[Qualitative and quantitative analysis of chemical components of Dracocephalum moldavica based on UPLC-Q-TOF-MS/MS and UPLC].

Q3 Pharmacology, Toxicology and Pharmaceutics
Ming-Lei Xu, Hui-Min Gao, Yong-Xin Zhang, Zhi-Jian Li, Yang Ding, Qing-Rong Wang, Shi-Xia Huo, Wei-Hong Feng, Yu-Tong Kang, Liang-Mian Chen, Zhi-Min Wang
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引用次数: 0

Abstract

Ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry(UPLC-Q-TOF-MS/MS) was used to rapidly identify the chemical components in Dracocephalum moldavica, and UPLC was employed to determine the content of its main components. MS analysis was performed using an electrospray ionization(ESI) source and data were collected in the negative ion mode. By comparing the retention time and mass spectra of reference compounds, and using a self-built compound database and the PubChem database, 68 compounds were identified from D. moldavica, including 36 flavonoids, 22 phenylpropanoids, 4 phenols, and 6 other compounds. On this basis, a UPLC quantitative method was established to simultaneously determine 8 main components, i.e., luteolin-7-O-glucuronide, apigenin-7-O-glucuronide, rosmarinic acid, diosmetin-7-O-glucuronide, tilianin, acacetin-7-O-glucuronide, acacetin-7-O-(6″-O-malonyl)-glucoside, and acacetin. A Waters ACQUITY BEH C_(18) column(2.1 mm × 100 mm, 1.7 μm) was used, with acetonitrile and a water solution containing 0.1% formic acid and 0.1% phosphoric acid as the mobile phase for gradient elution. The detection wavelength was set at 330 nm, with a flow rate of 0.4 mL·min~(-1), and the column temperature was maintained at 35 ℃. The 8 components demonstrated good linearity(r≥0.999 9) over a wide mass concentration range(50 or 100 times). The average recovery rate ranged from 97.5% to 105.1%, and the relative standard deviations(RSDs) were 0.90% to 3.4%(n= 6), indicating that the method was simple, accurate, and reliable. In 17 batches of D. moldavica samples, the content of these 8 components ranged from 0.405 to 2.10, 0.063 to 0.342, 0.446 to 2.43, 0.415 to 1.47, 1.57 to 4.34, 0.173 to 0.386, 1.00 to 5.40, and 0.069 to 0.207 mg·g~(-1), respectively. These results indicate significant differences in the internal quality of the samples, highlighting the need for strict quality control to ensure their pharmacodynamic efficacy. This study provides a scientific basis for the rapid discovery of pharmacodynamic substances, comprehensive quality control, and the formulation or revision of quality standards for D. moldavica.

[基于UPLC- q - tof -MS/MS和UPLC的龙头草化学成分定性定量分析]。
采用超高效液相色谱-四极杆飞行时间质谱联用技术(UPLC- q - tof -MS/MS)对龙头草中的化学成分进行快速鉴定,并采用超高效液相色谱法测定其主要成分的含量。质谱分析采用电喷雾电离(ESI)源,在负离子模式下采集数据。通过比较参比化合物的保留时间和质谱,并结合自建的化合物数据库和PubChem数据库,从moldavica中鉴定出68种化合物,其中黄酮类化合物36种,苯丙类化合物22种,酚类化合物4种,其他化合物6种。在此基础上,建立了UPLC定量方法,同时测定木犀草素-7- o -葡糖苷、芹菜素-7- o -葡糖苷、迭香香酸、薯蓣皂苷-7- o -葡糖苷、天青素、棘球葡糖苷-7- o -葡糖苷(6″- o -丙二醇基)、棘球葡糖苷等8种主要成分。采用Waters ACQUITY BEH C_(18)色谱柱(2.1 mm × 100 mm, 1.7 μm),以乙腈和0.1%甲酸、0.1%磷酸水溶液为流动相梯度洗脱。检测波长为330 nm,流速为0.4 mL·min~(-1),柱温为35℃。在较宽的质量浓度范围内(50倍或100倍),8种成分均表现出良好的线性关系(r≥0.999 9)。平均加样回收率为97.5% ~ 105.1%,相对标准偏差(rsd)为0.90% ~ 3.4%(n= 6),方法简便、准确、可靠。17批moldavica样品中8种成分的含量分别为0.405 ~ 2.10、0.063 ~ 0.342、0.446 ~ 2.43、0.415 ~ 1.47、1.57 ~ 4.34、0.173 ~ 0.386、1.00 ~ 5.40和0.069 ~ 0.207 mg·g~(-1)。这些结果表明,样品的内部质量存在显著差异,强调需要严格的质量控制,以确保其药效学效果。本研究为快速发现药效学物质、进行全面的质量控制以及制定或修订石竹药材质量标准提供了科学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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