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洛汀烟酸缓释片中两组分的含量测定
引用本文:吕凌,刘羽,李珠婧,陆忠祥,孙备,费勤志.洛汀烟酸缓释片中两组分的含量测定[J].中国药业,2008,17(4):27-29.
作者姓名:吕凌  刘羽  李珠婧  陆忠祥  孙备  费勤志
作者单位:安徽省药物研究所,安徽,合肥,230022
摘    要:目的建立复方洛汀烟酸缓释片中洛伐他汀和烟酸的含量测定方法。方法采用高效液相色谱(HPLC)法,色谱柱为ODS柱(250mm×4.6mm,5μm);流动相为水-乙腈-四丁基氢氧化铵(80.5:18:1.5);检测波长为263nm;流速为1.0mL/min;进样量为20μL。结果洛伐他汀和烟酸的质量浓度线性范围分别为25~150μg/mL和25~250μg/mL,平均回收率分别为100.1%和99.22%,RSD分别为1.5%和1.37%。结论HPLC法准确可靠,简单可行,可用于复方洛汀烟酸缓释片的质量控制。

关 键 词:复方洛汀烟酸缓释片  洛伐他汀  烟酸  高效液相色谱法
文章编号:1006-4931(2008)04-0027-03
修稿时间:2007年6月26日

Determination of Lovastain and Nicotinic Acid in Compound Lovastatin-Nicotinic Acid Sustained-Release Tablets
Lv ling,Liu Yun,Li Zhujing,Lu Zhongxiang,Sun Bei,Fei Qinzhi.Determination of Lovastain and Nicotinic Acid in Compound Lovastatin-Nicotinic Acid Sustained-Release Tablets[J].China Pharmaceuticals,2008,17(4):27-29.
Authors:Lv ling  Liu Yun  Li Zhujing  Lu Zhongxiang  Sun Bei  Fei Qinzhi
Institution:(Anhui Institute of Materia Medica, Hefei, Anhui, China 230022)
Abstract:Objective To establish the determination method of lovastatin and nicotinic acid in Compound Lovastatin - Nicotinic Acid Sustainde - Release Tablet. Methods ODS column (250 mm × 4.6 mm, 5μm) with water - acetonitrile - tetrabutyl ammonium hydroxide (80. 5 : 18 : 1, 5) as the mobile phase was used. The wavelength was at 265 nm and the flow rate was 1.0 mL/min. Results The lovastatin and nicotinic acid curves were linear at the ranges of 25 - 150 μg/mL and 25 - 250 μg/mL. The average recovery rates were 100. 1% with RSD 1.5% for lovastatin and 99.22% with RSD 1.37% for nicotinic acid. Conclusion This method is reliable and simple. It can be used for the quality control of Compound Lovastatin- Nicotnic Acid Sustained- Release Tablet.
Keywords:Compound Lovastatin - Nicotinic Acid Sustained - Release Tablet  lovastain  nicotinic acid  HPLC
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