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Table 3 Comparison of the performance of the microscale synthesis reported in this work to literature methods

From: A simple and efficient automated microvolume radiosynthesis of [18F]Florbetaben

Reference

This work

(Zhang et al. 2005)

(Rowe et al. 2008)

(Wang et al. 2011)

(Rominger et al. 2013)

(Patt et al. 2010)

(Collins et al. 2017)

(Brendel et al. 2015)

Number of replicates

n = 3

NR

NR

n = 4

NR

n = 10

n = 3

NR

Precursor amount (mg)

0.052

4

NR

5

5

NRa

7

5

Reaction solvent

DMSO

DMSO

NR

DMSO

MeCN

NRa

MeCN

MeCN

Reaction volume (mL)

0.01

0.2

NR

0.5

1

NRa

1.8

1

Formulated productyield (%; d.c.)

49 ± 3

30c

NR

23 ± 3

18

7.8 ± 2.6

60 ± 9 b

18

Formulation method

SPE (micro C18 cartridge)

NR

SPE (Sep-pak C18)

SPE (Sep-pakplus C18)

SPE (Sep-paklight C18)

SPE (Strata-X 33 μm,reversed phase)

NR

SPE (Sep-pak light C18)

Synthesis time (min)

55

90c

60

45d

75

50

44b

75

Molar activity at EOS(GBq/μmol)

340 ± 60

48–56

170

25–30

80

220 ± 170

NR

50–90

  1. Abbreviations: NR Not reported, EOS End of synthesis, SPE solid-phase extraction
  2. aThe conditions are not reported precisely, but method by Zhang et. al. is cited as a reference
  3. bThe reported data is up to the end of HPLC purification (excluding formulation). Yield is therefore overestimated and synthesis time underestimated
  4. cThe formulation procedure is not reported or discussed. Yield may be an overestimate and synthesis time an underestimate
  5. dIn this rapid method, purification was performed with SPE (no HPLC), but not all impurities were removed