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Abstract

Development and validation of different ultraviolet-spectrophotometric methods for the estimation of besifloxacin in different simulated body fluids

Author(s): CL Singh1, A Singh1, S Kumar1, M Kumar2, PK Sharma3, DK Majumdar4
1R. V. Northland Institute, Chithera, Dadri, Gautam Budh Nagar-203 207, India 2KPS, Clinical Services, Greater Noida, Gautam Budh Nagar-201 306, India 3Galgotias University, Yamuna Expressway, Greater Noida, Gautam Budh Nagar-201 306, India 4Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar-III, New Delhi-110 017, India

Correspondence Address:
C L Singh R. V. Northland Institute, Chithera, Dadri, Gautam Budh Nagar-203 207 India E-mail: [email protected]


In the present study a simple, accurate, precise, economical and specific UV-spectrophotometric method for estimation of besifloxacin in bulk and in different pharmaceutical formulation has been developed. The drug shows maximum λmax 289 nm in distilled water, simulated tears and phosphate buffer saline. The linearity range of developed methods were in the range of 3-30 µg/ml of drug with a correlation coefficient (r2) 0.9992, 0.9989 and 0.9984 with respect to distilled water, simulated tears and phosphate buffer saline, respectively. Reproducibility by repeating methods as %RSD were found to be less than 2%. The limit of detection in different media was found to be 0.62, 0.72 and 0.88 µg/ml, respectively. The limit of quantification was found to be 1.88, 2.10, 2.60 µg/ml, respectively. The proposed method was validated statically according to International Conference on Harmonization guidelines with respect to specificity, linearity, range, accuracy, precision and robustness. The proposed methods of validation were found to be accurate and highly specific for the estimation of besifloxacin in different pharmaceutical formulations.



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