- Author:
Kwon-Yeon WEON
1
;
Min Gi KIM
2
;
Soyoung SHIN
3
;
Tae Hwan KIM
2
;
Sang Hoon JOO
1
;
Eunsook MA
1
;
Seok Won JEONG
1
;
Sun Dong YOO
2
;
Yu Seok YOUN
2
;
Beom Soo SHIN
4
Author Information
- Publication Type:Journal Article
- Keywords: Bawu Decoction; Guipi Decoction; gefitinib; herb-drug interaction; pharmacokinetics
- MeSH: Animals; Chromatography, Liquid; Dose-Response Relationship, Drug; Drugs, Chinese Herbal; pharmacology; Male; Quinazolines; administration & dosage; blood; pharmacokinetics; Rats, Sprague-Dawley; Tandem Mass Spectrometry; Time Factors
- From: Chinese journal of integrative medicine 2018;24(6):460-466
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo evaluate the potential pharmacokinetic interactions of the anticancer agent gefitinib (Iressa®) and the oriental medications Guipi Decoction (, GPD, Guibi-tang in Korean) and Bawu Decoction (, BWD, Palmul-tang in Korean).
METHODSMethylcellulose (MC, control), GPD (1,200 mg/kg), or BWD (6,000 mg/kg) was orally administered to rats either as a single dose or multiple doses prior to gefitinib administration. To examine the effects of a single dose of the herbal medicines, gefitinib (10 mg/kg) was orally administered after 5 min or 1 h of MC or the herbal medicine pretreatments. To examine the effects of the multiple doses of the herbal medicines, gefitinib (10 mg/kg) was orally administered following 7 consecutive days of the administration of MC or each herbal medicine. The plasma concentrations of gefitinib were determined with liquid chromatography-tandem mass spectrometry assay. The plasma concentration-time profiles of gefitinib were analyzed with a noncompartmental analysis.
RESULTSGefitinib was rapidly absorbed and showed a monoexponential decline with an elimination half-life of 3.7-4.1 h. The pharmacokinetics of gefitinib was not affected by GPD pretreatment. However, a significantly lower maximum plasma concentration (C, P<0.05) and area under the curve (P<0.05), and a delayed time to reach C (T, P<0.01) were observed in both single- and multipledose BWD-pretreated rats compared with the control rats.
CONCLUSIONSBWD and not GPD might delay and interfere with gefitinib absorption. Further evaluations of the clinical significance of these findings are needed.