[PDF] Top 20 FORMULATION, EVALUATION AND DEVELOPMENT OF FAST RELEASE TABLETS OF ROSUVASTATIN CALCIUM USING SUBLIMATION METHOD

... optimized formulation of Rosuvastatin calcium (F10), and Marketed Formulation (Crestor) were carried out using male Wistar rats ...tablet formulation containing Complexation of ... See full document

... showed the highest swelling indices throughout the study period. This may be related to the high affinity of Xanthan gum containing matrices to the test medium. The maximum swelling index of this formula 243.69 was ... See full document

... stomach using propranolol hydrochloride as a model ...compressed using a single station rotary ...drug release from the tablet was controlled by the amount of HPMC in the sustained release ... See full document

... [r] ... See full document

... Finally, tablets of these powders were prepared by direct compression and wet granulation technique using tamarind gum (~3 %) as the ...tribasic calcium phosphate, magnesium stearate, and sodium ... See full document

... prepare fast dissolving tablets of Fosinopril with increased rate of dissolution may leads to increase ...The fast dissolving tablets of Fosinopril were prepared by using ... See full document

... and Rosuvastatin Calcium along with two amino acids is developed using Fenofibrate, Rosuvastatin Calcium, Microcrystalline Cellulose, Magnesium Stearate, Sodium Lauryl Sulfate, Cross ... See full document

... 16 Formulation, development and evaluation of immediate release tablets containing atorvastatin calcium drug was studied by Patel Dipika, Patel Vijayakumar 16 to develop ... See full document

... immediate release formulation of Atorvastatin calcium for oral drug delivery by using suitable concentration of ...the release of drug. Special care was taken for Atorvastatin ... See full document

... evaluate fast dissolving tablets of Rosuvastatin (BCS Class II drug) to enhance solubility, improve bioavailability and patient compliance especially for the paediatric and geriatric patients with ... See full document

... In-vitro Release Study: The United States Pharmacopeia (USP) XXIII rotating paddle method was used to study the drug release from the bilayered and multilayered ...The release study was ... See full document

... as tablets and capsules, are formulated to release the active drug immediately after oral administration, to obtain rapid and complete systemic drug ...and development of new drug ...Sustained ... See full document

... the fast dissolving tablets of ...by sublimation method. The tablets were evaluated for weight variation, hardness, wetting time, friability, water absorption ratio and disintegration ... See full document

... Five tablets were weighed individually, then placed in a mortar and powdered with a ...blank using UV-visible spectrophotometer (1700, Shimadzu, Kyoto, Japan) and drug content per tablet was ... See full document

... prepared tablets were shown good post compression parameters and they passed all the quality control evaluation parameters as per ...F1 formulation showed maximum % drug release ...drug ... See full document

... to release the medication in a prolonged rate to maintain plasma drug ...drug release profile in matrix systems by different ...sustained release had made a new phase for the novel drug delivery ... See full document

... When formulation F-3 is prepared by taking drug along with HPMC (E 15), HPC (M) and ethyl cellulose all the peaks corresponding to the four constituents were found to be present in its higher spectra indicating ... See full document

... matrix tablets as sustained release (SR) has given a new breakthrough for novel drug delivery system (NDDS) in the field of pharmaceutical ...drug release rate from the dosage form is controlled ... See full document

... a release modifier to develop Glimepiride sustained release ...sustain release properties of tamrind. These polymers were used as modifier using model drug ... See full document

... drug release over a prolonged period of time, reduction in systemic toxicity of drug, enhanced drug absorption due to longer residence time of nanoparticles on the corneal surface, higher drug concentrations in ... See full document