The sub-chronic toxicity of regular White Spirit in rats

被引:12
|
作者
Carrillo, Juan-Carlos [1 ]
Adenuga, M. David [2 ]
Mckee, Richard H. [2 ]
机构
[1] Shell Int BV, Shell Hlth, NL-2501 AN The Hague, Netherlands
[2] ExxonMobil Biomed Sci Inc, Annandale, NJ 08801 USA
关键词
Alkanes; Aromatic hydrocarbons; Sub-chronic toxicity; Inhalation toxicity; Occupational exposure limit; Liver enlargement; UVCB; Hydrocarbon solvent; Stoddard solvent; White spirit; TERM INHALATION EXPOSURE; EXPERIMENTAL-ANIMALS; DOSE LEVELS;
D O I
10.1016/j.yrtph.2014.07.007
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Hydrocarbon solvents are mostly complex substances (UVCB) with carbon numbers in the range of approximately C5-C20. One of the most common types is a C9-C14 aliphatic solvent containing approximately 20% aromatics and commonly known as White Spirit in Europe and mineral spirits in the US. In previous repeated inhalation toxicity studies, White Spirit was reported to cause minimal systemic effects in most animal species with few effects other than male rat-specific kidney changes at levels up to approximately 2000 mg/m(3). In the present study male and female rats were exposed to White Spirit vapors, 6 h/day, 5 days/week for 13 weeks at levels of approximately 2000, 4000, or 8000 mg/m(3) to assess the potential for effects at higher exposure levels. All of the rats survived the treatment period. In life observations were largely restricted to acute central nervous system (CNS) effects in the high exposure group. Terminal body weights of high exposure groups animals were significantly below control values. Statistically significant differences in the clinical and hematological observations were small and within normal physiological limits. Weights of some organs including liver, spleen and kidneys were elevated, but microscopic examination indicated that the only pathological effects were changes in the kidneys of the male rats, consistent with an alpha 2u-globulin-mediated process, which is gender and species-specific and not relevant to humans. The overall no observed adverse effect level (NOAEC) was 4000 mg/m(3). (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:222 / 230
页数:9
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