Journal
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
Volume 31, Issue 5, Pages 683-694Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/10826070701853867
Keywords
microextraction in packed syringe; sample preparation; cyclophosphamide; plasma; LC-UV; LC-MS/MS
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The aim of the present investigation was to develop a simple and fast method for the determination of cyclophosphamide in human plasma samples. Microextraction in packed syringe (MEPS) was used as an online rapid sample preparation method, followed by liquid chromatography with tandem mass spectrometry (LC-MS-MS) for the quantification of cyclophosphamide. The new method reduced the sample handling and the analysis time by several folds compared to liquid chromatography and UV detection. The limit of detection (LOD) was 0.005 mu g/mL and the lower limit of quantification was 0.5 mu g/mL. The accuracy of the quality control (QC) samples ranged from 95 to 106%. The inter-day variation was within the range 5-9% while the intra day variation was between 1-5%. The calibration curve in plasma was constructed within the concentration range 0.5-150 mu g/mL. The regression correlation coefficient (r) was 0.99 for all runs. The limit of detection improved by 100 time using MEPS-LC-MS/MS (0.005 mu g/mL) compared to LLE-LC-UV (0.5 mu g/mL). The present method was employed for the analysis of human plasma samples for more 170 patient samples. The concentrations obtained from LC-MS-MS were in good agreement with these obtained from LC-UV with the ratio of 1.02 +/- 0.11. The present method is rapid, reliable, and robust and may be used for therapeutic drug monitoring of cyclophosphamide.
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