Hoar D R, Bowen M H
J Pharm Sci. 1977 May;66(5):725-6. doi: 10.1002/jps.2600660530.
A method is presented for the quantitative determination of free triclocarban in rat or human blood. The procedure involves the extraction from blood with acetone, a TLC cleanup, derivatization with N,O-bis (trimethylsily) acetonide, and GLC using an electron-capture detector. GLC-mass spectral analysis confirmed that the structure of the derivative was a bis (trimethylsilyl) molecule with one group on a nitrogen and the second group attached to the enol tautomer. The method is sensitive to 25 ng (12.5 microgram/liter of blood). Recoveries of added triclocarban in the 12.5--50-microgram/liter range weree between 80 and 90%.
本文介绍了一种定量测定大鼠或人血液中游离三氯卡班的方法。该程序包括用丙酮从血液中萃取、薄层层析净化、用N,O-双(三甲基硅基)乙酰胺衍生化,以及使用电子捕获检测器的气相色谱法。气相色谱-质谱分析证实,衍生物的结构是一个双(三甲基硅基)分子,一个基团连接在氮上,第二个基团连接到烯醇互变异构体上。该方法对25纳克(12.5微克/升血液)敏感。添加的三氯卡班在12.5 - 50微克/升范围内的回收率在80%至90%之间。