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[Radiosensitizer: hypoxic cell radiosensitizer].

There is a world-wide demand for a clinically usable sensitizer for radio-resistant hypoxic cells. After unsuccessful clinical trials of misonidazole, many efforts have been made to develop new sensitizers. In the U.S., Brown and others reported a new drug named SR-2508 (ethanidazole), which is now in phase II and III clinical trials. In Japan, many drugs were synthesized and tested with the screening systems using EMT6 and SCCVII tumor. Since the failure with misonidazole is due to its neurotoxicity, two methods have been applied to find new sensitizers. The first one is to increase the sensitizing effects and the other is to decrease the neurotoxicity. KU-2285 is fluorinated nitroimidazole, and it has a higher sensitizing effect than misonidazole or SR-2508. Its sensitizing effect is 1.65 at 200 mg/kg, and the LD50 value is 2.3 g/kg. Hoping for less neurotoxicity, RK-28, RP-170 and KIH-801 were synthesized. RP-170 demonstrated less toxicity than Miso, and KIH-801 demonstrated an unexpectedly high sensitizing effect especially is in vivo experiments. Although RK-28 has a low LD50 value, it shows rapid clearance rate from serum and is supposed to have less cumulative neurotoxicity. KU-2285, RK-28, RP-170 and KIH-801 all await further clinical trials.

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Contribution to some radiobiological aspects of the investigation of chemical radiosensitizers of hypoxic cells. Part V: Metronidazole--dependence of its radiosensitizing effect on the dose, time interval of administration and hypoxia degree of the bone marrow evaluated according to the changes of its cellularity in rats.

In the experiments on female rats of Wistar strain the effect of metronidazole (Entizol - Polfa) was studied administrated in aqueous solution with a gastric pipette into the stomach. Dependence was analyzed on the dose of metronidazole, on the time interval of administration before irradiation and on the degree of hypoxia of bone marrow during irradiation induced in the lower part of the body and graded by the abdomen compression with an inflatable rubber cuff with overpressure 4, 6.7, 13.3 and 20 kPa. The effect of whole body irradiation (60Co source) was evaluated according to the changes of bone marrow cellularity (BMC) the third day after irradiation. The sensitizing effect of metronidazole increases rapidly up to dose of 30 mg/kg with rising dose of the drug, then at higher doses only slowly. With prolonging interval of the application of 600 mg/kg body weight the sensibilization increases and reaches the peak after 1-2 hours, then it gradually decreases till the complete disappearance after 10-15 hours. In both cases irradiation was carried out at abdomen compression corresponding to 20 kPa of overpressure in the rubber cuff. The induced hypoxia of bone marrow demonstrated a significant, protective effect, corresponding to the degree of abdomen compression which was reduced by metronidazole administration in the dose of 600 mg/kg. The reduction represents one half to one third of the protective value and is proportional to the degree of induced bone marrow hypoxia during irradiation.

Animals↗

Polyfunctional radiosensitizers. VII. Radiosensitization by conformationally-restricted isomers of a nitroxyl biradical in vitro.

Bothtrans-N,N'-bis(2,2,6,6-tetramethyl-1-oxyl-4-piperidinyl)-1, 2-diaminocyclopropane[Ro31-2269] and its cis isomer [Ro 31-2778] selectively sensitized hypoxic Chinese hamster cells, line V-79-753B, to radiation by decreasing both the D0 value and extrapolation number, whereas a related dibasic monoradical Ro 31-2655 decreased D0 alone. Although sensitization was maximal after a 1-hr cell-drug contact time, cells continued to accumulate both Ro 31-2269 and Ro 31-2778 when this contact time was increased up to 3 hr. There was no evidence for competition between either biradical and 2,2,6,6-tetramethyl-4-piperidinol-N-oxyl (TMPN) at equimolar concentration or biradical and 0.82 microM oxygen when cells were equilibrated with the biradicals for 3 hr prior to irradiation in the presence of mixtures of either oxygen and biradical, TMPN and biradical, or TMPN alone. Furthermore, when cells were equilibrated with an equimolar radical concentration of the trans isomer Ro 31-2269 and TMPN for 1 hr prior to irradiation in the presence of the mixture, there was no appreciable effect on sensitization of the slope of the hypoxic cell survival curve, but shoulder modification was reduced. When cells were equilibrated with the trans isomer Ro 21-2269 prior to irradiation in combination with 2.92 microM oxygen, cell survival was similar to that seen for cells irradiated with this concentration of oxygen alone. Examination of the plasma membrane from cells equilibrated with the trans biradical Ro 31-2269 showed that the drug accumulated in the membrane when compared with the concentration found in whole cells. Experiments with the conformationally-unrestricted biradical bis(2,2,6,6-tetramethyl-1-oxy-4-piperidinyl) succinate [Ro 03-6061] showed that when cells were equilibrated with the compound for 1 hr prior to irradiation in hypoxia in the presence of a mixture containing an equimolar radical concentration of TMPN, there was an increase in both the slope and the extrapolation number compared with values for hypoxic cells irradiated in the presence of this biradical alone. Furthermore, when cells which had been equilibrated with Ro 03-6061 were washed free of the drug, there was a residual decrease in both the D0 and extrapolation number of the hypoxic cell survival curve for at least 3 hr after removal of the compound. The results are discussed in terms of a model to account for sensitization by these compounds.

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