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作 者:王芳[1] 王斌[1] 张贺[1] 葛平[1] 李泽庚[1] 孟楣[1,2]
机构地区:[1]安徽中医药大学研究生部,安徽合肥230038 [2]安徽中医药大学第一附属医院 国家中医药管理局中药制剂三级实验室,安徽合肥230031
出 处:《安徽中医学院学报》2013年第5期72-75,共4页Journal of Anhui Traditional Chinese Medical College
基 金:安徽省高校省级自然科学研究项目(KJ2011Z218);安徽省2012年中医发展省级专项(皖中医药[2012]10号)
摘 要:目的采用高效液相色谱法测定芪白平肺胶囊中人参皂苷Rg1与Rb1的含量,为其质量控制提供依据。方法采用WelchMaterialIncC18色谱柱(4.6mm×250mm,5μm)。其流动相:水-乙腈;梯度洗脱(0~10min,81:19;11~35min,81:19—71:29;36~50min,71:29—50:50);流速:1.2ml/min;检测波长:203nm;柱温:30℃。结果人参皂苷Rg1、Rb1在0.16~2.40μg范围内与其峰面积呈线性关系,r=0.9999(n=8);人参皂苷Rg1、Rb1的平均加样回收率分别为102.31%、98.55%(n=9);芪白平肺胶囊中人参皂苷Rg1、Rb1的3批样品测定结果,人参皂苷Rg1平均含量分别为0.332、0.326、0.336mg/g,人参皂苷Rb1平均含量分别为0.496、0.509、0.511mg/g。结论所建立的高效液相色谱方法简便、灵敏度高、重现性好,可用于芪白平肺胶囊中人参皂苷的含量测定。Objective To establish a method for simultaneous determination of ginsenosides Rg1 and Rb1 in Qibai Pingfei Capsules by high-performance liquid chromatography (HPLC) and to provide a basis for the quality control of Qibai Pingfei Capsules. Methods HPLC was performed on a Welch Material Inc C18 column (4.6 mm × 250 mm, 5 μm) with a mobile phase of wateacetonitrile for gradient elution at a flow rate of 1..2 ml/min, a detection wavelength of 203 nm, and a column temperature of 30 ℃. The water/acetonitrile ratio was 81:19 at 0-10 min, ranged from 81:19 to 71:29 at 11-35 min, and ranged from 71:29 to 50:50 at 36-50 min. Results Ginsenosides Rg, and Rb1 showed a linear relationship between concentration and peak area within 0.16-2.40 μg (r= 0. 999 9, n=8); the average recovery rates of ginsenosides Rg1 and Rb1 were 102.31% and 98.55%, respectively (n=9). In the three batches of Qibai Pingfei Capsule samples, the average contents of ginsenoside Rg1 were 0. 332, 0. 326, and 0. 336 mg/g, respectively, and the average contents of ginsenoside Rb1 were 0. 496, 0. 509, and 0. 511 mg/g, respectively. Conclusion This HPLC method is simple, with high sensitivity and good repeatability. It can be used for the determination of ginsenosides ig1 and Rb1 in Qibai Pingfei Capsules.
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