Kobayashi Toshimi, Homma Masato, Momo Kenji, Kobayashi Daisuke, Kohda Yukinao
Department of Pharmaceutical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba, Ibaraki, Japan.
Biomed Chromatogr. 2011 Apr;25(4):435-8. doi: 10.1002/bmc.1488.
We developed a simple assay method for the determination of serum and urine norfloxacin and enoxacin using reversed-phase high-performance liquid chromatography and perchloric acid precipitation for sample pre-treatment. Optimized conditions can permit detection of norfloxacin and enoxacin in the same chromatogram, so either compound can be used as an internal standard for another determinant. Supernatants of the precipitated samples were analyzed by the octadecylsilyl silica-gel column under ambient temperature and an ultraviolet wavelength of 272 nm. A mobile phase solvent consisting of 20 mm sodium dihydrogenphosphate (pH 3.0) and acetonitrile (85:15, v/v) was pumped at a flow rate of 1.0 mL/min. The calibration curves for norfloxacin and enoxacin at a concentration of 62.5-1000 ng/mL for serum and 250-4000 ng/mL for urine were linear (r > 0.9997). The recoveries of norfloxacin and enoxacin from serum and urine were >94% with the coefficient of variations (CV) <5%. The CVs for intra- and inter-day assay of norfloxacin and enoxacin were <4.2 and <5.5%, respectively. This method can be applied to the pharmacokinetic study of norfloxacin and enoxacin after repeated administration to assess changes in CYP1A2 activity in healthy subjects.
我们开发了一种简单的检测方法,用于测定血清和尿液中的诺氟沙星和依诺沙星,该方法采用反相高效液相色谱法,并使用高氯酸沉淀法进行样品预处理。优化后的条件可使诺氟沙星和依诺沙星在同一色谱图中被检测到,因此任一化合物都可作为另一种测定物的内标。沉淀样品的上清液在室温及272 nm紫外波长下,通过十八烷基硅烷硅胶柱进行分析。以20 mM磷酸二氢钠(pH 3.0)和乙腈(85:15,v/v)组成的流动相溶剂,以1.0 mL/min的流速泵送。血清中诺氟沙星和依诺沙星浓度为62.5 - 1000 ng/mL、尿液中浓度为250 - 4000 ng/mL时的校准曲线呈线性(r > 0.9997)。诺氟沙星和依诺沙星在血清和尿液中的回收率>94%,变异系数(CV)<5%。诺氟沙星和依诺沙星日内和日间检测的CV分别<4.2%和<5.5%。该方法可应用于健康受试者多次给药后诺氟沙星和依诺沙星的药代动力学研究,以评估CYP1A2活性的变化。