Pharmacokinetic study of multicomponent in Hong-Hua-Xiao-Yao tablet

© 2024 John Wiley & Sons, Ltd..

Hong-Hua-Xiao-Yao tablet (HHXYT) is attracting attention increasingly because of its use in treatment of mammary gland hyperplasia (MGH) and menopausal syndrome. However, its pharmacokinetics remains unclear. This study developed a sensitive and rapid method for simultaneous determination of 10 compounds of HHXYT in rat plasma by liquid chromatography-tandem mass spectrometry and to compare the pharmacokinetics of these compounds in MGH rats and sham operated rats. The linearity, accuracy, precision, stability and matrix effect were within acceptable ranges. This established method was successfully applied to a pharmacokinetics study of 10 compounds in sham operated and MGH rats. According to the results, the bioavailability of glycyrrhetinic acid was highest in MGH rats and sham operated rats. The mean residence times of glycyrrhetinic acid and glycyrrhetinic acid 3-O-glucuronide were higher than those of the other compounds while the mean residence time and half-life of liquiritin, isoliquiritin and paeoniflorin were lower. Some pharmacokinetic parameters of ormononetin, liquiritigenin, isoliquiritigenin, liquiritin, isoliquiritin, paeoniflorin, protocatechuic acid and senkyunolide I were significantly different between MGH rats and sham operated rats. This study elucidated the dynamic changes of multiple components in rats after oral administration of HHXYT systematically and comprehensively, which provided guidance for clinical application.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - year:2024

Enthalten in:

Biomedical chromatography : BMC - (2024) vom: 06. März, Seite e5830

Sprache:

Englisch

Beteiligte Personen:

Li, Xiaofeng [VerfasserIn]
Huang, Leyi [VerfasserIn]
Xiao, Junping [VerfasserIn]
Zhang, Xuemei [VerfasserIn]

Links:

Volltext

Themen:

HPLC-MS/MS
Hong-Hua-Xiao-Yao tablet (HHXYT)
Journal Article
Mammary gland hyperplasia (MGH)
Non-compartment model
Pharmacokinetics (PK)

Anmerkungen:

Date Revised 06.03.2024

published: Print-Electronic

Citation Status Publisher

doi:

10.1002/bmc.5830

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM369351878