Solid carriers for improved solubility of glipizide in osmotically controlled oral drug delivery system

A Mehramizi, B Alijani, M Pourfarzib… - Drug development …, 2007 - Taylor & Francis
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 …

Fabrication and optimization of novel glipizide sustained release matrices for solubility and dissolution enhancement by solid dispersion through hydrophillic carriers

MA Shende, PV Fiske - Journal of Drug Delivery and Therapeutics, 2017 - jddtonline.info
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 …

Development of controlled release osmotic pump tablet of glipizide solid dispersion

GC Patel, KV Asodaria, HP Patel… - Current drug …, 2014 - ingentaconnect.com
Purpose: To develop controlled release osmotic pump tablets (COPT) of glipizide (GZ) solid
dispersion (SD). Methods: In elementary osmotic pump (EOP) tablets, an osmotic core with …

[HTML][HTML] Formulation and characterization of glipizide solid dosage form with enhanced solubility

BS Alotaibi, MA Khan, K Ullah, H Yasin, A Mannan… - Plos one, 2024 - journals.plos.org
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 …

Development and optimization of multi-unit solid dispersion systems of poorly water soluble drug

G Tiwari, R Tiwari, B Srivastava… - Research Journal of …, 2008 - indianjournals.com
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 …

[PDF][PDF] Comparative dissolution study of glipizide by solid dispersion technique

MHG Dehghan, M Saifee… - Journal of pharmaceutical …, 2010 - academia.edu
The aim of this study was to increase the solubility and dissolution of Glipizide in water by
solid dispersion. The solid dispersion of glipizide was prepared using water soluble carriers …

Development and evaluation of osmotically controlled oral drug delivery system of glipizide

RK Verma, S Garg - European journal of pharmaceutics and …, 2004 - Elsevier
Extended release formulation of glipizide based on osmotic technology was developed and
evaluated. The effect of different formulation variables, namely, level of solubility modifier in …

[PDF][PDF] Preparation and in vitro characterization of a non-effervescent floating drug delivery system for poorly soluble drug, glipizide

VS Meka, S Pillai, SR Dharmalingham, R Sheshala… - Acta Pol. Pharm, 2015 - ptfarm.pl
The aim of the present study was to formulate a non-effervescent floating drug delivery
system of glipizide, a poorly water soluble drug. The solubility of glipizide was initially …

Cyclodextrin complex osmotic tablet for glipizide delivery

Y Gan, W Pan, M Wei, R Zhang - Drug development and industrial …, 2002 - Taylor & Francis
Poorly soluble glipizide was selected as the model drug to prepare osmotic pump tablets
(OPT) with proper accessorial material after it was made an inclusion complex by kneading …

Formulation and evaluation of glimepiride solid dispersion tablets

B Gill, T Kaur, S Kumar… - Asian Journal of …, 2010 - asiapharmaceutics.info
Glimepiride (GMP) is poorly water soluble drug, so solubility is the main constraint for oral its
bioavailability. An attempt has been made to increase the solubility of this model drug by …