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反相高效液相色谱法同时测定芪香胶囊中红景天苷、芍药苷及毛蕊异黄酮葡萄糖苷的含量
引用本文:刘桂花,邢建国,何承辉,王云飞,帕依曼&#,亥米提,席梅. 反相高效液相色谱法同时测定芪香胶囊中红景天苷、芍药苷及毛蕊异黄酮葡萄糖苷的含量[J]. 中国医院药学杂志, 2017, 37(15): 1440-1443. DOI: 10.13286/j.cnki.chinhosppharmacyj.2017.15.05
作者姓名:刘桂花  邢建国  何承辉  王云飞  帕依曼&#  亥米提  席梅
作者单位:1. 新疆维吾尔自治区药物研究所, 新疆 乌鲁木齐 830004;2. 新疆医科大学中医学院, 新疆 乌鲁木齐 830004
基金项目:新疆维吾尔自治区中医民族医药管理局项目-新疆地产中药民族药新药研发项目(编号:Q2015-01-03)
摘    要:
目的:建立高效液相色谱法同时测定芪香胶囊(黄芪、红景天、赤芍、红花)中红景天苷、芍药苷、毛蕊异黄酮葡萄糖苷3种活性成分的含量。方法:采用Phenomenex Luna色谱柱(250 mm×4.6 mm,5 μm),以乙腈(A)和水(B)为流动相,梯度洗脱[0~11 min,A-B(10:90),11~40 min,A-B(18:82),40~45 min,A-B(10:90)],流速1.0 mL·min-1,柱温为35℃,检测波长:230 nm。结果:红景天苷在55.07~192.8 μg·mL-1、芍药苷在65.45~229.1 μg·mL-1、毛蕊异黄酮葡萄糖苷在10.74~64.44 μg·mL-1 范围内均呈良好线性关系;相关系数分别为0.999 8,0.999 7,0.999 8;红景天苷、芍药苷和毛蕊异黄酮葡萄糖苷的回收率分别为99.90%,100.88%,100.06%,样品溶液在24 h内稳定,含量分别为1.422 2,3.183 3,0.250 0 mg·g-1结论:该方法经验证,可为芪香胶囊多指标质量评价及控制提供科学依据。

关 键 词:芪香胶囊  高效液相色谱法  红景天苷  芍药苷  毛蕊异黄酮葡萄糖苷  质量控制  方法学验证  含量测定  
收稿时间:2016-11-22

Simultaneous determination of salidroside,paeoniflorin and calycosin-7-O-β-D-glucoside in Qixiang Capsules by HPLC
LIU Gui-hua,XING Jian-guo,HE Cheng-hui,WANG Yun-fei,Payiman-Haimiti,XI Mei. Simultaneous determination of salidroside,paeoniflorin and calycosin-7-O-β-D-glucoside in Qixiang Capsules by HPLC[J]. Chinese Journal of Hospital Pharmacy, 2017, 37(15): 1440-1443. DOI: 10.13286/j.cnki.chinhosppharmacyj.2017.15.05
Authors:LIU Gui-hua  XING Jian-guo  HE Cheng-hui  WANG Yun-fei  Payiman-Haimiti  XI Mei
Affiliation:1. Xinjiang Institute of Meteria Medica, Xinjiang Urumqi 830004, China;2. College of Traditional Chinese Medicine, Xinjiang Medical University, Xinjiang Urumqi 830004, China
Abstract:
OBJECTIVE To establish an HPLC method for simultaneous determination of salidroside, paeoniflorin and calycosin-7-O-β-D-glucoside in Qixiang Capsules (Astragalus membranaceus, Rhodiola hobsonii, Paeonia veitchii Lynch, Cdrthamus tinctorius L.).METHODS The determination was carried out over Phenomenex Luna column (250 mm×4.6 mm, 5μm) at the column temperature (35℃). The mobile phase consisted of acetonitrile (A)-water (B) solution with the gradient elution[0-11 min, A-B(10:90), 11-40 min, A-B(18:82), 40-45 min, A-B(10:90)], the flow rate was 1.0 mL min-1 and detection wavelength was 230 nm.RESULTS The method had good linear relationship within the range of 55.07-192.8 μg·mL-1 for salidroside (r=0.999 8), 65.45-229.1 μg·mL-1 for paeoniflorin (r=0.999 7) and 10.74-64.44 μg·mL-1 for calycosin-7-O-β-D-glucoside (r=0.999 8). The average recovery was 99.90% for salidroside, 100.88% for paeoniflorin and 100.06% for calycosin-7-O-β-D-glucoside. The sample solution was stable within 24 h. Contents were 1.422 2, 3.183 3 and 0.250 0 mg·g-1.CONCLUSION The method can be used to provide scientific evidence for the comprehensive quality evaluation and control of Qixiang Capsule through the methodological validation.
Keywords:Qixiang Capsules  HPLC  salidroside  paeoniflorin  calycosin-7-O-β-D-glucoside  quality control  methodological validation  quantitative determination  
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