Hasanuddin University

Validation of analysis method for determining ketoprofen concentration in pharmaceutical dosage form using high performance liquid chromatography

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dc.contributor.author Naid, Tadjuddin
dc.contributor.author Syukur, WR
dc.contributor.author Ilyas, Amran
dc.contributor.author Dali, Seniwati
dc.contributor.author Hamzah, Baharuddin
dc.date.accessioned 2013-09-24T05:52:51Z
dc.date.available 2013-09-24T05:52:51Z
dc.date.issued 2013-09-24
dc.identifier.issn 2153‐2249
dc.identifier.uri http://repository.unhas.ac.id/handle/123456789/6460
dc.description.abstract 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 en_US
dc.subject Conformity Optimization Ketoprofen Phosphate buffer Validation method High performance liquid chromatography en_US
dc.title Validation of analysis method for determining ketoprofen concentration in pharmaceutical dosage form using high performance liquid chromatography en_US
dc.UNHAS.email seniwatid@gmail.com en_US
dc.UNHAS.Fakultas MIPA en_US
dc.UNHAS.Prodi KIMIA en_US
dc.UNHAS.idno 195812311988032003 en_US


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