Robert T A, Hagardorn A N
J Chromatogr. 1983 Aug 12;276(1):77-84.
Five groups of six ICR mice were orally dosed with 22.5 mg/kg 2,4-dinitrophenol. Groups were sacrificed at 1, 3, 6, 12, and 24 h post treatment, and serum, liver, and kidney tissues were collected for analysis of dinitrophenol content. Quantitation was performed via a capillary gas chromatography--mass spectrometry technique after liquid--liquid extraction of biological specimens spiked with a trideuterated dinitrophenol internal standard. Concentration versus time data for each tissue were subjected to pharmacokinetic analysis. Similar two-compartment open models were found to characterize most phases of the disposition of this compound. The kidney appears to maintain a more persistent low concentration of 2,4-dinitrophenol.
将五组每组六只ICR小鼠口服给予22.5mg/kg的2,4 - 二硝基苯酚。在治疗后1、3、6、12和24小时处死各组小鼠,并收集血清、肝脏和肾脏组织用于分析二硝基苯酚含量。在用氘代二硝基苯酚内标加标的生物标本进行液 - 液萃取后,通过毛细管气相色谱 - 质谱技术进行定量分析。对每个组织的浓度 - 时间数据进行药代动力学分析。发现相似的二室开放模型可表征该化合物处置的大多数阶段。肾脏似乎维持着2,4 - 二硝基苯酚更持久的低浓度。