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

• Published in: Bioconjugate chemistry Vol. 2; no. 6; pp. 435 - 440
• Main Authors: Hylarides, Mark D, Wilbur, D. Scott, Reed, Michael W, Hadley, Stephen W, Schroeder, Joan R, Grant, Leah M
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01-11-1991
• Subjects: Animals; Antigens, Neoplasm - immunology; Dithiothreitol; Female; Immunoglobulin Fab Fragments; Iodine Radioisotopes; Iodobenzenes - chemical synthesis; Iodobenzenes - chemistry; Iodobenzenes - pharmacokinetics; Isotope Labeling - methods; Maleimides - chemical synthesis; Maleimides - chemistry; Maleimides - pharmacokinetics; Melanoma - immunology; Melanoma, Experimental - metabolism; Mice; Mice, Nude; Stomach - metabolism; Thyroid Gland - metabolism; Tissue Distribution
• DOI: 10.1021/bc00012a010
• EISSN: 1520-4812
• ISSN: 1043-1802

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.