Validation of analysis method for determining ketoprofen concentration in pharmaceutical dosage form using high performance liquid chromatography
Tadjuddin Naid (1) , Wahyu Rizandi Syukur (2) , Amran Ilyas (3) , Seniwati Dali (4) , Baharuddin Hamzah (5,*)
(1) Faculty of Pharmacy, Hasanuddin University, Makassar, 90245, Indonesia
(2) Faculty of Pharmacy, Hasanuddin University, Makassar, 90245, Indonesia
(3) Faculty of Pharmacy, Hasanuddin University, Makassar, 90245, Indonesia
(4) Chemistry Department, Faculty of Mathematics and Natural Sciences, Hasanuddin University, Makassar, 90245, Indonesia
(5) Chemistry Education Study Program, Faculty of Teacher Training and Education, Tadulako University, Palu, 94118, Indonesia
(*) Corresponding Author
Received: 14 Sep 2012, Accepted: 02 Nov 2012, Published: 31 Mar 2013
The study was conducted with the purpose to develop and validate a high performance liquid chromatography method with UV detector to determine ketoprofen content in tablet preparation using ethanol-phosphate buffer (pH = 6.0, 80:20, v:v). The method was validated toward parameters of accuracy, precision, linearity, selectivity, LOD and LOQ. The results obtained fulfill the validation requirement of the ketoprofen tablet in the form of LOD = 0.5302 ppm and LOQ = 1.7676 ppm.
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DOI Link: https://doi.org/10.5155/eurjchem.4.1.58-60.678
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