Author:
Leis H. J.,Windischhofer W.,Fauler G.
Abstract
AbstractA sensitive and specific method for the quantitative determination of morphine in human plasma is presented. Morphine was extracted from plasma by solid phase extraction on C18 and converted to its pentafluorobenzyl carbonate trimethylsilyl derivative. The derivatives were analysed without further purification. Using gas chromatography/negative ion chemical ionisation mass spectrometry, a useful diagnostic fragment ion at m/z 356 is obtained at high relative abundance. Deuterated morphine was used as internal standard. Calibration graphs were linear within the range 1.25 to 320 nmol/L. Intra‐day precision was 3.82% (15 nmol/L), 2.85% (75 nmol/L) and 4.13% (225 nmol/L), inter‐day variability was found to be 1.77% (15 nmol/L), 4.95% (75 nmol/L) and 9.88% (225 nmol/L). Inter‐day accuracy showed deviations of 2.18% (15 nmol/L), −0.72% (75 nmol/L) and −0.13% (225 nmol/L). The method is rugged and robust and has been applied to the batch analysis of morphine during pharmacokinetic profiling of the drug. Copyright © 2002 John Wiley & Sons, Ltd.
Reference25 articles.
1. World Health Organization Cancer Pain Relief Program WHO Geneva 1986.
2. The Metabolism of Morphine and Heroin in Man
3. Morphine: Radioimmunoassay
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献