Ebastine (EBS) is a non-sedating antihistamine with long duration of action. This drug has predominantly hydrophobic property causing low solubility and bioavailability. Surface solid dispersions (SSD) an effective technique for improving the dissolution rate poorly soluble drugs by using hydrophilic water insoluble carriers.
 The present study aims to enhance EBS surface dispersion techni...

The objective of this investigation was to prepare orodispersible tablets (ODTs) of ondansetron HCl using a direct compression method. A combination of glycine and chitosan was used as a disintegrating system and these tablets were compared for mechanical strength and disintegration time with those containing superdisintegrants. The Plackett-Burman screening design was used to screen the indepe...

The disintegration process of pharmaceutical tablets is a crucial step in the oral delivery drug. Tablet does not only refer to break up interparticle bonds, but also relates liquid absorption and swelling behaviour tablet. This study demonstrates use sessile drop method coupled with image processing models analyse surface kinetics four filler combinations (microcrystalline cellulose (MCC)/mann...

The purpose of the study was to formulate immediate release tablets using various types of disintegrants (crospovidone, sodium starch glycolate and sodium carboxymethylcellulose), in order to investigate the effect of mode of incorporation (intragranular, extragranular, intra and extragranularly) of disintegrants on release mechanism from tablets. Flecainide acetate, a class IC anti-arrhythmic ...

Diabetes mellitus (DM) and hypertension are two common diseases that often coexist. The most common cause of death in the diabetic patient is heart disease. In the present investigation we combine Nebivolol and Nateglinide for better patient compliance. IR layer was formulated using various superdisintegrants like Crospovidone, Croscarmellose sodium, and sodium starch glycolate and SR layer was...

A potent non-sulfhydryl prodrug, trandolapril is transformed into the active substance, trandolaprilat, in liver. For obese individuals with mild-to-moderate essential hypertension, Trandolapril effective and safe. The elimination t1/2 of trandolaprilat are approximately 6 hours 16–24 hours, respectively. goal present work to develop immediate release tablet using various superdisintegrants. Cr...

Quetiapine (QT) is a short acting atypical antipsychotic drug effective in schizophrenia and bipolar disorder. This study aims at designing a novel dosage form of sustained release taste-masked QT orally disintegrating tablets (ODTs) based on solid lipid micro-pellets (SLMPs). QT SLMPs were prepared using the hot melt extrusion technique and utilizing three lipid carriers: Compritol, Precirol a...