Abstract | BACKGROUND: METHODS: We labeled chimeric (human/mouse) Fab fragments of Mab A7 (chA7Fab) with (99m)Tc and examined the distribution of (99m)Tc-labeled chA7Fab in nude mice bearing human pancreatic carcinoma. RESULTS: The tumor accumulation of (99m)Tc-labeled chA7Fab was larger than that of (99m)Tc-labeled A7 from 2 to 6 hr after injection. (99m)Tc-labeled chA7Fab disappeared from blood more rapidly than (99m)Tc-labeled A7. For all resected normal tissues except kidney, the accumulation of (99m)Tc-labeled chA7Fab was low and similar to that of (99m)Tc-labeled A7. CONCLUSIONS: Because the half-life of (99m)Tc is short (6 hr), chA7Fab, which accumulates rapidly in tumors, may be a better carrier of (99m)Tc than intact Mab A7.
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Authors | Eigo Otsuji, Hiroomi Matsumura, Kazuma Okamoto, Atsushi Toma, Yoshiaki Kuriu, Daisuke Ichikawa, Akeo Hagiwara, Hisakazu Yamagishi |
Journal | Journal of surgical oncology
(J Surg Oncol)
Vol. 84
Issue 3
Pg. 160-5
(Nov 2003)
ISSN: 0022-4790 [Print] United States |
PMID | 14598360
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2003 Wiley-Liss, Inc. |
Chemical References |
- Antibodies, Monoclonal
- Immunoglobulin Fab Fragments
- Technetium
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Topics |
- Animals
- Antibodies, Monoclonal
(pharmacokinetics)
- Cell Line, Tumor
- Humans
- Immunoglobulin Fab Fragments
(immunology)
- Mice
- Mice, Nude
- Pancreatic Neoplasms
(diagnostic imaging, metabolism)
- Radioimmunodetection
- Technetium
(pharmacokinetics)
- Tissue Distribution
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