COMPARISON OF A NEW HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY METHOD WITH FLUORESCENCE POLARIZATION IMMUNOASSAY FOR ANALYSIS OF METHOTREXATE

Citation
Tao. Najjar et al., COMPARISON OF A NEW HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY METHOD WITH FLUORESCENCE POLARIZATION IMMUNOASSAY FOR ANALYSIS OF METHOTREXATE, Therapeutic drug monitoring, 14(2), 1992, pp. 142-146
Citations number
18
Journal title
ISSN journal
01634356
Volume
14
Issue
2
Year of publication
1992
Pages
142 - 146
Database
ISI
SICI code
0163-4356(1992)14:2<142:COANHL>2.0.ZU;2-Y
Abstract
A simple high-performance liquid chromatography (HPLC) method for the determination of methotrexate (MTX) in biological fluids is described. The assay is rapid, the time required for analysis is < 30 min, and i t is sensitive up to 0.01-mu-g/ml, which is three times below the toxi c MTX concentration. Fifty plasma samples drawn from acute lymphocytic leukemia (ALL) patients were used to compare this method with that of fluorescence polarization immunoassay (FPIA). A good correlation (r = 0.979) was obtained between the results of the two analyses. FPIA con stantly overestimates the concentration in samples collected during el imination and underestimates those collected during infusion. The diff erence between the means of the two methods was 29% and 13% for the el imination and infusion samples, respectively. The means of the peak he ight ratio of the metabolite to MTX in the HPLC chromatograms were 3.3 9 and 0.33 during elimination and infusion, respectively. The results therefore indicate that HPLC is more specific when tracing the washout of MTX concentration. Because of this specificity and simplicity, the method is recommended for therapeutic drug monitoring. The stability of MTX in human saliva was investigated in this study. MTX was found t o be stable at room temperature and at -20-degrees-C for a minimum of 3 h and 3 weeks, respectively.