A novel kinetic spectrophotometric method was developed for the simultaneous determination of caffeine,
theobromine and theophylline in food samples. This method was based on the different kinetic
characteristics between the reactions of analytes with cerium sulphate in sulphuric acid and the associated
change in absorbance at 320 nm. Experimental conditions, the effects of sulphuric acid, cerium sulphate
and temperature, were optimised. Linear ranges (0.4–8.4 lgmL1) for all three analytes were
established, and the limits of detection were: 0.30 lgmL1 (caffeine), 0.33 lgmL1 (theobromine) and
0.16 lgmL1 (theophylline). The recorded data were processed by partial least squares and artificial neural
network, and the developed mathematical models were then used for prediction. The proposed, novel
method was applied to determine the analytes in commercial food samples, and there were no significant
differences between the results from the proposed method and those obtained by high-performance
liquid chromatography.
A novel kinetic spectrophotometric method was developed for the simultaneous determination of caffeine,theobromine and theophylline in food samples. This method was based on the different kineticcharacteristics between the reactions of analytes with cerium sulphate in sulphuric acid and the associatedchange in absorbance at 320 nm. Experimental conditions, the effects of sulphuric acid, cerium sulphateand temperature, were optimised. Linear ranges (0.4–8.4 lgmL1) for all three analytes wereestablished, and the limits of detection were: 0.30 lgmL1 (caffeine), 0.33 lgmL1 (theobromine) and0.16 lgmL1 (theophylline). The recorded data were processed by partial least squares and artificial neuralnetwork, and the developed mathematical models were then used for prediction. The proposed, novelmethod was applied to determine the analytes in commercial food samples, and there were no significantdifferences between the results from the proposed method and those obtained by high-performanceliquid chromatography.
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