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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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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