Dinç E
Department of Analytical Chemistry, Faculty of Pharmacy, University of Ankara, Turkey.
J Pharm Biomed Anal. 1999 Dec;21(4):723-30. doi: 10.1016/s0731-7085(99)00186-7.
Two spectrophotometric methods and high-performance liquid chromatography were proposed for the simultaneous analysis of caffeine and paracetamol in a tablet formulation. The ratio spectra derivative method is based on the use of the analytical signals obtained by measuring at 267.9 and 291.0 nm for caffeine and 237.0 and 251.8 nm for paracetamol in the first derivative of the ratio spectra. Calibration graphs were prepared in the range 4-40 microg/ml for caffeine and 8-48 microg/ml for paracetamol. In Vierordt's method, A1(1) (1%, 1cm) values of paracetamol and caffeine were determined at 242.9 and 273.0 nm in zero-order spectra. The matrix for A1(1) (1%, 1cm) values was written and the amounts of both drugs were calculated by means of the program 'Matlab' software. The results obtained by these spectrophotometric methods were compared with the results of HPLC method.
提出了两种分光光度法和高效液相色谱法用于同时分析片剂制剂中的咖啡因和对乙酰氨基酚。比率光谱导数法基于在比率光谱的一阶导数中,分别在267.9和291.0 nm处测定咖啡因的分析信号以及在237.0和251.8 nm处测定对乙酰氨基酚的分析信号。咖啡因的校准曲线在4 - 40μg/ml范围内制备,对乙酰氨基酚的校准曲线在8 - 48μg/ml范围内制备。在菲尔奥德特法中,在零阶光谱中于242.9和273.0 nm处测定对乙酰氨基酚和咖啡因的A1(1)(1%,1cm)值。编写了A1(1)(1%,1cm)值的矩阵,并通过“Matlab”软件程序计算两种药物的含量。将这些分光光度法获得的结果与高效液相色谱法的结果进行了比较。