成分分析

咳清胶囊HPLC特征图谱及多成分含量测定研究*

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  • 1.贵州医科大学 贵州省天然药物资源高效利用工程中心,贵州省普通高等学校天然药物药理与成药性评价特色重点实验室,贵州医科大学-贵阳市联合重点实验室,天然药物资源优效利用重点实验室,药学院,贵阳 550025;
    2.贵州中医药大学,贵阳 550025;
    3.贵州省食品药品检验所,贵阳 550004;
    4.贵州省药品审评查验中心,贵阳 550081
第一作者 Tel:13158042081;E-mail:1217190211@qq.com
**茅向军 Tel:(0851)86811378;E-mail:1074459931@qq.com;许乾丽 Tel:(0851)86617052;E-mail:1500368608@qq.com;陶玲 Tel:(0851)88416160;E-mail:649511230@qq.com

收稿日期: 2020-09-03

  网络出版日期: 2024-07-12

基金资助

*国家药典委员会 2017 年度药品标准提高工作(中药)[项目编号 462]

Study on HPLC characteristic chromatogram and multi-component determination of Keqing capsules*

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  • 1. High Efficacy Application of Natural Medicinal Resources Engineering Center of Guizhou Province, The High Educational Key Laboratory of Natural Medicinal Pharmacology and Drugability, The Key Lab of Optimal Utilization of Natural Medicine Resources, School of Pharmaceutical Sciences, Guizhou Medical University, Guiyang 550025, China;
    2. Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China;
    3. Guizhou Provincial Food and Drug Inspection Institute, Guiyang 550004, China;
    4. Guizhou Drug Evaluation and Inspection Center, Guiyang 550081, China

Received date: 2020-09-03

  Online published: 2024-07-12

摘要

目的: 建立咳清胶囊的 HPLC 特征图谱,并同时测定没食子酸、吗啡、原儿茶酸、可待因、岩白菜素、绿原酸6个指标性成分的含量。方法: 采用 Ultimate® AQ-C18 色谱柱(250 mm×4.6 mm,5 µm),以乙腈(A)-0.1% 磷酸水(B)为流动相,梯度洗脱,流速 1.0 mL·min-1,检测波长 220 nm,柱温 30 ℃。以岩白菜素为参照峰,用中药色谱指纹图谱相似度评价软件(2012 版)对 11 批制剂进行相似度分析。结果: 建立了咳清胶囊的 HPLC 特征图谱,标定了 19 个共有特征峰,指认了其中 6 个化学成分,相似度均在 0.92 以上。没食子酸、吗啡、原儿茶酸、可待因、岩白菜素、绿原酸进样量分别在 0.050 4~1.260 0 µg(r=0.999 8)、0.100 4~2.510 0 µg(r=0.999 9)、0.050 8~1.270 0 µg(r=0.999 9)、0.050 4~1.260 0 µg(r=0.999 9)、0.300 8~7.520 0 µg(r=0.999 8 )、0.140 8~3.520 0 µg( r =0.999 9 )范围内线性关系良好,平均回收率(n=6)分别为 97.2%(RSD=1.6%)、97.5%(RSD=1.0%)、100.9%(RSD=1.3%)、104.0%(RSD=1.5%)、96.7%(RSD=1.3%)、95.9%(RSD=1.9%)。11 批制剂中上述 6 个成分的含量范围分别为 0.346 6~0.545 3、0.774 7~1.073 0、0.096 9~ 1.021 0、0.314 6~0.687 3、2.687 1~3.073 0、1.065 0~1.535 6 mg·g-1结论: 本研究所建立的咳清胶囊 HPLC特征图谱和定量测定分析方法可全面有效地评价该制剂的质量。

本文引用格式

刘学, 肖婷, 曲书阅, 马莹, 吴林菁, 周威, 沈祥春, 陶玲, 许乾丽, 茅向军 . 咳清胶囊HPLC特征图谱及多成分含量测定研究*[J]. 药物分析杂志, 2021 , 41(5) : 779 -787 . DOI: 10.16155/j.0254-1793.2021.05.04

Abstract

Objective: To establish an HPLC characteristic chromatogram of Keqing capsules and to simultaneously determine six index components including gallic acid,morphine,protocatechuic acid,codeine,bergenin and chlorogenic acid. Methods: The HPLC separation was carried out on Ultimate® AQ-C18 column(250 mm×4.6 mm,5 µm). The mobile phase was acetonitrile(A)-0.1% phosphoric acid solution(B)with gradient elution. The flow rate was 1.0 mL·min-1,the detection wavelength was 220 nm and the column temperature was 30 ℃. Similarity analysis of 11 batches of preparations was performed by Chinese medicine chromatographic fingerprint similarity evaluation software(2012 version)with bergenin as the reference peak. Results: The HPLC characteristic chromatogram of Keqing capsules was established,19 common characteristic peaks were demarcated, 6 chemical components were identified,and the similarities were above 0.92. The linear ranges of gallic acid,morphine, protocatechuic acid,codeine,bergenin and chlorogenic acid were 0.050 4-1.260 0 µg(r=0.999 8),0.100 4-2.510 0µg(r=0.999 9),0.050 8-1.270 0 µg(r=0.999 9),0.050 4-1.260 0 µg(r=0.999 9),0.300 8-7.520 0 µg(r=0.999 8)and 0.140 8-3.520 0 µg(r=0.999 9),respectively. The average recoveries(n=6)were 97.2%(RSD=1.6%),97.5%(RSD=1.0%),100.9%(RSD=1.3%),104.0%(RSD=1.5%),96.7%(RSD=1.3%)and 95.9%(RSD=1.9%),respectively. The contents of the above-mentioned components in 11 batches of preparations were 0.346 6-0.545 3,0.774 7-1.073 0,0.096 9-1.021 0,0.314 6-0.687 3,2.687 1-3.073 0 and 1.065 0-1.535 6 mg·g-1,respectively. Conclusion: The established HPLC characteristic chromatograms and quantitative analysis methods offered comprehensive and effective evaluation approach for quality control of the Keqing capsules.

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