Journal :   Asian Journal of Research in Chemistry

Volume No. :   4

Issue No. :  11

Year :  2011

Pages :   1685-1687

ISSN Print :  0974-4169

ISSN Online :  0974-4150


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Development and Validation of RP-HPLC Method for the Estimation of Gemifloxacin Mesylate in Bulk and Pharmaceutical Dosage Forms



Address:   Khan Hajera*, Mirza Shahed Baig, Zahid Zaheer and Khan Nazia
Y.B. Chavan College of Pharmacy, Rauza Baugh, Aurangabad.
*Corresponding Author
DOI No:

ABSTRACT:
A reverse phase high performance liquid chromatography (RP-HPLC) has been developed for the estimation of Gemifloxacin mesylate in bulk drug and pharmaceutical dosage form. The quantification was carried out using C18 column (250mm × 4.6mm i.d, 5 mm) in an isocratic mode with a mobile phase consisting of methanol: 7% formic acid (80:20v/v), pH was adjusted to 2.1, at a flow rate of 1 ml/min. The separation was performed at ambient temperature and detection was carried out at 260nm. The retention time of the drug was found to be 2.36min and method produced linear response in the concentration range of 10-60 µg/ml (R~0.9991). As per ICH guidelines, the method was validated for linearity, precision, accuracy, LOD, LOQ and robustness for bulk drug and pharmaceutical dosage form.
KEYWORDS:
Gemifloxacin mesylate, RP-HPLC method, validation.
Cite:
Khan Hajera, Mirza Shahed Baig, Zahid Zaheer, Khan Nazia. Development and Validation of RP-HPLC Method for the Estimation of Gemifloxacin Mesylate in Bulk and Pharmaceutical Dosage Forms. Asian J. Research Chem. 4(11): Nov., 2011; Page 1685-1687.
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