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引用本文:王钰琦,邓思韵,吴毅丹,何秋毅,陈杰.HPLC测定吉米沙星血药浓度[J].中国现代应用药学,2014,31(3):346-349.
WANG Yuqi,WU Yidan,DENG Siyun,HE Qiuyi,CHEN Jie.Determination of Gemifloxacin in Plasma by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2014,31(3):346-349.
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HPLC测定吉米沙星血药浓度
王钰琦, 邓思韵, 吴毅丹, 何秋毅, 陈杰
中山大学附属第一医院,广州 510080
摘要:
目的 建立高效液相色谱法快速测定人血浆中吉米沙星药物浓度。方法 色谱柱为Kromasil C18(250 mm×4.6 mm,5 mm);流动相为乙腈-10 mmol·L-1醋酸铵缓冲液(pH 2.2,含10 mmol·L-1高氯酸)(22∶78);柱温40 ℃;流速1.5 mL·min-1;检测波长为338 nm。血浆样品经5%硫酸锌甲醇溶液沉淀蛋白后进样测定。结果 本测定方法的线性范围:0.05~5 μg·mL-1,r=0.999 9。方法回收率93.2%~104.8%,批内RSD为1.8%~5.1%,批间RSD为7.7%~8.5%。吉米沙星的最低检测浓度为0.02 μg·mL-1。结论 本方法简单、快速、灵敏、重复性好,适用于吉米沙星生物利用度及人体药动学研究。
关键词:  吉米沙星  血药浓度  高效液相色谱法
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Determination of Gemifloxacin in Plasma by HPLC
WANG Yuqi, WU Yidan, DENG Siyun, HE Qiuyi, CHEN Jie
The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China
Abstract:
OBJECTIVE To establish a rapid HPLC method for determination of gemifloxacin in plasma. METHODS A Kromasil C18 column(4.6 mm×250 mm, 5μm) was used at 40 ℃. Mobile phase was a mixture of CH3CN and 10 mmol·L-1 ammonium acetate buffer (pH=2.2, containing 10 mmol·L-1 perchloric acid) (22∶78). The flow rate was 1.5 mL·min-1. The UV detector was operated at 338 nm. Plasma samples were treated by direct protein precipitation with 5% zinc sulfate-methanol solution. RESULTS The assay procedure was shown to produce linear calibration curves over the range of 0.05 μg·mL-1 to 5 μg·mL-1 of gemifloxacin in plasma(r=0.999 9). Within the range, the recovery rate was 93.2%-104.8%, and the RSD within-batch and between-batch were 1.8%~5.1% and 7.7%~8.5%, respectively. The detection limit of gemifloxacin was 0.02 μg·mL-1. CONCLUSION This method is found to be reproducible, convenient and sensitive for bioavailability and clinical pharmacokinetics study of gemifloxacin.
Key words:  gemifloxacin  plasma concentration  HPLC
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