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机构地区:[1]浙江杭州红十字会医院,浙江杭州310009 [2]浙江嘉兴学院医学院,浙江嘉兴314001
出 处:《中国现代应用药学》2005年第2期163-165,共3页Chinese Journal of Modern Applied Pharmacy
摘 要:目的建立RP-HPLC测定复方氟脲嘧啶二甲亚砜溶液中氟脲嘧啶和氢化可的松的含量.方法以水为溶剂,采用RPHPLC法,以Supelco discovery C18(150mm×4.6mm,5μm)为色谱柱,甲醇-0.5%醋酸(内含0.005mol/L庚烷磺酸钠)(60:40)为流动相,检测波长为248nm.结果氟脲嘧啶浓度在61.6~143.8μg·mL-1与氢化可的松浓度在6.3~14.6μg·mL-1之间与峰面积呈良好线性关系,日内、日间精密度(RSD)氟脲嘧啶为0.52%和0.63%,氢化可的松为0.49%和0.76%,平均回收率(n=6)氟脲嘧啶为(101.0±0.32)%,氢化可的松为(100.1±0.23)%.结论本法简便、快速、结果准确,适于该制剂的质量控制.OBJECTIVE To establish an ion-pair RP- HP LC method for determination of fluoruracil and dimethy sulfoxy in compound fluor ouracil and dimethy sulfoxy solution.METHOD Analytical column was discovery C 18(150mm×4.6mm,5 μm),Mobile phase consisted of methanol -0.5% acetic acid (contained 0.005mol ·L -1 of heptanesulfonic sodium) (60∶40),detection wavelength was 248nm.RESULTS The linearities were obtained in the ranges of 61.6~14 3.8μg·mL -1 (r=0.9998) from fluorouracil and 6.3~14.6μg·mL -1 (r=0.9999) from hydrocortisone.The precisions (RSD) of intra-day and inter -day were 0.52% and 0.63% from fluorouracil and 0.49% and 0.76% from hydroc ortisone.The mean recoveries (n=6) were (101.0±0.32)% fro fluorouracil and (100.1±0.23)% for hydrocortisone.CONCLUSION The method is simple,accurate,rapid and suitable for the quality control of this preparation.
关 键 词:离子对反相高效液相色谱法 氢化可的松 复方氟脲嘧啶 二甲亚砜 同时测定 含量 溶液 RP-HPLC测定 HPLC法 平均回收率 线性关系 检测波长 质量控制 色谱柱 流动相 磺酸钠 峰面积 精密度 浓度
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