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作 者:魏丽[1] 王静静[2] 杨艳梅[1] 赵丽艳[1] 张万明[1] 张丹参[1]
机构地区:[1]河北北方学院药学系,河北张家口075000 [2]河北北方学院附属第一医院,河北张家口075000
出 处:《时珍国医国药》2017年第4期815-817,共3页Lishizhen Medicine and Materia Medica Research
基 金:国家自然科学基金(No.81274005);河北北方学院基金资助项目(No.GZ1405)
摘 要:目的建立RP-HPLC法测定瑞香狼毒药材中伞形花内酯和狼毒色原酮的含量。方法采用反相高效液相色谱法,PDA检测器,选用Hypersil GOLDaQ-C_(18)(250mm×4.6mm,5μm),色谱柱;流动相为乙腈(A)-0.1%磷酸水溶液(B),进行梯度洗脱;检测波长伞形花内酯为327 nm,狼毒色原酮为297nm;流速1.0ml/min;进样量10μl,柱温25℃。结果2种活性成分在13 min内实现良好分离,伞形花内酯、狼毒色原酮的线性范围分别为1.22~19.6μg·ml^(-1)(r=0.9998)、20.0~320μg·ml^(-1)(r=0.9997),平均回收率分别为100.5%,101.8%,RSD分别为1.2%,1.5%。13批不同产地瑞香狼毒药材中伞形花内酯的含量范围为:0~0.57mg/g;狼毒色原酮的含量范围6.46~30.92mg/g。结论该方法操作简便、重现性好、结果准确可靠,可用于中药瑞香狼毒的质量控制。Objective A RP - HPLC method was established to detect the content of umbelliferone and chamechromone in 13 bat- ches SteUera chamaejasme from different areas in this paper. Methods A Hypersil Gold aQ - C18 (4.6 mmx 150 mm, 5txm) column was selected in this experiment; the mobile phase was acetonitrile (A) -0.1% phosphate aqueous solution (B) with gradient elution; the wavelength was umbelliferone 327 nm, chamechromone 297nm; the flow rate was 1.0 mL/min; the column temperature was 25℃. Results The 2 constituents were separated within 13min. The linear ranges of umbelliferone and cha- mechromone were 38.5 - 166.7 ug mL-1 ( r = 0. 9998 ) , 15.9 - 254.5 ug ml - l ( r = 0. 9997 ) respectively. The average re- coveries were 100.5% ,101.8% respectively. The RSD were 1.2% , 1.5% respectively. The content range of umbelliferone in Stellera chamaejasme was: 0 -0. 57mg/g; the content range of chamechromone in Stellera chamaejasme was 6.46 -30.92mg/g. Conclusion The method is simple, accurate and reliable, and could be used for quality control of traditional Chinese medicine Stellera chamaejasme.
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