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基于 UPLC/Q-TOF-MS 的青风藤提取物及代谢物在大鼠体内综合特征分析的整合策略的建立。

Development of an integrated strategy for comprehensive characterization of Sinomenii Caulis extract and metabolites in rats based on UPLC/Q-TOF-MS.

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.

出版信息

J Pharm Biomed Anal. 2024 Oct 15;249:116391. doi: 10.1016/j.jpba.2024.116391. Epub 2024 Aug 3.

DOI:10.1016/j.jpba.2024.116391
PMID:39116504
Abstract

Sinomenii Caulis (SC), a commonly used traditional Chinese medicine for its therapeutic effects on rheumatoid arthritis, contains rich chemical components. At present, most studies mainly focus on sinomenine, with little research on other alkaloids. In this study, a comprehensive profile of compounds in SC extract, and biological samples of rats (including bile, urine, feces, and plasma) after oral administration of SC extract was conducted via ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC/Q-TOF-MS). The fragmentation patterns and potential biotransformation pathways of six main types of alkaloids in SC were summarized, and the corresponding characteristic product ions, relative ion intensity, and neutral losses were obtained to achieve rapid classification and identification of complex components of SC from in vitro to in vivo. As a result, a total of 114 alkaloid compounds were identified, including 12 benzyl alkaloids, 4 isoquinolone alkaloids, 32 aporphine alkaloids, 28 protoberberine alkaloids, 34 morphinan alkaloids and 4 organic amine alkaloids. After administration of SC extract to rats, a total of 324 prototypes and metabolites were identified from rat plasma, urine, feces and bile, including 81 aporphines, 95 protoberberines, 117 morphinans and 31 benzylisoquinolines. The main types of metabolites were demethylation, hydrogenation, dehydrogenation, aldehydation, oxidation, methylation, sulfate esterification, glucuronidation, glucose conjugation, glycine conjugation, acetylation, and dihydroxylation. In summary, this integrated strategy provides an additional approach for the incomplete identification caused by compound diversity and low abundance, laying the foundation for the discovery of new bioactive compounds of SC against rheumatoid arthritis.

摘要

青风藤(SC)是一种常用于治疗类风湿关节炎的传统中药,其含有丰富的化学物质。目前,大多数研究主要集中在青藤碱上,对其他生物碱的研究较少。本研究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)对 SC 提取物的化合物及大鼠生物样品(胆汁、尿液、粪便和血浆)进行了全面分析。总结了 SC 中 6 种主要类型生物碱的裂解模式和潜在的生物转化途径,得到了相应的特征产物离子、相对离子强度和中性丢失,实现了从体外到体内 SC 复杂成分的快速分类和鉴定。共鉴定出 114 种生物碱化合物,包括 12 种苄基生物碱、4 种异喹啉生物碱、32 种阿朴啡生物碱、28 种原小檗碱生物碱、34 种吗啡烷生物碱和 4 种有机胺生物碱。SC 提取物给大鼠灌胃后,从大鼠血浆、尿液、粪便和胆汁中共鉴定出 324 个原型和代谢产物,包括 81 个阿朴啡类、95 个原小檗碱类、117 个吗啡烷类和 31 个苄基异喹啉类。主要代谢类型为去甲基化、加氢、脱氢、醛化、氧化、甲基化、硫酸酯化、葡萄糖醛酸化、葡萄糖结合、甘氨酸结合、乙酰化和二羟基化。综上所述,该综合策略为由于化合物多样性和丰度低导致的不完全鉴定提供了一种补充方法,为发现 SC 治疗类风湿关节炎的新生物活性化合物奠定了基础。

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