Gold Cluster Drugs for Glaucoma Beyond Intraocular Pressure

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Solution Overview

Problem

Current clinical treatments for glaucoma primarily focus on reducing intraocular pressure, which is insufficient to prevent progressive optic nerve damage and retinal ganglion cell apoptosis, as evidenced by the continued worsening of optic nerve function despite controlled pressure, and no effective drugs exist to inhibit amyloid-beta (Aβ) aggregation that contributes to optic nerve damage.

Innovation Solution

The application of gold clusters (AuCs) with specific ligands, such as L-cysteine derivatives, to inhibit Aβ aggregation and protect optic nerve function, administered through oral, injection, or local eye drops, demonstrating efficacy in in vitro and animal models by reducing RGCs apoptosis and improving visual function.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Stress or pressure

If intraocular pressure is reduced through clinical treatment, then the early predisposing factor for optic nerve damage is addressed, but progressive optic nerve damage and retinal ganglion cell apoptosis continue to worsen

Engineering Contradiction:
Improveintraocular pressureVSAvoidoptic nerve function
Core Design Contradiction:
Stress or pressureVSReliability

Solution Approach 1:

The patent uses small molecule compounds as intermediaries that can cross the blood-retina barrier and blood-brain barrier to directly act on retinal ganglion cells and optic nerve tissue. These compounds serve as mediators between systemic administration and the protected neural tissue, enabling neuroprotection independent of intraocular pressure control.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent changes the therapeutic approach from pressure-based treatment to molecular-based treatment by administering specific small molecule compounds that modify cellular parameters such as apoptosis resistance, oxidative stress resistance, and neurotrophic factor expression in retinal ganglion cells.

Inventive Principle:
Principle #35Parameter changes

2Device complexity

If no effective drugs are used to inhibit Aβ aggregation, then the current treatment regimen is simple, but optic nerve damage progresses due to Aβ accumulation and aggregation

Engineering Contradiction:
Improvetreatment regimen complexityVSAvoidAβ aggregation
Core Design Contradiction:
Device complexityVSObject-affected harmful factors

Solution Approach 1:

The patent extracts and targets the specific pathological mechanism of Aβ aggregation in glaucoma by using small molecule compounds that selectively bind to and inhibit Aβ aggregation. This extracts the harmful Aβ aggregation process from the complex glaucoma pathology and addresses it directly.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent employs composite therapeutic compounds that combine multiple functional moieties - including Aβ aggregation inhibition, antioxidant activity, and neurotrophic support - into single small molecule entities that can simultaneously address multiple pathological factors in glaucoma.

Inventive Principle:
Principle #40Composite materials

Data Source

PatentUS12377167B2Application of AuCs or substances containing AuCs in the preparation of drugs for preventing and/or treating glaucoma
Publication Date: 2025.08.05 SHENZHEN PROFOUND VIEW PHARMA TECH CO LTD
  • US12377167B2 patent drawing
  • US12377167B2 patent drawing
  • US12377167B2 patent drawing

AI summary

Disclosed is the use of a gold cluster or a gold cluster-containing substance in the preparation of a drug for preventing and/or treating glaucoma.