首页|基于UPLC-Q-TOF-MS/MS和UPLC的香青兰化学成分定性与定量分析

基于UPLC-Q-TOF-MS/MS和UPLC的香青兰化学成分定性与定量分析

扫码查看
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)快速鉴别香青兰的化学成分,并对其主要成分进行UPLC含量测定.质谱分析采用电喷雾离子源(ESI),负离子模式下采集数据,结合对照品的保留时间和质谱信息、自建化合物数据库、PubChem数据库等,从香青兰中鉴定化合物68个,其中黄酮类36个、苯丙素类22个,苯酚类4个、其他类化合物6个.在此基础上,建立同步测定木犀草素-7-O-葡萄糖醛酸苷、芹菜素-7-O-葡萄糖醛酸苷、迷迭香酸、香叶木素-7-O-葡萄糖醛酸苷、田蓟苷、金合欢素-7-O-葡萄糖醛酸苷、金合欢素-7-O-(6″-O-丙二酸单酰)-葡萄糖苷和金合欢素等8种主要成分的UPLC定量方法.采用Waters ACQUITY BEH C18色谱柱(2.1 mm×100 mm,1.7μm),以乙腈-含0.1%甲酸和0.1%磷酸的水溶液为流动相进行梯度洗脱,检测波长330 nm,流速0.4 mL·min-1,柱温35℃.上述8种成分在较宽的质量浓度范围(50或100倍)内,呈现良好的线性关系(r≥0.9999),平均回收率为97.5%~105.1%,RSD为0.90%~3.4%(n=6),该法简便、准确、可靠.17批香青兰样品中,上述8种成分的质量分数分别为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、0.069~0.207 mg·g-1,说明其内在质量存在较大差异,需进行良好的质量控制以保障其药效.该研究为香青兰的药效物质快速发现、整体质量控制与评价以及质量标准的制修订提供科学依据.
Qualitative and quantitative analysis of chemical components of Dracocephalum moldavica based on UPLC-Q-TOF-MS/MS and UPLC
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 C18 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≥0.9999) 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.

Dracocephalum moldavicaultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS/MS)qualitative analysiscontent determinationquality control

胥明磊、高慧敏、张永欣、李治建、丁阳、王清荣、霍仕霞、冯伟红、康雨彤、陈两绵、王智民

展开 >

中国中医科学院中药研究所,北京 100700

新疆维吾尔自治区维吾尔医医院,新疆乌鲁木齐 830049

新疆中药医院制剂循证与转化重点实验室,新疆乌鲁木齐 830049

香青兰 超高效液相色谱-四极杆-飞行时间质谱联用技术 定性分析 含量测定 质量控制

2024

中国中药杂志
中国药学会

中国中药杂志

CSTPCD北大核心
影响因子:1.718
ISSN:1001-5302
年,卷(期):2024.49(23)