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作 者:周逸芝[1] 刘训红[1] 许虎[1] 傅兴圣[1] 陈菲[1] 张奉苏[1]
机构地区:[1]南京中医药大学,南京210046
出 处:《中国药学杂志》2013年第2期139-142,共4页Chinese Pharmaceutical Journal
基 金:江苏省科技厅"科技基础实施建设计划"专项(BM2009903);江苏高校优势学科建设工程资助项目(ysxk-2010)
摘 要:目的建立HPLC测定龙柴方及其组方药材甘草中5种指标成分含量的方法,控制该方药的质量。方法 ODS C18色谱柱(4.6 mm×250 mm,5μm),流动相为乙腈和0.05%的磷酸水溶液,梯度洗脱;柱温为30℃;流速1 mL.min-1;检测波长237 nm。结果此方法可以使样品达到基线分离,阴性样品无干扰,甘草苷、异甘草苷、甘草素、甘草酸和异甘草素分别在0.156 8~1.568μg(r=0.999 7)、0.157 1~1.571μg(r=0.999 8)、0.155 8~1.558μg(r=0.999 6)、0.187 1~1.871μg(r=0.996 9)和0.158 1~1.581μg(r=0.999 5)内与各自峰面积积分值呈良好的线性关系;平均回收率分别为101.47%(RSD=1.272%)、101.09%(RSD=1.937%)、101.14%(RSD=2.388%)、100.38%(RSD=1.448%)及100.86%(RSD=1.759%)(n=5)。结论该方法分离良好、精密准确,可用于龙柴方及其组方药材甘草的质量控制。OBJECTIVE To establish a determination method of five index components to control the quality of Glycyrrhizae Radix et Rhizoma and Longchai Decoction. METHODS An ODS Cls column (4. 6 mm × 250 mm, 5 um) was adopted; the mobile phase consisted of acetonitrile-0.05% phosphoric acid with gradient elution at the flow rate of 1 mL . min-1 ;the detection wavelength was 237 nm,and the column temperature was 30 ℃ . RESULTS The five index components achieved baseline separation, and the negative sample showed no interference. The linear ranges were 0. 156 8 - 1. 568 ug for liquiritin (r =0. 999 7), 0. 157 1 - 1. 571 ug for isoliquiritin (r = 0. 999 8), 0. 155 8 - 1. 558 ug for liquiritigenin ( r = 0. 999 6), 0. 187 1 - 1. 871 ug for glycyrrhizic ( r = 0. 996 9) and 0. 158 1 - 1.58 1 ug for isoliquiritigenin (r =0. 999 5 ), respectively. The average recoveries were 101.47% ( RSD =1.272%), 101.09% (RSD = 1.937%), 101.14% (RSD = 2. 388%), 100.38% (RSD = 1.448%) and 100.86% (RSD = 1. 759% ) , respectively ( n = 5 ). CONCLUSION This method has good resolution and high precision, and can be used for the quality control of Glycyrrhizae Radix et Rhizoma and Longehai decoction.
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