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Transdermal Delivery Formulations

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Summary

USPTO published patent application US20260090981A1 for LifeActive, Inc., covering transdermal delivery formulations combining weak organic acids with fatty acid microemulsions for epicutaneous administration of therapeutic agents, drugs, and nutrients. The formulations are designed for use in high humidity conditions such as showers or saunas.

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What changed

USPTO published patent application US20260090981A1 (Application No. 19411114, filed December 5, 2025) for LifeActive, Inc. The application discloses transdermal delivery formulations comprising a homogeneous mixture of a transdermal accelerant (weak organic acid with pKa greater than 2.0) and a microemulsion (nonionic emulsifier, water, cis-unsaturated long-chain fatty acid). The formulations create fatty acid micelles and liposomes for encapsulating drugs, nutrients, or therapeutic compounds, with pH typically ranging from 1.5 to 2.5.

This is a patent application publication providing intellectual property notice. No compliance actions, deadlines, or penalties are associated with this document. Entities developing transdermal delivery technologies may wish to conduct freedom-to-operate analyses to assess potential infringement risks. Patent prosecution timelines vary and do not create regulatory obligations.

Archived snapshot

Apr 2, 2026

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TRANSDERMAL DELIVERY FORMULATIONS

Application US20260090981A1 Kind: A1 Apr 02, 2026

Assignee

LifeActive, Inc.

Inventors

Calvin Dexter MORRIS, Burgess A. THOMASSON, JR., Scott A. JENKINS

Abstract

Provided are transdermal delivery formulations, and methods for the manufacture thereof, for the epicutaneous administration of therapeutic agents, drugs, and nutrients to human subjects; veterinary animals; domesticated or undomesticated animals, plants or insects; or agricultural animals, plants, or insects. Transdermal delivery formulations disclosed herein comprise a homogenous mixture of (a) a transdermal accelerant comprising a weak organic acid having a pKa greater than 2.0 and (b) a microemulsion comprising a nonionic emulsifier, water, and a cis-unsaturated long-chain fatty acid. Fatty acid microemulsions are combined with the acidified transdermal accelerants having a pH greater than 1.0 (typically from 1.5 to 2.5) to yield a homogenous transdermal delivery formulation comprising fatty acid micelles and/or liposomes that encapsulate one or more compound, such as a nutrient or a drug, and incorporate one or more cis-unsaturated fatty acid having a 12 to 26 carbon chain that includes one or more double bond in a cis configuration. Transdermal delivery formulations exhibit ideal solubility and absorption properties in high humidity conditions, such as in a warm to hot shower or sauna.

CPC Classifications

A61K 9/0014 A61K 9/1075 A61K 31/201 A61K 31/375 A61K 36/185 A61K 47/12 A61K 47/26

Filing Date

2025-12-05

Application No.

19411114

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Last updated

Classification

Agency
USPTO
Published
April 2nd, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260090981A1
Docket
19411114

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent Application Drug Formulation Transdermal Delivery
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Legal
Topics
Drug Delivery Healthcare

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