Abstract:
A simple, selective, linear, precise and accurate UV-VIS method was
developed and validated for rapid assay of glibenclamide in
pharmaceutical dosage forms.
The validation parameter such as (linearity, precision, accuracy
detection limit, quantitation limit) was validated according to the
international conference of Harmonization.
In the linearity the regression equation found to be Y= 0.0575X with a
correlation coefficient R2 =09996
Statistical data reveals the method is accurate, selective and precise for
the quantitation of Glibenclamide.
The method was successfully applied for the routine analysis of
Glibenclamide in tablet dosage.