Cargando…

An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study

A sensitive and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated to simultaneously determine the toxic and other active components including isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex pe...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zhen, Li, Yang, Li, Jin, Liu, Rui, Hao, Jia, He, Jun, Chang, Yan-xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393897/
https://www.ncbi.nlm.nih.gov/pubmed/30894874
http://dx.doi.org/10.1155/2019/1639619
_version_ 1783398780491530240
author Li, Zhen
Li, Yang
Li, Jin
Liu, Rui
Hao, Jia
He, Jun
Chang, Yan-xu
author_facet Li, Zhen
Li, Yang
Li, Jin
Liu, Rui
Hao, Jia
He, Jun
Chang, Yan-xu
author_sort Li, Zhen
collection PubMed
description A sensitive and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated to simultaneously determine the toxic and other active components including isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex periplocae extract to rats. Plasma samples were prepared by protein precipitation with methanol. All compounds were separated on a C(18) column with gradient elution using acetonitrile and formic acid aqueous solution (0.1%, v/v) as the mobile phase at a flow rate of 0.3 mL/min. The detection of all compounds was accomplished by multiple-reaction monitoring (MRM) in the positive electrospray ionization mode. The LC-MS/MS method exhibited good linearity for five analytes. The lower limit of quantification (LLOQ) was 0.48 ng/mL for scopoletin, periplogenin, and periplocymarin; 2.4 ng/mL for isovanillin and periplocin. The extraction recoveries of all compounds were more than 90% and the RSDs were below 10%. It was found that the absorption of scopoletin and periplocin was rapid in vivo after oral administration of cortex periplocae extract. Furthermore, periplocymarin possessed abundant plasma exposure. The results demonstrated that the validated method was efficiently applied for the pharmacokinetic studies of isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex periplocae extract.
format Online
Article
Text
id pubmed-6393897
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-63938972019-03-20 An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study Li, Zhen Li, Yang Li, Jin Liu, Rui Hao, Jia He, Jun Chang, Yan-xu Int J Anal Chem Research Article A sensitive and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated to simultaneously determine the toxic and other active components including isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex periplocae extract to rats. Plasma samples were prepared by protein precipitation with methanol. All compounds were separated on a C(18) column with gradient elution using acetonitrile and formic acid aqueous solution (0.1%, v/v) as the mobile phase at a flow rate of 0.3 mL/min. The detection of all compounds was accomplished by multiple-reaction monitoring (MRM) in the positive electrospray ionization mode. The LC-MS/MS method exhibited good linearity for five analytes. The lower limit of quantification (LLOQ) was 0.48 ng/mL for scopoletin, periplogenin, and periplocymarin; 2.4 ng/mL for isovanillin and periplocin. The extraction recoveries of all compounds were more than 90% and the RSDs were below 10%. It was found that the absorption of scopoletin and periplocin was rapid in vivo after oral administration of cortex periplocae extract. Furthermore, periplocymarin possessed abundant plasma exposure. The results demonstrated that the validated method was efficiently applied for the pharmacokinetic studies of isovanillin, scopoletin, periplocin, periplogenin, and periplocymarin after oral administration of cortex periplocae extract. Hindawi 2019-02-13 /pmc/articles/PMC6393897/ /pubmed/30894874 http://dx.doi.org/10.1155/2019/1639619 Text en Copyright © 2019 Zhen Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Zhen
Li, Yang
Li, Jin
Liu, Rui
Hao, Jia
He, Jun
Chang, Yan-xu
An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
title An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
title_full An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
title_fullStr An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
title_full_unstemmed An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
title_short An LC-MS/MS Method for Simultaneous Determination of the Toxic and Active Components of Cortex Periplocae in Rat Plasma and Application to a Pharmacokinetic Study
title_sort lc-ms/ms method for simultaneous determination of the toxic and active components of cortex periplocae in rat plasma and application to a pharmacokinetic study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393897/
https://www.ncbi.nlm.nih.gov/pubmed/30894874
http://dx.doi.org/10.1155/2019/1639619
work_keys_str_mv AT lizhen anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT liyang anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT lijin anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT liurui anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT haojia anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT hejun anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT changyanxu anlcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT lizhen lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT liyang lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT lijin lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT liurui lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT haojia lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT hejun lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy
AT changyanxu lcmsmsmethodforsimultaneousdeterminationofthetoxicandactivecomponentsofcortexperiplocaeinratplasmaandapplicationtoapharmacokineticstudy