Nakagawa T, Higuchi T, Haslam J L, Shaffer R D, Mendenhall D W
J Pharm Sci. 1979 Jun;68(6):718-21. doi: 10.1002/jps.2600680617.
An assay was developed for determining mefloquine (quinolinemethanol) and pyridinemethanol derivative concentrations in whole blood. The method involved ion-pair extraction or usual solvent extraction for drug recovery from whole blood followed by trimethylsilylation. The silylated compounds were then submitted to GLC with electron-capture or flame-ionization detection. Mass spectrometry combined with GLC of the trimethylsilyl derivatives indicated that substitution of one trimethylsilyl group had occurred on the hydroxyl group. A phenyl methyl silicone column with temperature programming separated the drugs from normal blood extracts. The determination limit was 10 ng/ml of whole blood when an electron-capture detector was used with ion-pair extraction. Quantitation was achieved by using one antimalarial as an internal standard for the assay of the other. The utility of the present method was demonstrated by following the whole blood level time course after a single oral 250-mg tablet in beagle dogs.
已开发出一种用于测定全血中甲氟喹(喹啉甲醇)和吡啶甲醇衍生物浓度的分析方法。该方法包括离子对萃取或常规溶剂萃取,用于从全血中回收药物,随后进行三甲基硅烷化。然后将硅烷化的化合物进行气相色谱分析,并采用电子捕获或火焰离子化检测。质谱联用三甲基硅烷基衍生物的气相色谱分析表明,在羟基上发生了一个三甲基硅烷基的取代。采用程序升温的苯基甲基硅氧烷柱可将药物与正常血液提取物分离。当使用电子捕获检测器和离子对萃取时,全血的测定限为10 ng/ml。通过使用一种抗疟药作为另一种抗疟药测定的内标来实现定量。在比格犬单次口服250 mg片剂后,通过跟踪全血水平随时间的变化过程,证明了本方法的实用性。