Andere Kunden interessierten sich auch für
![Design and Development of Cefpodoxime Proxetil Dispersible Tablet]( "Design and Development of Cefpodoxime Proxetil Dispersible Tablet")
Design and Development of Cefpodoxime Proxetil Dispersible Tablet32,99 €![Formulation and Development of Dispersible Tablet and Dry Syrup]( "Formulation and Development of Dispersible Tablet and Dry Syrup")
Formulation and Development of Dispersible Tablet and Dry Syrup40,99 €![Formulation and Evaluation of Pantoprazole Sodium EC Tablets]( "Formulation and Evaluation of Pantoprazole Sodium EC Tablets")
Formulation and Evaluation of Pantoprazole Sodium EC Tablets42,99 €![Novel Co-Processed Superdisintegrants for Sublingual Tablets]( "Novel Co-Processed Superdisintegrants for Sublingual Tablets")
Novel Co-Processed Superdisintegrants for Sublingual Tablets36,99 €![Fast dissolving tablet of Metoprolol Tartrate using superdisintegrants]( "Fast dissolving tablet of Metoprolol Tartrate using superdisintegrants")
Fast dissolving tablet of Metoprolol Tartrate using superdisintegrants32,99 €![The Bioequivalence of Doxazosin Slow Release Tablets: A Pilot Study]( "The Bioequivalence of Doxazosin Slow Release Tablets: A Pilot Study")
The Bioequivalence of Doxazosin Slow Release Tablets: A Pilot Study44,99 €![Matrix Tablets: An Approach Towards Sustained Release Drug Delivery]( "Matrix Tablets: An Approach Towards Sustained Release Drug Delivery")
Matrix Tablets: An Approach Towards Sustained Release Drug Delivery36,99 €
The purpose of this research was to develop orodispersible tablet of fluoxetine hydrochloride. Fluoxetine hydrochloride is a selective serotonin reuptake inhibitor drug which is used in psychiatric disorder like depression. Orodispersible tablet prepared using various concentrations (1.5%, 3% & 4.5%) of superdisintegrates like crosscarmellose, crospovidone, sodium starch glycolate by wet granulation method & sublimation method. The preformulation studies by FTIR confirmed no interactions between drug and polymers. The prepared formulations were evaluated for the pre-compression parameters & the values were within prescribed limits. The tablets prepared by wet granulation & sublimation method were evaluated for physical parameters, wetting time, disintegration time, content uniformity and in vitro dissolution.Upon comparison sublimation method was showed good results for disintegration time ,wetting time & in vitro drug release studies because sublimation of camphor increases the porosity of the tablets. The tablets prepared with crospovidone at 4.5% concentration (FS-6) by sublimation method was found to be best suitable formulation.