Lu J, Cwik M, Kanyok T
Clinical Research Laboratory, College of Pharmacy, University of Illinois at Chicago, 60612, USA.
J Chromatogr B Biomed Sci Appl. 1997 Aug 1;695(2):329-35. doi: 10.1016/s0378-4347(97)00192-8.
A sensitive high-performance liquid chromatographic method for the determination of paromomycin in human plasma and urine was developed. Paromomycin was quantitated following pre-column derivatization with 2,4-dinitrofluorobenzene (DNFB). The chromatographic separation was carried out on a C18 column at 50 degrees C using a mobile phase consisting of 64% methanol in water adjusted to pH 3.0 with phosphoric acid. The eluents were monitored by UV detection at 350 nm. The linearity of response for paromomycin was demonstrated at concentrations from 0.5 to 50 microg/ml in plasma and 1 to 50 microg/ml in urine. The relative standard deviation of the assay procedure is less than 5%.
建立了一种灵敏的高效液相色谱法用于测定人血浆和尿液中的巴龙霉素。巴龙霉素经2,4-二硝基氟苯(DNFB)柱前衍生化后进行定量分析。色谱分离在C18柱上于50℃进行,流动相为含64%甲醇的水溶液,用磷酸调至pH 3.0。洗脱液在350 nm处用紫外检测进行监测。巴龙霉素在血浆中浓度为0.5至50μg/ml、尿液中浓度为1至50μg/ml时呈现线性响应。该测定方法的相对标准偏差小于5%。