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作 者:谭丹[1] 朱迪[1] 陆苑[1,2] 王爱民[1,3] 黄跃伟 李勇军[1,3] 兰燕宇[1,3]
机构地区:[1]贵州医科大学药学院,贵州贵阳550004 [2]贵州医科大学贵州省药物制剂重点实验室,贵州贵阳550004 [3]贵州医科大学民族药与中药开发应用教育部工程研究中心,贵州贵阳550004 [4]贵州德良方药业股份有限公司,贵州兴义562409
出 处:《贵阳医学院学报》2015年第10期1036-1039,共4页Journal of Guiyang Medical College
基 金:贵州省中药现代化专项项目[黔科合中药字(2013)5062号;黔科合重G字(2013)4001];贵州省高等学校创新能力提升计划[黔教合协同创新字(2013)04]
摘 要:目的:建立益肾养元颗粒中陈皮的薄层色谱鉴别与橙皮苷含量的测定方法。方法:采用薄层色谱法对陈皮的定性鉴别,采用高效液相色谱法测定橙皮苷的含量;色谱柱为迪马C18柱(150×4.6,5μm),流动相为乙腈-0.1%磷酸(20∶80),流速1 m L/min,柱温45℃,检测波长283 nm。结果:薄层色谱鉴别斑点清晰,阴性对照无干扰;橙皮苷进样量为0.114~2.29μg,与峰面积呈良好线性关系(r=0.999 4),平均回收率为99.67%,平均峰面积(RSD)为2.1%。结论:所建立的方法简便、准确、重复性好,可用于益肾养元颗粒中陈皮的鉴别和橙皮苷的含量测定。Objective : To establish the method for the identification of Pericarpium citri reticuLatae in Yishenyangyuan granules and the hesperidin content determination. Methods: Pericarpium cirri reticu- latae were identified by TLC and the content of hesperidin was determined by HPLC. A Diamonsil C18 column (150 mm ×4.6,5μm,5 p,m) was used with a mobile phase consisting of acetonitrile -0.1% phosphoric acid (20: 80) at a flow rate of 1.0 mL/min, the column temperature was 45 ℃ and the de- tection wave length was 283 nm. Result: The bilirubin spot of TLC were clear, and there was no inter- ference in negative control. The sample size of hesperidin was in the range of 0. 114 - 2.29 μg, dem- onstrating a good linear relationship with the peak area (r = 0. 999 4). The average recovery rate was 99.67% , and RSD was 2.1%. Conclusion: The above established methods were simple and accurate with good reproducible characteristic, which can be used for the identification of Pericarpium citri retic- ulatae and content determination of hesperidin in Yishenyangyuan granules.
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