Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction

A novel bioanalytical method was developed and validated for the quantitative determination of darunavir (DRV) in rat plasma by employing hydrophilic interaction chromatography and tandem mass spectrometry (HILICâMS/MS) with supported liquid extraction (SLE). Irbesartan (IRB) was used as an internal...

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Main Authors: Bokka Ramesh, Nemali Manjula, Sistla Ramakrishna, Potturi Sita Devi
Format: Article
Language:English
Published: Elsevier 2015-02-01
Series:Journal of Pharmaceutical Analysis
Online Access:http://www.sciencedirect.com/science/article/pii/S2095177914000422
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spelling doaj-e58d04f026a0403ca71264fbae09378d2021-04-02T10:38:23ZengElsevierJournal of Pharmaceutical Analysis2095-17792015-02-01514350Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extractionBokka Ramesh0Nemali Manjula1Sistla Ramakrishna2Potturi Sita Devi3Natural Products Chemistry Division, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, IndiaNatural Products Chemistry Division, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, IndiaMedicinal Chemistry & Pharmacology Division, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, IndiaNatural Products Chemistry Division, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, India; Corresponding author. Tel.: +91 40 27160123x1733.A novel bioanalytical method was developed and validated for the quantitative determination of darunavir (DRV) in rat plasma by employing hydrophilic interaction chromatography and tandem mass spectrometry (HILICâMS/MS) with supported liquid extraction (SLE). Irbesartan (IRB) was used as an internal standard (IS). The analyte in rat plasma (200 µL) was isolated through SLE using ethyl acetate as the eluting solvent. The chromatographic separation was achieved on Luna-HILIC (250 mmÃ4.6 mm, 5 μm) column with a mobile phase of 0.1% of formic acid in water:acetonitrile (5: 95, v/v), at a constant flow rate of 1.0 mL/min. The MS/MS ion transitions for DRV (548.1â392.0) and IS (429.2â207.1) were monitored on an ion trap mass spectrometer, operating in the multiple reaction monitoring (MRM) mode. The lower limit of quantitation (LLOQ) was 0.2 ng/mL and quantitation range was 0.2â5000 ng/mL. The method was validated for its selectivity, sensitivity, carryover, linearity, precision, accuracy, recovery, matrix effect and stability. The method was successfully applied to pharmacokinetic study in rats. Keywords: Darunavir, HILICâMS/MS, Rat plasma, Supported liquid extractionhttp://www.sciencedirect.com/science/article/pii/S2095177914000422
collection DOAJ
language English
format Article
sources DOAJ
author Bokka Ramesh
Nemali Manjula
Sistla Ramakrishna
Potturi Sita Devi
spellingShingle Bokka Ramesh
Nemali Manjula
Sistla Ramakrishna
Potturi Sita Devi
Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction
Journal of Pharmaceutical Analysis
author_facet Bokka Ramesh
Nemali Manjula
Sistla Ramakrishna
Potturi Sita Devi
author_sort Bokka Ramesh
title Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction
title_short Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction
title_full Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction
title_fullStr Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction
title_full_unstemmed Direct injection HILICâMS/MS analysis of darunavir in rat plasma applying supported liquid extraction
title_sort direct injection hilicâms/ms analysis of darunavir in rat plasma applying supported liquid extraction
publisher Elsevier
series Journal of Pharmaceutical Analysis
issn 2095-1779
publishDate 2015-02-01
description A novel bioanalytical method was developed and validated for the quantitative determination of darunavir (DRV) in rat plasma by employing hydrophilic interaction chromatography and tandem mass spectrometry (HILICâMS/MS) with supported liquid extraction (SLE). Irbesartan (IRB) was used as an internal standard (IS). The analyte in rat plasma (200 µL) was isolated through SLE using ethyl acetate as the eluting solvent. The chromatographic separation was achieved on Luna-HILIC (250 mmÃ4.6 mm, 5 μm) column with a mobile phase of 0.1% of formic acid in water:acetonitrile (5: 95, v/v), at a constant flow rate of 1.0 mL/min. The MS/MS ion transitions for DRV (548.1â392.0) and IS (429.2â207.1) were monitored on an ion trap mass spectrometer, operating in the multiple reaction monitoring (MRM) mode. The lower limit of quantitation (LLOQ) was 0.2 ng/mL and quantitation range was 0.2â5000 ng/mL. The method was validated for its selectivity, sensitivity, carryover, linearity, precision, accuracy, recovery, matrix effect and stability. The method was successfully applied to pharmacokinetic study in rats. Keywords: Darunavir, HILICâMS/MS, Rat plasma, Supported liquid extraction
url http://www.sciencedirect.com/science/article/pii/S2095177914000422
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