HPLC -质量设计法同时检测托尔塞米、螺内酯及其降解杂质

Unnati Bihola, P. Prajapati, Y. K. Agrawal
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引用次数: 5

摘要

建立了高效液相色谱-质谱联用技术同时分离、鉴定和定量Torsemide (TOR)、螺内酯(SPI)及其降解杂质的简便、可靠的质量设计(QbD)方法。药物和杂质的色谱分离采用ODS-3µm C18,尺寸为150 mm × 4.6 mm,采用甲醇、乙腈和水的三元流动相(5:3:2 v/v/v)等容洗脱,流速为0.2 mL/min,达到最佳分离效果。采用254 nm紫外分光光度法测定torsemide和螺内酯的含量,用质谱仪比较相同质量对降解物进行鉴定。在良好的验证参数下,旋塞米和螺内酯的回收率均大于98%;TOR的LOD和LOQ分别为10和33 ng, SPI的LOD和LOQ分别为75和248 ng。设计质量(QbD)方法的成功应用证明了该方法的鲁棒性,即使故意改变关键参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HPLC – Quality by Design Approach for Simultaneous Detection of Torsemide, Spironolactone and Their Degradant Impurities
Abstract A simple, highly robust (quality by design (QbD) approach), precise and accurate method using high performance liquid chromatography coupled to mass spectrometry has been established for the simultaneous separation, identification and quantitation of a Torsemide (TOR), spironolactone (SPI) and their degradant impurities. The chromatographic separations of drugs and impurities were achieved on a inertsil ODS-3 µm C18, 150 mm × 4.6 mm, while the isocratic elution using a ternary mobile phase mixture of methanol, acetonitrile and water (5:3:2 v/v/v) at a flow rate of 0.2 mL/min was adopted for achieving optimum separations. The quantitation of torsemide and spironolactone was accomplished by UV detection at 254 nm and identification of the degradants were done by comparing identical mass in mass spectrometer. The recoveries of the torsemide and spironolactone were obtained higher than 98 % with good validation parameters; linearity (r2>0.994), LOD and LOQ was 10 and 33 ng for TOR and 75 and 248 ng for SPI respectively. The quality by design (QbD) approach has been successfully utilized to prove the method is robust even deliberate changes in critical parameters.
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