2016Asian Journal of Pharmaceutical AnalysisRequires access

Development and Validation of analytical method for Simultaneous estimation of Ornidazole and Cefixime trihydrate tablet dosage forms by UV spectroscopy

Saravanan Selvakumar, Subramanian Ravichandran, L. Matsyagiri

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Abstract

A simple, specific, accurate, precise and economic Simultaneous spectrophotometric method in UV region have been developed for the determination of Ornidazole and Cefixime in bulk and pharmaceutical tablet formulations. The optimum conditions for the analysis of the drug were established. Linearity was found over the concentration range of 5–30 μg/ml for Ornidazole and 2–20 μg/ml for Cefixime. The Simultaneous UV method has been successfully applied for the analysis of drugs in tablet formulation. The results of the tablet analysis were in the range of 99.57 to 100.2% for Ornidazole and 99.25 to 100.8% for Cefixime, which indicated repeatability of the method. The percentage recoveries were found be 100.3% for both the drugs indicated that the Simultaneous UV method is precise and reproducible. The Ruggdness Interday variation were found be in mean of 100.25 for Ornidazole and 99.85 for Cefixime. The Ruggedness Intraday Variation were found be in mean of 100.2 for Ornidazole and 100.18 for Cefixime.

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What this paper is about

A simple, specific, accurate, precise and economic Simultaneous spectrophotometric method in UV region have been developed for the determination of Ornidazole and Cefixime in bulk and pharmaceutical tablet formulations. The optimum conditions for the analysis of the drug were established. Linearity was found over the concentration range of 5–30 μg/ml for Ornidazole and 2–20 μg/ml for Cefixime. The Simultaneous UV method has been successfully applied for the analysis of drugs in tablet formulation. The results of the tablet analysis were in the range of 99.57 to 100.2% for Ornidazole and 99.25 to 100.8% for Cefixime, which indicated repeatability of the method. The percentage recoveries were found be 100.3% for both the drugs indicated that the Simultaneous UV method is precise and reproducible. The Ruggdness Interday variation were found be in mean of 100.25 for Ornidazole and 99.85 for Cefixime. The Ruggedness Intraday Variation were found be in mean of 100.2 for Ornidazole and 100.18 for Cefixime.

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Available abstract

A simple, specific, accurate, precise and economic Simultaneous spectrophotometric method in UV region have been developed for the determination of Ornidazole and Cefixime in bulk and pharmaceutical tablet formulations. The optimum conditions for the analysis of the drug were established. Linearity was found over the concentration range of 5–30 μg/ml for Ornidazole and 2–20 μg/ml for Cefixime. The Simultaneous UV method has been successfully applied for the analysis of drugs in tablet formulation. The results of the tablet analysis were in the range of 99.57 to 100.2% for Ornidazole and 99.25 to 100.8% for Cefixime, which indicated repeatability of the method. The percentage recoveries were found be 100.3% for both the drugs indicated that the Simultaneous UV method is precise and reproducible. The Ruggdness Interday variation were found be in mean of 100.25 for Ornidazole and 99.85 for Cefixime. The Ruggedness Intraday Variation were found be in mean of 100.2 for Ornidazole and 100.18 for Cefixime.

Key concepts: Ornidazole, Cefixime, Biomedical engineering, Dosage form, Ultraviolet visible spectroscopy, Chromatography, Mathematics, Materials science

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