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作 者:刘晓哲[1]
机构地区:[1]河南省南阳市药品检验所,河南南阳473059
出 处:《中成药》2014年第1期98-101,共4页Chinese Traditional Patent Medicine
摘 要:目的建立同时测定肥儿丸(煨肉豆蔻、木香等)中木香烃内酯、去氢木香内酯、去氢二异丁香酚的方法。方法采用HPLC法,C18色谱柱;以乙腈-水(70:30)为流动相;体积流量1.0mL/min;检测波长225nm(木香烃内酯、去氢木香内酯),274nm(去氢二异丁香酚)。结果根据回归方程,3种成分线性范围分别为木香烃内酯10.834—216.68μg/mL,r^2=0.9996;去氢木香内酯9.506~190.12μg/mL,r^2=0.9994;去氢二异丁香酚5.782—115.64μg/mL,r^2=0.9989。平均回收率分别为木香烃内酯98.4%,RSD为0.66%(n=6);去氢木香内酯99.1%,RSD为1.16%(n:6);去氢二异丁香酚98.1%,RSD为1.25%(n=6)。结论该方法经济适用,操作简便、准确,重复性好,可用于肥儿丸的质量控制。AIM To establish a method for simultaneously determining the levels of costunolide, dehydrocostus lactone, and dehydrodiisoeugenol in Feier Pills (Myristicae Semen, Aucklandiae Radix, etc. ). METH- ODS The quantitative analysis was carried out on a column of Kromasil C18 by HPLC, by using a mobile phase of acetonitrilewater under a flow rate of 1.0 mL/min. 225 nm for costunolide and dehydrocostus lactone, 274 nm for dehydrodiisoeugenol as the detection wavelength. RESULTS The linear ranges of eostunolide, dehydro- costus laetone, and dehydrodiisoeugenol fell within the ranges of 10. 834-216.68 μg/mL, 9. 506-190.12μg/mL, 5. 782-115.64 p.g/mL, respectively. The three components showed good linear correlations (r^2 = 0. 999 6, 0. 999 4, 0. 998 9). The recoveries were 98.4% for costunolide, 99.1% for dehydrocostus laetone, 98. 1% for dehydrodiisoeugenol, respectively. The relative standard deviations were 0.66% , 1. 16% , and 1.25% , respectively. CONCLUSION The method is simple, economical, accurate, reproducible and con- venient for the quality control over Feier Pills.
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