Modified gum karaya (MGK), a recently developed excipient was evaluated as carrier for
dissolution enhancement of poorly soluble drug, nimodipine (NM). The advantages of MGK …

Glyburide is a poorly water‐soluble oral hypoglycemic agent, with problems of variable
bioavailability and bio‐inequivalence related to its poor water‐solubility. This work …

Solid dispersions of PEG6000 and loperamide—a poorly water-soluble agent—were
prepared by spray drying. Their physicochemical properties were evaluated immediately …

The aim of the present study was to prepare controlled-release tablets of poorly-soluble
drug, felodipine, and various erodable lipophilic excipients. Spray chilling was used to …

The aim of the present study was to prepare controlled-release tablets of poorly-soluble
drug, felodipine. Spray chilling was used to formulate the drug, the polar lipids and the …

This work describes a new approach to prepare solvent-free solid dispersions (SDs) for
Nimesulide (NMS), involving the use of microwaves irradiation (MW). In particular, the …

The physicochemical properties of spray dried micro-complexes of cefuroxime axetil (CFA)
with hydroxypropyl-β-cyclodextrin (HPβCD) in presence and/or absence of ternary …

A number of trained models based on the Jouyban-Acree model were proposed for
prediction of naproxen (NAP) solubility in the cosolvency systems. The predictive cosolvency …

The aim of this study was to investigate the effect of the presence of the water-soluble
polymer polyethylene glycol (PEG)—MW= 35000g/mol—on the complexation of the …

Purpose: Naproxen CR tablets have been obtained from its microspheres prepared by
coprecipitation with Eudragit L100-55. The purpose of this work was to evaluate the main …