Validation of direct injection electrospray LC-MS/MS for confirmation of opiates in urine drug testing

被引:66
作者
Gustavsson, E. [1 ]
Andersson, M. [1 ]
Stephanson, N. [1 ]
Beck, O. [1 ]
机构
[1] Karolinska Univ Hosp, Dept Med, Div Clin Pharmacol, SE-17176 Stockholm, Sweden
来源
JOURNAL OF MASS SPECTROMETRY | 2007年 / 42卷 / 07期
关键词
drugs of abuse; urine drug testing; confirmation; opiates; liquid chromatography; tandem mass spectrometry; CHROMATOGRAPHY-MASS-SPECTROMETRY; PERFORMANCE LIQUID-CHROMATOGRAPHY; SAMPLE PREPARATION; ILLICIT DRUGS; MORPHINE; 6-MONOACETYLMORPHINE; IDENTIFICATION; BIOANALYSIS; TOXICOLOGY; CRITERIA;
D O I
10.1002/jms.1219
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method based on the direct injection of diluted urine for the identification and quantification of morphine, morphine-3-glucuronide, morphine-6-glucuronide, codeine, codeine-6-glucuronide, ethylmorphine, ethylmorphine-6-glucuronide and 6-acetylmorphine (6AM) in human urine by electrospray ionisation liquid chromatography-tandem mass spectrometry was validated for use as a confirmation procedure in urine drug testing. Four deuterium labelled analogues were used as internal standards: morphine-3-glucuronideD3, morphine-133, codeine-D3 and 6AM-D3. Twenty microlitre aliquots of urine were mixed with 80 mu l of the internal standard solution in autosampler vials and 10 mu l was injected. The chromatographic system consisted of a 2.0 x 100 mm C18 column and the gradient elution buffers used acetonitrile and 25 mmol/l formic acid. Two product ions produced from the protonated molecular ions were monitored in the selected reaction monitoring mode. The intra- and inter-assay variability (coefficient of variation) was below 10% at higher levels for all analytes, but at the reporting limits the variation was above 20% for 6AM, morphine-3-glucuronide and codeine-6-glucuronide. Ion suppression occurred early after injection but did not affect the identification and quantification of the analytes in authentic samples.The method was further validated by comparison with a reference gas chromatographic-mass spectrometric method using authentic urine samples. The two methods agreed almost completely (99%) regarding the identified analytes, but for the quantitative results there were slightly lower levels when measuring glucuronides directly as compared to total determination after hydrolysis by gas chromatography-mass spectrometry. We conclude that the presented liquid chromatographic-tandem mass spectrometric method is robust and reliable, and suitable for use as a confirmation method in urine drug testing for opiates. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:881 / 889
页数:9
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