Biomedical Chromatography, volume 34, issue 1
Analysis of plasma migration components inPatrinia villosa(Thunb.) Juss. effective parts by UPLC–Q‐TOF–MS
Xiao Han
1
,
Shuai Wang
1, 2, 3
,
Xin-Xin Yang
1
,
Tian-Jiao Li
1, 2, 3
,
Huan Jun Zhao
1
,
Li-Ping Zhou
1
,
Zhao Lin
1
,
Yong-Rui Bao
1, 2, 3
,
Xiansheng Meng
1, 2, 3
2
Component Medicine Engineering Research Center of Liaoning Province Dalian China
|
3
Liaoning Province Modern Chinese Medicine Research Engineering Laboratory Dalian China
|
Publication type: Journal Article
Publication date: 2019-11-11
Journal:
Biomedical Chromatography
scimago Q3
SJR: 0.384
CiteScore: 3.6
Impact factor: 1.8
ISSN: 02693879, 10990801
DOI:
10.1002/bmc.4701
PubMed ID:
31596954
Drug Discovery
Biochemistry
Molecular Biology
General Medicine
Pharmacology
Clinical Biochemistry
Analytical Chemistry
Abstract
Patrinia villosa (Thunb.) Juss. (PVJ) is described as pungent, bitter and slightly cold in Chinese medicine, and is associated with the large intestine, stomach and liver meridians. The preliminary experiments of our research team proved that PVJ total flavonoids have excellent inhibitory effects on liver cancer cells. The present experiment uses the UPLC-Q-TOF-MS technology and serum pharmacochemistry methods to analyze the chemical components in vitro and in vivo of PVJ antiliver tumors. A total of 14 chemical components were identified in the total flavonoids extract of PVJ, and it is mainly composed of flavonoids, flavonones, flavonols and phenolic acids. At the same time, seven prototypical components and seven metabolic components were detected in the drug-containing plasma. Hydrocaffeate and scutellarein are the phase I metabolites of caffeic acid and scutellarin, respectively. Sulfated apigenin, sulfated luteolin, sulfated kaempferol and methylated kaempferol are the II phase metabolites of apigenin, luteolin, kaempferol, respectively. The experiment provides a reference for the research and development of antitumor drug candidates, and provides a basis for revealing the bioactive components of PVJ and the antitumor mechanism.
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