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American Journal of Pharmacy and Health Research

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Development and Validation of a New UV Method for Analysis of Balofloxacin

Published in September 2013 Issue 6 (Vol. 1, Issue 6, 2013)

Development and Validation of a New UV Method for Analysis of Balofloxacin - Issue cover

Abstract

A new, rapid sensitive, simple and cost effective UV method was developed for the estimation of balofloxacin in bulk as well as in pharmaceutical formulations. The absorbance of balofloxacin was measured in 0.1N sodium hydroxide at new wave length (λmax 290). The linearity range was found to be 1-9 μg/ml.The method was tested and validated for various parameters as per ICH specification. The result demonstrates that the developed procedure is accurate, precise and reproducible. Proposed method is applicable for the estimation of balofloxacin in different dosage forms and results are in good agreement with label claim. Key words: Balofloxacin, 0.1N Sodium hydroxide, UV method.

Authors (1)

S. Malathi*1 T.Sivakumar

NANDHA College of Pharmacy, Er...

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Article Information

AJPHR16007

AJPHR-01-000007

2013-09-01

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Malathi*1, S., (2013). Development and Validation of a New UV Method for Analysis of Balofloxacin. American Journal of Pharmacy and Health Research, 1(6), xx-xx. https://ajphr.com/articles/AJPHR16007

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