- Development of automated synthesis procedures for radiopharmaceuticals with high molar activity (Am) and quality according to GMP regulations
- Optimising 18F-radiofluorination methods (electrophilic, transition metal mediated and nucleophilic) for simplicity and high Am (Fig. 1)
- Optimising target performance, 11C-labelling agent pathways and synthesis methods for simplicity, high yields and Am (Fig. 2)
![](https://radchem.utu.fi/wp-content/uploads/2019/04/Fluori_TPC_Fig1-1024x664.png)
![](https://radchem.utu.fi/wp-content/uploads/2019/04/Hiili_TPC_Fig2-1024x485.png)