Development and Validation of Rp-hplc Method for the Estimation of Rosuvastatin Calcium in Bulk and Tablet Dosage Form
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چکیده
A validated simple, sensitive, specific and precise RP-HPLC method was developed for the determination of Rosuvastatin in pure and pharmaceutical formulations. Method was carried on Symmetry C18 column (100 X 4.6 mm i.d., particle size 3.5um,ACE) using acetontrile: phosphate buffer as mobile phase in the ratio of 60:40v/v/. The detection was carried out at 243nm using Waters (2659) UV-Visible detector.The proposed method obeyed linearity in the range of 20-60 μg/mL and met all specifications as per ICH guidelines. Statistical analysis revealed that this method can be used in routine quality control studies of Rosuvastatin in pure and its pharmaceutical formulations.
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تاریخ انتشار 2014