Assessing the interrelationship of microstructure, properties, drug release performance, and preparation process for amorphous solid dispersions via noninvasive …

W Jia, PD Yawman, KM Pandya, K Sluga, T Ng… - Pharmaceutical …, 2022 - Springer
Purpose The purpose of this work is to evaluate the interrelationship of microstructure,
properties, and dissolution performance for amorphous solid dispersions (ASDs) prepared …

[HTML][HTML] Advancing Drug Delivery Paradigms: Polyvinyl Pyrolidone (PVP)-Based Amorphous Solid Dispersion for Enhanced Physicochemical Properties and …

A Rusdin, A Mohd Gazzali, N Ain Thomas… - Polymers, 2024 - mdpi.com
Background: The current challenge in drug development lies in addressing the
physicochemical issues that lead to low drug effectiveness. Solubility, a crucial …

Production of nano-solid dispersions using a novel solvent-controlled precipitation process—Benchmarking their in vivo performance with an amorphous micro-sized …

Í Duarte, ML Corvo, P Serôdio, J Vicente… - European Journal of …, 2016 - Elsevier
A novel solvent controlled precipitation (SCP) process based on microfluidization was
assessed to produce solid dispersions of carbamazepine, a poorly water-soluble drug with …

Molecular-level examination of amorphous solid dispersion dissolution

MA Faiz Afzal, K Lehmkemper, E Sobich… - Molecular …, 2021 - ACS Publications
Amorphous solid dispersions (ASDs) are commonly used to orally deliver small-molecule
drugs that are poorly water-soluble. ASDs consist of drug molecules in the amorphous form …

Co-amorphous Drug Delivery Systems: a Review of Physical Stability, In Vitro and In Vivo Performance

Q Shi, Y Wang, SM Moinuddin, X Feng, F Ahsan - AAPS PharmSciTech, 2022 - Springer
Over the past few decades, co-amorphous solids have been used as a promising approach
for delivering poorly water-soluble drugs. Co-amorphous solids, comprising …

A mechanistic model for predicting the physical stability of amorphous solid dispersions

AT Ojo, PI Lee - Journal of Pharmaceutical Sciences, 2021 - Elsevier
In this paper, we establish a mechanistic model for the prediction of amorphous solid
dispersion (ASD) stability. The novel approach incorporates fundamental physical …

Refining stability and dissolution rate of amorphous drug formulations

H Grohganz, PA Priemel, K Löbmann… - Expert opinion on …, 2014 - Taylor & Francis
Introduction: Poor aqueous solubility of active pharmaceutical ingredients (APIs) is one of
the main challenges in the development of new small molecular drugs. Additionally, the …

Investigation into the solid-state properties and dissolution profile of spray-dried ternary amorphous solid dispersions: a rational step toward the design and …

S Baghel, H Cathcart, NJ O'Reilly - Molecular pharmaceutics, 2018 - ACS Publications
The formulation of oral amorphous solid dispersions (ASD) includes the use of excipients to
improve physical stability and enhance bioavailability. Combinations of excipients (polymers …

Relationship between amorphous solid dispersion in vivo absorption and in vitro dissolution: phase behavior during dissolution, speciation, and membrane mass …

V Wilson, X Lou, DJ Osterling, DF Stolarik… - Journal of controlled …, 2018 - Elsevier
Enzalutamide is a fast crystallizing, hydrophobic compound that has solubility limited
absorption in vivo. Given the low aqueous solubility of this compound, it was of interest to …

Regulatory considerations in development of amorphous solid dispersions

Z Rahman, A Siddiqui, A Gupta, M Khan - Amorphous Solid Dispersions …, 2014 - Springer
There is a growing interest in the pharmaceutical industry to develop amorphous solid
dispersions (ASDs) of poorly aqueous soluble drugs due to their higher supersaturation …