Determination of amphenicol antibiotics and their glucuronide metabolites in urine samples using liquid chromatography with quadrupole time-of-flight mass spectrometry

被引:16
作者
Pastor-Belda, Marta [1 ]
Campillo, Natalia [1 ]
Arroyo-Manzanares, Natalia [1 ]
Hernandez-Cordoba, Manuel [1 ]
Vinas, Pilar [1 ]
机构
[1] Univ Murcia, Dept Analyt Chem, Fac Chem, Reg Campus Int Excellence Campus Mare Nostrum, E-30100 Murcia, Spain
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2020年 / 1146卷
关键词
Amphenicols; Glucuronide; Human urine; Dispersive liquid-liquid microextraction; Liquid chromatography; Quadrupole time-of-flight mass spectrometry; POLYMER MONOLITH MICROEXTRACTION; WATER SAMPLES; SELECTIVE DETERMINATION; ASSISTED EXTRACTION; LC DETERMINATION; CHLORAMPHENICOL; THIAMPHENICOL; HONEY; MILK; FOOD;
D O I
10.1016/j.jchromb.2020.122122
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid procedure for the determination of amphenicol antibiotics in human urine by liquid chromatography with quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) is proposed. The presence of thiamphenicol (TAP), florfenicol (FF) and chloramphenicol (CAP) in the human body can be attributed to their administration to treat certain diseases or by eating food of animal origin. The TAP, FF and CAP excreted in urine is mainly in the form of glucuronide conjugates, although their free forms may also be excreted to a lesser extent. In the procedure described, the enzymatic hydrolysis of amphenicol glucuronide forms in urine was carried out using beta-glucuronidase and sulfatase at pH 5 (37 degrees C, overnight) in order to discriminate the free and conjugated forms. Then, amphenicol antibiotics were submitted to dispersive liquid-liquid microextraction (DLLME) for preconcentration. All the parameters affecting DLLME efficiency were optimized, and the following conditions were selected: 0.9 g NaCl in 10 mL of urine, to which 1.2 mL methanol (as dispersant solvent) and 1 mL of 4-methyl-2-pentanone (as extractant solvent) were added. The absence of a matrix effect allowed quantification of the samples against aqueous standards. Detection limits were 29, 6 and 3 pg mL(-1) for TAP, FF and CAP, respectively. Relative standard deviations were calculated to evaluate the infra- and inter-day precision and values lower than 10% were obtained in all cases. The trueness of the method was tested through recovery studies, obtaining satisfactory values (83-104%). Ten urine samples obtained from volunteers were analysed and all of them were free of the studied antibiotics.
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页数:7
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