Spectrofluorimetric determination of dipyridamole in serum — a comparison of two methods

Two spectrofluorimetric methods for the determination of dipyridamole in plasma are described. The thin-layer chromatographic—fluoridensitometric method utilizes 1 ml of plasma which is extracted at pH 10 with diethyl ether—dichloromethane (80:20). The organic phase is evaporated to dryness, reconstituted in 250 μl dichloromethane and 5 μl are spotted on a silica gel 60 plate. The plate is developed in ethyl acetate—methanol—ammonia (85:10:5), dried, dipped in a paraffin wax solution, dried, and scanned using 380 nm as excitation wavelength, a 430 nm cut-off filter, and collecting all emitted light on the photomultiplier. Quantitation was done by the external standard method, peak heights being measured and a calibration graph constructed. For the spectrofluorimetric method 1 ml of plasma is extracted at pH 10 with 8 ml of hexane—isoamyl alcohol (95:5) and the organic phase used directly for the measurement of the fluorescence intensity (excitation 405 nm, emission 495 nm). Quantitation was done by measuring the fluorescence of standards that were treated as above and constructing a calibration graph of concentration versus fluorescence intensity. Concentrations of unknowns were found by interpolation from this graph. The two methods were found to exhibit good correlation but the spectrofluorimetric method proved to be more amenable to the analysis of a large number of samples.