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Pharmacokinetics and Tissue Distribution of Anwuligan in Rats after Intravenous and Intragastric Administration by Liquid Chromatography-Mass Spectrometry.
Song, Yang; Zhang, Yuan; Duan, Xiao-Yi; Cui, Dong-Wei; Qiu, Xin; Bian, Yu; Wang, Ke-Fei; Feng, Xue-Song.
  • Song Y; School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Zhang Y; Department of Pharmacy, National Cancer Center/National Clinical Research Center for Cancer, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
  • Duan XY; School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Cui DW; School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Qiu X; School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Bian Y; School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Wang KF; School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Feng XS; School of Pharmacy, China Medical University, Shenyang 110122, China.
Molecules ; 25(1)2019 Dec 20.
Article en En | MEDLINE | ID: mdl-31861927
ABSTRACT
Anwuligan, a natural 2,3-dibenzylbutane lignan from the nutmeg mace of Myristica fragans, has been proved to possess a broad range of pharmacological effects. A rapid, simple, and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method has been established and successfully applied to the study of pharmacokinetics and tissue distribution of anwuligan after intravenous or intragastric administration. Sample preparation was carried out through a liquid-liquid extraction method with ethyl acetate as the extraction reagent. Arctigenin was used as the internal standard (IS). A gradient program was employed with a mobile phase consisting of 0.1% formic acid aqueous solution and acetonitrile. The mass spectrometer was operated in a positive ionization mode with multiple reaction monitoring. The transitions for quantification were m/z 329.0→205.0 for anwuligan and m/z 373.0→137.0 for IS, respectively. Calibration curves were linear over the ranges of 0.5-2000 ng/mL for both plasma samples and tissue samples (r > 0.996). The absolute bioavailability is 16.2%, which represented the existing of the obvious first-pass effect. An enterohepatic circulation was found after the intragastric administration. Anwuligan could be distributed rapidly and widely in different tissues and maintained a high concentration in the liver. The developed and validated LC-MS/MS method and the pharmacokinetic study of anwuligan would provide reference for the future investigation of the preclinical safety of anwuligan as a candidate drug.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lignanos / Myristica / Hígado Límite: Animals Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lignanos / Myristica / Hígado Límite: Animals Idioma: En Año: 2019 Tipo del documento: Article