Capillary electrophoresis-tandem mass spectrometry combined with molecularly imprinted solid phase extraction as useful tool for the monitoring of 5-nitroimidazoles and their metabolites in urine samples

被引:15
作者
Hernandez-Mesa, Maykel [1 ]
Cruces-Blanco, Carmen [1 ]
Garcia-Campana, Ana M. [1 ]
机构
[1] Univ Granada, Fac Sci, Dept Analyt Chem, Av Fuentenueva S-N, E-18071 Granada, Spain
关键词
Capillary electrophoresis; Mass spectrometry; 5-nitroimidazoles; Molecularly imprinted polymers; Urine samples; MICELLAR ELECTROKINETIC CHROMATOGRAPHY; CORRESPONDING HYDROXY METABOLITES; LIQUID-LIQUID MICROEXTRACTION; VETERINARY DRUG RESIDUES; TIME-OF-FLIGHT; NITROIMIDAZOLE RESIDUES; ELECTROSPRAY-IONIZATION; VOLATILE SURFACTANT; METRONIDAZOLE; ANTIMICROBIALS;
D O I
10.1016/j.talanta.2016.10.092
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel capillary electrophoresis-tandem mass spectrometry approach is proposed for the determination of eleven 5-nitroimidazoles in urine samples for therapeutical drug monitoring purposes. A comparison between two separation modes, namely micellar electrokinetic chromatography and capillary zone electrophoresis was carried out, obtaining higher selectivity when 1 M formic acid (pH 1.8) was selected as background electrolyte. 5-Nitroimidazoles were hydrodynamically injected in water for 40 s at 50 mbar and their separation was performed at 28 kV and 25 degrees C. To improve migration time repeatability, a pressure of 50 mbar was applied to the inlet vial during runs without any loss of peak resolution. Electrospray ionization parameters were established as follow: 6 L/min, dry gas flow rate; 51,021.2 Pa, nebulization pressure; 160 degrees C, dry gas temperature. Sheath liquid consisted of a mixture of propan-2-ol/water/acetic acid (60.0:38.8:0.2% v/v/v) supplied at 3.3 mu L/min. MS parameters were optimized for analyte identification through their MS2 and MS3 spectra. The method was applied to the determination of 5-nitroimidazoles in urine samples, applying molecularly imprinted solid phase extraction for sample clean-up. Recoveries higher than 79.2% demonstrated the suitability of the procedure. Limits of detection ranged from 9.6 to 130.2 mu g/L while precision assays resulted in relative standard deviations for peak areas lower than 16.1%.
引用
收藏
页码:111 / 120
页数:10
相关论文
共 42 条
[21]   Metronidazole Is Still the Drug of Choice for Treatment of Anaerobic Infections [J].
Lofmark, Sonja ;
Edlund, Charlotta ;
Nord, Carl Erik .
CLINICAL INFECTIOUS DISEASES, 2010, 50 :S16-S23
[22]   Analytical methodologies for the determination of nitroimidazole residues in biological and environmental liquid samples: A review [J].
Mahugo-Santana, Cristina ;
Sosa-Ferrera, Zoraida ;
Esther Torres-Padron, Ma ;
Juan Santana-Rodriguez, Jose .
ANALYTICA CHIMICA ACTA, 2010, 665 (02) :113-122
[23]   Multiple response optimization of a liquid chromatographic method for determination of fluoroquinolone and nitroimidazole antimicrobials in serum and urine [J].
Mannemala, Sai Sandeep ;
Kannappan, Valliappan .
CLINICAL BIOCHEMISTRY, 2016, 49 (7-8) :587-595
[24]   Strategies for the assessment of matrix effect in quantitative bioanalytical methods based on HPLC-MS/MS [J].
Matuszewski, BK ;
Constanzer, ML ;
Chavez-Eng, CM .
ANALYTICAL CHEMISTRY, 2003, 75 (13) :3019-3030
[25]   Use of molecularly imprinted solid-phase extraction sorbent for the determination of four 5-nitroimidazoles and three of their metabolites from egg-based samples before tandem LC-ESIMS/MS analysis [J].
Mohamed, Rayane ;
Mottier, Pascal ;
Treguier, Laureen ;
Richoz-Payot, Janique ;
Yilmaz, Ecevit ;
Tabet, Jean-Claude ;
Guy, Philippe A. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (10) :3500-3508
[26]   Micellar electrokinetic chromatography-electrospray ionization mass spectrometry employing a volatile surfactant for the analysis of amino acids in human urine [J].
Moreno-Gonzalez, David ;
Torano, Javier Sastre ;
Gamiz-Gracia, Laura ;
Garcia-Campana, Ana M. ;
de Jong, Gerhardus J. ;
Somsen, Govert W. .
ELECTROPHORESIS, 2013, 34 (18) :2615-2622
[27]   Dispersive liquid-liquid microextraction using a low density extraction solvent for the determination of 17 N-methylcarbamates by micellar electrokinetic chromatography-electrospray-mass spectrometry employing a volatile surfactant [J].
Moreno-Gonzalez, David ;
Gamiz-Gracia, Laura ;
Bosque-Sendra, Juan M. ;
Garcia-Campana, Ana M. .
JOURNAL OF CHROMATOGRAPHY A, 2012, 1247 :26-34
[28]   On-line partial filling micellar electrokinetic chromatography electrospray ionization mass spectrometry [J].
Nelson, WM ;
Tang, Q ;
Harrata, AK ;
Lee, CS .
JOURNAL OF CHROMATOGRAPHY A, 1996, 749 (1-2) :219-226
[29]   Structural characterization of product ions by electrospray ionization and quadrupole time-of-flight mass spectrometry to support regulatory analysis of veterinary drug residues in foods. Part 2: Benzimidazoles, nitromidazoles, phenothiazines, and mectins [J].
Nunez, Alberto ;
Lehotay, Steven J. ;
Geis-Asteggiante, Lucia .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2015, 29 (08) :719-729
[30]   Direct coupling of micellar electrokinetic chromatography to mass spectrometry using a volatile buffer system based on perfluorooctanoic acid and ammonia [J].
Petersson, P ;
Jörntén-Karlsson, M ;
Stålebro, M .
ELECTROPHORESIS, 2003, 24 (06) :999-1007