Ultrafast Measurement of Metformin in the Clinical Setting Using Probe Electrospray Ionization Mass Spectrometry

被引:1
|
作者
Griffeuille, Pauline [1 ]
El Balkhi, Souleiman [1 ]
Bodeau, Sandra [2 ]
Lamoureux, Fabien [3 ]
Marquet, Pierre [1 ,4 ]
Dulaurent, Sylvain [1 ]
Saint-Marcoux, Franck [1 ,5 ]
机构
[1] Limoges Univ Hosp, Dept Pharmacol & Toxicol, 2 Ave Martin Luther King, F-87042 Limoges, France
[2] Amiens Univ Hosp, Dept Pharmacol & Toxicol, 1 Rond Point Prof Christian Cabrol, F-80054 Amiens, France
[3] Rouen Univ Hosp, Dept Pharmacol & Toxicol, 37 Blvd Gambetta, F-76000 Rouen, France
[4] Univ Limoges, Pharmacol & Transplantat, INSERM, UMR1248, Rue Pr Bernard Descottes, F-87025 Limoges, France
[5] Fac Pharm, Dept Toxicol, 2 Rue Dr Marcland, F-87025 Limoges, France
关键词
LACTIC-ACIDOSIS; MORTALITY;
D O I
10.1093/jat/bkac034
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Metformin (MtF) is a treatment used for type 2 diabetes. Lactic acidosis (LA) is a frequent complication that can be either induced by or associated with elevated MtF plasma concentrations. When coupled with a mass spectrometry (MS) system, the probe electrospray ionization (PESI) method allows direct and rapid analysis of different types of matrices without pretreatment. In this study, we developed a PESI-MS method for the determination of MtF in plasma. We used a tandem mass spectrometer equipped with a PESI source in the reaction monitoring mode for the quantitation of MtF. MtF-D6 was chosen as the internal standard (IS), following an isotope dilution (ID) approach. The method was fully validated with six concentration levels (0.5-50 mg/L). The matrix effect was evaluated for each level, and the specificity was tested with a mix of potential co-medications. Using patient samples, the performance was compared with two classical LC-MS-MS and LC-diode array detector (DAD) methods used in external labs. Sample preparation consisted in mixing 10 mu L plasma in 1,000 mu L ethanol/ammonium formate buffer including MtF-D6 at a fixed concentration of 5 mg/L. The total run time was 0.31 min. ID gave satisfactory results of accuracy and precision (min-max: -12.1 to 15.8% and 1.0-17.1%, respectively). The matrix effect was fully corrected by the internal standard (bias < 1%). The specificity study also reported satisfactory results. Finally, in a representative group of 29 patients (55% with a concentration <5 mg/L, 38% with a concentration >5 mg/L and 7% not detected), we observed almost identical results when comparing LC-DAD and LC-MS-MS to PESI-MS (r(2) > 0.99). We propose a specific, sensitive, accurate and ultrafast solution for the measurement of MtF in patient plasma, with no sample preparation or calibration curve building. This could be helpful in a core lab when rapid diagnosis of LA is needed.
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页码:89 / 95
页数:7
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