首页|期刊导航|兰州大学学报(医学版)|保元颗粒分时段多波长融合指纹图谱及7个指标性成分含量测定

保元颗粒分时段多波长融合指纹图谱及7个指标性成分含量测定OA

Determination of the multi-wavelength fusion fingerprint and seven marker components in Bao Yuan granules at different time periods

中文摘要英文摘要

目的 建立保元颗粒高效液相色谱法的分时段多波长融合指纹图谱,构建其主要功效成分的含量测定方法.方法 采用高效液相色谱法-二极管阵列检测法全波长扫描构建10批保元颗粒的指纹图谱,基于该图谱中所包含的主要色谱峰,测定保元颗粒中人参皂苷Rg1、人参皂苷Re、人参皂苷Rb1、毛蕊异黄酮苷、甘草苷、6-姜辣素、桂皮醛7个指标性成分的含量.结果 指纹图谱测定的色谱条件为色谱柱Spursil C18(250 mm×4.6 mm,5 µm);流动相乙腈-水,梯度洗脱;流速0.8 mL/min;柱温25°C;选择203、237、260、280、290 nm共5个波长获得融合指纹图谱.10批样品的融合指纹图谱包含29个共有峰,分别来自保元颗粒组方中的不同药材,其中7个共有峰来自人参,15个共有峰来自黄芪,11个共有峰来自甘草,1个共有峰来自肉桂,8个共有峰来自生姜.10批保元颗粒相似度为0.878~0.985.7个指标成分的标准曲线相关系数R2均大于0.990 0,线性良好.方法学考察发现,构建的指纹图谱和7个指标成分含量测定方法的精密度、重复性、稳定性相对标准偏差均小于5%,7个指标成分加样回收率为97.21%~103.10%.结论 构建的多波长融合指纹图谱能较全面地反映保元颗粒的整体信息,还可用于组方药味的鉴别,为保元颗粒质量标准研究提供了方法学基础.

Objective To establish a multi-wavelength fusion fingerprint of Baoyuan Granules by high perfor-mance liquid chromatography at different time periods,and develop a method for determining the content of its main active ingredients.Methods The fingerprints of 10 batches of Baoyuan Granules were constructed through high performance liquid chromatography-diode array detector full-wavelength scanning.Based on the identification of the main chromatographic peaks in these fingerprints,the contents of seven indicator compo-nents in Baoyuan Granules,namely ginsenoside Rg1,ginsenoside Re,ginsenoside Rb1,calycosin-7-O-β-D-glu-coside,liquiritin,6-gingerol and cinnamaldehyde were determined.Results The chromatographic condi-tions for fingerprint determination were that the chromatographic column was Spursil C18(250 mm×4.6 mm,5 µm),the mobile phase was acetonitrile-water with gradient elution,the flow rate was 0.8 mL/min and the column temperature was 25 °C.A fusion fingerprint was obtained by selecting five wavelengths(203,237,260,280,and 290 nm).The fusion fingerprints of the 10 batches of samples contained 29 common peaks,which origi-nated from different medicinal materials in the formula of Baoyuan Granules.Specifically,7 common peaks were from ginseng,15 from astragalus membranaceus,11 from licorice,1 from cinnamon and 8 from ginger.The similarity of the 10 batches of Baoyuan Granules was between 0.878 and 0.985.The correlation coeffi-cients R2 of the standard curves of the seven indicator components were all above 0.990 0,indicating a good linearity.The methodological investigation showed that the relative standard deviations of precision,repeat-ability,and stability of the constructed fingerprint and the content determination methods of the seven indica-tor components were all less than 5%.The spiked recoveries of the seven indicator components were between 97.21%and 103.10%.Conclusion The multi-wavelength fusion fingerprint constructed could not only com-prehensively reflect the overall information of Baoyuan Granules,but also be used to identify the medicinal materials in the formula.This method provides a methodological basis for the research on the quality standard of Baoyuan Granules.

牛艺鸽;孙科;王燕萍;杨惠妮;葛雯蓉;柴国林;胡芳弟

甘肃中医药大学 药学院,甘肃 兰州 730000兰州佛慈制药股份有限公司,甘肃 兰州 730000兰州大学 药学院,甘肃 兰州 730000兰州大学 药学院,甘肃 兰州 730000南华大学 药学院,湖南 衡阳 421001兰州佛慈制药股份有限公司,甘肃 兰州 730000兰州大学 药学院,甘肃 兰州 730000

医药卫生

保元颗粒高效液相色谱指纹图谱含量测定多波长融合组方药

Bao Yuan granuleshigh performance liquid chromatographyfingerprintcontent determinationMulti-wavelength fusionformula

《兰州大学学报(医学版)》 2026 (1)

33-41,58,10

甘肃省中医药科研课题(GZKZ-2024-30)兰州市科技计划项目(2024-2-24,2024-8-1)

10.13885/j.issn.2097-681X.M20250141

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