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USPTO Publishes A1 Application for Mucoadhesive Polymeric Prodrug Delivery System

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Summary

The USPTO published application US20260108615A1 on April 23, 2026, covering a mucoadhesive polymeric prodrug system using partially succinated polyvinyl alcohol (PVA-SA) that self-assembles into 50–260 nm particles for controlled drug delivery. The prodrug forms ester and/or amide linkages with biologically active compounds including doxorubicin (DOX), cysteamine (CYS), ketoprofen (KETO), and 4-hydroxybenzyl alcohol (HBA), enabling adjustable drug release and improved mucoadhesive properties. The application (No. 18697611) was originally filed on September 29, 2022, by inventors Abdelghafour, Szabó, Janovák, Dékány, and Rovó.

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About this source

USPTO classification A61K covers pharmaceutical preparations: formulations, dosage forms, combination therapies, delivery systems, and the vehicles that carry active ingredients. Every newly published application in A61K lands in this feed, around 245 a month. Applications publish 18 months after filing, so this feed reveals what pharma formulators at major sponsors and generics were working on in the prior year and a half. Watch this if you compete in drug formulation, file freedom-to-operate analyses, scout competitive drug products before clinical readouts, or follow novel delivery platforms like nanoparticles, lipid carriers, and long-acting injectables.

What changed

The USPTO published application US20260108615A1 discloses a self-assembled mucoadhesive biopolymer particle release system based on partially succinated polyvinyl alcohol (PVA-SA). The polymer contains both hydroxyl and carboxyl pendant groups that form ester and/or amide linkages with amino, carboxyl, and hydroxyl groups of active compounds such as doxorubicin, cysteamine, ketoprofen, and 4-hydroxybenzyl alcohol. The simultaneous hydroxyl and carboxyl groups enable the macromolecules to self-assemble into 50–260 nm nanoparticles, prolonging and regulating drug release.

For parties in the pharmaceutical and drug delivery sector, this published application marks the entry of a novel mucoadhesive prodrug platform into the public patent record, with potential implications for formulation strategies in antitumor, anti-fibrotic, and anti-inflammatory therapies. Inventors named include Mohamed M. Abdelghafour, Diána Szabó, László Janovák, Imre Dékány, and László Rovó. No compliance obligations or deadlines are imposed by this publication; it is informational in nature.

Archived snapshot

Apr 23, 2026

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SELF-ASSEMBLED MUCOADHESIVE BIOPOLYMER PARTICLE RELEASE SYSTEM AND PREPARATION METHOD THEREOF

Application US20260108615A1 Kind: A1 Apr 23, 2026

Inventors

Mohamed M ABDELGHAFOUR, Diána SZABÓ, László JANOVÁK, Imre DÉKÁNY, László ROVÓ

Abstract

The present invention relates to a mucoadhesive polymeric prodrug comprising a partially succinated polyvinyl alcohol (PVA-SA) with adjusted amount of hydroxyl and carboxyl pendant groups, which form an ester and/or amide linkage with amino and/or carboxyl and/or hydroxyl groups of biologically active compounds such as proteins, peptides, synthetic chemical, or natural products compounds (e.g. doxorubicin as an antitumor agent and antifibrotic drug). Preferably, said biologically active compounds are cysteamine (CYS) as the aminothiol compound and one compound selected from the group consisting of doxorubicin (DOX), ketoprofen (KETO), or 4-hydroxybenzyl alcohol (HBA). Moreover, the simultaneous presence of both hydroxyl and carboxyl groups in the partially succinated polyvinyl alcohol (PVA-SA) chain of the prodrug enables the self-assembled formation of 50-260 nm particles from the linear macromolecules and thus the drug release can be prolonged or adjusted. The present invention also relates to improving the mucoadhesive properties of the polymeric prodrug by the regulation of the amount of conjugated aminothiol compound. Further, the present invention relates to the method for producing said mucoadhesive polymeric prodrug, and nanoparticles of the said mucoadhesive polymeric prodrug.

CPC Classifications

A61K 47/58 A61K 9/006 A61K 9/5192 A61K 31/05 A61K 31/145 A61K 31/192 A61K 31/704 A61K 47/6937 B82Y 5/00 B82Y 40/00

Filing Date

2022-09-29

Application No.

18697611

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Last updated

Classification

Agency
USPTO
Published
April 23rd, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260108615A1

Who this affects

Applies to
Pharmaceutical companies Manufacturers Healthcare providers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent filing publication Drug delivery formulation Nanoparticle technology
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Regulatory Affairs
Topics
Pharmaceuticals Healthcare Product Safety

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