Literature DB >> 22004675

Determination of sunitinib and its active metabolite N-desethylsunitinib in sweat of a patient.

Nienke A G Lankheet1, Christian U Blank, Henk Mallo, Sandra Adriaansz, Hilde Rosing, Jan H M Schellens, Alwin D R Huitema, Jos H Beijnen.   

Abstract

Skin reactions are side effects of sunitinib therapy with an adverse impact on quality of life often necessitating dose reductions. For conventional antineoplastic agents, such as doxorubicin, previous studies have indicated a possible relationship between sweat excretion and the development of skin toxicity. However, the determination of sunitinib and its active metabolite in sweat has not yet been reported. A sensitive and accurate method for the determination of sunitinib and its active metabolite N-desethylsunitinib in human sweat was developed using high-performance liquid chromatography coupled to tandem mass spectrometry detection (LC-MS-MS). Sweat samples of a patient treated with sunitinib were collected using Pharmchek™ Drugs of Abuse patches to determine cumulative amounts of sunitinib and metabolite. Validation of the LC-MS-MS method was performed over a range from 1.0 to 200 ng/patch with good intra- and interassay accuracies for sunitinib and N-desethylsunitinib. Ranges of 76-119 and 7.9-10.5 ng/patch for cumulative secretion of sunitinib and metabolite, respectively, were found in patient samples. To our knowledge, this is the first method for determination of cumulative secretion of sunitinib and N-desethylsunitinib in human sweat samples. Sunitinib and its metabolite were easily detectable in sweat patches of a patient treated with sunitinib.

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Year:  2011        PMID: 22004675     DOI: 10.1093/anatox/35.8.558

Source DB:  PubMed          Journal:  J Anal Toxicol        ISSN: 0146-4760            Impact factor:   3.367


  7 in total

1.  The effect of seasonal variation and secretion of sunitinib in sweat on the development of hand-foot syndrome.

Authors:  Nienke A G Lankheet; Alwin D R Huitema; Henk Mallo; Sandra Adriaansz; John B A G Haanen; Jan H M Schellens; Jos H Beijnen; Christian U Blank
Journal:  Eur J Clin Pharmacol       Date:  2013-08-31       Impact factor: 2.953

2.  Oestrogen enhances cardiotoxicity induced by Sunitinib by regulation of drug transport and metabolism.

Authors:  Pamela Ann Harvey; Leslie Anne Leinwand
Journal:  Cardiovasc Res       Date:  2015-05-25       Impact factor: 10.787

3.  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

4.  Therapeutic drug monitoring and tyrosine kinase inhibitors.

Authors:  Pauline Herviou; Emilie Thivat; Damien Richard; Lucie Roche; Joyce Dohou; Mélanie Pouget; Alain Eschalier; Xavier Durando; Nicolas Authier
Journal:  Oncol Lett       Date:  2016-06-24       Impact factor: 2.967

5.  Quantitative mass spectrometry of unconventional human biological matrices.

Authors:  Ewelina P Dutkiewicz; Pawel L Urban
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-10-28       Impact factor: 4.226

6.  Dietary phytoestrogens present in soy dramatically increase cardiotoxicity in male mice receiving a chemotherapeutic tyrosine kinase inhibitor.

Authors:  Pamela Ann Harvey; Leslie Anne Leinwand
Journal:  Mol Cell Endocrinol       Date:  2014-10-30       Impact factor: 4.102

Review 7.  Regorafenib-associated hand-foot skin reaction: practical advice on diagnosis, prevention, and management.

Authors:  B McLellan; F Ciardiello; M E Lacouture; S Segaert; E Van Cutsem
Journal:  Ann Oncol       Date:  2015-06-01       Impact factor: 32.976

  7 in total

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