Pacha W, Delaborde C, Keller H P, Meier J, Rietsch H
Arzneimittelforschung. 1981;31(5a):893-6.
A rapid and sensitive fluorimetric assay was developed for the quantitative determination of 4-(p-fluorophenyl)-1-isopropyl-7-methyl-2(1H)-quinazolinone(fluproquazone) in plasma and urine. The unchanged drug was extracted from alkalinized plasma or urine into n-heptane containing 0--1.5% isoamyl alcohol followed by a back extraction into 5 N HCl. After oxidation with potassium persulfate the fluorescence measurements were taken at 326 nm excitation and 520 nm emission. Detection limits were about 15 ng/ml plasma and 6 ng/ml urine, using 1 ml plasma and 2 ml urine, respectively. The automated assay had a five times higher sample capacity and better reproducibility (+/- 3%) than the manual assay (+/- 5%). The method was applied to animal studies including assays in milk and proved to be suitable in human studies after oral doses in the therapeutical range.
开发了一种快速灵敏的荧光分析法,用于定量测定血浆和尿液中的4-(对氟苯基)-1-异丙基-7-甲基-2(1H)-喹唑啉酮(氟丙喹唑)。将未变化的药物从碱化的血浆或尿液中萃取到含有0-1.5%异戊醇的正庚烷中,随后反萃取到5N盐酸中。用过硫酸钾氧化后,在激发波长326nm和发射波长520nm处进行荧光测量。分别使用1ml血浆和2ml尿液时,检测限约为血浆15ng/ml和尿液6ng/ml。自动化分析的样品处理能力比手动分析高五倍,重现性更好(分别为±3%和±5%)。该方法应用于动物研究,包括牛奶中的分析,并且在口服治疗剂量范围内的人体研究中证明是适用的。