[Pharmacokinetics of arsenic trioxide in the mouse].

C Brunet, M Luyckx, M Cazin
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Abstract

Considering the diversity of previous observations given by literature about the metabolic fate or arsenic, the authors using a radioactive tracer, study the pharmacokinetics of that arsenical derivative after giving the mouse a non toxic dose. By the oral route, this compound is quickly absorbed and resorbed. The elimination process mainly occurs by renal route then by the faecal route. The blood results or the concentrations in the tissues do not reveal any retention process though the latter always rise above blood levels. During the first two hours the concentrations in the thymus seem to be particularly interesting.

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三氧化二砷在小鼠体内的药代动力学。
考虑到先前文献中关于砷代谢命运的观察结果的多样性,作者使用放射性示踪剂,在给予小鼠无毒剂量后研究砷衍生物的药代动力学。通过口服途径,这种化合物被迅速吸收和再吸收。清除过程主要通过肾脏途径,然后通过粪便途径。血液结果或组织中的浓度没有显示任何滞留过程,尽管后者总是高于血液水平。在头两个小时胸腺的浓度似乎特别有趣。
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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