The aim of this study was to enhance the kinetic solubility and dissolution rate of ibuprofen
by co-milling with different excipients and to establish the underlying mechanism (s) for such …

The wetting and dissolution of a BCS class II drug (Ibuprofen) is enhanced by solventless
solid dispersion technique using co-milling. The co-milling is performed in a planetary ball …

Co-milling of a drug with a co-former is an efficient technique to improve the solubility of
drugs. Besides the particle size reduction, the co-milling process induces a structural …

To improve its solubility, dissolution, and bioavailability; Ibuprofen–polyethylene glycol 8000
(PEG 8000) solid dispersions (SDs) with different drug loadings were prepared …

Ibuprofen: Eudragit coprecipitates were prepared in 10: 3 ratios and their physical properties
and related dissolution characteristics were determined. The Eudragit polymers used for the …

In this work the effects of citric acid and of two common fillers, lactose (soluble) and
tricalcium phosphate (insoluble) are examined on the release profiles from pellets, using …

To improve its oral absorption, rapidly dissolving ibuprofen solid dispersions (SD) were
prepared in a relatively easy, simple, quick, inexpensive, and reproducible manner …

This study investigates the effects of a variety of coating materials on the flowability and
dissolution of dry-coated cohesive ibuprofen powders, with the ultimate aim to use these in …

The influence of cellulose ether derivatives on ibuprofen release from matrix tablets was
investigated. Raman spectroscopy and differential scanning calorimetry (DSC) experiments …

This work investigates the possibility of increasing the dissolution properties of ibuproxam (a
poorly water‐soluble anti‐inflammatory drug) using hydrophilic carriers such as …