王秀, 王冬云, 张文静, 张劲, 余婷婷, 李见春. 高效液相色谱法测定家兔血浆中安妥沙星浓度及药代动力学参数[J]. 蚌埠医科大学学报, 2015, 40(11): 1545-1547,1566. DOI: 10.13898/j.cnki.issn.1000-2200.2015.11.028
    引用本文: 王秀, 王冬云, 张文静, 张劲, 余婷婷, 李见春. 高效液相色谱法测定家兔血浆中安妥沙星浓度及药代动力学参数[J]. 蚌埠医科大学学报, 2015, 40(11): 1545-1547,1566. DOI: 10.13898/j.cnki.issn.1000-2200.2015.11.028
    WANG Xiu, WANG Dong-yun, ZHANG Wen-jing, ZHANG Jin, YU Ting-ting, LI Jian-chun. Determination of antofloxacin concentration in rabbits plasma by high performance liquid chromatography and its pharmacokinetics[J]. Journal of Bengbu Medical University, 2015, 40(11): 1545-1547,1566. DOI: 10.13898/j.cnki.issn.1000-2200.2015.11.028
    Citation: WANG Xiu, WANG Dong-yun, ZHANG Wen-jing, ZHANG Jin, YU Ting-ting, LI Jian-chun. Determination of antofloxacin concentration in rabbits plasma by high performance liquid chromatography and its pharmacokinetics[J]. Journal of Bengbu Medical University, 2015, 40(11): 1545-1547,1566. DOI: 10.13898/j.cnki.issn.1000-2200.2015.11.028

    高效液相色谱法测定家兔血浆中安妥沙星浓度及药代动力学参数

    Determination of antofloxacin concentration in rabbits plasma by high performance liquid chromatography and its pharmacokinetics

    • 摘要: 目的:建立测定家兔血浆中安妥沙星浓度的高效液相色谱方法,探讨安妥沙星在家兔体内的药代动力学特征。方法:取安妥沙星片,按25 mg/kg剂量,研细,分散于0.5%羧甲基纤维素钠溶液中,给家兔灌胃,采血,血样经高氯酸处理后进行高效液相色谱法分析。色谱柱条件:Phenomenex C18柱(250 mm×4.6 mm,4μm);乙腈:50 mmol/L枸橼酸溶液:1 mol/L醋酸胺溶液(19:80:1,体积比)为流动相,流速1.0ml/min;检测波长为295nm,柱温40℃。结果:安妥沙星在家兔血浆中的线性范围为0.164~10.5μg/ml,最低定量限为0.164μg/ml。日内及日间变异均<10%,准确度相对误差<5%。血浆中回收率>80%。实验条件下安妥沙星在家兔体内的药代动力学参数:血药浓度时间曲线下面积为(46.17±13.99)mg·L-1·h-1,达峰时间为(0.9±0.14)h,峰浓度为(5.15±0.54)mg/L,生物半衰期为(11.98±4.02)h,清除率为(0.58±0.19)L·kg-1·h-1结论:该方法经考察符合生物样品的测定要求,可用于测定家兔血浆安妥沙星浓度和药代动力学的研究。

       

      Abstract: Objective: To develop a high performance liquid chromatography method to assess the concentration of antofloxacin in rabbit plasma,and explore the drug metabolism of antofloxacin in rabbits Kinetic characteristics.Methods: Antofloxacin tablets were taken,powdered,added to 0.5% sodium carboxymethyl cellulose solution and mixed.The solution was intragastric administrated to rabbits at a dose of 25 mg/kg.Blood samples were collected.Following protein precipitation,the analytes were separated on a Phenomenex C18 column(250 mm×4.6 mm,4μm),with a mobile phase consisting of acetonitrile 50 mmol/L,citric acid solution 1 mmol/L,ammonium acetate solution(19:80:1,volume/volume) at a flow rate of 1.0 ml/min,and the eluent was detected at 295 nm,column temperature was 40℃.Results: Linear calibration was generated over antofloxacin's concentration range of 0.164 to 10.5μg/ml for plasma samples.Intra-and inter-days precision was<10%,and the accuracy of the relative error was <5%,which were acceptable for all quality control.Samples with relative errors were within the prescribed scopes,including the lowest limit of quantification of 0.164μg/ml.The mean recovery of antofloxacin from plasma was >80%.Pharmacokinetic parameters of antofloxacin in rabbits were estimated as follows:the area under concentration-time curve was(46.17±13.99) mg·L-1·h-1,the time peak was(0.9±0.14) h,the peak concentration was(5.15±0.54) mg/L,the half time was(11.98±4.02) h,and the clearance rate was(0.58±0.19) L·kg-1·h-1.Conclusions: This specific,sensitive and precise method is suitable for the pharmacokinetic study of antofloxacin in rabbits.

       

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