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Simultaneous Determination of 32 Pyrrolizidine Alkaloids in Two Traditional Chinese Medicine Preparations by UPLC-MS/MS

机译:UPLC-MS/MS 同时测定两种中药制剂中的 32 种吡咯里西啶生物碱

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摘要

Pyrrolizidine alkaloids (PAs) constitute a class of phytotoxin which demonstrates strong hepatotoxicity. In China, many plants containing PAs are used as traditional medicines or medicinal preparations, which could harm human health and safety. Xiaoyao Tablet (XYT) is an antidepressant drug registered in the European Union (EU), Compound Danshen Dropping Pills (CDDP) is a commonly used drug for coronary heart disease, and phase III clinical study is ongoing in the United States. The purpose of this study is to provide data to support the use of Chinese medicine preparations internationally and to establish analytical methods for 32 PAs in XYT and CDDP. The extraction parameters that were optimized include solid-phase extraction (SPE) cartridge, extraction method, and extraction solvent. Then ultra-performance liquid chromatography coupled with triple-quadrupole linear ion-traptandem mass spectrometry (UPLC-MS/MS) was developed to effectively and efficiently quantify the 32 PAs of the XYT and CDDP. The analytical methods for XYT and CDDP were verified respectively. For XYT, the analytical method for 32 PAs was linear, and the correlation coefficient r was greater than 0.994; the recovery (REC%) at 10–2000 μg/kg was 73.3%–118.5%, and the relative standard deviation (RSD%) was 2.1%–15.4%. The CDDP REC% was 71.8%–112.0%, and the RSD% was 2.0%–17.1%. This study provides technical and data support for the registration of Chinese patented medicines in the EU, controls quality and ensures safety, and is committed to the internationalization and standardization of Chinese patented medicines.
机译:吡咯里西啶生物碱 (PAs) 是一类植物毒素,具有很强的肝毒性。在中国,许多含有 PA 的植物被用作传统药物或药物制剂,这可能会危害人类健康和安全。逍遥片(XYT)是在欧盟(EU)注册的抗抑郁药,复方丹参滴丸(CDDP)是冠心病的常用药物,在美国正在进行III期临床研究。本研究的目的是提供数据以支持中药制剂在国际上的使用,并建立 XYT 和 CDDP 中 32 种 PA 的分析方法。优化的萃取参数包括固相萃取 (SPE) 小柱、萃取方法和萃取溶剂。然后,开发了超高效液相色谱法与三重四极杆线性离子阱串联质谱 (UPLC-MS/MS) 联用,以有效且高效地定量 XYT 和 CDDP 的 32 种 PA。分别验证了 XYT 和 CDDP 的分析方法。对于 XYT,32 种 PAs 的解析方法是线性的,相关系数 r 大于 0.994;10–2000 μg/kg 时的回收率 (REC%) 为 73.3%–118.5%,相对标准偏差 (RSD%) 为 2.1%–15.4%。CDDP REC% 为 71.8%–112.0%,RSD% 为 2.0%–17.1%。本研究为中成药在欧盟的注册提供技术和数据支持,控制质量,确保安全,致力于中成药的国际化和标准化。

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