建立了以反相高效液相色谱法测定人血浆中硫普罗宁浓度的方法.采用Agilent C8(250mm×4.6mm,5μm)色谱柱,乙腈:水(用磷酸调pH至2.5)=8:92(v/v),为流动相,检测波长203nm,流速1.0mL·min^-1.硫普罗宁浓度在1.5-1600“g·mL。浓度范围内,峰面积与浓度呈良好线性关系(r=0.9998),提取回收率在74.26%-76.35%之间,方法回收率在101.95%-106.86之间,2.5、50和1000“g·mL^-1 3种浓度的日内、日问RSD分别为2.83%-3.75%、5.92%-6.85%均小于10%.本方法操作简便、快速、准确、重现性好,适用于硫普罗宁的药动学研究.
A HPLC method is established to determine the concentration of tiopronin in human plasma. The sample separation is performed on a Agilent Ca column (250 minx 4.6 ram, 5 tam). The mobile phase is acetontrile -- water(pH2.5 by phosphate) (8 : 92 ,v/v)wit h a flow rate of 1.0 mL · min-l and a detection wavelength of 203 nm. The linear range of tiopro- nin is 1.5-1 600 μg · mL-1 , (r= 0. 999 8) . The extraction recovery of tiopronin is 74.26%-76.35% and the methodological recovery of it is 101.95-106.86%. The intra- day RSD and inter- day RSD are 2.83%-3.75% and 5.92%-6.85%, re- spectively. This method is simple , rapid ,accurate and reproducible, and it is applicable for the pharmacokinetic study of tio- pronin in human plasma1.