Transdermal Patch for TBI Neuropsychiatric Symptoms

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current treatments lack effective methods for preventing or alleviating neuropsychiatric symptoms and psychiatric disorders associated with traumatic brain injury (TBI) and related disorders, particularly with no FDA-approved medication-based therapies for acute stress reactions or cognitive symptoms.

Innovation Solution

A matrix-type transdermal patch containing opipramol, administered in effective dosages ranging from 5-500 mg per day, which can increase bioavailability by 20-50% to 5-fold compared to oral forms, and can be used alone or in combination with additional therapeutic agents to treat TBI-related disorders.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If oral dosage form of opipramol is used, then the treatment is simple to administer, but the bioavailability is low (20-50% lower than transdermal)

Engineering Contradiction:
Improveease of administrationVSAvoidbioavailability
Core Design Contradiction:
Ease of operationVSQuantity of substance

Solution Approach 1:

The patent introduces the skin as an intermediary delivery route between oral administration and systemic circulation. The transdermal patch uses the skin's natural permeability to deliver opipramol directly into the bloodstream, bypassing the gastrointestinal tract and first-pass metabolism, thereby achieving higher bioavailability while maintaining ease of use through simple patch application.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent changes the administration route parameter from oral to transdermal. This parameter change fundamentally alters the pharmacokinetic profile of opipramol, increasing bioavailability by 20-50% while maintaining simplicity of administration through the user-friendly patch application process.

Inventive Principle:
Principle #35Parameter changes

2Device complexity

If oral dosage form of opipramol is used, then the formulation is simple, but the drug delivery is not sustained

Engineering Contradiction:
Improveformulation complexityVSAvoidduration of drug delivery
Core Design Contradiction:
Device complexityVSDuration of action of moving object

Solution Approach 1:

The patent segments the drug delivery process into controlled stages through the transdermal patch structure. The patch contains opipramol in a matrix that gradually releases the drug through the skin over an extended period, providing sustained delivery without requiring complex formulation changes to the active ingredient itself.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The transdermal patch enables continuous drug delivery through the skin, maintaining therapeutic levels of opipramol in the bloodstream over an extended period. This continuous delivery mechanism addresses the limitation of oral dosing intervals while avoiding the need for complex sustained-release oral formulations.

Inventive Principle:
Principle #20Continuity of useful action

3Quantity of substance

If transdermal patch is used, then the bioavailability is increased (20-50% increase), but the device complexity increases

Engineering Contradiction:
ImprovebioavailabilityVSAvoiddevice complexity
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The patent employs a disposable transdermal patch that is applied once and removed after a set period. This disposable approach achieves high bioavailability through transdermal delivery while keeping the device relatively simple in structure. The patch is designed for single-use, eliminating the need for complex reusable components, storage systems, or adjustment mechanisms.

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

4Duration of action of moving object

If transdermal patch is used, then the drug delivery is sustained, but the manufacturing complexity increases

Engineering Contradiction:
Improveduration of drug deliveryVSAvoidmanufacturing ease
Core Design Contradiction:
Duration of action of moving objectVSEase of manufacture

Solution Approach 1:

The transdermal patch utilizes a porous or semi-permeable matrix material that allows controlled diffusion of opipramol from the patch reservoir through the skin. This porous structure enables sustained drug delivery through passive diffusion gradients, achieving extended release without requiring complex manufacturing processes such as controlled-release coating applications or multi-layer lamination systems.

Inventive Principle:
Principle #31Porous 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 transdermal patch effectively reduces neuropsychiatric symptoms and psychiatric disorders associated with TBI by increasing bioavailability and providing sustained drug delivery, offering a potential solution for treating TBI-related disorders with improved efficacy compared to oral administration.

Implementation Method 1

administering a matrix-type transdermal patch with a composition consisting of opipramol

Methodology Applied
Scientific EffectTransdermal absorption: Absorption (physical)

Data Source

PatentUS20230381195A1Methods and compositions for the treatment of traumatic brain injury (TBI) and related disorders
Publication Date: 2023.11.30 MEHRA AKHIL

AI summary

The present invention relates to methods for the treatment or prevention of symptoms associated with traumatic brain injury (TBI) and related disorders. The present disclosure provides compositions and methods for preventing, ameliorating, or alleviating neuropsychiatric symptoms and psychiatric disorders associated with TBI and related disorders consisting of administering a matrix-type transdermal patch with a composition consisting of opipramol, excluding any other component such as a pharmaceutical carrier or excipient.