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

机译:皮肤接触后无毛大鼠的全身吸收和清除氯仿的方法:II。吸收纯溶剂。

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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.
机译:将无毛大鼠小面积(约5.5 cm2)的背部暴露于过量的溶剂中1分钟,3分钟或8分钟后,监测氯仿的血药浓度。通过将血液浓度的曲线下面积(AUC)与时间图相比较,以已知浓度的氯仿水溶液注入30分钟后获得的AUC(阳性对照)来量化吸收量。氯仿迅速穿透真皮屏障,皮肤的角质层和较深的皮肤组织仅在短时间内充当氯仿的储库。一旦从表面除去氯仿,从这些储层的蒸发和生理清除很快。用于限制接触影响的摄取模板的压力。对于血液水平,达到最大血药浓度的时间随着暴露时间的延长而增加。吸收的量还取决于暴露时间。血药水平表明,暴露3分钟后全身吸收的氯仿比暴露1分钟高约1.3倍(不显着),而暴露8分钟产生的AUC比3分钟时高约3.8倍。最小值(p = 0.026)。从大鼠血液中快速清除氯仿(终末清除速率常数= 0.009 / min)。计算表明,从这些区域受限的接触中吸收的氯远远超过了将氯仿以饱和水溶液形式存在于皮肤中所吸收的吸收。

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