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Preparation and in vivo evaluation of an N-(p-[125I]iodophenethyl)maleimide-antibody conjugate

Authors :
D. Scott Wilbur
Stephen W. Hadley
Leah M. Grant
Michael W. Reed
Mark D. Hylarides
Joan R. Schroeder
Source :
Bioconjugate Chemistry. 2:435-440
Publication Year :
1991
Publisher :
American Chemical Society (ACS), 1991.

Abstract

Protein sulfhydryl reactive N-(4-[125I]iodophenethyl)maleimide (IPEM, 5) was obtained from N-[4-(tri-n-butylstannyl)phenethyl]maleimide in 59-100% radiochemical yield. Conjugation of 5 to NR-ML-05 Fab, a murine anti-melanoma antibody Fab fragment that had been previously reduced with dithiothreitol (DTT), was effected in an average of 85% yield. Results from in vitro chemical challenges and serum stability studies on the IPEM conjugate of NR-ML-05 Fab (6) indicated a stable covalent attachment of the radioiodine. A biodistribution study of the IPEM conjugate in tumor-bearing athymic nude mice showed lack of significant accumulation of radioiodine in the thyroid and stomach which was an indication of in vivo stability. The observed uptake in tumor was consistent with that obtained for Chloramine-T- or p-iodobenzoate-labeled NR-ML-05 Fab conjugates.

Details

ISSN :
15204812 and 10431802
Volume :
2
Database :
OpenAIRE
Journal :
Bioconjugate Chemistry
Accession number :
edsair.doi.dedup.....a9b3559bac4173d0770148fd10861648