Abstract | INTRODUCTION: METHODS: Two 5-nitroimidazole derivatives, and were synthesized. Preparation of [(68)Ga]complexes [(68)Ga]-Nit1 and [(68)Ga]-Nit2 was performed at pH 4.5 and 95 °C during 15 minutes and radiochemical purity (RP) was evaluated by reverse phase HPLC. Stability, lipophilicity and plasma protein binding were studied. Biological behaviour in HCT-15 cells both in normoxia and hypoxia has been assessed. Biodistribution in animals bearing induced 3LL Lewis murine lung carcinoma was studied. Comparison with [(18)F] FMISO is also presented. RESULTS: Nit1 and Nit2 have been successfully synthesized. Labelling in high radiochemical purity was achieved for both ligands. Complexes are stable in labelling milieu for at least four hours and in human plasma or in the presence of an excess of DTPA for at least two hours. Both compounds showed high uptake in hypoxic cells in vitro and a very favourable biodistribution profile in mice bearing induced tumours. Results are comparable to those obtained for [(18)F] FMISO. CONCLUSIONS: Selective uptake and retention in tumour together with favourable tumour/muscle ratio make these compounds promising candidates for further evaluation as potential hypoxia imaging agents.
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Authors | Soledad Fernández, Sylvia Dematteis, Javier Giglio, Hugo Cerecetto, Ana Rey |
Journal | Nuclear medicine and biology
(Nucl Med Biol)
Vol. 40
Issue 2
Pg. 273-9
(Feb 2013)
ISSN: 1872-9614 [Electronic] United States |
PMID | 23218939
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Elsevier Inc. All rights reserved. |
Chemical References |
- Gallium Radioisotopes
- Ligands
- Nitroimidazoles
- 4-nitroimidazole
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Topics |
- Animals
- Biological Transport
- Carcinoma, Lewis Lung
(diagnostic imaging, metabolism, pathology)
- Cell Hypoxia
- Cell Line, Tumor
- Cell Transformation, Neoplastic
- Chemistry Techniques, Synthetic
- Gallium Radioisotopes
- Humans
- Hydrophobic and Hydrophilic Interactions
- Isotope Labeling
- Ligands
- Mice
- Nitroimidazoles
(chemical synthesis, chemistry, pharmacokinetics)
- Positron-Emission Tomography
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