HPLC法测定高良姜中原儿茶酸的含量

来源 :沈阳药科大学学报 | 被引量 : 0次 | 上传用户:loogog
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
目的建立高良姜中原儿茶酸的含量测定方法。方法采用HPLC法。色谱柱为D iamonsilODS C18柱(200 mm×4.6 mm,5μm),流动相为甲醇-质量分数为0.05%的磷酸水溶液(体积比为12∶88),流速为1.0 mL.m in-1,检测波长为258 nm,柱温为35℃,进样量为20μL。结果原儿茶酸在0.902~14.432 mg.L-1内与峰面积呈良好的线性关系,平均回收率为99.2%,RSD=1.8%(n=9)。结论该方法可为高良姜药材质量控制提供新指标。 Objective To establish a method for determining the content of protocatechuic acid in Galangal. Method using HPLC method. The column was a Diamonsil ODS C18 column (200 mm×4.6 mm, 5 μm). The mobile phase consisted of methanol-mass fraction 0.05% phosphoric acid (volume ratio 12:88) and flow rate 1.0 mL.m in-1. The wavelength is 258 nm, the column temperature is 35°C, and the injection volume is 20 μL. Results There was a good linear relationship between protocatechuic acid and peak area within the range of 0.902-14.432 mg.L-1. The average recovery was 99.2% and RSD was 1.8% (n=9). Conclusion This method can provide new indicators for quality control of Galangal medicine.
其他文献
目的为探讨骨髓辐射损伤的分子机理,研究了整体照射条件下,辐射前后骨髓基因表达的变化.方法小鼠7 Gyγ射线照射后4 h提取骨髓总RNA为实验方(tester),对照组动物骨髓总RNA为驱动方(driver);实验方、驱动方总RNA由SMART cDNA合成方法合成双链cDNA,进而由抑制消减杂交(SSH)方法获得消减杂交产物,消减杂交产物克隆到T载体建立消减文库;对部分克隆进行杂交筛选及序列比对.