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The Joint Research Centre: EU Science Hub
  • 30 December 2020

Method for producing 225Actinium from 226Radium

Short technical description of the invention

The main seven steps for Ac-225 production method are presented below. For more information, see full patent description on the World Intellectual Property Organization (WIPO) website.

  1. 1. Preparation
    Solution Mixing

    Liquid target solution with Ra-226 and nitric acid is prepared 

  2. 2. Irradiation
    Ac-225 Generation

    Solution is irradiated to produce Ac-225 

  3. 3. Extraction
    Ac-225 Separation

    Ac-225 is extracted while Ra-226 is retained 

  4. 4. Recirculation
    Continuous Production

    Irradiated solution is recirculated to generate more Ac-225 

  5. 5. Purification
    Ac-225 Refinement

    Ac-225 is purified and concentrated using extraction columns 

  6. 6. Radon Removal
    Decay Product Filtering

    Radon and other decay products are removed using activated carbon filters

  7. 7. Radium Recycling
    Waste Minimization

    Ra-226 is recycled to reduce waste and optimize production 

Reference

Patent: WO2020260210

Developed by: The EU, represented by European Commission

Publication date: 30 December 2020

Countries covered: European Unitary Patent, China, Canada, India, Japan 

Licensing terms: Negotiable royalties, upfront fees, and technical support 

Contact: JRC-TechTransferatec [dot] europa [dot] eu (JRC-TechTransfer[at]ec[dot]europa[dot]eu)

Why 225actinium production matters

  • Medical Demand: Ac-225 is a “gold standard” for targeted alpha therapy (TAT) due to its short half-life (10 days) and high-energy alpha particles, which destroy cancer cells while sparing healthy tissue. Ac-225 clinical trials increase every year
  • Critical Shortage/ Supply Crisis: Global supply falls drastically short of demand. Scaling production unlocks therapies for thousands awaiting treatment
  • Regulatory Push: Medical regulations support Ac-225-based therapies, but supply bottlenecks hinder clinical trial, research demands and commercialization

Key advantages/ unique selling points:

  • Efficient Recycling: Recycle radium targets efficiently, enabling continuous production
  • No Drying and Re-dissolving: Skip drying and re-dissolving steps, streamlining the process
  • Enhanced Safety: Reduce radon gas emission and contamination risks
  • Improved Separation: Easily separate actinium from radium without extra steps
  • Continuous Production: Circulate liquid targets in a closed loop for non-stop production
  • Cost-effectiveness: Save on expensive equipment and complex processes
  • Purity: Avoid long-lived contaminants like Ac-227
  • Scalability: Scale up or down with commercial cyclotrons for high-yield production
  • Flexibility: Adapt production to changing demand with ease

Technology readiness level

The technical readiness level (TRL) of this technology is TRL 4: "Technology validated in a laboratory".

Justification: The technology has been demonstrated in laboratory setting, with a high level of sophistication. However, further development, validation and optimization are required to achieve operational/ commercial-scale production.

Competitive landscape

Producing Ac-225 is a highly complex and challenging process, requiring significant expertise and resources to overcome the numerous technical and logistical hurdles that exist. Despite these challenges, the demand for Ac-225 is growing rapidly, driven by its potential in cancer treatment and research. 

However, current production methods are often limited by their scalability, cost-effectiveness, and ability to produce high-purity Ac-225, making it difficult for producers to meet the increasing demand. 

Below is a table showing the competitive landscape of existing Ac-225 production technologies, highlighting the advantages and disadvantages of each method.

Table 1. Competitive landscape of the Ac-225 production methods

 PRODUCTION MethodDescriptionAdvantagesLimitations
1Thorium-229 DecayUses Th-229 to produce Ac-225 through radioactive decayWell-established method; high purity Ac-225Limited availability of Th-229
2Proton irradiation of Th-232Uses protons to irradiate Th-232 High yield of Ac-225Co-produces Ac-227; difficult target handling after irradiation; requires complex isotopic separation and radiation protection
3Photon irradiation of solid Ra-226Uses photons to irradiate solid Ra-226 targetsNon charged particle irradiation; easier target systemRequires handling of solid Ra-226 targets; requires electron accelerators (which are less abundant than cyclotrons)
4Proton irradiation of solid Ra-226Uses protons to irradiate solid Ra-226 High yields of Ac-225 in commercially available cyclotrons Requires handling of solid Ra-226 targets 
5Neutron irradiation of solid Ra-226Uses neutrons to irradiate solid Ra-226 targetsIrradiation without charged particlesRequires large Ra-226 targets; neutron source required; reactor or accelerator required 
6Deuteron irradiation of a beryllium target with a Ra-226 capsuleSecondary neutrons are formed which irradiate a Ra-226 capsule to transmute Ra-226 into Ac-225Potentially safer than direct charged particle irradiation of Ra-226 Requires handling of solid Ra-226 targets. Requires acceleration of deuterons to 
7

Our Patent: 

Liquid Ra-226 irradiation method

Uses a liquid target of Ra-226 and irradiation with protons, deuterons or gamma to produce Ac-225Closed system, no handling of solid Ra-226 targets; improved safety and radiation protectionRequires development of specialized equipment and expertise

Market potential

Market Size & Growth

  • 2025 Market Value: $1.6 billion (projected for radiopharmaceuticals using Ac-225)
  • Market expected to reach $5.5 billion by 2033 globally
  • Compound Annual Growth Rate (CAGR): 15–20.6% (2025–2033) 

Key Growth Drivers

  • Rising cancer incidence / rising adoption of Targeted Alpha Therapy (TAT); 10 million deaths globally in 2023; 60% projected increase in new cases by 2040
  • Ac-225’s high linear energy transfer (LET) destroys cancer cells with minimal damage to healthy tissue, making it ideal for resistant cancers
  • Regulatory Prioritization: The FDA’s prioritization of Ac-225 reflects its transformative potential in oncology, with Fast Track designations accelerating therapies for prostate, lung and rare cancers 

Market Opportunity

  • Supply-Demand Gap: Current global Ac-225 production is less than the clinical demand
  • Untapped Applications: e.g. in theranostics (combining Ac-225’s therapeutic α-particles with imaging γ-emissions for real-time monitoring) 

Key Customers for Ac-225 Production

  • Pharmaceutical/ Biotechnology Companies
  • Research Institutions
  • Hospitals and Cancer Centers
  • Radiopharmaceutical Manufacturers

These customers will use the produced Ac-225 to develop and manufacture various products, including: radiopharmaceuticals for cancer treatment, targeted alpha therapies for cancer treatment, diagnostic agents for cancer imaging, research tools for cancer research.

Ideal licensee profile 

To license our Ac-225 production method, the licensee will need the following infrastructure: technical expertise, facilities and equipment, radiation protection and safety, quality control and assurance/ regulatory compliance, etc.

What JRC offers

The European Commission's Joint Research Centre (JRC) may provide technical support and collaboration to licensees, including, but not limited to: training and capacity building to support the development of the licensee's technical expertise and infrastructure, troubleshooting analysis, collaboration on R&D, etc. For more information, contact the JRC Technology Transfer Team: JRC-TechTransferatec [dot] europa [dot] eu (JRC-TechTransfer[at]ec[dot]europa[dot]eu)