SGLT2 Transdermal Patch With Acrylic Adhesive for Sustained Delivery

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Solution Overview

Problem

Current oral administration of SGLT2 inhibitors for Type 2 diabetes is invasive and can cause liver metabolism-related side effects, necessitating a minimally invasive and effective alternative delivery method.

Innovation Solution

A transdermal patch comprising a mixture of SGLT2 inhibitors and an acrylic adhesive, designed with specific adhesion properties and permeation profiles to deliver the drug through the skin over an extended period.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If oral administration of SGLT2 inhibitors is used, then the drug can be delivered systemically, but liver metabolism-related side effects occur

Engineering Contradiction:
Improvetherapeutic efficacyVSAvoidliver metabolism side effects
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent uses the skin and transdermal patch as an intermediary delivery system to transport SGLT2 inhibitors directly into the bloodstream, bypassing the liver's first-pass metabolism. This mediator approach eliminates liver metabolism-related side effects while maintaining therapeutic efficacy through sustained drug release.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Object-affected harmful factors

If transdermal delivery is used, then liver metabolism is bypassed, but sustained delivery over extended periods is challenging

Engineering Contradiction:
Improveliver metabolism side effectsVSAvoiddrug delivery duration
Core Design Contradiction:
Object-affected harmful factorsVSDuration of action of moving object

Solution Approach 1:

The patent employs drug-in-adhesive formulations with carefully controlled drug loading concentrations and adhesive properties to achieve sustained transdermal delivery. By adjusting formulation parameters such as drug concentration, adhesive composition, and patch design, the system maintains stable drug release rates over extended periods (7 days or longer), bypassing liver metabolism while ensuring prolonged therapeutic action.

Inventive Principle:
Principle #35Parameter changes

3Ease of operation

If transdermal patch with drug-in-adhesive is used, then minimally invasive delivery is achieved, but adhesion and permeation properties must be precisely controlled

Engineering Contradiction:
Improveminimally invasive deliveryVSAvoidadhesion and permeation control
Core Design Contradiction:
Ease of operationVSManufacturing precision

Solution Approach 1:

The patent utilizes composite drug-in-adhesive formulations combining SGLT2 inhibitors with specialized acrylic adhesives. This composite material approach integrates both adhesion function and drug delivery capability into a single layer, ensuring precise control over both skin attachment and drug permeation properties while maintaining ease of application as a minimally invasive patch.

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 transdermal patch provides sustained delivery of SGLT2 inhibitors for at least 7 days with reduced liver metabolism, minimizing side effects and maintaining therapeutic efficacy.

Implementation Method 1

designed with specific adhesion properties and permeation profiles to deliver the drug through the skin over an extended period

Methodology Applied
Scientific EffectPermeation: Permeation

Data Source

PatentUS20260069550A1Transdermal delivery of antidiabetic agents
Publication Date: 2026.03.12 RITTENHOUSE CHRISTINE
  • US20260069550A1 patent drawing
  • US20260069550A1 patent drawing
  • US20260069550A1 patent drawing

AI summary

Disclosed herein are compositions and methods for transdermal formulations of antidiabetic agents. An example transdermal formulation contains a SGLT2 inhibitor, and is used for the treatment of Type 2 diabetes.