NLP-1: a DNA intercalating hypoxic cell radiosensitizer and cytotoxin
- 1. Univ. of Toronto, Ontario (Canada)
Description
The 2-nitroimidazole linked phenanthridine, NLP-1 (5-[3-(2-nitro-1-imidazoyl)-propyl]-phenanthridinium bromide), was synthesized with the rationale of targeting the nitroimidazole to DNA via the phenanthridine ring. The drug is soluble in aqueous solution (greater than 25 mM) and stable at room temperature. It binds to DNA with a binding constant 1/30 that of ethidium bromide. At a concentration of 0.5 mM, NLP-1 is 8 times more toxic to hypoxic than aerobic cells at 37 degrees C. This concentration is 40 times less than the concentration of misonidazole, a non-intercalating 2-nitroimidazole, required for the same degree of hypoxic cell toxicity. The toxicity of NLP-1 is reduced at least 10-fold at 0 degrees C. Its ability to radiosensitize hypoxic cells is similar to misonidazole at 0 degrees C. Thus the putative targeting of the 2-nitroimidazole, NLP-1, to DNA, via its phenanthridine group, enhances its hypoxic toxicity, but not its radiosensitizing ability under the present test conditions. NLP-1 represents a lead compound for intercalating 2-nitroimidazoles with selective toxicity for hypoxic cells
Additional details
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 16
- Journal Issue
- 4
- Series
- Int. J. Radiat. Oncol., Biol. Phys.
- Journal Page Range
- 1039-1043
- ISSN
- 0360-3016
- CODEN
- IOBPD
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 20068201
- Subject category
- S63: RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS; S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANOXIA; CELL CULTURES; EVALUATION; OXYGEN; RADIOSENSITIZERS; TOXICITY
- Descriptors DEC
- DRUGS; ELEMENTS; NONMETALS; RESPONSE MODIFYING FACTORS