Literature DB >> 19797000

A routine feasible HPLC analysis for the anti-angiogenic tyrosine kinase inhibitor, sunitinib, and its main metabolite, SU12662, in plasma.

Marie-Christine Etienne-Grimaldi1, Nicole Renée, Hassan Izzedine, Gérard Milano.   

Abstract

Sunitinib is an oral inhibitor of multiple tyrosine kinase receptors with antitumor activity in metastatic renal cell carcinoma. So far, published methods for analysis of sunitinib and its active metabolite (SU12662) in plasma are exclusively based on mass spectrometry. In the context of a large-scale feasibility pharmacokinetic analysis, we developed an original, simple, high-performance liquid chromatography (HPLC) assay with UV detection. A stability study of sunitinib and SU12662 in different light exposure conditions is presented. Due to photo-instability of the compounds, blood sampling and the whole handling procedure have to be performed quickly and with minimal light exposure (6-7 lx). Following single organic extraction with tert-butyl methyl ether, HPLC analysis was performed on an ODS column and UV detection was monitored at 369 nm (run time 15 min). This assay was selective and sensitive enough (limit of detection approximately 1 ng/ml) to quantify minimal concentrations at steady state (Css min) of sunitinib and SU12662 in treated patients.

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Year:  2009        PMID: 19797000     DOI: 10.1016/j.jchromb.2009.09.011

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  6 in total

1.  Localization of sunitinib, its metabolites and its target receptors in tumour-bearing mice: a MALDI-MS imaging study.

Authors:  S Torok; A Vegvari; M Rezeli; T E Fehniger; J Tovari; S Paku; V Laszlo; B Hegedus; A Rozsas; B Dome; G Marko-Varga
Journal:  Br J Pharmacol       Date:  2015-01-12       Impact factor: 8.739

2.  Clinical pharmacokinetics of tyrosine kinase inhibitors: focus on pyrimidines, pyridines and pyrroles.

Authors:  Paola Di Gion; Friederike Kanefendt; Andreas Lindauer; Matthias Scheffler; Oxana Doroshyenko; Uwe Fuhr; Jürgen Wolf; Ulrich Jaehde
Journal:  Clin Pharmacokinet       Date:  2011-09       Impact factor: 6.447

3.  Association of drug exposure with toxicity and clinical response in metastatic renal cell carcinoma patients receiving an attenuated dosing regimen of sunitinib.

Authors:  Yi Ling Teo; Xiu Ping Chue; Noan Minh Chau; Min-Han Tan; Ravindran Kanesvaran; Hwee Lin Wee; Han Kiat Ho; Alexandre Chan
Journal:  Target Oncol       Date:  2014-12-13       Impact factor: 4.493

4.  Quantitation of unbound sunitinib and its metabolite N-desethyl sunitinib (SU12662) in human plasma by equilibrium dialysis and liquid chromatography-tandem mass spectrometry: application to a pharmacokinetic study.

Authors:  Rana Rais; Ming Zhao; Ping He; Linping Xu; John F Deeken; Michelle A Rudek
Journal:  Biomed Chromatogr       Date:  2012-01-18       Impact factor: 1.902

5.  Effect of the CYP3A5 and ABCB1 genotype on exposure, clinical response and manifestation of toxicities from sunitinib in Asian patients.

Authors:  Y L Teo; H L Wee; X P Chue; N M Chau; M-H Tan; R Kanesvaran; H L Wee; H K Ho; A Chan
Journal:  Pharmacogenomics J       Date:  2015-03-17       Impact factor: 3.550

6.  HLA-G 3'UTR Polymorphisms Predict Drug-Induced G3-4 Toxicity Related to Folinic Acid/5-Fluorouracil/Oxaliplatin (FOLFOX4) Chemotherapy in Non-Metastatic Colorectal Cancer.

Authors:  Marica Garziera; Saverio Virdone; Elena De Mattia; Lucia Scarabel; Erika Cecchin; Jerry Polesel; Mario D'Andrea; Nicoletta Pella; Angela Buonadonna; Adolfo Favaretto; Giuseppe Toffoli
Journal:  Int J Mol Sci       Date:  2017-06-27       Impact factor: 5.923

  6 in total

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