Direct quantification of morphine glucuronides and free morphine in urine by liquid chromatography-tandem mass spectrometry

被引:9
|
作者
Deventer, K. [1 ]
Pozo, O. J. [2 ]
Delbeke, F. T. [1 ]
Van Eenoo, P. [1 ]
机构
[1] Ghent Univ UGent, Doping Control Lab DoCoLab, Dept Clin Chem Microbiol & Immunol, B-9052 Ghent, Belgium
[2] IMIM Hosp Mar, Bioanal Res Grp, Barcelona 08003, Spain
关键词
Morphine; Opiate; Urine; Detection; Doping; LC-MS; DIRECT-INJECTION; ELECTROSPRAY-IONIZATION; ENZYMATIC-HYDROLYSIS; PRESCRIPTION OPIOIDS; INCOMPLETE RECOVERY; LC-MS/MS; METABOLITES; VALIDATION; OPIATES; 6-GLUCURONIDE;
D O I
10.1007/s11419-012-0135-8
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
A simple and robust liquid chromatographic-tandem mass spectrometric method was developed and validated for the direct quantification of the structural isomers morphine-3-glucuronide (M3G), morphine-6-glucuronide (M6G), and morphine in urine. Method development showed that dilution of the urine samples was mandatory to obtain reproducible chromatography and that the use of deuterated internal standards was needed to compensate for ion suppression. Sample preparation consisted of a 20-fold dilution of urine into the internal standard solution. Chromatography was performed on a C-8-column using gradient conditions. The mobile phase consisted of water/methanol, both containing 0.1 % acetic acid and 1 mM ammonium acetate. Calibration curves were constructed between 0.05 and 2 mu g/ml. Validation data showed biases ranging from 1.5 to 5.2 % for M3G, -2.7 to -5.9 % for M6G, and 3.7 to 7.1 % for morphine. Imprecision never exceeded 5.2, 5.9, and 5.7 % for M3G, M6G, and morphine, respectively. The applicability of the method was checked by the analysis of 20 urine samples that were analyzed concurrently with a routine gas chromatography-mass spectrometry method. Results showed good correlation between the methods with a correlation coefficient of approximately 0.95.
引用
收藏
页码:106 / 113
页数:8
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