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Updated: Apr 28, 2026
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Automated Preparation of [68Ga]Ga-3BP-3940 on a Synthesis Module for PET Imaging of the Tumor Microenvironment
Published on: April 25, 2025
Development of (166)Ho-phytate Complex for Radiosynovectomy.
Amir R Jalilian1, Akbar Anvari2, Ali Bahrami-Samani1
1Radiopharmaceutical Research and Development Laboratory (RRDL), Nuclear Science and Technology Research Institute (NSTRI), Tehran, Iran 14155-1339.
Holmium-166 phytate demonstrated excellent retention at the injection site for two days post-intraarticular administration in rats. This suggests its potential as a targeted radiotherapeutic agent for joint conditions.
Area of Science:
- Nuclear Medicine
- Radiochemistry
- Biomedical Engineering
Background:
- Holmium-166 chloride ((166)Ho-chloride) was synthesized via neutron bombardment of holmium nitrate.
- The synthesis utilized a thermal neutron flux of 4-5 × 10(13) n.cm(-2).s(-1).
Purpose of the Study:
- To prepare and characterize a stable (166)Ho-phytate complex for potential radiotherapeutic applications.
- To evaluate the in vivo behavior of the (166)Ho-phytate complex following intraarticular injection in a rat model.
Main Methods:
- A high radiochemical purity ((166)Ho-phytate complex) was achieved using (166)Ho-chloride.
- Complex stability and viscosity were assessed over two days.
- Intraarticular injection into rat knee joints was performed, followed by monitoring of radioactivity leakage and organ distribution for 48 hours.
Main Results:
- The prepared (166)Ho-phytate complex exhibited high radiochemical purity (>99.9%).
- The complex remained stable and its viscosity was acceptable for injection.
- Nearly all injected radioactivity was retained at the injection site 48 hours post-injection, with minimal distribution to other organs.
Conclusions:
- The (166)Ho-phytate complex is a stable and effective agent for intraarticular injection.
- This complex shows promise as a feasible agent for cavitary radiotherapy in both oncology and rheumatology.
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