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HPLC法测定莲芝消炎片中穿心莲内酯和脱水穿心莲内酯的含量 被引量:2

Determination of Lianzhi Xiaoyan Pill by HPLC
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摘要 建立莲芝消炎片中脱水穿心莲内酯、穿心莲内酯含量的HPLC测定方法.色谱柱为SUNTEKKromasil C18柱;流动相为甲醇-水(60∶40),流速为0.8 mL·min^-1,检测波长为250 nm.线性范围为脱水穿心莲内酯0.8000~2.240μg,r=0.9999,穿心莲内酯0.1011~0.2831μg,r=0.9995,平均回收率脱水穿心莲内酯为98.99%,RSD为1.4%,穿心莲内酯为101.48%,RSD为1.5%.方法准确可靠,简单易行,适用于莲芝消炎片中脱水穿心莲内酯、穿心莲内酯的含量测定. A HPLC method for the determination of Lianzhi Xiaoyan Pill was established. A SUNTEK Kromasil C18 column was used with methanol-water (60 : 40) as mobile phase. The flow rate was 0. 8 mL · min^-1 and detection wavelength was 250 nm, The linear range for deoxyandrographolide was 0. 8000- 2. 240μg (r=0. 9999) and those for andrographolide was 0. 1011 -0. 2831μg (r= 0. 9995) . The average recovery and RSD for deoxyandrographolide were 98.99 % and 1.4 %, and those for andrographolide were 101.48% and 1.5% respectively. The method was accurate, reliable, simple and feasible, it could be used for the content determination of Lianzhi Xiaoyan Pill.
出处 《中国药事》 CAS 2007年第8期594-595,共2页 Chinese Pharmaceutical Affairs
关键词 莲芝消炎片 高效液相色谱法 含量测定 Lianzhi Xiaoyan Pill HPLC determination
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  • 1卫生部药品标准[S].WS3-B-3977-98

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