Literature DB >> 26517852

Development and validation of an enantioselective LC-MS/MS method for the analysis of the anthelmintic drug praziquantel and its main metabolite in human plasma, blood and dried blood spots.

Isabel Meister1, Anna Leonidova1, Jana Kovač1, Urs Duthaler1, Jennifer Keiser2, Jörg Huwyler3.   

Abstract

Praziquantel (PZQ) is the treatment of choice against various trematode and cestode infections. To study the pharmacokinetics of PZQ in patients infected with the liver fluke Opisthorchis viverrini, we developed and validated an enantioselective liquid chromatography coupled to tandem mass spectrometry method for the analysis of R - and S -PZQ and its R -trans-4-OH-PZQ metabolite in human plasma, blood and dried blood spots (DBS). The analytes were detected in the positive mode using selected reaction monitoring (R- and S-PZQ: m/z 312.2 → 202.2; R-trans -4-OH-PZQ: m/z 328.0 → 202.0). Prior to the chiral separation with a cellulose tris(3-chloro-4-methylphenylcarbamate) column, the analytes were purified from matrix contaminants and concentrated on a C-18 trapping column. The analytical range for each PZQ enantiomer was 0.01-2.5 μg/mL, and 0.1-25 μg/mL for the metabolite. The method met the requirements regarding precision (± 15%, ± 20% at the lower limit of quantification-LLOQ), intra- and inter-assay accuracy (85-115%, 80-120% at LLOQ), and linearity (R(2) ≥ 0.998). The analytes were stable in stock solutions as well as in plasma, blood and DBS. For DBS, the influences of hematocrit and blood spot size were considered as minor. Our validation results show that the method presented here is precise, accurate and selective, and can be used for pharmacokinetic studies. Moreover, the enantioselective separation was achieved with a run time of 11.5 min and a simple sample processing method.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Dried blood spot; Enantiomer; LC–MS/MS; Pharmacokinetics; Praziquantel; R-trans-4-OH-PZQ

Mesh:

Substances:

Year:  2015        PMID: 26517852     DOI: 10.1016/j.jpba.2015.10.011

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  5 in total

Review 1.  Praziquantel for Schistosomiasis: Single-Drug Metabolism Revisited, Mode of Action, and Resistance.

Authors:  Nuno Vale; Maria João Gouveia; Gabriel Rinaldi; Paul J Brindley; Fátima Gärtner; José M Correia da Costa
Journal:  Antimicrob Agents Chemother       Date:  2017-04-24       Impact factor: 5.191

2.  Pharmacokinetics of Ascending Doses of Praziquantel in Adults Infected with Opisthorchis felineus in Western Siberia, Russian Federation.

Authors:  Alexandra Probst; Daniela Hofmann; Olga S Fedorova; Sofia V Mazeina; Tatiana S Sokolova; Ekaterina Golovach; Jennifer Keiser
Journal:  Antimicrob Agents Chemother       Date:  2022-09-12       Impact factor: 5.938

3.  Pharmacokinetics of Praziquantel in Schistosoma mansoni- and Schistosoma haematobium-Infected School- and Preschool-Aged Children.

Authors:  Jana Kovač; Isabel Meister; Anna Neodo; Gordana Panic; Jean T Coulibaly; Christine Falcoz; Jennifer Keiser
Journal:  Antimicrob Agents Chemother       Date:  2018-07-27       Impact factor: 5.191

4.  Pharmacokinetic Study of Praziquantel Enantiomers and Its Main Metabolite R-trans-4-OH-PZQ in Plasma, Blood and Dried Blood Spots in Opisthorchis viverrini-Infected Patients.

Authors:  Isabel Meister; Jana Kovac; Urs Duthaler; Peter Odermatt; Jörg Huwyler; Fiona Vanobberghen; Somphou Sayasone; Jennifer Keiser
Journal:  PLoS Negl Trop Dis       Date:  2016-05-06

5.  Extrapolation of praziquantel pharmacokinetics to a pediatric population: a cautionary tale.

Authors:  Peter L Bonate; Tianli Wang; Paul Passier; Wilhelmina Bagchus; Howard Burt; Christian Lüpfert; Nada Abla; Jana Kovac; Jennifer Keiser
Journal:  J Pharmacokinet Pharmacodyn       Date:  2018-09-14       Impact factor: 2.745

  5 in total

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