Experimental exposure to methyl tertiary-butyl ether -: I.: Toxicokinetics in humans

被引:45
|
作者
Nihlén, A [1 ]
Löf, A
Johanson, G
机构
[1] Natl Inst Working Life, Dept Toxicol & Chem, S-17184 Solna, Sweden
[2] Univ Uppsala Hosp, Dept Occupat & Environm Med, S-75185 Uppsala, Sweden
关键词
biological monitoring; exposure; gasoline; human; methyl tertiary-butyl ether; MTBE; oxygenated fuels; MBA; tertiary-butyl alcohol; toxicokinetics;
D O I
10.1006/taap.1997.8333
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Methyl tertiary-butyl ether (MTBE) is widely used in gasoline as an oxygenate and octane enhancer. The aim of this study was to evaluate the uptake, distribution, metabolism, and elimination of MTBE in humans. Ten healthy male volunteers were exposed to MTBE vapor (5, 25, and 50 ppm) on three different occasions during 2 h of light physical exercise (50 W). MTBE and the metabolite tertiary-butyl alcohol (TEA) were monitored in exhaled air, blood, and urine. Blood and urine were collected at selected time intervals, during and up to 3 days after the exposure, and analyzed by head space gas chromatography. MTBE in exhaled air was collected with sorbent sample tubes and subsequently analyzed by gas chromatography. The respiratory uptake of MTBE was rather low (42-49%), and the respiratory exhalation was high (32-47%). A relatively low metabolic blood clearance (0.34-0.52 L/h/kg) was seen compared to many other solvents. The kinetic profile of MTBE in blood could be described by four phases, and the average half-lives were 1 min, 10 min, 1.5 h, and 19 h. The post-exposure decay curve of MTBE in urine was separated into two linear phases, with average half-lives of 20 min and 3 h. The average post-exposure half-lives of TEA in blood and urine were 10 and 8.2 h, respectively. The urinary excretion of MTBE and TEA was less than 1% of the absorbed dose, indicating further metabolism of TEA, other routes of metabolism, or excretion. The kinetics of MTBE and TEA were linear up to the highest exposure level of 50 ppm. We suggest that TEA in blood or urine is a more appropriate biological exposure marker for MTBE than the parent ether itself. (C) 1998 Academic Press.
引用
收藏
页码:274 / 280
页数:7
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