Introduction of five potentially metabolizable linking groups between 111In-cyclohexyl EDTA derivatives and F(ab′)2 fragments of anti-carcinoembryonic antigen antibody—II. Comparative pharmacokinetics and biodistribution in human colorectal carcinoma-bearing nude mice
- 31 August 1993
- journal article
- research article
- Published by Elsevier in Nuclear Medicine and Biology
- Vol. 20 (6) , 763-771
- https://doi.org/10.1016/0969-8051(93)90163-o
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Introduction of five potentially metabolizable linking groups between 111In-cyclohexyl EDTA derivatives and F(ab′)2 fragments of anti-carcinoembryonic antigen antibody—I. A new reproducible synthetic methodNuclear Medicine and Biology, 1993
- A novel bifunctional metabolizable linker for the conjugation of antibodies with radionuclidesBioconjugate Chemistry, 1991
- Metabolizable 111in chelate conjugated anti-idiotype monoclonal antibody for radioimmunodetection of lymphoma in miceEuropean Journal of Nuclear Medicine and Molecular Imaging, 1986