Inagaki K, Takagi J, Lor E, Okamoto M P, Gill M A
Faculty of Pharmacy, Meijo University, Aichi, Japan.
Ther Drug Monit. 1992 Aug;14(4):306-11. doi: 10.1097/00007691-199208000-00008.
A simple, rapid, and accurate reversed-phase octadecylsilyl high-performance liquid chromatographic method using solid-phase column extraction is described for measuring fluconazole in human serum. The column eluent was monitored by ultraviolet absorption at 210 nm. Fluconazole was extracted from diluted serum by adsorption on a small Bond-Elut C18 cartridge after the addition of UK48,134 as the internal standard and recovered by elution with methanol. The methanol was then evaporated to dryness and the residue reconstituted in 200 microliters of mobile phase and filtered prior to injecting an aliquot (50 microliters) onto an Adsorbosphere C18 column (4.6 x 250 mm, 5 microns particle size), using a mobile phase of 25 mM tris(hydroxymethyl)aminomethane-phosphate buffer (pH 7.0):acetonitrile (75:25, vol/vol). The retention times were 6.6 min for fluconazole and 9.0 min for the internal standard. The assay was precise, with inter- and intraassay coefficients of variation of less than or equal to 2.9% and less than or equal to 2.1%, respectively, and with good linearity (r = 1.000) in the range of 0.1 to 25 micrograms/ml. The duration of each analysis was 15 min and the minimum detectable serum concentration was 0.1 microgram/ml.
本文描述了一种采用固相柱萃取的简单、快速且准确的反相十八烷基硅烷键合硅胶高效液相色谱法,用于测定人血清中的氟康唑。通过在210nm处的紫外吸收监测柱洗脱液。加入UK48,134作为内标后,氟康唑通过吸附在小型Bond-Elut C18柱上从稀释血清中萃取出来,并用甲醇洗脱回收。然后将甲醇蒸发至干,残渣用200微升流动相复溶并过滤,取50微升注入Adsorbosphere C18柱(4.6×250mm,粒径5微米),流动相为25mM三(羟甲基)氨基甲烷-磷酸盐缓冲液(pH 7.0):乙腈(75:25,体积/体积)。氟康唑的保留时间为6.6分钟,内标的保留时间为9.0分钟。该测定方法精密度良好,批间和批内变异系数分别小于或等于2.9%和小于或等于2.1%,在0.1至25微克/毫升范围内线性良好(r = 1.000)。每次分析时长为15分钟,最低可检测血清浓度为0.1微克/毫升。