首页> 外文期刊>Journal of Liquid Chromatography & Related Technologies >RAPID AND SENSITIVE DETERMINATION OF KETOPROFEN IN MICRO-WHOLE BLOOD SAMPLES BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY AND ITS APPLICATION IN A PHARMACOKINETIC STUDY IN RATS
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RAPID AND SENSITIVE DETERMINATION OF KETOPROFEN IN MICRO-WHOLE BLOOD SAMPLES BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY AND ITS APPLICATION IN A PHARMACOKINETIC STUDY IN RATS

机译:高效液相色谱法快速灵敏地测定微孔血液样品中的酮洛芬及其在大鼠药动学中的应用

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A new simple and sensitive method for determination of ketoprofen in micro-whole blood samples was developed, and its usefulness was demonstrated by the characterization of the oral pharmacokinetics of this drug in rats. Whole blood samples were added with perchloric acid to precipitate proteins, and supernatant was injected into the chromatographic system. Separation of compounds was achieved with a Symmetry C18 column eluted with a mixture of acetonitrile and 0.1 M potassium dihydrogen phosphate solution pH 3.5 (48:52 v/v) as the mobile phase at flow rate of 1.0 mL/min. Detection was carried out by absorbance at 260 nm. Under these conditions the method was linear in the range 0.1-15 µg/mL. In order to demonstrate the usefulness of this method, oral pharmacokinetics of ketoprofen after administration of 1, 3.2, and 10 mg/kg was evaluated in rats. Blood samples were obtained at selected times during 24 hr and successfully analyzed by the method described. It is concluded that the method is suitable for pharmacokinetic studies of ketoprofen using small volume of sample.View full textDownload full textKeywordsHPLC, ketoprofen, micro-whole blood samples, pharmacokineticsRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10826076.2011.551611
机译:建立了一种测定微量全血中酮洛芬的简便,灵敏的新方法,并通过表征该药物在大鼠中的口服药代动力学,证明了其有效性。向全血样品中添加高氯酸以沉淀蛋白质,然后将上清液注入色谱系统。化合物的分离通过用乙腈和0.1 M磷酸二氢钾溶液pH 3.5(48:52 v / v)的混合物作为流动相以1.0 mL / min的流速洗脱的Symmetry C18色谱柱实现。通过在260 nm的吸光度进行检测。在这些条件下,该方法在0.1-15 µg / mL范围内呈线性。为了证明此方法的有效性,在大鼠中评估了酮洛芬1、2、3和10 mg / kg的给药后的口服药代动力学。在24小时内的选定时间获取了血液样本,并通过上述方法成功进行了分析。结论是该方法适用于使用少量样品进行酮洛芬的药代动力学研究。查看全文下载全文关键词高效液相色谱法,酮洛芬,微全血样品,药代动力学相关的var addthis_config = {ui_cobrand:“ Taylor&Francis Online”,services_compact:“ citeulike,netvibes,twitter,technorati,美味,linkedin,facebook,stumbleupon,digg,google,更多”,发布:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10826076.2011.551611

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