Spectrophotometric and RP-HPLC methods for simultaneous estimation of ofloxacin and satranidazole from tablets
Rahul Keshav Godge, Leena R. Bhat, Asfak T. Vora, Mrinalini C. Damle
Abstract
Rahul Keshav Godge, Leena R. Bhat, Asfak T. Vora, Mrinalini C. Damle
Abstract
Two simple, accurate and sensitive validatedUVspectrophotometricmethods and one HPLC method for simultaneous estimation of ofloxacin and satranidazole in combined tablet dosage form has been developed. The first developed spectroscopic method employs ÂÂarea under curve using 292-296nmand 316-320nmfor estimation of ofloxacin and satranidazole, respectively. The second spectrophotometric method employedwas ÂÂDual wavelengthmethod using 300.2, 338.8nm for ofloxacin and 276.2, 307.6nm for satranidazole. BeerÂÂs law is obeyed in the concentration range of 2.0 to 20.0iÂg/mL-1 and 3.0 to 30iÂg/mL-1 of ofloxacin and satranidazole, respectively. DevelopedHPLCmethod is reverse-phase chromatographicmethod using Jasco HPLC systemwith HiQ Sil C18Wcolumn (250i´4.6mmi.d.), using acetonitrile: 0.005mol. L-1 tetra butyl ammoniumhydrogen sulphate 70:30 v/v as a mobile phase. The detection was carried out using UV detector set at 320nm. Clonazepamwas used as internal standard. BeerÂÂs law is obeyed in the concentration range of 2.0 to 30.0iÂg/mL-1 and 3.0 to 45iÂg/mL-1 of ofloxacin and satranidazole, respectively.All the three methods have been successfully applied for the analysis of drugs in pharmaceutical formulations. Results of analysis were validated statistically and by recovery studies.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Two simple, accurate and sensitive validatedUVspectrophotometricmethods and one HPLC method for simultaneous estimation of ofloxacin and satranidazole in combined tablet dosage form has been developed. The first developed spectroscopic method employs ÂÂarea under curve using 292-296nmand 316-320nmfor estimation of ofloxacin and satranidazole, respectively. The second spectrophotometric method employedwas ÂÂDual wavelengthmethod using 300.2, 338.8nm for ofloxacin and 276.2, 307.6nm for satranidazole. BeerÂÂs law is obeyed in the concentration range of 2.0 to 20.0iÂg/mL-1 and 3.0 to 30iÂg/mL-1 of ofloxacin and satranidazole, respectively. DevelopedHPLCmethod is reverse-phase chromatographicmethod using Jasco HPLC systemwith HiQ Sil C18Wcolumn (250i´4.6mmi.d.), using acetonitrile: 0.005mol. L-1 tetra butyl ammoniumhydrogen sulphate 70:30 v/v as a mobile phase. The detection was carried out using UV detector set at 320nm. Clonazepamwas used as internal standard. BeerÂÂs law is obeyed in the concentration range of 2.0 to 30.0iÂg/mL-1 and 3.0 to 45iÂg/mL-1 of ofloxacin and satranidazole, respectively.All the three methods have been successfully applied for the analysis of drugs in pharmaceutical formulations. Results of analysis were validated statistically and by recovery studies.
Key concepts: Ofloxacin, Chromatography, High-performance liquid chromatography, Acetonitrile, Chemistry, Biochemistry, Antibiotics, Ciprofloxacin