Abstract
A (13)C-enriched phosphorylcholine polymer ((13)C-PMPC) as a self-traceable MR (magnetic resonance) tag was conjugated with a fragment (scFv) of Herceptin, a clinical antibody against antigen Her2. When injected in model mice bearing Her2(+) (gastric) and Her2(-) (pancreatic) tumors, the antibody-tag conjugate (13)C-PMPC-scFv selectively accumulated in the Her2(+) tumor with a rapid build-up/decay (accumulation/clearance) profile and, with the use of the (1)H-(13)C double-resonance (heteronuclear correlation) technique, the Her2(+) gastric tumor was clearly MR imaged.
Keywords:
Active targeting; Anti-Her2 antibody; MRI; Self-traceable polymer; Tumor imaging.
Copyright © 2015 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Carbon Isotopes / pharmacokinetics
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Cell Line, Tumor
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Female
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Humans
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Immunoconjugates / chemistry
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Immunoconjugates / pharmacokinetics*
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Magnetic Resonance Imaging
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Mice
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Mice, Inbred BALB C
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Mice, Nude
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Pancreatic Neoplasms / diagnosis*
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Pancreatic Neoplasms / metabolism
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Phosphorylcholine / analogs & derivatives
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Phosphorylcholine / pharmacokinetics
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Polymethacrylic Acids / pharmacokinetics
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Receptor, ErbB-2 / immunology
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Receptor, ErbB-2 / metabolism
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Single-Chain Antibodies / pharmacokinetics
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Stomach Neoplasms / diagnosis*
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Stomach Neoplasms / metabolism
Substances
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Carbon Isotopes
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Immunoconjugates
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Polymethacrylic Acids
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Single-Chain Antibodies
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poly(2-methacryloyloxyethyl-phosphorylcholine)
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Phosphorylcholine
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ERBB2 protein, human
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Receptor, ErbB-2