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海军军医大学第三附属医院药剂科,上海 200438
药师。研究方向:药物分析。电话:021-81887226。E-mail:wxlcpu09@sina.com
副主任药师,硕士生导师。研究方向:中药药理学、天然产物抗肿瘤活性成分筛选及耐药机制。电话:021-81875571。E-mail:annabao212@126.com
纸质出版日期:2023-09-30,
收稿日期:2023-03-20,
修回日期:2023-08-09,
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王晓丽,朱平,周燕妮等.肝泰舒胶囊的成分鉴别及指标成分含量测定方法建立 Δ[J].中国药房,2023,34(18):2198-2203.
WANG Xiaoli,ZHU Ping,ZHOU Yanni,et al.Method establishment of components identification and content determination of index components in Gantaishu capsules[J].ZHONGGUO YAOFANG,2023,34(18):2198-2203.
王晓丽,朱平,周燕妮等.肝泰舒胶囊的成分鉴别及指标成分含量测定方法建立 Δ[J].中国药房,2023,34(18):2198-2203. DOI: 10.6039/j.issn.1001-0408.2023.18.05.
WANG Xiaoli,ZHU Ping,ZHOU Yanni,et al.Method establishment of components identification and content determination of index components in Gantaishu capsules[J].ZHONGGUO YAOFANG,2023,34(18):2198-2203. DOI: 10.6039/j.issn.1001-0408.2023.18.05.
目的
2
建立分别鉴别肝泰舒胶囊的化学成分以及甘草酸等6种指标成分的含量测定方法。
方法
2
采用高效液相-飞行时间质谱技术鉴别肝泰舒胶囊中的化学成分;采用超高效液相-串联质谱技术测定甘草酸等6种指标成分的含量。
结果
2
肝泰舒胶囊中共鉴别出41种化学成分。甘草酸、芒果苷、木犀草苷、木香烃内酯、齐墩果酸和小檗碱检测质量浓度的线性范围均为200~10 000 ng/mL(
r
均大于0.999);定量限分别为200、20、10、1、10、0.5 ng/mL,检测限分别为100、10、5、0.5、5、0.25 ng/mL;精密度、稳定性(24 h)、重复性试验的RSD均小于5.0%(
n
=6或
n
=3);加样回收率为99.05%~101.08%(RSD均小于2.0%,
n
=6);含量分别为2.42~2.66、0.85~1.16、0.35~0.46、6.18~6.46、0.99~1.29、5.22~5.56 mg/g。
结论
2
本研究所建立的鉴别和含量测定方法快速、简便,可用于肝泰舒胶囊化学成分的鉴别和指标成分的含量测定。
OBJECTIVE
2
To establish methods to identify the chemical components of Gantaishu capsule, and determine the contents of 6 index components including glycyrrhizic acid.
METHODS
2
The chemical components of Gantaishu capsule were determined by HPLC-TOF/MS; the contents of 6 index components including glycyrrhizic acid were determined by UPLC-MS/MS.
RESULTS
2
A total of 41 chemical components were identified in Gantaishu capsules. The linear ranges of glycyrrhizic acid, mangiferin, luteolin, costunolide, oleanolic acid and berberine were 200-10 000 ng/mL(
r
were all greater than 0.999). The limits of quantification were 200, 20, 10, 1, 10, 0.5 ng/mL, and the limits of detection were 100, 10, 5, 0.5, 5, 0.25 ng/mL, respectively; RSDs of precision, stability (24 h) and reproducibility tests were all less than 5.0% (
n
=6 or
n
=3); the recoveries were 99.05%-101.08% (RSD were all less than 2.0%,
n
=6). The contents of them were 2.42-2.66, 0.85-1.16, 0.35-0.46, 6.18-6.46, 0.99-1.29, 5.22-5.56 mg/g.
CONCLUSIONS
2
The established methods for identification and content determination are rapid and simple, and can be used for the identification of chemical components and the content determination of index components in Gantaishu capsule.
肝泰舒胶囊成分鉴别含量测定高效液相-飞行时间质谱技术超高效液相-串联质谱技术
component identificationcontent determinationHPLC-TOF/MSUPLC-MS/MS
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