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机构地区:[1]中山大学附属第六医院药剂科,广州510655 [2]中山大学附属第一医院药学部,广州510080
出 处:《国际医药卫生导报》2010年第4期477-479,共3页International Medicine and Health Guidance News
摘 要:目的建立RP—HPI.c法测定人血浆巾头孢吡肟的浓度。方法色谱柱:NueleodurC18分析柱(4.6mm×250mm,5μm),流动相:0.03%三氟乙酸缓冲液/乙腈(81/19,V/V,冰醋酸调节pH=5),流速1.0ml/min,检测波长270nm,柱温30℃,进样量20μl。结果头孢吡肟线性范围为0.02~5.0μg/ml。头孢吡肟的最低检测限为0.02μg/ml,日内、日间RSD均小于5%,相对回收率为97.6%~104.5%,提取回收率均大于91.3%。结论该方法灵敏、简便、准确度高,可用于头孢吡肟的血药浓度测定。Objective To establish a RP-HPLC method for determination of Cefepime concentration in human plasma. Methods Nucleodur C18 was used with the mobile phase of 0.03 % trifluoro acetic acid buffer / acetonitrile (81/19, v/v PH=5) at the detection wavelength of 270 nm. The flow rate was 1.0 ml/min. Results Under the condition of this cefditoren in plasma was well separated, the calibration curve was linear in the range of 0.02 - 5.0 μ g/ml. The limit of quantification was 0.02 μg/ml. The RSD of intra- and inter-day were less than 5%, the relative recovery was 97.6% - 104.5% and the extraction recovery was above 91.3%. Conclusion This validated method is sensitive, simple and repeatable enough to he used in pharmacokinetic studies.
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