Simultaneous Quantification of Psychotropic Drugs in Human Plasma and Breast Milk and Its Application in Therapeutic Drug Monitoring and Peripartum Treatment Optimization

Author:

Le Marois Marguerite123,Doudka Natalia1,Tzavara Eleni456,Delaunay Laurence1,Quaranta Sylvie7,Blin Olivier12,Belzeaux Raoul368,Guilhaumou Romain12

Affiliation:

1. Service de Pharmacologie Clinique et Pharmacovigilance, Hôpital de la Timone, Marseille Cedex 5 13385, France;

2. Aix Marseille Université, Institut de Neurosciences des Systèmes, Inserm UMR 1106, Marseille 13385, France;

3. Aix Marseille Univ, CNRS, Inst Neurosci Timone, Marseille, France;

4. Pôle de Psychiatrie, Hôpital Sainte-Marguerite, AP-HM, Marseille, France;

5. Université Paris Cité, CNRS, Integrative Neuroscience and Cognition Center, Paris 75006, France;

6. Fondation FondaMental, Créteil, France;

7. Laboratoire de Pharmacocinétique et Toxicologie, Hôpital de la Timone, Marseille Cedex 5 13385, France; and

8. Pôle Universitaire de Psychiatrie, CHU de Montpellier, Montpellier, France.

Abstract

Background: Therapeutic drug monitoring is recommended for several psychotropic drugs, particularly in sensitive situations such as the peripartum period. This study aimed to develop an ultra-high-performance liquid chromatography–tandem spectrometry method for the simultaneous quantification of 14 psychotropic drugs in human plasma and 4 in breast milk. Methods: The samples were precipitated with methanol containing the stable isotope-labeled analogs. Chromatographic separation was performed using a Phenomenex Luna Omega Polar C18 column. Detection was performed using a triple-quadrupole mass spectrometer equipped with an electrospray ionization interface. The method was fully validated in plasma according to the European Guidelines on Bioanalytical Method Validation and partially validated in breast milk by determining the intraday precision and accuracy, linearity, lower limit of quantification, and matrix effect. Results: The correlation coefficients of the calibration curves were greater than 0.99. Coefficients of variation ranged from 3.05% to 14.66% and 0.62%–14.90% for internal standard-normalized matrix effect, 1.4%–14.1% and 2.1%–10.4% for intraday precision, and 3.2%–13.9% and 4.1%–9.6% for interday precision, in plasma and milk, respectively. The relative error in accuracy did not exceed ±15% for any analyte. The method was successfully applied clinically to measure the concentrations of psychotropic drugs in 952 plasma samples, among which 43% of the concentrations were out of the therapeutic range, and 13 breast milk samples, with calculated relative infant doses ranging from 0.32% to 8.18%. Conclusions: To the best of the authors' knowledge, this is the first routine technique validated for the quantification of psychotropic drugs in both plasma and breast milk, allowing for treatment optimization and prevention of adherence issues, including those in breastfeeding patients.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Pharmacology

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