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引用本文:陈林,赵培敬.螺内酯片有关物质检测方法的优化[J].中国现代应用药学,2023,40(1):112-115.
CHEN Lin,ZHAO Pei-jing.Improvement of Determination Method for Related Substance in Spironolactone Tablets[J].Chin J Mod Appl Pharm(中国现代应用药学),2023,40(1):112-115.
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螺内酯片有关物质检测方法的优化
陈林, 赵培敬
南阳市食品药品检验所, 河南 南阳 473061
摘要:
目的 优化螺内酯片有关物质的测定方法和供试品溶液制备方法。方法 采用Welch Materials Eclipse XB-C18色谱柱(4.6mm×250mm,5μm),以乙腈-水(54∶46)为流动相,流速1.0mL·min-1,检测波长254nm和283nm,柱温35℃。样品以流动相为提取溶剂,超声提取。结果 主峰与各杂质峰均能良好分离。螺内酯、坎利酮分别在1.00~100.38,1.03~102.53μg·mL-1内线性关系良好(r均为1.000),回收率分别为99.52%和99.23%。结论 本方法结果准确、重复性好、专属性强,比中国药典方法操作更简便,可为螺内酯片有关物质检测方法的优化提供参考依据。
关键词:  螺内酯片  有关物质检测  优化
DOI:10.13748/j.cnki.issn1007-7693.2023.01.015
分类号:R917
基金项目:
Improvement of Determination Method for Related Substance in Spironolactone Tablets
CHEN Lin, ZHAO Pei-jing
Nanyang Institute for Food and Drug Control, Nanyang 473061, China
Abstract:
OBJECTIVE To improve the method for related substance determination and sample preparation of spironolactone tablets.METHODS The detection method was performed on the column of Welch Materials Eclipse XB-C18column(4.6 mm×250 mm,5μm) with mobile phase of acetonitrile-water(54∶46) at flow rate of 1.0 mL·min-1,detection wavelengths was 254 nm and 283 nm,column temperature was 35℃.The samples were extracted by flow phase ultrasonic method.RESULTS Related substances were completely separated from the principal component.The linear range of spironolactone and canrenone were 1.00-100.38μg·mL-1 and 1.03-102.53μg·mL-1(r=1.000),respectively.The average recovery rates were 99.52%and 99.23%,respectively.CONCLUSION The method is simple,accurate,reproducible and more convenient than the Chinese Pharmacopoeia method,which can provide reference for the optimization of the determination method of spironolactone tablets in the future.
Key words:  spironolactone tablets  related substance determination  improvement
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