Validation of a novel UPLC-MS/MS method for estimation of metformin and empagliflozin simultaneously in human plasma using freezing lipid precipitation approach and its application to pharmacokinetic study

被引:12
作者
Omar, M. N. Abou [1 ]
Kenawy, M. [2 ]
Youssef, A. O. [2 ]
Alharthi, Sarah [3 ]
Attia, M. S. [2 ]
Mohamed, Ekram H. [4 ]
机构
[1] Ain Shams Univ, Fac Women Arts Sci & Educ, Dept Chem, Cairo, Egypt
[2] Ain Shams Univ, Fac Sci, Chem Dept, Cairo 11566, Egypt
[3] Taif Univ, Collage Sci, Dept Chem, POB 11099, At Taif 21944, Saudi Arabia
[4] British Univ Egypt, Fac Pharm, Chem Dept, Pharmaceut Analyt, Cairo 11837, Egypt
关键词
Empagliflozin; Metformin; Matrix effect; Antidiabetic drugs; UPLC-MS/MS; Pharmacokinetic; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION;
D O I
10.1016/j.jpba.2021.114078
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fast, sensitive one step UPLC ESI-MS/MS method was successfully applied for the simultaneous estimation of two concurrently administrated antidiabetic drugs, Metformin (MET) and Empagliflozin (EMPA) in human plasma. Metformin-d6 (MET-d6) and Empagliflozin-d4 (EMPA-d4) were utilized as internal standards. Extraction of the analytes from the human plasma was performed through acetonitrile precipitation technique followed by freezing the precipitated plasma proteins and lipids to minimize the matrix effect. Chromatographic analysis was developed on Acquity UPLC BEH C-18 column (1.7 mu m, 2.1 x 50 mm) using isocratic elution mode. A mobile phase of formic acid (0.01 %): acetonitrile (70:30 v/v) with a flow rate of 0.3 mL/min achieved optimum separation. Multiple reaction monitoring (MRM) in positive ion mode, with transitions at (m/z) 130.14 -> 71.08 for (MET), 451.72 -> 71.29 for (EMPA), 136.03 -> 77.02 for (MET-d6), and 455.43 -> 75.05 for (EMPA-d4) was used for quantification. The obtained linearity covered the concentration ranges of 10-1500 ng/mL and 2.0-250.0 ng/mL for MET and EMPA, respectively. The run time of the proposed Method didn't exceed 3.0 min allowing faster analysis and determination of larger number of samples per day without affecting accuracy and sensitivity. The presented chromatographic method could be successfully applied in pharmacokinetics studies and therapeutic monitoring of MET and EMPA in patients' plasma administrating fixed dose combination of both drug with high reproducibility and ruggedness. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:9
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