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Research Article Open Access
In this study, a new and rapid spectrofluorometry and UV spectrophotometry methods were developed for determination of flurbiprofen in pure and pharmaceutical preparations. The solvent system and wavelength of detection were optimized in order to maximize the sensitivity of both the proposed methods. The linearity was established over the concentration range of 50- 350 ng ml-1 for spectrofluorometry and 1-14 μg ml-1 for UV spectrophotometry method. The intra- and inter-day relative standard deviation (RSD) was less than 3.80 and 3.20% for spectrofluorometry and UV spectrophotometry, respectively. Limits of quantification (LOQ) were determined as 0.03 and 0.60 μg ml-1 for spectrofluorometry and UV spectrophotometry, respectively. No interference was found from tablet excipients at the selected assay conditions. Also, the methods were applied for the quality control of five commercial flurbiprofen dosage forms to quantify the drug and to check the formulation content uniformity.
Flurbiprofen, Spectrofluorometry, UV Spectrophotometry,Validation, Pharmaceutical Analysis