RP-HPLC and UV-derivative spectrophotometry technique for the
simultaneous estimation of ibuprofen and famotidine in pharmaceutical
dosage form
A Reversed Phase High Performance Liquid Chromatography and UV ̢̮Ãâââ¬Ãâââ¬Å Derivative Spectrophotometric method has
been developed for the simultaneous estimation of Famotidine and Ibuprofen in Pharmaceutical dosage forms. For
RP ̢̮Ãâââ¬Ãâââ¬Å HPLC method, Methanol and 25 mM Heptane Sulfonate Sodium were selected as mobile phase at a flow rate
of 1 ml/min using gradient elution. The detection wavelength was set at 267 nm. The responses were linear in the
range of 1- 8 ÃÆÃ Â½Ãâüg/ml for Famotidine and 40 ̢̮Ãâââ¬Ãâââ¬Å 180 ÃÆÃ Â½Ãâüg/ml for Ibuprofen. The correlation coefficient for both drugs was
0.9991. The percentage recovery of Ibuprofen was 99.72 ̢̮Ãâââ¬Ãâââ¬Å 101.8 % and that of Famotidine was 98.2 ̢̮Ãâââ¬Ãâââ¬Å 99.33%. The
% RSD for the precision studies was below 2%. The UV method was developed in derivative mode setting the
detection wavelength for each drug at zero crossing points of the other. Famotidine was analyzed at 226 nm and
Ibuprofen at 244 nm. The linearity range for Famotidine is 2- 16 ÃÆÃ Â½Ãâüg/ml with a correlation coefficient of 0.9989 and
that of Ibuprofen is 80 ̢̮Ãâââ¬Ãâââ¬Å 280 ÃÆÃ Â½Ãâüg/ml with correlation coefficient of 0.9994. The percentage recovery for Ibuprofen
was 98.9 ̢̮Ãâââ¬Ãâââ¬Å 102.2 and Famotidine was 98.25 ̢̮Ãâââ¬Ãâââ¬Å 99.95 % and the % RSD for the precision studies was below 2%.Both
methods are reliable, accurate and precise and can be adopted for routine analysis. Author(s): V. Rajani Sekhar, Y. Padmanabha Reddy, P. Ramalingam and D. Harihara Theja Abstract |
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