Pfaffenberger C D, Peoples A J, Enos H F
Int J Environ Anal Chem. 1980;8(1):55-65. doi: 10.1080/03067318008071879.
A 31-day rat-dosing sequence was used to study some aspects of the physiological distribution, metabolism, storage and rate of elimination of chloroform, trichloroethylene, carbon tetrachloride and bromodichloromethane from rat adipose tissue and blood serum. Data points were collected nine times during the dosing period and twice after dosing had ceased. Purge/trap/desorb methodology was employed using a liquid sample concentrator, a gas-liquid chromatograph and a Hall electrolytic conductivity detector in series. Compound identities were confirmed using a GC/MS analytical system. For these volatile compounds, tissue levels fluctuated but did not indicate increased storage with time. Adipose tissue to blood serum levels never differed by more than a factor of three. Within 3-6 days after dosing was terminated, practically all of the halogenated compounds had left the examined tissues. Metabolic conversion of trichloroethylene and carbon tetrachloride into chloroform and/or a chloroform precursor was observed; bromodichloromethane-dosed animals did not have serum chloroform levels exceeding those observed for the control animals.
采用31天的大鼠给药序列,研究了氯仿、三氯乙烯、四氯化碳和溴二氯甲烷在大鼠脂肪组织和血清中的生理分布、代谢、储存及消除速率等方面。在给药期间收集了9次数据点,给药停止后收集了2次。采用吹扫/捕集/解吸方法,串联使用液体样品浓缩器、气液色谱仪和霍尔电解电导率检测器。使用GC/MS分析系统确认化合物的身份。对于这些挥发性化合物,组织水平有波动,但未显示随时间增加而储存。脂肪组织与血清中的水平差异从未超过三倍。给药终止后3至6天内,几乎所有卤代化合物都已离开被检查的组织。观察到三氯乙烯和四氯化碳代谢转化为氯仿和/或氯仿前体;给予溴二氯甲烷的动物血清氯仿水平未超过对照动物。