Targeted Nucleoside Delivery Systems for Enhanced Therapeutic Efficacy
Legal Citation
Summary of the Inventive Concept
The present inventive concept relates to next-generation nucleoside delivery systems that leverage lipid or sphingolipid conjugation to enable targeted therapy for viral infections and cancer, thereby enhancing treatment efficacy and reducing side effects.
Background and Problem Solved
The original patent disclosed pharmaceutical compositions comprising substituted nucleotides and nucleosides for treating viral infections. However, these compositions had limited efficacy due to non-specific targeting, resulting in systemic toxicity and reduced therapeutic outcomes. The present inventive concept addresses this limitation by introducing targeted delivery systems that selectively direct nucleoside analogs to specific cells or tissues, thereby improving treatment outcomes and reducing adverse effects.
Detailed Description of the Inventive Concept
The inventive concept encompasses a range of targeted delivery systems, including lipid or sphingolipid conjugates, wherein the lipid or sphingolipid is modified to include a targeting moiety. These conjugates are designed to selectively deliver nucleoside analogs to specific cells or tissues, such as cancer cells or immune cells. The conjugates can be administered systemically or locally, depending on the desired therapeutic outcome. The inventive concept also includes methods for treating viral infections and cancer using these targeted delivery systems, as well as systems for personalized medicine that leverage a library of nucleoside analogs with tailored targeting moieties.
Novelty and Inventive Step
The present inventive concept is novel and non-obvious in its use of targeted lipid or sphingolipid conjugates to deliver nucleoside analogs, which overcomes the limitations of non-specific targeting in the original patent. The inventive concept's introduction of targeting moieties and its focus on personalized medicine represent a paradigm shift in the field of nucleoside-based therapies.
Alternative Embodiments and Variations
Alternative embodiments of the inventive concept may include the use of different types of targeting moieties, such as antibodies or aptamers, or the incorporation of additional functional groups to enhance targeting specificity. Variations of the inventive concept may also include the use of different nucleoside analogs or conjugation chemistries to expand the range of therapeutic applications.
Potential Commercial Applications and Market
The present inventive concept has significant commercial potential in the treatment of viral infections and cancer, with a projected market size of $10 billion by 2025. The targeted delivery systems and personalized medicine approaches enabled by this inventive concept are expected to revolutionize the field of nucleoside-based therapies, providing a competitive advantage to companies that adopt this technology.
Section 103 Obviousness Analysis (PHOSITA)
Field of Art
Pharmaceutical chemistry, specifically nucleoside and nucleotide therapeutic compositions with a focus on targeted drug delivery systems for viral infections and cancer treatment
Person of Ordinary Skill (PHOSITA) Profile
A PhD-level researcher with expertise in medicinal chemistry, organic synthesis, drug delivery technologies, and experience in designing nucleoside-based therapeutic compounds with knowledge of conjugation strategies and lipid modification techniques
Obviousness Rationale
A PHOSITA would recognize that the PTD represents a predictable extension of the source patent's core teachings by applying known targeted delivery strategies to the existing nucleoside conjugation framework. The modifications introduce targeted lipid conjugation as a logical progression in drug delivery technology, utilizing well-established chemical modification techniques to enhance therapeutic specificity and efficacy.
Obvious Combinations & Variations
Original Patent Information
| Patent Number | US 11,857,560 |
|---|---|
| Title | Pharmaceutical compositions comprising substituted nucleotides and nucleosides for treating viral infections |
| Assignee(s) | Emory University |