Literature DB >> 24619951

Liquid chromatography-tandem mass spectrometric assay for the multikinase inhibitor regorafenib in plasma.

Dino Luethi1, Selvi Durmus, Alfred H Schinkel, Jan H M Schellens, Jos H Beijnen, Rolf W Sparidans.   

Abstract

Regorafenib has recently been approved for the treatment of colorectal cancer. A bioanalytical liquid chromatography-tandem mass spectrometric assay for this multikinase inhibitor was developed and validated in plasma. The concentration range of the assay was 25-25,000 ng/mL. Protein precipitation with acetonitrile was used as sample pre-treatment with sorafenib as internal standard. The extract was diluted with methanol (25%, v/v) and then injected onto the sub-2 µm particle, bridged ethylsilicia hybrid trifunctional bonded C18 column. Isocratic elution using 0.02% (v/v) formic acid in a methanol-water mixture was used. Compounds were monitored by a triple quadrupole mass spectrometer in the selected reaction monitoring mode after positive electrospray ionization. Double logarithmic calibration was used; within-day precisions, between-day precisions, and accuracies were 3.2-9.2, 4.1-12.3 and 94.8-103.0%, respectively. High drug stability was observed under all relevant storage conditions. The assay was used to measure drug concentrations in a pharmacokinetic study in wild-type FVB mice.
Copyright © 2014 John Wiley & Sons, Ltd.

Entities:  

Keywords:  LC-MS/MS; bioanalytical assay; multikinase inhibitor; regorafenib

Mesh:

Substances:

Year:  2014        PMID: 24619951     DOI: 10.1002/bmc.3176

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  6 in total

1.  Brain and Testis Accumulation of Regorafenib is Restricted by Breast Cancer Resistance Protein (BCRP/ABCG2) and P-glycoprotein (P-GP/ABCB1).

Authors:  Anita Kort; Selvi Durmus; Rolf W Sparidans; Els Wagenaar; Jos H Beijnen; Alfred H Schinkel
Journal:  Pharm Res       Date:  2015-01-08       Impact factor: 4.200

2.  Therapeutic drug monitoring and tyrosine kinase inhibitors.

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Journal:  Oncol Lett       Date:  2016-06-24       Impact factor: 2.967

3.  Development and validation of an analytical method for regorafenib and its metabolites in mouse plasma.

Authors:  Qiang Fu; Mingqing Chen; Shuiying Hu; Craig A McElroy; Ron H Mathijssen; Alex Sparreboom; Sharyn D Baker
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2018-05-05       Impact factor: 3.205

4.  Associations among plasma concentrations of regorafenib and its metabolites, adverse events, and ABCG2 polymorphisms in patients with metastatic colorectal cancers.

Authors:  Kazuo Kobayashi; Erika Sugiyama; Eiji Shinozaki; Takeru Wakatsuki; Masataka Tajima; Hiyori Kidokoro; Takeshi Aoyama; Yasuhiro Nakano; Kazuyoshi Kawakami; Koki Hashimoto; Mitsukuni Suenaga; Takashi Ichimura; Mariko Ogura; Keisho Chin; Izuma Nakayama; Akira Ooki; Daisuke Takahari; Wataru Suzuki; Takashi Yokokawa; Yuichi Minowa; Tomoko Hiraoka; Kenichi Suzuki; Hitoshi Sato; Toshihiro Hama; Kensei Yamaguchi
Journal:  Cancer Chemother Pharmacol       Date:  2021-02-26       Impact factor: 3.333

5.  Highly Sensitive Electrochemical Sensor for Anticancer Drug by a Zirconia Nanoparticle-Decorated Reduced Graphene Oxide Nanocomposite.

Authors:  Manthrapudi Venu; Sada Venkateswarlu; Yenugu Veera Manohara Reddy; Ankireddy Seshadri Reddy; Vinod Kumar Gupta; Minyoung Yoon; Gajulapalli Madhavi
Journal:  ACS Omega       Date:  2018-11-01

6.  Quantification of cobimetinib, cabozantinib, dabrafenib, niraparib, olaparib, vemurafenib, regorafenib and its metabolite regorafenib M2 in human plasma by UPLC-MS/MS.

Authors:  Stefanie D Krens; Eric van der Meulen; Frank G A Jansman; David M Burger; Nielka P van Erp
Journal:  Biomed Chromatogr       Date:  2020-01-13       Impact factor: 1.902

  6 in total

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