Objective: To develop and validate a simple, accurate, and precise HPLC method for the determination of caffeine in green coffee beans (Coffea arabica L.) from three districts of West Java, Indonesia.
Methods:The analytical method was conducted using Enduro C-18 (250 x 4.6 mm) column with methanol: water (37: 63) as a mobile phase, the flow rate was 1.0 ml/min, and the detector wavelength was set at 274 nm. The selectivity, linearity, limit of detection (LOD), limit of quantification (LOQ), accuracy, precision, and system suitability testing
Results:The retention time of caffeine was 6.36 min. % RSD for precision was 0.192. The linearity of the method was obtained using a concentration range of 1-200 ppm with the correlation coefficient of 0.998. The limit of detection was 9 ppm and the limit of quantitation was 28 ppm. The accuracy was in between were evaluated as the parameters of validation.
90.723%-102.853Conclusion: The proposed HPLC method meets the acceptance criteria of validation parameters and can be applied for routine analysis. %. Caffeine levels from Garut, Pangalengan, and Tasikmalaya were 1.454 ± 0.004%, 1.574 ± 0.082%, and 2.280 ± 0.004%.Caffeine (1,3,7-trimethylxanthine) is a central nervous system stimulant that prevents drowsiness, improves short-term memory, influences human circadian timing, and improves the effectiveness of particular drugs. It is an alkaloid which naturally found in the seeds, leaves or fruits of more than 63 plants species worldwide [1][2][3]. Caffeine is widely consumed by humans for many years as foods and beverages containing caffeine including coffee beverage [4][5][6]. The world's major source of caffeine is the coffee bean, that is the seed of the coffee plant [2]. I In nt te er rn na at ti io on na al l J Jo ou ur rn na al l o of f A Ap pp pl li ie ed d P Ph ha ar rm ma ac ce eu ut ti ic cs s