Development and characterization of fast-dissolving tablet formulations of glyburide based on solid self-microemulsifying systems

M Cirri, A Roghi, M Valleri, P Mura - European Journal of Pharmaceutics …, 2016 - Elsevier
The aim of this work was to develop effective fast-dissolving tablet formulations of glyburide,
endowed with improved dissolution and technological properties, investigating the actual …

Fast-dissolving tablets of glyburide based on ternary solid dispersions with PEG 6000 and surfactants

M Cirri, F Maestrelli, G Corti, P Mura, M Valleri - Drug delivery, 2007 - Taylor & Francis
Marketed glyburide tablets present unsatisfying dissolution profiles that give rise to variable
bioavailability. With the purpose of developing a fast-dissolving tablet formulation able to …

New solid self-microemulsifying systems to enhance dissolution rate of poorly water soluble drugs

P Mura, M Valleri, M Cirri, N Mennini - Pharmaceutical …, 2012 - Taylor & Francis
Context: An adequate drug dissolution behavior is essential for the therapeutic effectiveness
of all solid dosage forms. Objective: To develop a new solid self-micro-emulsifying drug …

Formulation of spray congealed microparticles with self-emulsifying ability for enhanced glibenclamide dissolution performance

B Albertini, MD Sabatino, C Melegari… - Journal of …, 2015 - Taylor & Francis
Purpose: To develop a novel preparation approach of solid Self-Emulsifying Drug Delivery
System (s-SEDDS) based on spray congealing as potential drug delivery technology for …

Development of a solid self-microemulsifying drug delivery system (SMEDDS) for solubility enhancement of naproxen

K Čerpnjak, A Zvonar, F Vrečer… - Drug development and …, 2015 - Taylor & Francis
Context: Comparative evaluation of liquid and solid self-microemulsifying drug delivery
systems (SMEDDS) as promising approaches for solubility enhancement. Objective: The …

Development and evaluation of glyburide fast dissolving tablets using solid dispersion technique

M Valleri, P Mura, F Maestrelli, M Cirri… - Drug development and …, 2004 - Taylor & Francis
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 …

Development of glyburide fast-dissolving tablets based on the combined use of cyclodextrins and polymers

M Cirri, MF Righi, F Maestrelli, P Mura… - Drug development and …, 2009 - Taylor & Francis
Commercial tablets of glyburide exhibit unsatisfactory dissolution profiles and, consequently,
problems of bioinequivalence and poor bioavailability. The aim of this work was to develop …

Granulated colloidal silicon dioxide-based self-microemulsifying tablets, as a versatile approach in enhancement of solubility and therapeutic potential of anti-diabetic …

V Pandey, RM Gilhotra, S Kohli - Drug Development and Industrial …, 2017 - Taylor & Francis
The current research work was executed with an aim to explore and promote the potential of
self-microemusifying drug delivery systems (SMEDDS) in the form of tablets, in order to …

Solid self microemulsifying drug deliviry system: a review

B Sanghai, G Aggarwal, SL HariKumar - Journal of Drug Delivery …, 2013 - jddtonline.info
Oral route still remains the favorite route of drug administration in many diseases and till
today it is the first way investigated in the development of new dosage forms. The major …

Stability‐Enhanced Ternary Solid Dispersions of Glyburide: Effect of Preparation Method on Physicochemical Properties

L Barghi, A Vekalati, A Jahangiri - … in Pharmacological and …, 2023 - Wiley Online Library
Introduction. Limited aqueous solubility and subsequent poor absorption and low
bioavailability are the main challenges in oral drug delivery. Solid dispersion is a widely …