Enhanced Pharmaceutical Compositions for Treating Viral Infections

Publication ID: 24-11857560_0001_PTD
Published: October 28, 2025
Category:Direct Improvements & Enhancements

Legal Citation

pr1or.art Inc., “Enhanced Pharmaceutical Compositions for Treating Viral Infections,” Published Technical Disclosure No. 24-11857560_0001_PTD, Published October 28, 2025, available at https://archive.pr1or.art/24-11857560_0001_PTD
This technical disclosure describes improvements that would be readily apparent to a Person Having Ordinary Skill In The Art (PHOSITA) when considered in combination with the foundational architecture disclosed in U.S. Patent No. 11,857,560.

Summary of the Inventive Concept

The inventive concept relates to improved pharmaceutical compositions comprising sulfur-containing nucleosides and nucleotides for treating viral infections, offering enhanced bioavailability, efficacy, and stability.

Background and Problem Solved

The original patent disclosed pharmaceutical compositions comprising sulfur-containing nucleosides and nucleotides for treating viral infections. However, these compositions had limitations in terms of bioavailability, efficacy, and stability. The new inventive concept addresses these limitations by introducing novel conjugate compounds, phosphorus oxide linkages, and lipid or sphingolipid modifications, thereby providing improved therapeutic outcomes.

Detailed Description of the Inventive Concept

The inventive concept encompasses pharmaceutical compositions comprising sulfur-containing nucleosides or nucleotides conjugated to phosphorus oxide, which can be a phosphorothioate or phosphoroamidate. These compositions may further comprise a lipid or sphingolipid linked to the nucleotide or nucleoside through an amino group or hydroxyl group. Additionally, the inventive concept includes conjugate compounds or salts thereof, where the conjugate compound comprises a nucleotide or nucleoside containing a sulfur-containing base linked by a phosphorus oxide to a sphingolipid or derivative. The phosphorus oxide can be a polyphosphate or polyphosphonate, providing improved stability and solubility of the composition. The inventive concept also includes methods for treating viral infections using these compositions, as well as systems for delivering nucleoside analogs for the treatment of infectious diseases and cancer.

Novelty and Inventive Step

The new inventive concept introduces novel conjugate compounds, phosphorus oxide linkages, and lipid or sphingolipid modifications that enhance the bioavailability, efficacy, and stability of the pharmaceutical compositions. These features are not obvious from the original patent and provide a significant improvement over the prior art.

Alternative Embodiments and Variations

Alternative embodiments of the inventive concept may include different types of phosphorus oxide linkages, such as phosphorodithioates or phosphoroselenoates. Additionally, the lipid or sphingolipid component may be varied to include different types of lipids or sphingolipids, such as cholesterol or ceramide. The inventive concept may also be adapted for use in different therapeutic areas, such as cancer treatment or gene therapy.

Potential Commercial Applications and Market

The inventive concept has significant commercial potential in the pharmaceutical industry, particularly in the areas of viral infection treatment and cancer therapy. The improved pharmaceutical compositions may offer enhanced therapeutic outcomes, reduced side effects, and improved patient compliance, making them attractive to pharmaceutical companies and healthcare providers.

Field of Art

Pharmaceutical chemistry, specifically nucleoside and nucleotide therapeutic compositions for viral infection treatment, requiring advanced organic synthesis skills, knowledge of medicinal chemistry, and expertise in drug delivery systems

Person of Ordinary Skill (PHOSITA) Profile

A PhD-level pharmaceutical chemist with expertise in organic synthesis, nucleoside chemistry, drug design, and experience in modifying molecular structures to improve pharmaceutical properties

Obviousness Rationale

A skilled practitioner would recognize that the PTD's variations represent predictable modifications to the source patent's core nucleoside composition technology. The disclosed conjugation strategies, phosphorus oxide linkage variations, and lipid modifications represent standard design approaches in pharmaceutical chemistry for enhancing drug delivery and stability. These technical extensions would be considered routine optimization techniques within the ordinary skill of a pharmaceutical chemist specializing in nucleoside therapeutics.

Obvious Combinations & Variations

Source Patent Element
Sulfur-containing nucleosides conjugated to phosphorus oxide
PTD Variation
Introducing phosphorothioate and phosphoroamidate specific linkage variations
Obviousness Reasoning
Phosphorus oxide linkage modifications are well-known techniques for altering drug pharmacokinetic properties, representing predictable variations a PHOSITA would recognize as routine design choices
Source Patent Element
Nucleoside pharmaceutical compositions
PTD Variation
Adding lipid and sphingolipid conjugation through amino or hydroxyl group linkages
Obviousness Reasoning
Lipid conjugation is a standard strategy for improving drug solubility, bioavailability, and targeted delivery, which would be an obvious extension to a skilled practitioner
Source Patent Element
Base nucleoside structure
PTD Variation
Introducing sulfur-containing base substitutions with thione, thiol, or thioether groups
Obviousness Reasoning
Systematic structural modifications of nucleoside bases are routine optimization techniques in medicinal chemistry, representing predictable variations a PHOSITA would consider
Source Patent Element
Pharmaceutical composition excipients
PTD Variation
Exploring alternative polyphosphate and polyphosphonate delivery mechanisms
Obviousness Reasoning
Exploring alternative phosphorus oxide derivatives represents a standard approach to improving drug stability and solubility, which would be obvious to a skilled pharmaceutical chemist
Source Patent Element
Viral infection treatment compositions
PTD Variation
Expanding potential therapeutic applications to include cancer treatment and gene therapy
Obviousness Reasoning
Identifying additional therapeutic applications for nucleoside analog compositions is a predictable scientific exploration that would be obvious to a skilled researcher in the field
35 U.S.C. § 103 Summary: Based on the teachings of US Patent 11857560 and the disclosed variations in the published technical disclosure, a person having ordinary skill in the art would find the claimed pharmaceutical compositions and methods obvious, as the technical extensions represent predictable modifications within the established knowledge of nucleoside therapeutic chemistry, thereby rendering potential patent claims anticipated and non-patentable under 35 U.S.C. Section 103.

Original Patent Information

Patent NumberUS 11,857,560
TitlePharmaceutical compositions comprising substituted nucleotides and nucleosides for treating viral infections
Assignee(s)Emory University