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A New, Rapid, Fully Automated Method for Determination of Fluconazole in Serum by Column-Switching Liquid Chromatography.

机译:一种快速,全自动的柱切换液相色谱法测定血清中氟康唑的方法。

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A sensitive and rapid HPLC assay for the determination of fluconazole in serum is described. HPLC-integrated sample preparation allows direct injection of serum samples without any pretreatment. The in-line extraction technique is carried out by automatically switching from the extraction column (Lichrospher ADS C8) to the analytic column (Nucleosil C18). After 6 minutes the matrix passes the extraction column, and the retained analyte is quantitatively transferred to the analytic column, where separation by isocratic HPLC is performed. The extraction eluent is sodium dihydrogen phosphate buffer, pH 5.0 (50 mM), and the analytic eluent is acetonitrile/sodium dihydrogen phosphate buffer, pH 5.0 (50 mM) (26.8/73.2, vol/vol). Fluconazole is detected according to its absorption maximum at 210 nm. The lower limit of quantification (LLOQ) is 0.65 microg/mL, the limit of detection (LOD) is 0.2 microg/mL, and the quantification range is 0.65-23.3 microg/mL. The assay was precise with a between-run coefficient of variation of
机译:描述了一种灵敏而快速的HPLC测定血清中氟康唑的方法。 HPLC集成的样品制备无需任何预处理即可直接注射血清样品。在线提取技术是通过自动从提取柱(Lichrospher ADS C8)切换到分析柱(Nucleosil C18)来进行的。 6分钟后,基质通过萃取柱,并将保留的分析物定量转移至分析柱,在此通过等度HPLC进行分离。萃取洗脱液为pH 5.0(50 mM)的磷酸二氢钠缓冲液,分析洗脱液为pH 5.0(50 mM)的乙腈/磷酸二氢钠缓冲液(26.8 / 73.2,vol / vol)。根据氟康唑在210 nm处的最大吸收进行检测。定量下限(LLOQ)为0.65微克/毫升,检测限(LOD)为0.2微克/毫升,定量范围为0.65-23.3微克/毫升。该测定精确,间运行变异系数为5.59%。对于23.3 microg / mL和1.3 microg / mL的浓度,批内准确度分别为99.8%和103.4%,批间准确度分别为99.2%和99.7%。回收率为78%。所描述的程序允许在20分钟内清理和确定样品,从而有助于临床常规中的药物监测。该方法已成功应用。

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