The aluminium fluoride-18 ([18F] AlF) radiolabelling procedure has generated great interest
because it is a simple, one-pot method that can be used to directly radiolabel small …

The construction of fully automated Al [18 F] F radiochemistry can enhance the
reproducibility and reliability of Al [18 F] F-based radiopharmaceuticals while promoting …

Due to its ideal physical properties, fluorine-18 turns out to be a key radionuclide for positron
emission tomography (PET) imaging, for both preclinical and clinical applications. However …

Background Fibroblast activation protein (FAP) is overexpressed in the stroma of many types
of cancer.[18F] AlF-FAPI-74 is a positron emission tomography tracer with high selectivity for …

Radiolabelled peptides are crucial tools for biomedical research purposes. Peptides are
usually labeled with fluorine-18 via an indirect prosthetic group approach, which requires a …

Radiolabeling compounds with positron-emitting radionuclides often involves a time-
consuming, customized process. Herein, we report a simple lyophilized kit formulation for …

To date the majority of 18F-peptide radiolabeling approaches are multi-step, low yielding
and time-consuming processes. Given the short half-life of 18F (109.8 min), it is critical that …

There is a great demand to develop more cost‐efficient and robust manufacturing processes
for fluorine‐18 (18F) labelled compounds and radiopharmaceuticals. Herein, we present to …

Two fully automated synthetic procedures of [18F] fluoroacetate ([18F] FAC) have been
developed using a modified commercial TRACERlab FXFN synthesizer. One was a two …

A novel, efficient, time-saving and reliable radiolabeling procedure via nucleophilic
substitution with [18F] fluoride is described. Different radiolabeled aliphatic and aromatic …