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1.广西中医药大学附属国际壮医医院壮瑶药研发中心,南宁 530201
2.广西中医药大学药学院,南宁 530200
3.广西中医药大学中药学国家级实验教学示范中心,南宁 530200
副主任药师。研究方向:药物分析、质量控制、民族药制剂研发。E-mail:84946936@qq.com
教授,博士。研究方向:中药、民族药的品质与药效研究。E-mail:rousel@126.com
收稿日期:2024-04-16,
修回日期:2024-07-23,
录用日期:2024-09-03,
纸质出版日期:2024-11-30
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陈松,李运容,农璐蔚,等.基于HPLC指纹图谱和多成分含量综合评价扶正胶囊的质量[J].中国药房,2024,35(22):2726-2731.
CHEN Song,LI Yunrong,NONG Luwei,et al.Quality evaluation of Fuzheng capsules based on HPLC fingerprint and multi-ingredient content determination[J].ZHONGGUO YAOFANG,2024,35(22):2726-2731.
陈松,李运容,农璐蔚,等.基于HPLC指纹图谱和多成分含量综合评价扶正胶囊的质量[J].中国药房,2024,35(22):2726-2731. DOI: 10.6039/j.issn.1001-0408.2024.22.04.
CHEN Song,LI Yunrong,NONG Luwei,et al.Quality evaluation of Fuzheng capsules based on HPLC fingerprint and multi-ingredient content determination[J].ZHONGGUO YAOFANG,2024,35(22):2726-2731. DOI: 10.6039/j.issn.1001-0408.2024.22.04.
目的
2
建立壮药制剂扶正胶囊指纹图谱和多指标成分含量的测定方法,并对其进行质量评价。
方法
2
采用高效液相色谱(HPLC)法,结合《中药色谱指纹图谱相似度评价系统(2004A)》建立12批扶正胶囊样品的指纹图谱,并进行相似度评价、共有峰确认;以指纹图谱共有峰峰面积为变量,采用SPSS 20.0软件进行聚类分析和主成分分析。采用同一HPLC法测定12批样品中甘草苷、特女贞苷、3,6′-二芥子酰基蔗糖、甘草酸铵的含量。
结果
2
12批扶正胶囊样品共有22个共有峰,相似度均大于0.91;指认出甘草苷(峰8)、特女贞苷(峰10)、3,6′-二芥子酰基蔗糖(峰11)、甘草酸铵(峰21)4个共有峰;12批样品可聚为3类,200801、200802、200803为Ⅰ类,样1~样8为Ⅱ类,221101为Ⅲ类;200802的综合得分(2.540)最高。12批样品中,甘草苷、特女贞苷、3,6′-二芥子酰基蔗糖、甘草酸铵的含量分别为0.44~0.73、1.28~2.47、0.08~0.12、1.31~1.81 mg/粒。
结论
2
12批扶正胶囊样品的主要成分相似但含量有所差别,以200802的质量最优;所建指纹图谱和多指标成分含量测定方法专属性强、准确度高,结合化学模式识别分析可用于扶正胶囊的质量评价。
OBJECTIVE
2
To establish the fingerprint of the Zhuang medicine preparation Fuzheng capsules and a method for the determination of multi-ingredient content for quality evaluation.
METHODS
2
High-performance liquid chromatography (HPLC) was used in conjunction with the
Similarity Evaluation System for Chromatographic Fingerprints of Traditional Chinese Medicine
(2004A edition) to establish the fingerprint of 12 batches of Fuzheng capsules, evaluate their similarity and confirm the common peaks. Cluster analysis and principal component analysis were performed using SPSS 20.0 software with the peak areas of the common peaks in the fingerprint as variables. The same HPLC method was adopted to determine the content of liquiritin, sp
ecnuezhenide, 3,6′-disinapoyl sucrose and ammonium glycyrrhizinate in the 12 batches of samples.
RESULTS
2
A total of 22 common peaks were identified in the fingerprints of the 12 batches of Fuzheng capsules, with the similarities greater than 0.91. Four common peaks were identified as liquiritin (peak 8), specnuezhenide (peak 10), 3,6′-disinapoyl sucrose (peak 11), and ammonium glycyrrhizinate (peak 21). The 12 batches of samples could be clustered into 3 categories, with 200801, 200802 and 200803 as category Ⅰ, samples 1 to 8 as category Ⅱ, and 221101 as category Ⅲ. The sample 200802 had the highest comprehensive score (2.540). The contents of liquiritin, specnuezhenide, 3,6′-disinapoyl sucrose and ammonium glycyrrhizinate in the 12 batches of samples were 0.44 to 0.73, 1.28 to 2.47, 0.08 to 0.12, and 1.31 to 1.81 mg per capsule, respectively.
CONCLUSIONS
2
The main components of the 12 batches of Fuzheng capsules were similar, but the content varied, with the sample 200802 indicating the highest quality. The established fingerprint and multi-ingredient content determination method were highly specific and accurate, which can be used for the quality evaluation of Fuzheng capsules in combination with chemical pattern recognition analysis.
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