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机构地区:[1]广西医科大学第四附属医院,广西柳州545005 [2]广西柳州市中医院,广西柳州545001
出 处:《中国药房》2012年第23期2165-2167,共3页China Pharmacy
摘 要:目的:建立抗乳腺小叶增生合剂的质量标准。方法:采用薄层色谱(TLC)法对处方中的白芍、当归和丹参进行定性鉴别;采用高效液相色谱法对芍药苷、阿魏酸和甘草酸进行含量测定。结果:TLC特征斑点明显、专属性强。芍药苷、阿魏酸和甘草酸的检测浓度分别在25.96~259.65、2.15~21.55、31.63~316.30μg.mL-1范围内与各自峰面积积分值呈良好线性关系(r分别为0.9995、0.9998、0.9996);平均加样回收率分别为100.82%、98.61%和100.39%,RSD分别为2.64%、2.43%和2.98%(n均为6)。结论:所建标准可用于抗乳腺小叶增生合剂的质量控制。OBJECTIVE: To establish a quality standard of Anti-lobular hypertrophy mixture. METHODS:Paeonia lactiflora, Angelica sinensis and Salvia miltiorrhiza in the formula were identified qualitatively by TLC. The contents of paeoniflorin, ferulic acid and glycyrrhizic acid were determined by HPLC. RESULTS: The TLC spots were clear and specific. The linear ranges for paeoniflorin, ferulic acid and glycyrrhizic acid were 25.96-259.65 μg. mL- t (r= 0.999 5), 2.15-21.55 μg mL- 1 (r: 0.999 8) and 31.63-316.30 μg.mL-1 (r=0.999 6) respectively. The average recoveries were 100.82%, 98.61% and 100.39% ,RSD were 2.64% - 2.43 % and 2.98% (n=6). CONCLUSION: The established standard can be used for the quality control of Anti-lobular hypertrophy mixture.
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