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High‐throughput protein precipitation method with 96‐well plate for determination of doxepin and nordoxepin in human plasma using LC–MS/MS
Author(s) -
Margaryan Tigran,
Sargsyan Mariam,
Gevorgyan Arpine,
Zakaryan Hasmik,
Aleksanyan Armine,
Harutyunyan Armen,
Armoudjian Yeghig,
Mikayelyan Astghik
Publication year - 2020
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/bmc.4844
Subject(s) - doxepin , chemistry , chromatography , protein precipitation , ammonium formate , selected reaction monitoring , mass spectrometry , triple quadrupole mass spectrometer , electrospray ionization , analyte , tandem mass spectrometry , pharmacology , medicine
The aim of this study was to establish a high‐throughput and sensitive LC–MS/MS method for the determination of doxepin and its major active metabolite nordoxepin in human plasma. It has been designed for bioequivalence study for formulations containing 25 mg of doxepin. Doxepin and nordoxepin were extracted from human plasma samples by protein precipitation with acetonitrile by using protein precipitation 96‐well plates. The analyte was separated using a Phenomenex Kinetex Biphenyl column (100 × 2.1 mm, 2.6 μm) using isocratic elution with a mobile phase of 20 mM ammonium formate (30%) and acetonitrile:methanol 3:7 v:v (70%) at a flow rate of 0.5 mL/min and an injection volume of 10 μL. The detection was performed using a triple quadrupole mass spectrometer by multiple reaction monitoring mode to monitor the precursor‐to‐product ion transitions of m / z 280.4 → 107.0 and 283.4 → 235.0 for doxepin and doxepin‐D3, respectively, and 266.3 → 106.9 and 269.3 → 235.0 for nordoxepin and nordoxepin‐D3, respectively, in positive electrospray ionization mode. The total run time was 3.5 min. The method was validated over a concentration range of 50–10,000 pg/mL using a Triple Quad 4500 MS System (Sciex) for both analytes. The developed and validated method can be successfully used to study the bioequivalence/pharmacokinetics of doxepin and nordoxepin.