SYNTHESIS OF N-SUCCINIMIDYL-4-~(18) F(FLUOROMETHYL)BENZOATE[J]. Journal of Nuclear and Radiochemistry, 2002, 24(3): 157-157.
    Citation: SYNTHESIS OF N-SUCCINIMIDYL-4-~(18) F(FLUOROMETHYL)BENZOATE[J]. Journal of Nuclear and Radiochemistry, 2002, 24(3): 157-157.

    SYNTHESIS OF N-SUCCINIMIDYL-4-~(18) F(FLUOROMETHYL)BENZOATE

    • N succinimidyl 4 18 F (fluoromethyl)benzoate ( 18 F SFMB) of labeling proteins has been synthesized. Laborious and time consuming HPLC is substituted by simple Sep pak silica during the process of isolation. Many factors affecting the radiochemical synthesis of 18 F SFMB including reaction solvents, temperature, the mole ratio of K/222 to K 2CO 3 and reaction time are studied. The better labeling conditions are as follows:dry acetonitrile as solvent, the mole ratio of K/222 to K 2CO 3 is 1∶1, reaction time is 5 min at 80 ℃. The radiochemical yield is about 57%(EOS) which is about 3 times higher than the published data. IgG is indirectly labeled by 18 F SFMB and the labeled yield are about 88% at room temperature.
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