Crosslinked MHA Hydrogel Hormone Delivery via Dual-Chamber Syringe

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Solution Overview

Problem

Existing hormone therapies face challenges such as inconsistent dosage delivery, adverse effects, and poor compliance due to methods like pills, patches, creams, and injections, while subcutaneous hydrogel formulations face absorption and bioavailability issues, affecting stability and shelf life.

Innovation Solution

A dual chamber syringe is used to administer a crosslinked methacrylate hyaluronic acid (MHA) polymer encapsulating hormones, which is injected subcutaneously to provide a controlled release of micronized testosterone or estradiol, utilizing a hydrogel polymer that forms microbeads for consistent medication delivery.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Duration of action of moving object

If subcutaneous hydrogel formulations are used for hormone delivery, then controlled release is achieved, but absorption and bioavailability issues occur

Engineering Contradiction:
Improvecontrolled release durationVSAvoidabsorption and bioavailability
Core Design Contradiction:
Duration of action of moving objectVSReliability

Solution Approach 1:

The patent uses a composite material system consisting of hydrogel microbeads embedded in a crosslinkable hydrogel matrix. The hydrogel microbeads contain the hormone (testosterone or estradiol) and are composed of biocompatible polymers such as PLGA, PLA, or gelatin. This composite structure enables controlled release through the hydrogel matrix while the microbead formulation improves absorption and bioavailability by protecting the hormone and facilitating gradual release into surrounding tissue.

Inventive Principle:
Principle #40Composite materials

2Stability of the object's composition

If hormone therapies are administered frequently to maintain effective levels, then consistent dosage is achieved, but patient compliance deteriorates

Engineering Contradiction:
Improvedosage consistencyVSAvoidpatient compliance
Core Design Contradiction:
Stability of the object's compositionVSEase of operation

Solution Approach 1:

The patent implements preliminary action by formulating hormones in pre-prepared hydrogel microbeads that are ready for single-step injection. The hydrogel matrix is designed to release the hormone over an extended period (weeks to months), eliminating the need for frequent administrations. This preliminary formulation approach maintains consistent dosage levels while significantly improving patient compliance by reducing the frequency of medical visits and injections.

Inventive Principle:
Principle #10Preliminary action

3Duration of action of moving object

If solubilized hormones are injected frequently, then hormone levels are maintained, but the need for repeated doctor visits increases

Engineering Contradiction:
Improvehormone level maintenanceVSAvoiddoctor visit frequency
Core Design Contradiction:
Duration of action of moving objectVSLoss of time

Solution Approach 1:

The patent extracts the hormone from its conventional solubilized form and incorporates it into solid hydrogel microbead matrices. This extraction from liquid solution to solid encapsulated form allows the hormone to be delivered in a single injection that releases the medication over an extended period. The hydrogel matrix acts as a reservoir, releasing the hormone gradually into the surrounding tissue, thereby maintaining hormone levels for weeks or months without requiring repeated doctor visits.

Inventive Principle:
Principle #2Taking out (Extraction)

4Ease of operation

If pills are used for hormone therapy, then administration is simple, but dosage delivery consistency deteriorates

Engineering Contradiction:
Improveadministration simplicityVSAvoiddosage delivery consistency
Core Design Contradiction:
Ease of operationVSStability of the object's composition

Solution Approach 1:

The patent introduces hydrogel microbeads as an intermediary between the hormone and the patient's body. Instead of administering pills that rely on gastrointestinal absorption (which varies significantly), the hydrogel microbeads are injected subcutaneously and serve as a controlled release mediator. The hydrogel matrix controls the release rate of the hormone, providing consistent dosage delivery while the injection method remains simple and can be performed in a single medical visit.

Inventive Principle:
Principle #24Intermediary (Mediator)

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 method offers a stable, extended-release hormone therapy with improved absorption and bioavailability, reducing the need for frequent doctor visits and enhancing patient compliance by providing consistent hormone levels for up to six months.

Implementation Method 1

a crosslinked methacrylate hyaluronic acid (MHA) polymer that encapsulates a hormone. The crosslinked MHA polymer is the hydrogel polymer

Methodology Applied
Scientific EffectHydrogel: Hydrogel

Implementation Method 2

subcutaneously inserted slow-release hormone therapies (e.g., hormone hydrogels or pellets)... deliver drugs over time in a therapeutically effective dosage

Methodology Applied
Scientific EffectDiffusion: Diffusion

Implementation Method 3

Piercing the separator generates a mixture that includes the diluent and the crosslinked MHA polymer that encapsulates the hormone

Methodology Applied
Scientific EffectMechanical mixing:

Data Source

PatentUS20250319099A1Method of administering a hormone encapsulated by a hydrogel with a dual chamber syringe
Publication Date: 2025.10.16 VITALTE LIFESCIENCES INC
  • US20250319099A1 patent drawing
  • US20250319099A1 patent drawing
  • US20250319099A1 patent drawing

AI summary

A method for administering a hormone encapsulated by a hydrogel polymer with a dual chamber syringe is described. The method includes providing a crosslinked methacrylate hyaluronic acid (MHA) polymer that encapsulates a hormone. The crosslinked MHA polymer is the hydrogel polymer. A dosage of the crosslinked MHA polymer that encapsulates the hormone to a subcutaneous tissue is administered with a dual chamber syringe. The dual chamber syringe includes a first chamber, a second chamber, a separator, and a plunger. The first chamber includes the crosslinked MHA polymer that encapsulates the hormone. The second chamber has a diluent for the crosslinked MHA polymer. The separator separates the first chamber from the second chamber. Piercing or bypassing the separator generates a mixture that includes the diluent and the crosslinked MHA polymer that encapsulates the hormone. The plunger forces the mixture through a needle.