The present research work was to improve the dissolution rate of glipizide which belongs to
BCS II drug by enhancing its aqueous solubility using different hydrophilic carriers like PEG …

The aim of this study was to increase the solubility and dissolution of glipizide-a practically
water insoluble drug. To achieve complete drug release, various batches of solid dispersion …

The aim of this research was to design and evaluate a hydrophilic matrix system for
sustained release of glipizide, a weakly acidic poor soluble drug. A combination of inclusion …

Glipizide, a poor water-soluble drug belongs to BCS class II. The proposed work aimed to
enhance the solubility of glipizide by preparing solid dispersions, using polyvinyl pyrrolidone …

The purpose of this study was to develop a new monolithic matrix system to completely
deliver glipizide, a Biopharmaceutics Classification System (BCS) Class II drug in a zero …

The purpose of this study was to increase the solubility of glipizide (gli) by solid dispersions
SDs technique with polyvinylpyrrolidone (PVP) in aqueous media. The gli–PVP solid …

Glipizide (GZ) is an oral blood-glucose-lowering drug of the sulfonylurea class characterized
by its poor aqueous solubility. Aiming for the production of GZ tablets with rapid onset of …

Glipizide is a class-II antidiabetic drug which is purely insoluble in water. Since only
dissolved drug can pass the gastro intestinal membrane, proper solubility of the drug is …

Glipizide (GPZ) and GPZ-HPC solid dispersion (SD) pellets were developed and
characterized for drug release mechanisms from a multi-unit erosion matrix system for …

ABSTRACT Objective: The Glipizide matrix tablet were prepared using different hydrophilic
polymers (HPMC different grades and sodium CMC) in various proportions as release …