Synthesis of radioiodinated N-succinimidyl iodobenzoate: optimization for use in antibody labelling.

Journal Article (Journal Article)

N-succinimidyl-3-(tri-n-butylstannyl)benzoate (m-BuATE), N-succinimidyl-3-(tri-methylstannyl)benzoate (m-MeATE) and N-succinimidyl-4-(tri-n-butylstannyl)benzoate (p-BuATE) were synthesized and radioiodinated using either N-chlorosuccinimide (NCS) or t-butylhydroperoxide (TBHP) as the oxidant. Radiohalogenation of m-MeATE proceeded more rapidly than m-BuATE. NCS was the more efficient oxidant at reaction times less than 15 min; use of both TBHP and NCS resulted in nearly quantitative yields after 15 min when m-MeATE was used. Using NCS, achieving optimal antibody coupling and specific binding required purification of the active ester by HPLC; in contrast, with TBHP, only Sep-Pak purification was needed.

Full Text

Duke Authors

Cited Authors

  • Garg, PK; Archer, GE; Bigner, DD; Zalutsky, MR

Published Date

  • 1989

Published In

Volume / Issue

  • 40 / 6

Start / End Page

  • 485 - 490

PubMed ID

  • 2551846

International Standard Serial Number (ISSN)

  • 0883-2889

Digital Object Identifier (DOI)

  • 10.1016/0883-2889(89)90131-7


  • eng

Conference Location

  • England