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. Author manuscript; available in PMC: 2015 Jul 7.
Published in final edited form as: J Nucl Med. 2013 Dec 23;55(2):321–328. doi: 10.2967/jnumed.113.121053

Figure 1.

Figure 1

Overall workflow of radiosynthesis of [18F]FLT on EWOD chip followed by cartridge purification to produce an injectable dose of [18F]FLT for mice imaging. Synthetic scheme of the radiosynthesis of [18F]FLT using a mixture of thexyl alcohol and DMSO in the fluorination reaction. The crude [18F]FLT product was extracted and purified via a simple cartridge purification to yield ∼ 52 MBq (non-decay corrected) of [18F]FLT.