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Radiosensitization and Hypoxic Cell Toxicity of NLA-1 and NLA-2, Two New Bioreductive Compounds
- Source :
- Japanese Journal of Cancer Research : Gann
- Publication Year :
- 1992
- Publisher :
- Wiley, 1992.
-
Abstract
- Two new bioreductive compounds, 9-[3-(2-nitro-1-imidazolyl)propylamino]acridine hydrochloride (NLA-1) and 9-[2-(2-nitro-1-imidazolyl)ethylamino]acridine hydrochloride (NLA-2), have been prepared. They feature an acridine ring to intercalate with DNA, a 2-nitroimidazole ring as the radiosensitizing moiety and an amino functionality for increased DNA-binding and hydrophilicity. Time and concentration dependent cytotoxicity as well as radiosensitization efficacy of the two compounds under hypoxic or aerobic conditions were determined in vitro using V-79 cells and an MTT colorimetric or clonogenic assay. The isosensitization point (ISP), defined as that drug concentration which results in the same survival decrement upon exposure of hypoxic or oxygenated cells to a given radiation dose, has been determined for both compounds at 7.5 Gy and the values are significantly lower than the ISPs of 5-[3-(2-nitro-1-imidazolyl)propyl]phenanthridinium bromide, 2-(2-nitro-1-imidazolyl)ethylamine or misonidazole (MISO). NLA-1 and NLA-2 are potent hypoxic cytotoxins and on a concentration basis, more potent than MISO as radiosensitizers in vitro. The sensitization enhancement ratios were significantly increased when 1 h drug preincubation under hypoxia at 37 degrees C was applied, before irradiation at room temperature.
- Subjects :
- Radiation-Sensitizing Agents
Cancer Research
Misonidazole
Radiosensitizer
Cell Survival
Hydrochloride
Article
Cell Line
chemistry.chemical_compound
Bioreductive Agent
Intercalation
Animals
Radiosensitivity
Key words
Acridine
Clonogenic assay
Molecular Structure
Aminoacridines
Chemistry
Bioreductive agent
Cell Hypoxia
Kinetics
Oncology
Biochemistry
Nitroimidazoles
Oxygen enhancement ratio
Nuclear chemistry
Subjects
Details
- ISSN :
- 09105050
- Volume :
- 83
- Database :
- OpenAIRE
- Journal :
- Japanese Journal of Cancer Research
- Accession number :
- edsair.doi.dedup.....c0e106fd77185a7737372056d3942962
- Full Text :
- https://doi.org/10.1111/j.1349-7006.1992.tb00123.x