Application of newly developed and validated UPLC-MS/MS method for pharmacokinetic study of ROS1/NTRK inhibitor taletrectinib in beagle dog plasma
•A validated UPLC-MS/MS assay for the measurement of taletrectinib in dog plasma.•Low sample volume is needed, as well as simple sample preparation by protein precipitation.•A high sensitivity (LLOQ 0.2 ng/mL) was achieved.•Excellent linearity was achieved between 0.2–200 ng/mL.•The assay was succes...
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creator | Zhu, Yunfeng Wang, Fangkai Wang, Xin Cheng, Ya Wang, Xingyu Fan, Ali Chang, Jiawei |
description | •A validated UPLC-MS/MS assay for the measurement of taletrectinib in dog plasma.•Low sample volume is needed, as well as simple sample preparation by protein precipitation.•A high sensitivity (LLOQ 0.2 ng/mL) was achieved.•Excellent linearity was achieved between 0.2–200 ng/mL.•The assay was successfully applied to a pharmacokinetic study in dogs.
Taletrectinib is a potent selective ROS and pan-NTRK tyrosine kinase inhibitor (TKI) and has been developed to treat non-small cell lung cancer (NSCLC). To facilitate pharmacokinetic and toxicokinetic studies of taletrectinib, we developed a procedure for ultra-high-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) to detect the plasma level of taletrectinib in dogs. This assay procedure was validated in compliance with FDA guidance. The dog plasma samples were spiked with internal standard (IS), followed by protein precipitation, and analyzed using a Waters ACQUITY BEH C18 column coupled to a Thermo triple quadrupole mass spectrometer. Separation was executed using the acetonitrile-0.1 % formic acid solution with gradient elution, at a flow rate of 0.4 mL/min. Taletrectinib and IS were monitored by multiple reaction monitoring (MRM) with m/z 406.2 > 349.2 and m/z 441.2 > 138.1, respectively. The procedure demonstrated excellent linearity with a correlation coefficient greater than 0.999 within the concentration range of 0.2–200 ng/mL. The inter- and intra-day accuracy ranged from −5.25 % to 5.26 %, and the precision was below 6.39 %. Acetonitrile-mediated protein precipitation showed high extraction efficiency and a recovery above 85 %. The procedure was then applied to quantify taletrectinib in beagle dog plasma after oral and intravenous doses and achieved success. The obtained pharmacokinetic parameters indicated high bioavailability of taletrectinib (>85 %) and extensive tissue distribution (>40 L/kg). |
doi_str_mv | 10.1016/j.jchromb.2024.124305 |
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Taletrectinib is a potent selective ROS and pan-NTRK tyrosine kinase inhibitor (TKI) and has been developed to treat non-small cell lung cancer (NSCLC). To facilitate pharmacokinetic and toxicokinetic studies of taletrectinib, we developed a procedure for ultra-high-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) to detect the plasma level of taletrectinib in dogs. This assay procedure was validated in compliance with FDA guidance. The dog plasma samples were spiked with internal standard (IS), followed by protein precipitation, and analyzed using a Waters ACQUITY BEH C18 column coupled to a Thermo triple quadrupole mass spectrometer. Separation was executed using the acetonitrile-0.1 % formic acid solution with gradient elution, at a flow rate of 0.4 mL/min. Taletrectinib and IS were monitored by multiple reaction monitoring (MRM) with m/z 406.2 > 349.2 and m/z 441.2 > 138.1, respectively. The procedure demonstrated excellent linearity with a correlation coefficient greater than 0.999 within the concentration range of 0.2–200 ng/mL. The inter- and intra-day accuracy ranged from −5.25 % to 5.26 %, and the precision was below 6.39 %. Acetonitrile-mediated protein precipitation showed high extraction efficiency and a recovery above 85 %. The procedure was then applied to quantify taletrectinib in beagle dog plasma after oral and intravenous doses and achieved success. The obtained pharmacokinetic parameters indicated high bioavailability of taletrectinib (>85 %) and extensive tissue distribution (>40 L/kg).</description><identifier>ISSN: 1570-0232</identifier><identifier>ISSN: 1873-376X</identifier><identifier>EISSN: 1873-376X</identifier><identifier>DOI: 10.1016/j.jchromb.2024.124305</identifier><identifier>PMID: 39293159</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Chromatography, High Pressure Liquid - methods ; Dogs ; Limit of Detection ; Linear Models ; Liquid Chromatography-Mass Spectrometry ; Male ; Pharmacokinetics ; Protein Kinase Inhibitors - blood ; Protein Kinase Inhibitors - chemistry ; Protein Kinase Inhibitors - pharmacokinetics ; Proto-Oncogene Proteins - antagonists & inhibitors ; Proto-Oncogene Proteins - blood ; Reproducibility of Results ; ROS1/NTRK inhibitor ; Taletrectinib ; Tandem Mass Spectrometry - methods ; UPLC-MS/MS</subject><ispartof>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2024-10, Vol.1247, p.124305, Article 124305</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c243t-7948a19cfe165f5c1622daa72fcb24e9f4686b4439f48f700ceed8070bbe18b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jchromb.2024.124305$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39293159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yunfeng</creatorcontrib><creatorcontrib>Wang, Fangkai</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Cheng, Ya</creatorcontrib><creatorcontrib>Wang, Xingyu</creatorcontrib><creatorcontrib>Fan, Ali</creatorcontrib><creatorcontrib>Chang, Jiawei</creatorcontrib><title>Application of newly developed and validated UPLC-MS/MS method for pharmacokinetic study of ROS1/NTRK inhibitor taletrectinib in beagle dog plasma</title><title>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</title><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><description>•A validated UPLC-MS/MS assay for the measurement of taletrectinib in dog plasma.•Low sample volume is needed, as well as simple sample preparation by protein precipitation.•A high sensitivity (LLOQ 0.2 ng/mL) was achieved.•Excellent linearity was achieved between 0.2–200 ng/mL.•The assay was successfully applied to a pharmacokinetic study in dogs.
Taletrectinib is a potent selective ROS and pan-NTRK tyrosine kinase inhibitor (TKI) and has been developed to treat non-small cell lung cancer (NSCLC). To facilitate pharmacokinetic and toxicokinetic studies of taletrectinib, we developed a procedure for ultra-high-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) to detect the plasma level of taletrectinib in dogs. This assay procedure was validated in compliance with FDA guidance. The dog plasma samples were spiked with internal standard (IS), followed by protein precipitation, and analyzed using a Waters ACQUITY BEH C18 column coupled to a Thermo triple quadrupole mass spectrometer. Separation was executed using the acetonitrile-0.1 % formic acid solution with gradient elution, at a flow rate of 0.4 mL/min. Taletrectinib and IS were monitored by multiple reaction monitoring (MRM) with m/z 406.2 > 349.2 and m/z 441.2 > 138.1, respectively. The procedure demonstrated excellent linearity with a correlation coefficient greater than 0.999 within the concentration range of 0.2–200 ng/mL. The inter- and intra-day accuracy ranged from −5.25 % to 5.26 %, and the precision was below 6.39 %. Acetonitrile-mediated protein precipitation showed high extraction efficiency and a recovery above 85 %. The procedure was then applied to quantify taletrectinib in beagle dog plasma after oral and intravenous doses and achieved success. The obtained pharmacokinetic parameters indicated high bioavailability of taletrectinib (>85 %) and extensive tissue distribution (>40 L/kg).</description><subject>Animals</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Dogs</subject><subject>Limit of Detection</subject><subject>Linear Models</subject><subject>Liquid Chromatography-Mass Spectrometry</subject><subject>Male</subject><subject>Pharmacokinetics</subject><subject>Protein Kinase Inhibitors - blood</subject><subject>Protein Kinase Inhibitors - chemistry</subject><subject>Protein Kinase Inhibitors - pharmacokinetics</subject><subject>Proto-Oncogene Proteins - antagonists & inhibitors</subject><subject>Proto-Oncogene Proteins - blood</subject><subject>Reproducibility of Results</subject><subject>ROS1/NTRK inhibitor</subject><subject>Taletrectinib</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>UPLC-MS/MS</subject><issn>1570-0232</issn><issn>1873-376X</issn><issn>1873-376X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkclu2zAQhoWiRZOmfYQWPPYim4skSqciMLohzoI4AXojuIxiupSokrQLv0afuDTs9NrTLPhmfsz8RfGe4BnBpJlvZhu9Dn5QM4ppNSO0Yrh-UZyTlrOS8ebHy5zXHJeYMnpWvIlxgzHhmLPXxRnraMdI3Z0Xfy6nyVktk_Uj8j0a4bfbIwM7cH4Cg-Ro0E46a2TK1ePdclFer-bXKzRAWnuDeh_QtJZhkNr_tCMkq1FMW7M_LLu_XZH5zcP9FbLj2iqbMpykgxRAJztalftIgXxygIx_QpOTcZBvi1e9dBHeneJF8fjl88PiW7m8_fp9cbksdb41lbyrWkk63QNp6r7WpKHUSMlprxWtoOurpm1UVbGctT3HWAOYFnOsFJBWteyi-HjcOwX_awsxicFGDc7JEfw2CkZwwxmta5zR-ojq4GMM0Isp2EGGvSBYHOwQG3GyQxzsEEc78tyHk8RWDWD-TT3_PwOfjgDkQ3cWgojawqjB2MOPhPH2PxJ_AYLLn50</recordid><startdate>20241015</startdate><enddate>20241015</enddate><creator>Zhu, Yunfeng</creator><creator>Wang, Fangkai</creator><creator>Wang, Xin</creator><creator>Cheng, Ya</creator><creator>Wang, Xingyu</creator><creator>Fan, Ali</creator><creator>Chang, Jiawei</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20241015</creationdate><title>Application of newly developed and validated UPLC-MS/MS method for pharmacokinetic study of ROS1/NTRK inhibitor taletrectinib in beagle dog plasma</title><author>Zhu, Yunfeng ; Wang, Fangkai ; Wang, Xin ; Cheng, Ya ; Wang, Xingyu ; Fan, Ali ; Chang, Jiawei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c243t-7948a19cfe165f5c1622daa72fcb24e9f4686b4439f48f700ceed8070bbe18b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Dogs</topic><topic>Limit of Detection</topic><topic>Linear Models</topic><topic>Liquid Chromatography-Mass Spectrometry</topic><topic>Male</topic><topic>Pharmacokinetics</topic><topic>Protein Kinase Inhibitors - blood</topic><topic>Protein Kinase Inhibitors - chemistry</topic><topic>Protein Kinase Inhibitors - pharmacokinetics</topic><topic>Proto-Oncogene Proteins - antagonists & inhibitors</topic><topic>Proto-Oncogene Proteins - blood</topic><topic>Reproducibility of Results</topic><topic>ROS1/NTRK inhibitor</topic><topic>Taletrectinib</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>UPLC-MS/MS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yunfeng</creatorcontrib><creatorcontrib>Wang, Fangkai</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Cheng, Ya</creatorcontrib><creatorcontrib>Wang, Xingyu</creatorcontrib><creatorcontrib>Fan, Ali</creatorcontrib><creatorcontrib>Chang, Jiawei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Yunfeng</au><au>Wang, Fangkai</au><au>Wang, Xin</au><au>Cheng, Ya</au><au>Wang, Xingyu</au><au>Fan, Ali</au><au>Chang, Jiawei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of newly developed and validated UPLC-MS/MS method for pharmacokinetic study of ROS1/NTRK inhibitor taletrectinib in beagle dog plasma</atitle><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><date>2024-10-15</date><risdate>2024</risdate><volume>1247</volume><spage>124305</spage><pages>124305-</pages><artnum>124305</artnum><issn>1570-0232</issn><issn>1873-376X</issn><eissn>1873-376X</eissn><abstract>•A validated UPLC-MS/MS assay for the measurement of taletrectinib in dog plasma.•Low sample volume is needed, as well as simple sample preparation by protein precipitation.•A high sensitivity (LLOQ 0.2 ng/mL) was achieved.•Excellent linearity was achieved between 0.2–200 ng/mL.•The assay was successfully applied to a pharmacokinetic study in dogs.
Taletrectinib is a potent selective ROS and pan-NTRK tyrosine kinase inhibitor (TKI) and has been developed to treat non-small cell lung cancer (NSCLC). To facilitate pharmacokinetic and toxicokinetic studies of taletrectinib, we developed a procedure for ultra-high-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) to detect the plasma level of taletrectinib in dogs. This assay procedure was validated in compliance with FDA guidance. The dog plasma samples were spiked with internal standard (IS), followed by protein precipitation, and analyzed using a Waters ACQUITY BEH C18 column coupled to a Thermo triple quadrupole mass spectrometer. Separation was executed using the acetonitrile-0.1 % formic acid solution with gradient elution, at a flow rate of 0.4 mL/min. Taletrectinib and IS were monitored by multiple reaction monitoring (MRM) with m/z 406.2 > 349.2 and m/z 441.2 > 138.1, respectively. The procedure demonstrated excellent linearity with a correlation coefficient greater than 0.999 within the concentration range of 0.2–200 ng/mL. The inter- and intra-day accuracy ranged from −5.25 % to 5.26 %, and the precision was below 6.39 %. Acetonitrile-mediated protein precipitation showed high extraction efficiency and a recovery above 85 %. The procedure was then applied to quantify taletrectinib in beagle dog plasma after oral and intravenous doses and achieved success. The obtained pharmacokinetic parameters indicated high bioavailability of taletrectinib (>85 %) and extensive tissue distribution (>40 L/kg).</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39293159</pmid><doi>10.1016/j.jchromb.2024.124305</doi></addata></record> |
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subjects | Animals Chromatography, High Pressure Liquid - methods Dogs Limit of Detection Linear Models Liquid Chromatography-Mass Spectrometry Male Pharmacokinetics Protein Kinase Inhibitors - blood Protein Kinase Inhibitors - chemistry Protein Kinase Inhibitors - pharmacokinetics Proto-Oncogene Proteins - antagonists & inhibitors Proto-Oncogene Proteins - blood Reproducibility of Results ROS1/NTRK inhibitor Taletrectinib Tandem Mass Spectrometry - methods UPLC-MS/MS |
title | Application of newly developed and validated UPLC-MS/MS method for pharmacokinetic study of ROS1/NTRK inhibitor taletrectinib in beagle dog plasma |
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