanical properties, allowing for effective corneal penetration and delivery.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If sodium hyaluronate eye drops with 0.1% concentration are used, then the formulation is simple and safe for mild corneal wounds, but the therapeutic effect is poor for severe corneal wounds due to short ocular surface retention time and poor corneal barrier penetration

Engineering Contradiction:
Improvetherapeutic effectVSAvoidocular surface retention time
Core Design Contradiction:
ReliabilityVSDuration of action of moving object

Solution Approach 1:

The patent changes the concentration parameter of sodium hyaluronate from 0.1% to 0.3%, and transforms the dosage form from liquid eye drops to microneedle patches. This parameter change increases the drug loading amount and enables sustained release, thereby extending ocular surface retention time and improving therapeutic effect for severe corneal wounds

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces polyvinyl alcohol (PVA) as a matrix material to form microneedle patches. PVA serves as an intermediary carrier that enables controlled release of sodium hyaluronate, extending its retention time on the ocular surface and improving corneal barrier penetration through the microneedle delivery system

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If commercial eye drops are used frequently to treat severe corneal wounds, then the ocular surface is continuously exposed to the drug, but patient compliance is poor due to frequent dropping requirements

Engineering Contradiction:
Improvetherapeutic effectVSAvoidpatient compliance
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent loads a high concentration of sodium hyaluronate (0.3%) into microneedle patches in advance, creating a reservoir of drug that releases slowly over time. This preliminary action eliminates the need for frequent application, improving patient compliance while maintaining continuous therapeutic effect for severe corneal wounds

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The microneedle patches are designed as disposable single-use devices. Each patch contains sufficient drug loading to treat severe corneal wounds without requiring repeated applications, simplifying the treatment regimen and improving patient compliance

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

3Ease of manufacture

If sodium hyaluronate is used to prepare microneedle patches alone, then the formulation is simple, but the needle formation rate is low and the hardness is insufficient

Engineering Contradiction:
Improveformulation simplicityVSAvoidneedle formation rate
Core Design Contradiction:
Ease of manufactureVSManufacturing precision

Solution Approach 1:

The patent creates a composite matrix system by combining sodium hyaluronate (0.3%) with polyvinyl alcohol (PVA). This composite material approach maintains formulation simplicity while significantly improving needle formation rate and mechanical hardness, enabling successful microneedle patch manufacturing

Inventive Principle:
Principle #40Composite materials

4Ease of manufacture

If sodium hyaluronate is used to prepare microneedle patches alone, then the formulation is simple, but the mechanical strength and flexibility are insufficient

Engineering Contradiction:
Improveformulation simplicityVSAvoidmechanical strength
Core Design Contradiction:
Ease of manufactureVSStrength

Solution Approach 1:

The patent develops a composite matrix comprising sodium hyaluronate and PVA in specific ratios. This composite material provides both mechanical strength for needle integrity and flexibility for comfortable ocular application, while keeping the formulation process simple and scalable

Inventive Principle:
Principle #40Composite materials

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 microneedle patch demonstrates strong mechanical properties, flexibility, and efficient delivery of sodium hyaluronate to the corneal tissue, effectively treating severe corneal wounds and reducing inflammation.

Implementation Method 1

Because carboxyl and hydroxyl groups in a molecular structure of sodium hyaluronate can form hydrogen bonds with water, sodium hyaluronate exhibits excellent water-retention properties

Methodology Applied
Scientific EffectHydrogen bonding:

Implementation Method 2

Microneedles are a minimally-invasive and painless drug delivery manner with a length of 25 μm to 2,000 μm, which can effectively break the physical barrier of a tissue and efficiently deliver a drug to a target site

Methodology Applied
Scientific EffectPhysical barrier disruption:

Implementation Method 3

Sodium hyaluronate eye drops can bind to fibronectin to enhance the adhesion and extensibility of corneal epithelial cells and improve the self-repair ability of corneas

Methodology Applied
Scientific EffectMolecular adhesion: Adhesive

Data Source

PatentUS20250367421A1Sodium hyaluronate-containing ophthalmic microneedle patch, and preparation method and use thereof
Publication Date: 2025.12.04 WENZHOU MEDICAL UNIV
  • US20250367421A1 patent drawing
  • US20250367421A1 patent drawing
  • US20250367421A1 patent drawing

AI summary

Provided is a sodium hyaluronate-containing ophthalmic microneedle patch, and a preparation method and use thereof. The preparation method includes: preparing a microneedle patch matrix solution, where the microneedle patch matrix solution includes sodium hyaluronate and polyvinyl alcohol (PVA); and dropping the microneedle patch matrix solution into a microneedle patch mold, drying, and then demolding to obtain the sodium hyaluronate-containing ophthalmic microneedle patch.