The pharmaceutical properties of clarithromycin (CAM) tablets containing the metastable
form I of crystalline CAM were investigated. Although the dissolution rate of form I was higher …

The purpose of this study is to improve in vitro dissolution and in vivo bioavailability of the
poorly soluble drug cilostazol (CLT) through amorphous solid dispersion technology, and …

Purpose: To develop simple, rapid and selective spectrophotometric methods for the
determination of cilostazol in tablet dosage form. Methods: Cilostazol was dissolved in 50 …

The cocrystal of celecoxib and nicotinamide (Cel: Nic) was crystallized from chloroform in a
1: 1 ratio, and the structure has been solved from powder X-ray diffraction data. The …

Variations in the physico-chemical properties of ketoconazole have been studied, following
polymorphic changes caused by fusion-cooling processes or by recrystallization in solvents …

The objective of the present study was to alter the crystal habit of itraconazole (ITZ) by
cooling and anti-solvent crystallization and characterize its properties. ITZ was recrystallized …

The aim of this study was to improve wettability and dissolution rate of a poorly water-soluble
drug, cilostazol, using the supercritical antisolvent (SAS) process. The solid state of particles …

A simple, selective, precise and stability-indicating high-performance liquid-
chromatographic method of analysis of cilostazol in pharmaceutical dosage form was …

Crystal structure prediction (CSP) is an invaluable tool in the pharmaceutical industry
because it allows to predict all the possible crystalline solid forms of small-molecule active …

Cilostazol is being developed for the treatment of intermittent claudication due to peripheral
arterial disease (PAD). This study was conducted to investigate the effects of age and …