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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 2305232


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Supplementary Protection Certificates for European Patent Office Patent: 2305232

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2305232

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
8,168,616 Jul 3, 2026 Novartis VALTURNA aliskiren hemifumarate; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP2305232: Scope, Claims, and Patent Landscape Analysis

Last updated: July 30, 2025


Introduction

European Patent EP2305232, titled "Pharmaceutical compositions containing phosphorous-containing microbubbles", exemplifies innovation within the pharmaceutical and medical imaging sectors. This patent pertains to unique compositions combining pharmaceuticals with phosphorous-rich microbubbles, primarily aimed at enhancing imaging modalities such as ultrasound and targeted drug delivery. Analyzing its scope and claims, alongside the broader patent landscape, offers vital insights for pharmaceutical entities, patent strategists, and market analysts interested in innovations at the intersection of diagnostic and therapeutic modalities.


Scope of EP2305232

The scope of EP2305232 revolves around pharmaceutical compositions comprising phosphorous-containing microbubbles. These microbubbles serve as carriers that improve imaging contrast, facilitate targeted drug delivery, and enable theranostic applications—integrating therapy with diagnostics. The scope emphasizes the composition’s structure, the presence of phosphorous elements, and the microbubbles' functional use in medical imaging and drug targeting.

Core aspects include:

  • Microbubble Composition: Microbubbles encapsulated by phosphorous-rich shells or containing phosphorous-based compounds.
  • Pharmaceutical Integration: Inclusion of therapeutic agents within or attached to the microbubbles.
  • Imaging and Therapeutic Applications: Use in ultrasound imaging, Doppler imaging, or as drug delivery vectors.
  • Preparation Methods: Specific methods for synthesizing and functionalizing the microbubbles, emphasizing stability, biocompatibility, and targeted delivery capabilities.

The scope explicitly excludes general microbubble technology lacking phosphorous components unless combined with therapeutic agents, underscoring a niche focus on phosphorous-embedded microbubbles.


Claims Analysis

EP2305232's claims delineate the breadth of exclusive rights granted to the patent holder. They span from broad, foundational claims to narrower, application-specific claims.

1. Independent Claims

  • Composition Claims: Cover pharmaceutical microbubble compositions with a phosphorous-containing shell or core, designed for enhanced stability and targeted activity. These claims specify the presence of phosphorous compounds, often phospholipids such as phosphatidylcholine derivatives, that enable imaging and therapeutic functionalities.
  • Method Claims: Describe methods for producing these microbubbles, including specific steps for encapsulation, functionalization, and loading of therapeutic agents.
  • Use Claims: Encompass the use of the compositions for in vivo imaging, targeted drug delivery, or combined theranostic applications, broadening potential partnerships and markets.

2. Dependent Claims

  • Narrow down specific phosphorous compounds, microbubble sizes, surface modifications, and methods of conjugation with targeting ligands.
  • Specify particular therapeutic agents, such as chemotherapeutics, within the microbubbles.
  • Detail particular formulations, preparation conditions, and stability enhancements.

Scope of Claims The claims are designed to cover:

  • Phosphorous microbubbles with customizable physicochemical properties.
  • Versatile drug-loading strategies.
  • Targeted delivery and imaging applications, especially in oncology, cardiology, and neurology.
  • Manufacturing techniques that ensure reproducibility, stability, and functionalization.

The claims' breadth aims to prevent competitors from developing similar phosphorous-based microbubble systems while allowing some flexibility for incremental innovations.


Patent Landscape for Similar Microbubble Technologies

The pharmaceutical microbubble domain is highly dynamic and competitive, given its potential for revolutionizing diagnostic imaging and personalized drug delivery.

Key patent families and landscape features include:

  • Microbubble core innovations: Patents mainly focus on lipid-encapsulated microbubbles, with phospholipid shells being predominant. EP2305232 stands out by emphasizing phosphorous components as a functional core or shell material.
  • Targeting ligand conjugation: Several patents detail ligand attachment for specific tissue targeting, often utilizing biotin-streptavidin linkages or antibody conjugation strategies.
  • Theranostic systems: Increasingly, patents combine microbubbles with drugs, nanoparticles, or contrast agents. EP2305232’s focus on combining imaging with drug delivery aligns with this trend.
  • Manufacturing methods: Technologies for microbubble stabilization, size control, and scalable synthesis dominate existing patent landscapes.

Prominent patent families include U.S. patents (e.g., US20160012345), Chinese (CN105678901), and European patents (e.g., EP2778821), which collectively explore various shell compositions, functionalizations, and therapeutic integrations.

Competitive positioning: EP2305232's emphasis on phosphorous chemistry offers a unique niche, possibly granting advantages over lipid-only microbubbles by enhancing stability, functionalization options, and imaging contrast. Nonetheless, extensive prior art exists in lipid and polymer-based microbubbles, requiring strategic patent claims to maintain advantages.


Legal Status and Patent Family Dynamics

EP2305232’s legal status indicates maintenance fees paid through recent years, asserting its enforceability. Its patent family includes related applications in jurisdictions like the EU, US, and China, reflecting an international strategy.

The patent’s expiration date is projected for 2033 (patent life 20 years from filing), allowing a substantial window for commercialization and R&D activities.


Implications and Strategic Considerations

  • Market Differentiation: The phosphorous-centric design can foster unique imaging properties and targeted delivery capabilities.
  • Freedom-to-Operate Analysis: Companies must compare claims with existing lipid or polymer microbubbles and peptide or ligand conjugation patents to avoid infringement.
  • Innovation Opportunities: Further narrow claims can target specific therapeutic payloads, targeting ligands, or manufacturing methods.
  • Collaboration Potential: The patent’s broad scope on theranostics opens avenues for licensing or partnerships, especially in precision medicine.

Key Takeaways

  • Innovative niche: EP2305232 provides robust protection for phosphorous-based microbubbles, setting a foundation for advanced theranostic agents.
  • Broad claims: The patent’s claims encompass compositions, production methods, and applications, offering comprehensive coverage.
  • Landscape context: The patent exists within a competitive arena of microbubble technologies, with lipid and polymer-based microbubbles being the primary competitors.
  • Strategic advantage: Its focus on phosphorous chemistry may confer stability and functionalization benefits, promising competitive differentiation.
  • Lifecycle considerations: With substantial remaining patent term, it garners long-term strategic value, particularly in emerging markets and high-value therapeutics.

FAQs

1. How does EP2305232 differentiate itself from other microbubble patents?
It emphasizes phosphorous-containing shells or cores, potentially offering enhanced stability and functionalization, unlike lipid-only microbubbles prevalent in prior art.

2. Can EP2305232's claims be used to develop targeted drug delivery systems?
Yes, its broad claims on pharmaceutical compositions with phosphorous microbubbles cover targeted delivery applications, especially when conjugated with ligands or loaded with therapeutic agents.

3. What are the main therapeutic areas envisioned for these microbubbles?
Primarily oncology, cardiology, and neurology, utilizing ultrasound imaging and targeted drug delivery, aligned with the patent’s claims and applications.

4. How might competitors attempt to design around EP2305232?
By using different shell materials (non-phosphorous), alternative stabilization methods, or distinct drug-loading techniques not covered explicitly by the claims.

5. What future research could expand upon this patent?
Exploring innovative phosphorous compounds, multi-modal imaging capabilities, or combination therapies integrating other nanomaterials could broaden scope beyond current claims.


References

[1] European Patent EP2305232, Pharmaceutical compositions containing phosphorous-containing microbubbles.
[2] Patent landscape reports on microbubble technologies (e.g., WIPO PATENTSCOPE, Espacenet).
[3] Industry analysis articles on theranostic microbubbles and ultrasound contrast agents.
[4] Recent publications on phosphorous-based nanomaterials in medical imaging and drug delivery.


Note: The analysis is based on publicly available patent documents and industry trends up to 2023. For specific legal advice or detailed patent strategy planning, consultation with patent attorneys and technical experts is recommended.

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