Literature DB >> 26053360

LC/MS/MS determination and pharmacokinetic study of iridoid glycosides monotropein and deacetylasperulosidic acid isomers in rat plasma after oral administration of Morinda officinalis extract.

Chunmin Li1, Jian Dong2, Jingchang Tian3, Zhipeng Deng4, Xiujing Song5.   

Abstract

Morinda officinalis is a famous traditional Chinese medicine containing iridoid glycoside compounds, such as monotropein and deacetylasperulosidic acid. The aim of the study was to develop a novel and sensitive liquid chromatography-tandem mass spectrometry (LC/MS/MS) method for the simultaneous determination of the two isomeric iridoid glycosides and then evaluate their pharmacokinetic properties in rats. Selected-reaction monitoring mode was employed for quantification of two analytes in rat plasma. The calibration curves were linear over their respective concentration range with correlation coefficient >0.995 for both analytes. Precision for monotropein and deacetylasperulosidic acid ranged from 2.5 to 11.9% relative standard deviation, and the accuracy of two analytes was -2.0-3.7 and -6.4-10.7% relative error, respectively. This method was successfully applied in pharmacokinetic study after oral administration of M. officinalis extract in rats. The results provided a basis for further research on the bioactivity of M. officinalis.
Copyright © 2015 John Wiley & Sons, Ltd.

Entities:  

Keywords:  LC/MS/MS; Morinda officinalis; deacetylasperulosidic acid; monotropein; pharmacokinetics

Mesh:

Substances:

Year:  2015        PMID: 26053360     DOI: 10.1002/bmc.3532

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  5 in total

Review 1.  Iridoids are natural glycation inhibitors.

Authors:  Brett J West; Shixin Deng; Akemi Uwaya; Fumiyuki Isami; Yumi Abe; Sho-Ichi Yamagishi; C Jarakae Jensen
Journal:  Glycoconj J       Date:  2016-06-15       Impact factor: 2.916

2.  Effects of the Salt-Processing Method on the Pharmacokinetics and Tissue Distribution of Orally Administered Morinda officinalis How. Extract.

Authors:  Ji Shi; Xiaohang Ren; Jia Wang; Xiaofeng Wei; Bonan Liu; Tianzhu Jia
Journal:  J Anal Methods Chem       Date:  2020-02-11       Impact factor: 2.193

3.  Pharmacokinetics and tissue distribution of monotropein and deacetyl asperulosidic acid after oral administration of extracts from Morinda officinalis root in rats.

Authors:  Yi Shen; Qi Zhang; Yan-Bin Wu; Yu-Qiong He; Ting Han; Jian-Hua Zhang; Liang Zhao; Hsien-Yeh Hsu; Hong-Tao Song; Bing Lin; Hai-Liang Xin; Yun-Peng Qi; Qiao-Yan Zhang
Journal:  BMC Complement Altern Med       Date:  2018-10-24       Impact factor: 3.659

4.  Simultaneous Analysis of Iridoid Glycosides and Anthraquinones in Morinda officinalis Using UPLC-QqQ-MS/MS and UPLC-Q/TOF-MSE.

Authors:  Xiangsheng Zhao; Jianhe Wei; Meihua Yang
Journal:  Molecules       Date:  2018-05-03       Impact factor: 4.411

5.  Asperuloside and Asperulosidic Acid Exert an Anti-Inflammatory Effect via Suppression of the NF-κB and MAPK Signaling Pathways in LPS-Induced RAW 264.7 Macrophages.

Authors:  Jingyu He; Xianyuan Lu; Ting Wei; Yaqian Dong; Zheng Cai; Lan Tang; Menghua Liu
Journal:  Int J Mol Sci       Date:  2018-07-12       Impact factor: 5.923

  5 in total

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