2012
DOI: 10.1016/j.jchromb.2012.08.021
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Liquid chromatography–tandem mass spectrometric assay for the ALK inhibitor crizotinib in mouse plasma

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Cited by 24 publications
(21 citation statements)
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References 11 publications
(26 reference statements)
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“…One of the main reasons for the absence of metabolite quantification is the lack of commercial standards at the time of development of the assay [84]. Alternatively, papers from Vikingsson et al [133] reported quantification of the metabolites relative to their parent compound, or a related metabolite of which an analytical standard is readily available [84,132,133]. For sunitinib, it has been demonstrated that the active metabolite is equally potent, but less dermatotoxic.…”
Section: Metabolite Analysismentioning
confidence: 99%
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“…One of the main reasons for the absence of metabolite quantification is the lack of commercial standards at the time of development of the assay [84]. Alternatively, papers from Vikingsson et al [133] reported quantification of the metabolites relative to their parent compound, or a related metabolite of which an analytical standard is readily available [84,132,133]. For sunitinib, it has been demonstrated that the active metabolite is equally potent, but less dermatotoxic.…”
Section: Metabolite Analysismentioning
confidence: 99%
“…TKIs [96,115,132,133,136], no recent analytical papers describing quantitative assays for these metabolites were published. Vikingsson et al described that a glucuronide and a glucosylation metabolite of vemurafenib were excluded from their method due to low concentrations and poor stability [132].…”
Section: Metabolite Analysismentioning
confidence: 99%
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“…Accordingly, reliable and accurate analytical methodology for CRZ determination is crucial for further pharmacokinetic studies. Literature review revealed that CRZ was assayed in plasma by liquid chromatography coupled with either tandem mass spectrometry [6][7][8][9] or fluorescence detection [10]. However, these chromatographic methods suffered from complexity and being expensive.…”
Section: Introductionmentioning
confidence: 99%
“…A recent report described the first validated assay for crizotinib in mouse plasma using protein precipitation and LC–MS/MS [16], however, no validated methods have been published for use with human samples. Therefore, in this paper we describe a rapid LC-MS/MS method that was developed and validated according to internal SOP’s to assay crizotinib concentrations in both human and mouse plasma using a 96-well solid phase extraction procedure.…”
Section: Introductionmentioning
confidence: 99%