Quantification of vincristine and tariquidar by liquid chromatography‐tandem mass spectrometry in mouse whole blood using volumetric absorptive microsampling for pharmacokinetic applications
A liquid chromatography‐tandem mass spectrometry method was developed and validated for the simultaneous quantification of vincristine and tariquidar in 10 μL of mouse whole blood using volumetric absorptive microsampling devices. Samples were extracted from the devices and quantified against calibr...
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| Veröffentlicht in: | Journal of separation science 2022-07, Vol.45 (14), p.2508-2519 |
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| container_title | Journal of separation science |
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| creator | Rosser, Sebastian P. A. Atkinson, Caroline Nath, Christa E. Fletcher, Jamie I. |
| description | A liquid chromatography‐tandem mass spectrometry method was developed and validated for the simultaneous quantification of vincristine and tariquidar in 10 μL of mouse whole blood using volumetric absorptive microsampling devices. Samples were extracted from the devices and quantified against calibrators prepared in a human blood plasma matrix. Separation of vincristine and tariquidar was achieved using a Shimpack XR ODS III C18 stationary phase and H2O and methanol mobile phase solvents containing 0.1% formic acid, running a gradient elution at a flow rate of 0.2 mL/min over 6.0 min. The method was linear up to 1200 ng/mL (R2 > 0.99 for both analytes), with calibrator accuracy within ± 15% of the nominal concentrations and analyte coefficient of variance |
| doi_str_mv | 10.1002/jssc.202101013 |
| format | Article |
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A. ; Atkinson, Caroline ; Nath, Christa E. ; Fletcher, Jamie I.</creator><creatorcontrib>Rosser, Sebastian P. A. ; Atkinson, Caroline ; Nath, Christa E. ; Fletcher, Jamie I.</creatorcontrib><description>A liquid chromatography‐tandem mass spectrometry method was developed and validated for the simultaneous quantification of vincristine and tariquidar in 10 μL of mouse whole blood using volumetric absorptive microsampling devices. Samples were extracted from the devices and quantified against calibrators prepared in a human blood plasma matrix. Separation of vincristine and tariquidar was achieved using a Shimpack XR ODS III C18 stationary phase and H2O and methanol mobile phase solvents containing 0.1% formic acid, running a gradient elution at a flow rate of 0.2 mL/min over 6.0 min. The method was linear up to 1200 ng/mL (R2 > 0.99 for both analytes), with calibrator accuracy within ± 15% of the nominal concentrations and analyte coefficient of variance <15% for both vincristine and tariquidar. Pharmacokinetic assessment of both analytes was successfully applied in mice as both single‐agent therapy and combination therapy over a 24‐h period, and a 2.3‐fold increase in vincristine drug exposure was observed in combination with tariquidar. 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A.</creatorcontrib><creatorcontrib>Atkinson, Caroline</creatorcontrib><creatorcontrib>Nath, Christa E.</creatorcontrib><creatorcontrib>Fletcher, Jamie I.</creatorcontrib><title>Quantification of vincristine and tariquidar by liquid chromatography‐tandem mass spectrometry in mouse whole blood using volumetric absorptive microsampling for pharmacokinetic applications</title><title>Journal of separation science</title><addtitle>J Sep Sci</addtitle><description>A liquid chromatography‐tandem mass spectrometry method was developed and validated for the simultaneous quantification of vincristine and tariquidar in 10 μL of mouse whole blood using volumetric absorptive microsampling devices. Samples were extracted from the devices and quantified against calibrators prepared in a human blood plasma matrix. Separation of vincristine and tariquidar was achieved using a Shimpack XR ODS III C18 stationary phase and H2O and methanol mobile phase solvents containing 0.1% formic acid, running a gradient elution at a flow rate of 0.2 mL/min over 6.0 min. The method was linear up to 1200 ng/mL (R2 > 0.99 for both analytes), with calibrator accuracy within ± 15% of the nominal concentrations and analyte coefficient of variance <15% for both vincristine and tariquidar. Pharmacokinetic assessment of both analytes was successfully applied in mice as both single‐agent therapy and combination therapy over a 24‐h period, and a 2.3‐fold increase in vincristine drug exposure was observed in combination with tariquidar. This study validates the use of this approach for longitudinal analysis of drug exposure in animal studies.</description><subject>Absorptivity</subject><subject>Blood plasma</subject><subject>Chromatography</subject><subject>Flow velocity</subject><subject>Formic acid</subject><subject>Ions</subject><subject>Liquid chromatography</subject><subject>liquid chromatography‐tandem mass spectrometry</subject><subject>Mass spectrometry</subject><subject>method validation</subject><subject>Pharmacokinetics</subject><subject>Pharmacology</subject><subject>P‐glycoprotein</subject><subject>Scientific imaging</subject><subject>Spectroscopy</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhSMEoj-wZYkssWEzU9uJk3iJRoWCKlWosI5uHLvjwT-p7UyVHY_AI_EsPAkOU2bBBt2Fr3S_e3SuT1G8InhNMKYXuxjFmmJKcK7ySXFKasJWvCTV02OP65PiLMYdxqRpOX5enJSM1U3DyGnx8_MELmmlBSTtHfIK7bUTQceknUTgBpQg6PtJDxBQPyPzp0diG7yF5O8CjNv51_cfKaPSIgsxojhKkfJcpjAj7ZD1U5ToYeuNRL3xfkBT1O4O7b2ZFkgLBH30YUx6L5HVIvgIdjQLo3xA4xaCBeG_ZUtpgcc8OxiOL4pnCkyULx_f8-Lr-8svm6vV9c2Hj5t31ytBectXALzGoGSlVINp3wsxUNbyqhS14pjykmOMmeqVJFBCj2EANqgSKEiW_60tz4u3B90x-PtJxtRZHYU0BpzM53W0rquGE9ryjL75B935KbjsLlOcsaZmjGZqfaCWa2OQqhuDthDmjuBuybZbsu2O2eaF14-yU2_lcMT_hpmB6gA8aCPn_8h1n25vN02d7f4G24S4Vg</recordid><startdate>202207</startdate><enddate>202207</enddate><creator>Rosser, Sebastian P. 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A.</au><au>Atkinson, Caroline</au><au>Nath, Christa E.</au><au>Fletcher, Jamie I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of vincristine and tariquidar by liquid chromatography‐tandem mass spectrometry in mouse whole blood using volumetric absorptive microsampling for pharmacokinetic applications</atitle><jtitle>Journal of separation science</jtitle><addtitle>J Sep Sci</addtitle><date>2022-07</date><risdate>2022</risdate><volume>45</volume><issue>14</issue><spage>2508</spage><epage>2519</epage><pages>2508-2519</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>A liquid chromatography‐tandem mass spectrometry method was developed and validated for the simultaneous quantification of vincristine and tariquidar in 10 μL of mouse whole blood using volumetric absorptive microsampling devices. Samples were extracted from the devices and quantified against calibrators prepared in a human blood plasma matrix. Separation of vincristine and tariquidar was achieved using a Shimpack XR ODS III C18 stationary phase and H2O and methanol mobile phase solvents containing 0.1% formic acid, running a gradient elution at a flow rate of 0.2 mL/min over 6.0 min. The method was linear up to 1200 ng/mL (R2 > 0.99 for both analytes), with calibrator accuracy within ± 15% of the nominal concentrations and analyte coefficient of variance <15% for both vincristine and tariquidar. Pharmacokinetic assessment of both analytes was successfully applied in mice as both single‐agent therapy and combination therapy over a 24‐h period, and a 2.3‐fold increase in vincristine drug exposure was observed in combination with tariquidar. 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| source | Wiley Online Library Journals Frontfile Complete |
| subjects | Absorptivity Blood plasma Chromatography Flow velocity Formic acid Ions Liquid chromatography liquid chromatography‐tandem mass spectrometry Mass spectrometry method validation Pharmacokinetics Pharmacology P‐glycoprotein Scientific imaging Spectroscopy |
| title | Quantification of vincristine and tariquidar by liquid chromatography‐tandem mass spectrometry in mouse whole blood using volumetric absorptive microsampling for pharmacokinetic applications |
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