Preparation and characterization of dipyridamole solid dispersions for stabilization of supersaturation: effect of precipitation inhibitors type and molecular weight

C Vora, R Patadia, K Mittal… - Pharmaceutical …, 2016 - Taylor & Francis
Dipyridamole (DPL) is a weakly basic BCS class II drug which precipitates upon entering
into intestine leading to pH dependant and variable absorption. Thus, research envisaged …

Effects of tablet formulation and subsequent film coating on the supersaturated dissolution behavior of amorphous solid dispersions

T Sakai, D Hirai, S Kimura, Y Iwao, S Itai - International Journal of …, 2018 - Elsevier
The effects of tablet preparation and subsequent film coating with amorphous solid
dispersion (ASD) particles that were composed of a drug with poor water solubility and …

Comparison of induction methods for supersaturation: amorphous dissolution versus solvent shift

J Plum, CG Bavnhøj, JN Eliasen, T Rades… - European Journal of …, 2020 - Elsevier
Simple solvent shift is often used to induce supersaturation and investigate precipitation
kinetics in early drug development as a substitute for amorphous dissolution. This study …

[PDF][PDF] Investigating the effect of molecular weight of polyvinylpyrrolidone and hydroxypropyl methyl cellulose as potential antiprecipitants on supersaturated drug …

SP Chaudhari, RH Dave - International Journal of Pharmaceutical …, 2016 - researchgate.net
Most of the drug discovered in past decade belongs to biopharmaceutical classification
system (BCS) class II. The solubility of these drugs is the limiting factor for oral …

The opposed effects of polyvinylpyrrolidone K30 on dissolution and precipitation for indomethacin supersaturating drug delivery systems

W Wang, M Li, Q Yang, Q Liu, M Ye, G Yang - AAPS PharmSciTech, 2020 - Springer
Amorphous solid dispersions (ASD) are one of the most important supersaturating drug
delivery systems (SDDS) for poorly water-soluble drugs to improve their bioavailability. As a …

Supersaturated controlled release matrix using amorphous dispersions of glipizide

Z Lu, Y Yang, RA Covington, YV Bi, T Dürig… - International journal of …, 2016 - Elsevier
Spray dried dispersions (SDDs) of glipizide, a BCS Class II model drug, were prepared
using various grades of hydroxypropyl methylcellulose acetate succinate (HPMCAS) and …

Revealing the roles of polymers in supersaturation stabilization from the perspective of crystallization behaviors: A case of nimodipine

P Zhao, G Hu, H Chen, M Li, Y Wang, N Sun… - International Journal of …, 2022 - Elsevier
Formulating drugs into amorphous solid dispersions (ASDs) represents an attractive means
to enhance the aqueous solubility of drugs. Furthermore, water-soluble polymers have …

Understanding the generation and maintenance of supersaturation during the dissolution of amorphous solid dispersions using modulated DSC and 1H NMR

S Baghel, H Cathcart, NJ O'Reilly - International journal of pharmaceutics, 2018 - Elsevier
In this study, the dissolution behaviour of dipyridamole (DPM) and cinnarizine (CNZ) spray-
dried amorphous solid dispersions (ASDs) using polyvinyl pyrrolidone (PVP) and polyacrylic …

Effect of Surfactants, Gastric Emptying, and Dosage Form on Supersaturation of Dipyridamole in an in Vitro Model Simulating the Stomach and Duodenum

A Mitra, HM Fadda - Molecular pharmaceutics, 2014 - ACS Publications
The purpose of this study was to investigate the influence of gastric emptying patterns,
surfactants, and dosage form on the supersaturation of a poorly soluble weakly basic drug …

Site specific solubility improvement using solid dispersions of HPMC-AS/HPC SSL–Mixtures

DE Zecevic, R Meier, R Daniels, KG Wagner - European journal of …, 2014 - Elsevier
Many upcoming drug candidates are pH-dependent poorly soluble weak bases in the pH
range of the gastrointestinal tract. This often leads to a high in vivo variability and …