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一种经过验证的稳定性指示超高效液相色谱法,用于测定依普利酮中潜在的工艺相关杂质。

A validated stability-indicating ultra performance liquid chromatography method for the determination of potential process-related impurities in eplerenone.

作者信息

Du Mingluo, Pan Chunyan, Chen Jing, Song Min, Zhu Tingting, Hang Taijun

机构信息

Department of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, Jiangsu, P. R. China.

出版信息

J Sep Sci. 2016 Aug;39(15):2907-18. doi: 10.1002/jssc.201600324. Epub 2016 Jul 4.

Abstract

A simple, sensitive, and accurate stability-indicating analytical method has been developed and validated using ultra high performance liquid chromatography. The developed method is used to evaluate the related substances of eplerenone (EP). The degradation behavior of EP under stress conditions was determined, and the major degradants were identified by ultra high performance liquid chromatography with tandem mass spectrometry. The chromatographic conditions were optimized using an impurity-spiked solution, and the samples, generated from forced degradation studies. The resolution of EP, its potential impurities, and its degradation products was performed on a Waters UPLC BEH C18 column (50 × 2.1 mm, 1.7 μm) by linear gradient elution using a mobile phase consisting of 10 mmol/L ammonium acetate adjusted to pH 4.5, methanol and acetonitrile. A photo-diode array detector set at 245 nm was used for detection. The flow rate was set at 0.3 mL/min. The procedure had good specificity, linearity (0.02-3.14 μg/mL), recovery (96.1-103.9%), limit of detection (0.01-0.02 μg/mL), limit of quantitation (0.03-0.05 μg/mL), and robustness. The correction factors of the process-related substances were calculated.

摘要

已开发并验证了一种使用超高效液相色谱法的简单、灵敏且准确的稳定性指示分析方法。所开发的方法用于评估依普利酮(EP)的有关物质。测定了EP在强制降解条件下的降解行为,并通过超高效液相色谱-串联质谱法鉴定了主要降解产物。使用加样杂质溶液对色谱条件进行了优化,该样品来自强制降解研究。在Waters UPLC BEH C18柱(50×2.1 mm,1.7μm)上,通过线性梯度洗脱,使用由pH值调至4.5的10 mmol/L醋酸铵、甲醇和乙腈组成的流动相,对EP、其潜在杂质及其降解产物进行分离。使用设置在245 nm的光电二极管阵列检测器进行检测。流速设定为0.3 mL/min。该方法具有良好的专属性、线性(0.02 - 3.14μg/mL)、回收率(96.1 - 103.9%)、检测限(0.01 - 0.02μg/mL)、定量限(0.03 - 0.05μg/mL)和耐用性。计算了工艺相关物质的校正因子。

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