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高效液相法测定氯尼达明的有关物质和含量
引用本文:金冲,许宁,陈景,周国防,焦小丽,余晓燕.高效液相法测定氯尼达明的有关物质和含量[J].中国医药,2010,5(6):537-538.
作者姓名:金冲  许宁  陈景  周国防  焦小丽  余晓燕
作者单位:扬子江药业集团有限公司质管部,江苏省泰州市,225321
摘    要:目的 测定氯尼达明的有关物质和含量.方法 在系统适用性和专属性试验的基础上,采用反相色谱柱Hypersil C18硅烷柱(ODS)(200×4.6 mm)]:流动相为甲醇-水-冰醋酸(80:11:1);柱温为:25℃;流速为1.0 ml/min;检测波长为298 nm,建立测定氯尼达明有关物质和含量的高效液相色谱法.结果 氯尼达明在2~16μg/ml 浓度范围内与其峰面积呈线性关系,回归方程为A=7043C-108353,r=0.9914,测得的氯尼达明含量在98.5%以上,有关物质含量均小于1%.结论 高效液相色谱法测定氯尼达明的有关物质和含量方法准确、简便、可行,重现性和稳定性好,可适用于氯尼达明的含量测定及其有关物质检测.

关 键 词:高效液相  氯尼达明  含量测定

High performance liquid chromatogaph determination of lonidamine's related substance and content
JIN Chong,XU Ning,CHEN Jing,ZHOU Guo-fang,JIAO Xiao-li,YU Xiao-yan.High performance liquid chromatogaph determination of lonidamine's related substance and content[J].China Medicine,2010,5(6):537-538.
Authors:JIN Chong  XU Ning  CHEN Jing  ZHOU Guo-fang  JIAO Xiao-li  YU Xiao-yan
Affiliation:. (Yangtze River Pharmaceutical Group, Taizhou 225321, China)
Abstract:Objective To observe the impurities and assay of Lonidamine.Methods Based on the system suitability and specificity, a reversed-phase column Hypersil C18 column silane (ODS) (200 × 4.6 mm)] and a methanol-water-glacial acetic acid (80: 11:1) mobile phase, Lonidamine's related substances and content were determined by HPLC with the column temperature 25℃, the flow rate 1.0 ml/min and the detection wave length 298 nm.Results Lonidamine is linear relationship with its peak area in in the concentration range of 2 ~ 16 μg/ml,its regression equation is A = 7043C-108353, r = 0.9914. All the contents were above 98.5%. Conclusion Determination of lonidamine related material and content by high performance liquid is accurate, simple, feasible,as well as of high reproducibility and stability.
Keywords:High performance liquid chromatography  Lonidamine  Related substances  Determination assay
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