TY - JOUR
T1 - No-Observed-Effect Level of Diborane on the Respiratory Organs of Male Mice in Acute and Subacute Inhalation Experiments
AU - Nomiyama, Tetsuo
AU - Omae, Kazuyuki
AU - Uemura, Takamoto
AU - Nakashima, Hiroshi
AU - Takebayashi, Toru
AU - Ishizuka, Chizuru
AU - Sakurai, Haruhiko
AU - Yamazaki, Kazuto
PY - 1995
Y1 - 1995
N2 - No-Observed-Effect Level of Diborance on the Respiratory Organs of Male Mice in Acute and Subacute Inhalation Experiments: Tetsuo NOMIYAMA, et al. Department of Preventive Medicine and Public Health, School of Medicine, Keio University-In order to clarify the acute and subacute toxicity of diborane (B2H6, CAS: 19287-45-7) at low concentrations, male ICR mice were exposed to diborane for 1, 2, 4 or 8 h at concentrations of 1 or 5 ppm (phase I study), and for 6 h/day, 5 days/wk, over 2 or 4 wk at concentrations of 0.2 or 0.7 ppm (phase II study). Hematological and biochemical tests, and histopathological examinations of the cornea, nasal mucosa, respiratory tract and lung were carried out. All mice in both studies survived until they were sacrificed. In the phase I study, lung weight increased significantly in mice exposed to 5 ppm of diborane for 8 h. Histopathologically diffuse panbronchiolitis-like lesion was observed in mice exposed to 5 ppm of diborane for 2, 4 or 8 h. In the phase II study, slight infiltration of polymorphous neutrophil was observed mainly in the peribronchiolar region in mice exposed to 0.2 ppm or 0.7 ppm of diborane for 2 or 4 wk. In both studies, hematological and biochemical examinations failed to reveal any exposure-related changes. These results suggest that no-observed-effect level of diborane inhalation on the respiratory organs were 1 ppm in acute exposure, but 0.2 ppm of diborane inhalation for 2 or 4 wk seems to be unsafe. [J Occup Health 1995; 37: 157-160).
AB - No-Observed-Effect Level of Diborance on the Respiratory Organs of Male Mice in Acute and Subacute Inhalation Experiments: Tetsuo NOMIYAMA, et al. Department of Preventive Medicine and Public Health, School of Medicine, Keio University-In order to clarify the acute and subacute toxicity of diborane (B2H6, CAS: 19287-45-7) at low concentrations, male ICR mice were exposed to diborane for 1, 2, 4 or 8 h at concentrations of 1 or 5 ppm (phase I study), and for 6 h/day, 5 days/wk, over 2 or 4 wk at concentrations of 0.2 or 0.7 ppm (phase II study). Hematological and biochemical tests, and histopathological examinations of the cornea, nasal mucosa, respiratory tract and lung were carried out. All mice in both studies survived until they were sacrificed. In the phase I study, lung weight increased significantly in mice exposed to 5 ppm of diborane for 8 h. Histopathologically diffuse panbronchiolitis-like lesion was observed in mice exposed to 5 ppm of diborane for 2, 4 or 8 h. In the phase II study, slight infiltration of polymorphous neutrophil was observed mainly in the peribronchiolar region in mice exposed to 0.2 ppm or 0.7 ppm of diborane for 2 or 4 wk. In both studies, hematological and biochemical examinations failed to reveal any exposure-related changes. These results suggest that no-observed-effect level of diborane inhalation on the respiratory organs were 1 ppm in acute exposure, but 0.2 ppm of diborane inhalation for 2 or 4 wk seems to be unsafe. [J Occup Health 1995; 37: 157-160).
KW - Diborane
KW - Inhalation toxicity
KW - Mouse
KW - Respiratory system
KW - Semiconductor
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U2 - 10.1539/sangyoeisei.37.3_157
DO - 10.1539/sangyoeisei.37.3_157
M3 - Article
C2 - 7796306
AN - SCOPUS:0029054751
SN - 1341-0725
VL - 37
SP - 157
JO - Journal of occupational health
JF - Journal of occupational health
IS - 3
ER -