Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration
Kuraridin is an active natural prenylated flavonoid ingredient originating from the well-known traditional Chinese medicine Sophora flavescens Ait., that possesses various bioactivities, such as antitumor activity, PLCγ1 inhibitory activity, glycosidase inhibitory activity, etc. However, there is no...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2018-01-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/23/2/132 |
_version_ | 1818982921930801152 |
---|---|
author | Yi Liu Lei Chen Wei Cai Lin-lin Zhao Zhi-xian Mo |
author_facet | Yi Liu Lei Chen Wei Cai Lin-lin Zhao Zhi-xian Mo |
author_sort | Yi Liu |
collection | DOAJ |
description | Kuraridin is an active natural prenylated flavonoid ingredient originating from the well-known traditional Chinese medicine Sophora flavescens Ait., that possesses various bioactivities, such as antitumor activity, PLCγ1 inhibitory activity, glycosidase inhibitory activity, etc. However, there is no report on the plasma metabolic profile and pharmacokinetic study of kuraridin. The current study was designed to use an ultra-performance liquid chromatography/tandem mass spectrometry (UHPLC-MS/MS) method for the quantification and characterization metabolites in rat plasma after oral administration of kuraridin. A liquid-liquid extraction method with ethyl acetate-acetonitrile (1:3) was used to extract the kuraridin from rat plasma samples. The chromatographic separation was carried out on a Hypersil GOLD UHPLC C18 column equipped with a C18 guard cartridge using a gradient elution with organic solvent-water as mobile phase. Based on comparing the retention times with reference standards or on the basis of MS2 fragmentation behaviors, a total of 19 metabolites were identified or tentatively characterized from rat plasma. Under the optimized conditions, the method showed good linearity (r2 > 0.99) over the ranges of 1–500 ng/mL for kuraridin. The inter- and intra-day precisions were less than 8.95%, and the accuracy was in the range of −6.27–6.48%. The recovery of kuraridin ranged from 90.1% to 100.4%. The developed UHPLC-MS/MS method was thus successfully applied in the qualitative of metabolites and quantitative analysis of kuraridin in rat plasma. |
first_indexed | 2024-12-20T17:54:54Z |
format | Article |
id | doaj.art-373b0def74a442bda08e0f5a6346d575 |
institution | Directory Open Access Journal |
issn | 1420-3049 |
language | English |
last_indexed | 2024-12-20T17:54:54Z |
publishDate | 2018-01-01 |
publisher | MDPI AG |
record_format | Article |
series | Molecules |
spelling | doaj.art-373b0def74a442bda08e0f5a6346d5752022-12-21T19:30:46ZengMDPI AGMolecules1420-30492018-01-0123213210.3390/molecules23020132molecules23020132Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral AdministrationYi Liu0Lei Chen1Wei Cai2Lin-lin Zhao3Zhi-xian Mo4School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, ChinaKey Laboratory of Digital Quality Evaluation of Chinese Materia Medica of State Administration of TCM, China; Engineering & Technology Research Center for Chinese Materia Medical Quality of the Universities of Guangdong Province, Guangdong Pharmaceutical University, Guangzhou 510006, ChinaDepartment of Pharmacy, Hunan University of Medicine, Huaihua 418000, ChinaKey Laboratory of Digital Quality Evaluation of Chinese Materia Medica of State Administration of TCM, China; Engineering & Technology Research Center for Chinese Materia Medical Quality of the Universities of Guangdong Province, Guangdong Pharmaceutical University, Guangzhou 510006, ChinaSchool of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, ChinaKuraridin is an active natural prenylated flavonoid ingredient originating from the well-known traditional Chinese medicine Sophora flavescens Ait., that possesses various bioactivities, such as antitumor activity, PLCγ1 inhibitory activity, glycosidase inhibitory activity, etc. However, there is no report on the plasma metabolic profile and pharmacokinetic study of kuraridin. The current study was designed to use an ultra-performance liquid chromatography/tandem mass spectrometry (UHPLC-MS/MS) method for the quantification and characterization metabolites in rat plasma after oral administration of kuraridin. A liquid-liquid extraction method with ethyl acetate-acetonitrile (1:3) was used to extract the kuraridin from rat plasma samples. The chromatographic separation was carried out on a Hypersil GOLD UHPLC C18 column equipped with a C18 guard cartridge using a gradient elution with organic solvent-water as mobile phase. Based on comparing the retention times with reference standards or on the basis of MS2 fragmentation behaviors, a total of 19 metabolites were identified or tentatively characterized from rat plasma. Under the optimized conditions, the method showed good linearity (r2 > 0.99) over the ranges of 1–500 ng/mL for kuraridin. The inter- and intra-day precisions were less than 8.95%, and the accuracy was in the range of −6.27–6.48%. The recovery of kuraridin ranged from 90.1% to 100.4%. The developed UHPLC-MS/MS method was thus successfully applied in the qualitative of metabolites and quantitative analysis of kuraridin in rat plasma.http://www.mdpi.com/1420-3049/23/2/132kuraridinUHPLC-MS/MSrat plasmametabolitespharmacokinetic |
spellingShingle | Yi Liu Lei Chen Wei Cai Lin-lin Zhao Zhi-xian Mo Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration Molecules kuraridin UHPLC-MS/MS rat plasma metabolites pharmacokinetic |
title | Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration |
title_full | Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration |
title_fullStr | Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration |
title_full_unstemmed | Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration |
title_short | Use of an UHPLC-MS/MS Method for Determination of Kuraridin and Characterization of Its Metabolites in Rat Plasma after Oral Administration |
title_sort | use of an uhplc ms ms method for determination of kuraridin and characterization of its metabolites in rat plasma after oral administration |
topic | kuraridin UHPLC-MS/MS rat plasma metabolites pharmacokinetic |
url | http://www.mdpi.com/1420-3049/23/2/132 |
work_keys_str_mv | AT yiliu useofanuhplcmsmsmethodfordeterminationofkuraridinandcharacterizationofitsmetabolitesinratplasmaafteroraladministration AT leichen useofanuhplcmsmsmethodfordeterminationofkuraridinandcharacterizationofitsmetabolitesinratplasmaafteroraladministration AT weicai useofanuhplcmsmsmethodfordeterminationofkuraridinandcharacterizationofitsmetabolitesinratplasmaafteroraladministration AT linlinzhao useofanuhplcmsmsmethodfordeterminationofkuraridinandcharacterizationofitsmetabolitesinratplasmaafteroraladministration AT zhixianmo useofanuhplcmsmsmethodfordeterminationofkuraridinandcharacterizationofitsmetabolitesinratplasmaafteroraladministration |