Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography

A novel, highly sensitive, simple, and rapid strategy was designed and developed for simultaneous determination of cabozantinib (CBZ) as an anticancer agent and its main metabolites including monohydroxy sulfate (EXEL-1646), N-oxide (EXEL-5162(, amide cleavage product (EXEL-5366), and 6-desmethyl am...

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Main Authors: Xiurong Qi, Shuping Zhang, Mei Yu, Suliman Khan
Format: Article
Language:English
Published: Elsevier 2021-07-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535221002215
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spelling doaj-3eb5b946acc74dda8b14868cf2e6c09d2021-06-25T04:47:25ZengElsevierArabian Journal of Chemistry1878-53522021-07-01147103206Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatographyXiurong Qi0Shuping Zhang1Mei Yu2Suliman Khan3Department of Radiation Oncology, Shanxi Provincial People's Hospital, Taiyuan 030012, ChinaDepartment of Radiation Oncology, Shanxi Provincial People's Hospital, Taiyuan 030012, ChinaDepartment of Blood Transfusion, Ankang Central Hospital, Ankang 725000, China; Corresponding authors at: No. 85, Jinzhou South Road, Hanbin District, Ankang, Shanxi 72500, China (M. Yu).Department of Cerebrovascular Diseases, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China; Corresponding authors at: No. 85, Jinzhou South Road, Hanbin District, Ankang, Shanxi 72500, China (M. Yu).A novel, highly sensitive, simple, and rapid strategy was designed and developed for simultaneous determination of cabozantinib (CBZ) as an anticancer agent and its main metabolites including monohydroxy sulfate (EXEL-1646), N-oxide (EXEL-5162(, amide cleavage product (EXEL-5366), and 6-desmethyl amide cleavage product sulfate) EXEL-1644). Measurements were done through a micellar liquid chromatography (MLC) method coupled with fluorescence detection. The high-performance liquid chromatography (HPLC) was performed using a Kinetex C18 100 Å column as well as acetonitrile, cetyltrimethylammonium bromide (CTAB; 0.2 mol.L−1), and tris buffer (pH 8.5) solutions as the mobile phase at a 40:50:10 (v/v) ratio. The method’s linearity (20 to 700 ng.mL−1), limit of detection (LOD; 2.11 to 3.69 ng.mL−1), limit of quantification (LOQ; 20 to 30 ng.mL−1), intra- and inter-day precisions (RSD < 4.00%), selectivity, recovery, and robustness were fully evaluated. According to the obtained results, the developed method can be used for simple and rapid (~35 min) quantification of CBZ as an anticancer drug and its major metabolites in human serum samples with high sensitivity and low cost.http://www.sciencedirect.com/science/article/pii/S1878535221002215CabozantinibMetabolitesMicellar chromatographyFluorescence detectionCetyltrimethylammonium bromid
collection DOAJ
language English
format Article
sources DOAJ
author Xiurong Qi
Shuping Zhang
Mei Yu
Suliman Khan
spellingShingle Xiurong Qi
Shuping Zhang
Mei Yu
Suliman Khan
Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
Arabian Journal of Chemistry
Cabozantinib
Metabolites
Micellar chromatography
Fluorescence detection
Cetyltrimethylammonium bromid
author_facet Xiurong Qi
Shuping Zhang
Mei Yu
Suliman Khan
author_sort Xiurong Qi
title Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
title_short Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
title_full Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
title_fullStr Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
title_full_unstemmed Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
title_sort concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography
publisher Elsevier
series Arabian Journal of Chemistry
issn 1878-5352
publishDate 2021-07-01
description A novel, highly sensitive, simple, and rapid strategy was designed and developed for simultaneous determination of cabozantinib (CBZ) as an anticancer agent and its main metabolites including monohydroxy sulfate (EXEL-1646), N-oxide (EXEL-5162(, amide cleavage product (EXEL-5366), and 6-desmethyl amide cleavage product sulfate) EXEL-1644). Measurements were done through a micellar liquid chromatography (MLC) method coupled with fluorescence detection. The high-performance liquid chromatography (HPLC) was performed using a Kinetex C18 100 Å column as well as acetonitrile, cetyltrimethylammonium bromide (CTAB; 0.2 mol.L−1), and tris buffer (pH 8.5) solutions as the mobile phase at a 40:50:10 (v/v) ratio. The method’s linearity (20 to 700 ng.mL−1), limit of detection (LOD; 2.11 to 3.69 ng.mL−1), limit of quantification (LOQ; 20 to 30 ng.mL−1), intra- and inter-day precisions (RSD < 4.00%), selectivity, recovery, and robustness were fully evaluated. According to the obtained results, the developed method can be used for simple and rapid (~35 min) quantification of CBZ as an anticancer drug and its major metabolites in human serum samples with high sensitivity and low cost.
topic Cabozantinib
Metabolites
Micellar chromatography
Fluorescence detection
Cetyltrimethylammonium bromid
url http://www.sciencedirect.com/science/article/pii/S1878535221002215
work_keys_str_mv AT xiurongqi concurrentdetectionofcabozantinibasananticanceragentanditsmajormetabolitesinhumanserumusingfluorescencecoupledmicellarliquidchromatography
AT shupingzhang concurrentdetectionofcabozantinibasananticanceragentanditsmajormetabolitesinhumanserumusingfluorescencecoupledmicellarliquidchromatography
AT meiyu concurrentdetectionofcabozantinibasananticanceragentanditsmajormetabolitesinhumanserumusingfluorescencecoupledmicellarliquidchromatography
AT sulimankhan concurrentdetectionofcabozantinibasananticanceragentanditsmajormetabolitesinhumanserumusingfluorescencecoupledmicellarliquidchromatography
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