An Optimized and Sensitive UHPLC-ESI-Q-TOF/HRMS Demonstrated the Dynamic Profiling of Allantoin, N-trans-Feruloyl-3-Methoxytyramine, and N-p-Coumaroyltyramine from Portulaca oleracea L. In Vivo in Rats

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL Journal of separation science Pub Date : 2024-12-31 DOI:10.1002/jssc.70055
Kexian Li, Wei Wang
{"title":"An Optimized and Sensitive UHPLC-ESI-Q-TOF/HRMS Demonstrated the Dynamic Profiling of Allantoin, N-trans-Feruloyl-3-Methoxytyramine, and N-p-Coumaroyltyramine from Portulaca oleracea L. In Vivo in Rats","authors":"Kexian Li,&nbsp;Wei Wang","doi":"10.1002/jssc.70055","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>This study revealed the dynamic profiling of three main components of <i>Portulaca oleracea</i> L. in vivo in rats, namely allantoin (<b>A</b>), <i>N</i>-<i>trans</i>-feruloyl-3-methoxytyramine (<b>M</b>), and <i>N</i>-<i>p</i>-coumaroyltyramine (<b>C</b>). A sensitive and efficient UHPLC-ESI-Q-TOF/HRMS, including an optimized separation process, was applied to their qualitative and quantitative analysis. The validation of the method presented the correlation coefficients, which were over 0.997. The mean matrix factors were 0.930. Recoveries ranged from 96.6% to 109.2%, and determination accuracy varied from 95% to 109.4%. The biological samples included rat plasma, liver, kidneys, bile, and excreta taken after a single oral administration of the saturated DMSO solution of <i>P. oleracea</i> extract. The contents of <b>A</b>, <b>M</b>, and <b>C</b> were of 2.5, 5.1, and 3.4 g/kg in the dry whole herb, respectively. <b>A</b> was identified in the liver and kidneys from 0 to 6 h. Allantoic acid, as one metabolite of <b>A</b>, was found to be kept in plasma for a short time, but another two successive metabolites of <b>A</b> remained over 6 h. It depicted a pharmacological material basis of the herb, regarded with <b>A</b>. The glucuronidation and/or sulfation of <b>M</b> and <b>C</b> were detected in rat bile from 0 to 12 h. The complicated but interesting metabolic schemes for <b>A</b>, <b>M</b>, and <b>C</b> were illustrated from their HRMS and MS/MS performance.</p>\n </div>","PeriodicalId":17098,"journal":{"name":"Journal of separation science","volume":"48 1","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of separation science","FirstCategoryId":"5","ListUrlMain":"https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/jssc.70055","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

This study revealed the dynamic profiling of three main components of Portulaca oleracea L. in vivo in rats, namely allantoin (A), N-trans-feruloyl-3-methoxytyramine (M), and N-p-coumaroyltyramine (C). A sensitive and efficient UHPLC-ESI-Q-TOF/HRMS, including an optimized separation process, was applied to their qualitative and quantitative analysis. The validation of the method presented the correlation coefficients, which were over 0.997. The mean matrix factors were 0.930. Recoveries ranged from 96.6% to 109.2%, and determination accuracy varied from 95% to 109.4%. The biological samples included rat plasma, liver, kidneys, bile, and excreta taken after a single oral administration of the saturated DMSO solution of P. oleracea extract. The contents of A, M, and C were of 2.5, 5.1, and 3.4 g/kg in the dry whole herb, respectively. A was identified in the liver and kidneys from 0 to 6 h. Allantoic acid, as one metabolite of A, was found to be kept in plasma for a short time, but another two successive metabolites of A remained over 6 h. It depicted a pharmacological material basis of the herb, regarded with A. The glucuronidation and/or sulfation of M and C were detected in rat bile from 0 to 12 h. The complicated but interesting metabolic schemes for A, M, and C were illustrated from their HRMS and MS/MS performance.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
优化且灵敏的 UHPLC-ESI-Q-TOF/HRMS 显示了大鼠体内马齿苋中尿囊素、N-反式-阿魏酰-3-甲氧基酪胺和 N-对香豆酰酪胺的动态轮廓。
研究了马蹄苋中尿囊素(A)、n -反式阿魏酰-3-甲氧基酪胺(M)和n -对- coumaryyyramine (C)三种主要成分在大鼠体内的动态特征,采用高效液相色谱- esi - q - tof /HRMS对其进行了定性和定量分析,并优化了分离工艺。方法验证的相关系数均在0.997以上。平均矩阵因子为0.930。加样回收率为96.6% ~ 109.2%,测定准确度为95% ~ 109.4%。生物样品包括单次口服马齿苋提取物饱和DMSO溶液后的大鼠血浆、肝脏、肾脏、胆汁和排泄物。干全草中A、M、C含量分别为2.5、5.1、3.4 g/kg。被发现在肝脏和肾脏从0到6小时,尿囊酸代谢产物之一,被发现在等离子体在短时间内,但另一个连续两个代谢物仍超过6 h。它描述了草药的药理物质基础,认为A . M和C的glucuronidation和/或硫酸盐化作用被发现在大鼠胆汁从0到12 h。复杂的但是有趣的代谢机制,M, C从,8经和MS / MS性能说明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
期刊最新文献
Trace determination of morphine and codeine in whole blood samples using pH-switchable hydrophobic deep eutectic solvents based liquid phase microextraction followed by HPLC-UV. How to Process Samples for Metabolomics in Ecology: A Comparative Study of Preanalytical Storage Methods Quantification of Monoclonal Antibodies in Pharmaceutical Matrices by Middle-Up Capillary Zone Electrophoresis-Mass Spectrometry Ultrasound-Assisted Combined With Natural Ternary Deep Eutectic Solvent Extraction Method for the Green Extraction of Squalene From Strobilanthes tonkinensis Spectral Pixel-Based Analysis and Clustering Workflow for the Exploration of the Composition of Gas Oil Samples by Comprehensive Two-dimensional Gas Chromatography Vacuum Ultraviolet Spectroscopy
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1