DEVELOPMENT AND VALIDATION STUDIES OF ZONISAMIDE BY RP-HPLC METHOD IN CAPSULE DOSAGE FORM
Bhagyashree Gaikwad*, Rashmi Wani and Shriram H. Bairagi
ABSTRACT
To develop simple, accurate, precise and cost effective UV-VIS Spectrophotometric method for the estimation of Zonisamide in bulk and pharmaceutical dosage form. Zonisamide is used to treat angina Pectoris. The solvent used was Methanol and the λmax or the absorption maxima of the drug was found to be 287nm. Zonisamide was subjected to stress degradation under different conditions recommended by ICH. The sample so generated was used for degradation studies using the developed method. A linear response was observed in the range of 5-35μg/ml with a regression coefficient of 0.998. The method was then validated for different parameters as per
the ICH guidelines. The stress degradation studies showed that Zonisamide undergoes degradation in acidic, oxidative and alkaline conditions whereas it is relatively stable to neutral. This method can be used for the determination of Ivabradine in quality control of formulation without interference of the excipients.
Keywords: Zonisamide, UV, Validation and Linearity.
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