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Development of UPLC-MS/MS method for the simultaneous quantification of valproic acid and phenytoin in human plasma and application to study pharmacokinetic interaction in epilepsy patients.
Nguyen, Sil Thanh; Ho, Duy Nguyen; Huynh, Thi Anh Huynh; Nguyen, Huyen Thu Thi; Thi Ly, Ngan Kim; Van Le, Minh; Minh Chau Do, Tho Vinh.
Afiliación
  • Nguyen ST; Faculty of Pharmacy, Can Tho University of Medicine and Pharmacy, Can Tho, 900000, Viet Nam.
  • Ho DN; Faculty of Pharmacy, Can Tho University of Medicine and Pharmacy, Can Tho, 900000, Viet Nam.
  • Huynh TAH; Department of Chemistry, College of Natural Sciences, Can Tho University, Can Tho, 900000, Viet Nam.
  • Nguyen HTT; Institute of Drug Quality Control Ho Chi Minh City, Ho Chi Minh City, 700000, Viet Nam.
  • Thi Ly NK; Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho, 900000, Viet Nam.
  • Van Le M; Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho, 900000, Viet Nam.
  • Minh Chau Do TV; Department of Analytical Chemistry - Toxicology - Drug Quality Control, Faculty of Pharmacy, Can Tho University of Medicine and Pharmacy, Can Tho, 900000, Viet Nam.
Heliyon ; 10(13): e33630, 2024 Jul 15.
Article en En | MEDLINE | ID: mdl-39040279
ABSTRACT
Valproic acid and phenytoin are two prevalent antiepileptic medications known for their narrow indices and propensity for cardiovascular and respiratory system toxicity. Therefore, therapeutic drug monitoring (TDM) of valproic acid (VAL) and phenytoin (PHE) concentrations in patient plasma is extremely beneficial for improving clinical choices, avoiding adverse reactions, and optimizing treatment for individual patients. In this study, a rapid and sensitive ultra-performance liquid chromatographic tandem mass spectrometer (UPLC-MS/MS) method was developed and validated for the simultaneous quantitative determination of valproic acid (VAL) and phenytoin (PHE) in human plasma. Negative electron spray ionization (ESI-) mode with selective ion recording (SIR) was employed to determine the transitions of m/z 142.98 and m/z 250.93 for VAL and PHE, respectively. The internal standard (IS) betamethasone (BETA) was ionized using positive electron spray ionization (ESI+) and detected by multi-reaction monitoring (MRM) mode to obtain precursor ions and specific fragment ions for quantification, and the MRM transition was chosen to be m/z 393.17 â†’ 355.16. The separation was performed using a Phenomenex Synergi Hydro-RP (4 µm, 250 × 4.6 mm, I.D.) with an isocratic mobile phase consisting of acetonitrile - water (7525, v/v) at a flow rate of 0.8 mL/min. The column temperature was maintained at 25 °C. The lower limit of quantification of VAL and PHE was 3.6 µg/mL and 0.72 µg/mL, respectively, which resulted in a recovery of more than 85 % for most analytes. According to US-FDA bioanalytical technique validation, the specificity, intra- and inter-day precision and accuracy, matrix effect, carryover, dilution, and stability of all analytes were within acceptable ranges. This analytical method was successful in evaluating the levels of valproic acid and phenytoin in human plasma from epileptic patients.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Heliyon Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Heliyon Año: 2024 Tipo del documento: Article