Literature DB >> 27606925

Stereoselective determination of citalopram and desmethylcitalopram in human plasma and breast milk by liquid chromatography tandem mass spectrometry.

Etienne Weisskopf1, Alice Panchaud2, Kim An Nguyen3, Delphine Grosjean4, Jean-Michel Hascoët5, Chantal Csajka2, Chin B Eap6, Nicolas Ansermot7.   

Abstract

A high performance liquid chromatography (HPLC) tandem mass spectrometry (MS/MS) method was developed for the simultaneous, stereoselective quantification of the antidepressant citalopram and its active metabolite desmethylcitalopram in human plasma and breast milk. Sample preparation was performed by a two-step approach, including generic protein precipitation with acetonitrile followed by solid phase extraction. Enantiospecific separation of analytes was achieved on a Phenomenex® Lux Cellulose-2 column (4.6mm×150mm; 5μm), using reversed phase chromatography conditions characterized by a gradient elution of ammonium acetate buffer (pH 9.0; 20mM) and acetonitrile at a flow rate of 0.6ml/min. The compounds were detected by a tandem quadrupole mass spectrometer equipped with an electrospray ionization source and operating in multiple reaction monitoring mode. The method was fully validated in both biological fluids over a large concentration range of 0.1-100ng/ml for S-(+)- and R-(-)-citalopram, and 0.3-100ng/ml for S-(+)- and R-(-)-desmethylcitalopram. Trueness (90.0-113.3% and 97.1-103.6%), repeatability (0.9-15.9% and 0.9-8.4%) and intermediate precision (1.3-17.8% and 0.9-9.6%) in plasma and breast milk, respectively, meet international guidelines for method validation. Internal standard-normalized matrix effects ranged between 99 and 101% and 98-105%, respectively. The accuracy profiles (total error of trueness and precision) were mostly within the acceptance limits for biological samples defined as ±30%. The method was successfully applied to patient samples in a clinical trial setting.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Breast milk; Citalopram; Enantiomer; LC–MS/MS; Plasma; Quantification

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Substances:

Year:  2016        PMID: 27606925     DOI: 10.1016/j.jpba.2016.08.014

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


  2 in total

1.  A population pharmacokinetic model for escitalopram and its major metabolite in depressive patients during the perinatal period: Prediction of infant drug exposure through breast milk.

Authors:  Etienne Weisskopf; Monia Guidi; Céline J Fischer; Myriam Bickle Graz; Etienne Beaufils; Kim An Nguyen; Mathilde Morisod Harari; Sylvie Rouiller; Sophie Rothenburger; Pascal Gaucherand; Behrouz Kassai-Koupai; Cristina Borradori Tolsa; Manuella Epiney; Jean-François Tolsa; Yvan Vial; Jean-Michel Hascoët; Olivier Claris; Chin B Eap; Alice Panchaud; Chantal Csajka
Journal:  Br J Clin Pharmacol       Date:  2020-04-14       Impact factor: 4.335

Review 2.  Enantioselectivity in Drug Pharmacokinetics and Toxicity: Pharmacological Relevance and Analytical Methods.

Authors:  Maria Miguel Coelho; Carla Fernandes; Fernando Remião; Maria Elizabeth Tiritan
Journal:  Molecules       Date:  2021-05-23       Impact factor: 4.411

  2 in total

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