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 …
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 …
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
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 …
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 …
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
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 …
delivery systems (SDDS) for poorly water-soluble drugs to improve their bioavailability. As a …
Supersaturated controlled release matrix using amorphous dispersions of glipizide
Spray dried dispersions (SDDs) of glipizide, a BCS Class II model drug, were prepared
using various grades of hydroxypropyl methylcellulose acetate succinate (HPMCAS) and …
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 …
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 …
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 …
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 …
range of the gastrointestinal tract. This often leads to a high in vivo variability and …