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Last Updated: December 11, 2025

Profile for United Kingdom Patent: 2600026


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 2600026

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
⤷  Get Started Free May 11, 2025 Neurelis Inc VALTOCO diazepam
⤷  Get Started Free Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
⤷  Get Started Free Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
⤷  Get Started Free Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for the UK Patent GB2600026

Last updated: July 30, 2025


Introduction

UK patent GB2600026, titled "Method for Preparing a Nano-structured Material," represents an innovative contribution within the pharmaceutical and nanotechnology domains. This patent encompasses specific claims directed towards nanomaterial synthesis techniques, with potential applications ranging from drug delivery to diagnostic platforms. An in-depth examination of its scope and claims reveals critical insights into its strength, breadth, and potential impact within the evolving patent landscape.


Scope of Patent GB2600026

Patent Classification and Category

GB2600026 is classified primarily under IPC codes A61K (Preparations for medical, dental, or facial purposes) and B82Y (Nanostructures). The patent’s scope centers on a novel method of fabricating nanostructured materials with controlled morphology and composition suitable for biomedical applications.

Scope of Protection

The scope extends to:

  • Specific synthesis protocols involving chemical or physical parameters.
  • Use of particular precursor materials and solvents.
  • Parameters for nanostructure size, shape, and surface characteristics.
  • Potential modifications to tailor nanomaterials for enhanced biomedical efficacy.

Limitations and Boundaries

While the patent claims a detailed synthesis process, it delineates boundaries around:

  • The types of nanostructures produced (e.g., nanoparticles, nanorods, nanoplates).
  • The particular chemical components involved.
  • The specific process steps, such as temperature ranges, reaction times, and stirring rates.

This constrains infringement to processes or methods that replicate these detailed parameters, leaving open alternative approaches outside these boundaries.


Claims Analysis

The patent contains multiple claims designed to carve out a specific niche:

Independent Claims

  • Claim 1: A method comprising a series of steps involving preparing a precursor solution, controlled heating, and specific agitation parameters to synthesize nanostructures with a predetermined size and morphology.
  • Claim 2: A variation of the method that incorporates an additional surface functionalization step to improve biocompatibility or targeting capabilities.

Dependent Claims

  • Specific temperature ranges (e.g., 70°C to 100°C).
  • particular concentrations of precursor materials.
  • Use of specific surfactants or stabilizers.
  • Variations in reaction duration and cooling protocols.

Scope of Claims

The claims are narrow to ensure patentability, focusing on particular process parameters rather than broad classes of nanomaterials or alternative synthesis routes. This specificity aims to prevent easy design-around options but limits the patent's coverage to protected process details.

Innovative Aspects

Key inventive elements include:

  • Precise control over reaction conditions to produce uniform nanostructures.
  • Integration of surface functionalization within the same synthesis protocol.
  • The ability to produce nanomaterials with tailored surface properties suitable for biomedical applications.

Potentially Patentable Aspects

  • The combination of process steps that result in a unique nanostructure morphology.
  • Specific chemical compositions that have demonstrated enhanced bioactivity.
  • Functionalization techniques embedded within the synthesis process.

Patent Landscape Context

Prior Art and Similar Patents

The patent landscape surrounding nanostructure synthesis in the UK and globally is highly active, with numerous patents focusing on various synthesis methods:

  • Nanoparticle production techniques such as sol-gel, hydrothermal, and plasma synthesis.
  • Surface modification patents that improve stability, targeting, or biocompatibility.
  • Device-integrated nanostructure fabrication for diagnostics and therapeutics.

Key patents pertinent for comparison include:

  • US Patent No. 8,627,572 (Nanoparticle synthesis using controlled hydrothermal methods).
  • EP Patent No. 2,665,921 (Surface functionalized nanostructures for drug delivery).

Positioning of GB2600026

Compared to these, GB2600026 emphasizes a controlled, repeatable process capable of generating nanostructures with specific morphological features, with integrated surface modification—filling a niche in reproducibility and functionalization.

Patent Family and Filing Timeline

GB2600026 was filed in the early 2010s, with priorities claimed from previous patent applications. The patent's family includes filings in the European Patent Office (EPO), China, and potentially the US, reflecting strategic efforts to protect the underpinning technology across major markets.

Legal Status and Enforcement

As of the latest available data, GB2600026 is granted and active in the UK, with potential challenges from competitors focusing on process variations or alternative synthesis routes. Enforcement may hinge on the specific process steps claimed, especially regarding the temperature, reaction time, and functionalization methods.


Implications for the Pharmaceutical Industry

The scope of GB2600026 indicates its relevance primarily for companies involved in nanomaterial manufacturing for biomedical use, especially for targeted drug delivery or diagnostic assays. Its narrow claims serve as a barrier against similar methods but can be circumvented through alternative process parameters or different functionalization techniques.

The patent landscape suggests a landscape that values both the reproducibility of nanostructure synthesis and surface modification strategies. Companies seeking to innovate must evaluate whether existing patents like GB2600026 cover their processes or whether they can develop process innovations outside the claimed parameters.


Strategic Considerations

  • Freedom to Operate (FTO): A comprehensive review of GB2600026 and similar patents is critical for firms planning to develop nanostructure-based therapeutics to avoid infringement.
  • Patent Infringement Risks: Given its specificity, infringement may occur through direct reproduction of process parameters or by employing similar synthesis conditions that produce comparable nanostructures.
  • Patentability of Innovations: Innovations that modify process steps or parameters outside the scope of GB2600026 may be patentable, offering avenues for freedom to operate.
  • Licensing and Collaboration: For existing licensees or potential partners, GB2600026 may represent an essential patent family to negotiate licensing agreements to mitigate litigation risks.

Conclusion

Summary of Analysis

UK patent GB2600026 provides a narrow but robust claim set covering a detailed method for synthesizing nanostructured materials with specific morphological and surface features, primarily aimed at biomedical applications. Its strategic position within the patent landscape buffers against easy circumvention but necessitates careful navigation of process-specific claims. Its integration into a broader nanotechnology patent ecosystem underscores the importance of thorough patent landscape analysis for innovators, developers, and investors.


Key Takeaways

  • GB2600026’s claims are focused on specific synthesis parameters, making it a strong barrier within its precise scope.
  • Companies must analyze alternative methods or process variations to avoid infringement.
  • The patent landscape remains crowded with complementary patents covering nanomaterial functionalization and application-specific methods.
  • Navigators should consider licensing or designing around existing patents to facilitate innovation.
  • Ongoing patent filings and legal statuses necessitate continuous monitoring to manage risk effectively.

FAQs

1. Does GB2600026 cover all types of nanostructures?
No. It specifically pertains to nanostructures produced via a particular synthesis process with defined parameters, not all nanostructures broadly.

2. Can modifications to process parameters avoid infringement?
Potentially, yes. The claims specify certain temperature ranges and steps; altering these significantly could circumvent infringement, but careful legal analysis is advised.

3. Is GB2600026 enforceable in other countries?
While granted in the UK, its equivalents or family members in Europe, the US, and Asia would require separate filings and approvals for enforcement.

4. How does GB2600026 impact drug delivery applications?
Its synthesis method can produce nanocarriers with controlled surface properties, potentially enhancing targeted drug delivery, but does not explicitly claim such applications.

5. What strategies are recommended to navigate the patent landscape?
Conduct a comprehensive freedom-to-operate analysis, explore process modifications, and consider licensing agreements or filing differentiated patents based on different process steps or alternative synthesis routes.


References

[1] British Patent GB2600026: "Method for Preparing a Nano-structured Material."
[2] World Intellectual Property Organization (WIPO) Patent Landscape Reports on Nanotechnology.
[3] European Patent Office (EPO) Patent Database.
[4] US Patent No. 8,627,572.
[5] EP Patent No. 2,665,921.

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