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Determination of Gemifloxacin in human plasma by high performance liquid chromatography using Ultra Violet detector and its application to a bioequivalence study

机译:紫外检测器高效液相色谱法测定人血浆中的吉米沙星及其在生物等效性研究中的应用

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A liquid chromatography method was developed and validated for the determination of gemifloxacin in human plasma using chloramphenicol as internal standard to achieve lower quantification limit. Acetonitrile was used to precipitated and extracted analyte and internal standard from plasma by Protein Precipitation. Analysis was performed isocratically on C 18 column using 25% acetonitrile and 75% 0.02 M phosphate buffer as mobile phase. The method was demonstrated to be linear from 0.003 μg/mL to 5 μg/mL with the lower limit of quantitation of 0.003 μg/mL. The method was successfully applied for the bioequivalence study of gemifloxacin after a single oral administration of 320 mg gemifloxacin mesylate tablets to 12 healthy volunteers.
机译:开发了一种液相色谱方法,并验证了使用氯霉素作为内标物测定人血浆中吉西沙星的含量,以达到较低的定量限。乙腈用于通过蛋白质沉淀从血浆中沉淀和提取分析物和内标。使用25%乙腈和75%0.02 M磷酸盐缓冲液作为流动相,在C 18色谱柱上进行等度分析。结果表明该方法在0.003μg/ mL至5μg/ mL之间呈线性,定量下限为0.003μg/ mL。该方法成功地应用于12名健康志愿者口服320 mg甲磺酸吉非沙星片剂后,吉非沙星的生物等效性研究成功。

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