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Optimization of chromatography to overcome matrix effect for reliable estimation of four small molecular drugs from biological fluids using LC–MS/MS
Author(s) -
Trivedi Vikas,
Shah Priyanka A.,
Shrivastav Pranav S.,
Sanyal Mallika
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.4777
Subject(s) - chemistry , chromatography , ammonium acetate , ammonium formate , elution , methanol , analyte , extraction (chemistry) , high performance liquid chromatography , organic chemistry
The article describes a systematic study to overcome the matrix effect during chromatographic analysis of gemfibrozil, rivastigmine, telmisartan and tacrolimus from biological fluids using LC–ESI–MS/MS. All four methods were thoroughly developed by the appropriate choice of analytical column, elution mode and pH of mobile phase for improved chromatography and overall method performance. Matrix effect was assessed by post‐column analyte infusion, slope of calibration line approach and post‐extraction spiking. The best chromatographic conditions established were: Acquity BEH C 18 (50 × 2.1 mm, 1.7 μm) column with 5.0 mm ammonium acetate, pH 6.0–methanol as the mobile phase under gradient program for gemfibrozil; Luna CN (50 × 2.0 mm, 3 μm) column with a mobile phase consisting of acetonitrile–10 m m ammonium acetate, pH 7.0 (90:10, v/v) for rivastigmine; Inertsustain C 18 (100 × 2.0 mm, 5 μm) column using methanol–2.0 m m ammonium formate, pH 5.5 (80: 20, v/v) as the mobile phase for isocratic elution of telmisartan; and Acquity BEH C 18 (50 × 2.1 mm, 1.7 μm) with methanol–10 m m ammonium acetate, pH 6.0 (95:5, v/v) as mobile phase for tacrolimus. The methods were thoroughly validated as per European Medicines Agency and US Food and Drug Administration guidance and were successfully applied for pharmacokinetic studies in healthy subjects.