Dr. Gampa Vijay Kumar*1, B. Sravanthi2, N. Swetha3
1Professor and Head, Dept. of Pharmacy, KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India.
2KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India.
3KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India.
A B S T R A C T
High performance liquid chromatography is at present one of the most sophisticated tool of the analysis. The estimation of Decitabine and Cedazuridine was done by RP-HPLC. The Phosphate buffer was pH 4.5 and the mobile phase was optimized with consists of Methanol: Phosphate buffer mixed in the ratio of PH 4.5(20:80 v/v). Kromosil C18 Column (250mm x 4.6mm) 5µg or equivalent chemically bonded to porous silica particles was used as stationary phase. The detection was carried out using UV detector at 254 nm. The solutions were chromatographed at a constant flow rate of 1 ml min-1. The linearity range of Decitabine and Cedazuridine were found to be from 100-500 mg/ml of Decitabine and 1-5mg/ml of Cedazuridine. Linear regression coefficient was not more than 0.999. The values of % RSD are less than 2% indicating accuracy and precision of the method. Decitabine %RSD 0.2 and Cedazuridine %RSD 0.6. Intermediate precision for Decitabine %RSD 0.2 and Cedazuridine %RSD 0.1. The percentage recovery varies from 98-102% of Decitabine and Cedazuridine. LOD and LOQ were found to be within limit. The results obtained on the validation parameters met ICH and USP requirements .it inferred the method found to be simple, accurate, precise and linear. The method was found to be having suitable application in routine laboratory analysis with high degree of accuracy and precision.
Keywords: Kromosil C18, Decitabine and Cedazuridine, RP-HPLC