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-Reference-Cited by-同舟云学术

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

Published:1993-08 Issue:6 Volume:20 Page:763-771
ISSN:0969-8051
Container-title:Nuclear Medicine and Biology
language:en
Short-container-title:Nuclear Medicine and Biology

Author:

Faivre-chauvet A.,Gestin J.F.,Mease R.C.,Sai-maurel C.,Thédrez P.,Slinkin M.,Meinken G.E.,Srivastava S.C.,Chatal J.F.

Publisher

Elsevier BV

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Molecular Medicine

Reference12 articles.

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2. Effect of different linkages between chelates and monoclonal antibodies on levels of radioactivity in the liver;Deshpande;Nucl. Med. Biol.,1989

3. 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 method;Gestin;Nucl. Med. Biol.,1993

4. Metabolizable 111In chelate conjugated anti-idiotype monoclonal antibody for radioimmunodetection of lymphoma in mice;Haseman;Eur. J. Nucl. Med.,1986

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