Document Type : Research Paper
Department of Chemistry, Holy Cross College (Autonomous), Affiliated to Bharathidasan University, Trichy-1, Tamil Nadu, India
Department of Chemistry, Faculty of Science, University of Botswana, Private Bag UB 00704 Gaborone, Botswana
Method validated using (RP-HPLC) reversed-phase high-performance liquid chromatographic method of this research was four selected Anti-Cancer standards. The newly developed method is novel, simple, precise, accurate, reproducible and less time consuming and it can be used for raw material of quantitative analysis and quality control. The separation of Rutin, Chrysin, Piperin and Berberine was conducted in less than 3 minutes and chromatographic separation was achieved using a stationary phase C18 J’Sphere column (internal diameter150 mm x 4.6 mm and particle size 4µ) and mobile phase contained acetonitrile: 0.1% formic acid (pH 2.7 ) in isocratic elution of (85:15 v/v) ratio, with a flow rate of 1mL/min and column temperature was maintained at 30 ̊ C with injection volume 20 µl, UV detection wavelength of at 336 nm were used.
Rutin, Chrysin, Piperine and Berberine had retention times of 1.3, 1.8, 2.1 and 2.6 minutes, respectively. Calibration curves were accepted and reported good linear correlation coefficients (r2 ˃ 0.999) within the range of 1-3.5µg/mL. Mean percent recoveries for the standards were found to be within the acceptance limits (80-115%). Relative standard deviation (according to FDA and ICH guidelines) which indicates the method is precise. The developed method was applied in various medicinal plants Solanum aculeastrum dunal, Elephantorrhiza elephantina, Cadaba aphylla (Thunb) and Adenia glauca used to manage by traditional doctors in Botswana. All three plants were reported Rutin and Chrysin compounds except S. aculeastrum, it was reported only Rutin present whereas, Piperine and Berberine was not detected in all four plants.