Systemic uptake and clearance of chloroform by hairless rats following dermal exposure: II. Absorption of the neat solvent.

M S Islam, L Zhao, J Zhou, L Dong, J N McDougal, G L Flynn
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引用次数: 3

Abstract

Blood concentrations of chloroform were monitored after exposing small areas (approximately 5.5 cm2) of the backs of hairless rats to liberal excesses of the solvent for either 1, 3, or 8 min. The amounts absorbed were quantified by comparing areas-under-the-curves (AUCs) of blood concentration versus time plots to the AUC obtained on infusing an aqueous chloroform solution of known concentration for 30 min (positive control). Chloroform penetrated the dermal barrier rapidly, the skin's horny layer and the deeper skin tissues acting as reservoirs for chloroform only for short durations. Evaporative and physiological clearance from these reservoirs was rapid once the chloroform was removed from the surface. Pressure of the template used to confine the exposure affected uptake. For blood levels, the time to reach the maximum blood concentration increased with increased exposure duration. Amounts absorbed also depended on exposure duration. Blood level profiles indicated systemic uptake of chloroform following a 3-min exposure was about 1.3-fold higher than for a 1-min exposure (not significant), while the 8-min exposure produced an AUC roughly 3.8-fold higher than found at 3 min (p = 0.026). Chloroform is rapidly cleared from rat blood (terminal elimination rate constant = 0.009/min). Calculations indicated that its absorption from these area-limited exposures far exceeds that which would be absorbed had the chloroform been presented to the skin as a saturated aqueous solution.

皮肤暴露后无毛大鼠对氯仿的全身摄取和清除:对纯溶剂的吸收。
将无毛大鼠背部的一小块区域(约5.5 cm2)暴露在过量的溶剂中1,3,8分钟后,监测氯仿的血液浓度。通过将血液浓度曲线下面积(AUC)与时间图的曲线下面积(AUC)与输注已知浓度氯仿水溶液30分钟(阳性对照)时获得的AUC进行比较,来定量吸收的量。氯仿迅速穿透真皮屏障,皮肤角质层和更深的皮肤组织作为氯仿的储存库只能持续很短的时间。一旦氯仿从表面除去,这些储层的蒸发和生理清除很快。模板的压力用来限制曝光影响吸收。对于血药浓度,达到最大血药浓度的时间随着暴露时间的增加而增加。吸收量也取决于暴露时间。血液水平谱显示,暴露3分钟后氯仿的全身摄取比暴露1分钟时高1.3倍(无显著性),而暴露8分钟后产生的AUC比暴露3分钟时高3.8倍(p = 0.026)。氯仿能迅速从大鼠血液中清除(最终清除速率常数= 0.009/min)。计算表明,从这些面积有限的暴露中吸收的氯仿远远超过以饱和水溶液形式暴露在皮肤上所吸收的氯仿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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