ISSN: 2157-7064
+44 1300 500008
Harikrishna KA
India
Research Article
Development and Validation of a Novel Stability Indicating UPLC Method
for Dissolution Analysis of Bexarotene Capsules: An Anti Cancer Drug
Author(s): Venkata Subba Rao D, Raghuram P and Harikrishna KA
Venkata Subba Rao D, Raghuram P and Harikrishna KA
A novel stability indicating liquid chromatographic method for dissolution analysis of Bexarotene capsules, 75 mg has been developed and validated. Efficient chromatographic separation was achieved on a C18 column (50 mm × 2.1 mm, 1.7-μm particles) with a simple isocratic mobile-phase at a flow rate of 1.0 mL min−1. Quantification was achieved by use of ultraviolet detection at 260 nm. After the determination of the solubility the conditions selected were paddle at 50 RPM, with 900 mL of 0.5% HDTMA (hexadecyltrimethylammonium bromide) in 0.05 M phosphate buffer, pH adjusted to 7.5 with 1 N Sodium hydroxide at 37°C ± 0.5°C. Under these conditions the in vitro release profile of Bexarotene capsules, 75 mg shown good results. The drug release was evaluated by Reverse phase HPLC using mixture of Acetonitrile, water and trifluro acetic acid 70:30:0.1 (v/v/v). .. View More»
DOI:
10.4172/2157-7064.1000364