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1 Toxicology Division, Directorate of Medical Research, U. S. Army Chemical Research and Development Laboratories, Edgewood Arsenal, Maryland
LC50 values of pentaborane were determined for mice at 0.5-, 2-, 5-, and 15-minute exposure periods, for dogs at 2-, 5-, and 15-minute exposure periods, and for monkeys at 2-minute exposure periods. All deaths occurred within 24 hours, although the observation period was 7 days. The LC50s of mice, calculated by the method of Bliss, were 1,034, 342, 136, and 50 mg/cu m for 0.5-, 2-, 5-, and 15-minute exposures, respectively. For dogs, LC50s of 734, 324, and 92 mg/cu m for 2-, 5-, and 15-minute exposures, respectively, were found. The 2-minute LC50 for monkeys was 640 mg/cu m.
Additional exposures of dogs and monkeys to concentrations approximating one-half, one-fourth, and one-eighth of their respective LC5Os at each exposure time listed above were conducted. Dogs were observed for toxic signs and for variation in a conditioned avoidance response (CAR) test. Monkeys were observed for toxic signs and for changes in blood components (erythrocytes, packed red blood cell volume, hemoglobin, total and differential leukocyte count) and bromsulphalein (BSP) retention. Histopathologic studies were made on monkeys sacrificed 1, 2, and 4 weeks after exposure. All animals showed severe signs of intoxication after exposure to one-half of their LC50s, but minimal or no signs were noted after exposures to one-fourth and one-eighth of their LC50s. CAR effects occurred only after
-LC50 exposures. No notable changes in the blood cell components and in BSP retention were seen. No gross or microscopic lesions were seen that could be considered compound-induced.