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Determination of Gliclazide in human plasma by RP-HPLC

机译:RP-HPLC法测定人血浆中格列齐特

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Aim To establish a simple and sensitive high performance liquid chromatographic (HPLC) method involving ultraviolet detecting for the determination of Gliclazide in human plasma. Methods A diamonsil C18 column (200X4.6mm ID, 5um) was used as stationary phase and the mobile phase consisted of acetonitrile and water (49:51, v/v, pH2.8) at a flow-rate of 1.2 mL min~(-1). The Ultraviolet absorbance was monitored at 229nm wavelength. Temperature control was kept at 45 癈 for the column. Results The lower limit of quantitation achieved was 50ng-mL~(-1), and the standard curve was found to be linear in the concentration range of 50-l0000ng-mL~(-1). Gliclazide and internal standard were eluted at 8.5min and 4.8min respectively. Conclusion The method was very good and suitable for determination of Gliclazide in human plasma.
机译:目的建立一种简单,灵敏的高效液相色谱(HPLC)方法,该方法涉及紫外检测,用于测定人血浆中格列齐特。方法使用diamonsil C18色谱柱(200X4.6mm ID,5um)作为固定相,流动相由乙腈和水(49:51,v / v,pH2.8)组成,流速为1.2 mL min〜 (-1)。在229nm波长下监测紫外线吸收。将该柱的温度控制在45℃。结果定量下限为50ng-mL〜(-1),标准曲线在50-10000ng-mL〜(-1)浓度范围内呈线性关系。格列齐特和内标分别在8.5min和4.8min洗脱。结论该方法非常准确,适用于人血浆中格列齐特的测定。

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