International Journal of Chemical and Analytical Science, Vol 1, No 7 (2010)
Spectrophotometric and Reversed-Phase High-Performance Liquid Chromatographic Method for the Determination of Doxophylline in Pharmaceutical Formulation
Abstract
Two methods described for determination of Doxophylline in solid dosage form. The first method was based on UV-Spectrophotometric determination of the drug. It involves absorbance measurement at 274 nm (lmax of Doxophylline) in 0.1 N Hydrochloric acid. Calibration curve was linear with the correlation coefficient between 0.99 to 1.0 over a concentration range of 0.20 to 30 mgmL-1 for the drug. The second method was based on HPLC separation of the drug in reverse phase mode using Hypersil ODS C18 column (250 X 4.6mm, 5mm). The mobile phase constituted of Buffer: Acetonitrile (80:20) and pH adjusted to 3.0 with dilute orthophosphoric acid was delivered at the flow rate 1.0 mL min-1. Detection was performed at 210 nm. Separation was completed within 7 min. Calibration curve was linear with the correlation coefficient between 0.99 to 1.0 over a concentration range of 0.165 to 30 mgmL-1 for the drug. The relative standard deviation (R.S.D) was found
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