Biologic Glaucoma Stent for Aqueous Outflow Without Tissue Damage

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Solution Overview

Problem

Current ab interno stenting devices for glaucoma treatment using non-biological hardware materials cause erosion, fibrosis, and ocular tissue damage such as endothelial cell loss.

Innovation Solution

Implantation of a minimally invasive, bio-tissue stent in the eye, positioned in suprachoroidal, trans-scleral, and/or supraciliary locations, utilizing biologically-derived materials like autograft, allograft, or xenograft tissue, engineered to provide aqueous humor drainage through the anterior chamber to uveoscleral pathways, with optional therapeutic agents.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Strength

If non-biological hardware materials are used for stenting devices, then structural strength and durability are improved, but tissue damage and biocompatibility worsen

Engineering Contradiction:
Improvestructural strengthVSAvoidtissue damage
Core Design Contradiction:
StrengthVSObject-affected harmful factors

Solution Approach 1:

The patent changes the material parameter from non-biological hardware materials to biologically-derived materials. This parameter change maintains sufficient structural strength for stenting while eliminating the harmful effects of erosion, fibrosis, and endothelial cell loss associated with synthetic materials.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses composite material structures where biologically-derived materials are combined with or replaced non-biological components. The implant may include biologically-derived material in combination with therapeutic agents or structural elements that provide both strength and biocompatibility.

Inventive Principle:
Principle #40Composite materials

2Manufacturing precision

If non-biological hardware materials are used for stenting devices, then manufacturing precision is improved, but biocompatibility and safety worsen

Engineering Contradiction:
Improvedevice precisionVSAvoidbiocompatibility
Core Design Contradiction:
Manufacturing precisionVSReliability

Solution Approach 1:

The patent changes the material composition parameter from synthetic polymers and metals to biologically-derived materials such as corneal stroma, scleral tissue, or other extracellular matrix materials. This maintains manufacturing precision through controlled tissue processing while dramatically improving biocompatibility and safety profiles.

Inventive Principle:
Principle #35Parameter changes

3Reliability

If biologically-derived materials are used for implants, then biocompatibility is improved, but material availability and processing complexity worsen

Engineering Contradiction:
ImprovebiocompatibilityVSAvoidprocessing complexity
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent employs preliminary action by pre-processing biologically-derived materials into implantable forms before surgery. Tissue patches are harvested, processed, and prepared in advance, allowing the actual surgical implantation to be simpler and more straightforward despite the complexity of material preparation.

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

Reduces tissue damage risks while enhancing aqueous outflow, improving biocompatibility and safety over conventional hardware-based implants.

Implementation Method 1

The biologically-derived material can have a permeability and/or firm structure allowing for aqueous outflow from the eye when the implant cut from the patch of material is positioned within a cyclodialysis cleft

Methodology Applied
Scientific EffectPermeability: Permeation

Data Source

PatentUS12558259B2Implantable biologic stent and system for biologic material shaping and preparation in the treatment of glaucoma
Publication Date: 2026.02.24 IANTREK INC
  • US12558259B2 patent drawing
  • US12558259B2 patent drawing
  • US12558259B2 patent drawing

AI summary

A system for preparation of an implant and ab interno insertion of the implant into an eye including a handle having one or more actuators and an elongated shaft having an outer sheath and an elongate member positioned within a lumen of the tubular outer sheath. The system includes a recess sized for holding a patch of material fixed relative to the handle and a cutting member movable relative to the handle and to the recess. The cutting member cuts the patch of material into an implant as the cutting member moves towards a cutting configuration. The implant, once cut, is axially aligned with the lumen of the tubular outer sheath. The inner elongate member is movable relative to the tubular outer sheath to advance the implant into a deployment position in the lumen of the tubular outer sheath for delivery into the eye. Related devices and methods are provided.