[HTML][HTML] Pharmaceutical amorphous solid dispersion: A review of manufacturing strategies

SV Bhujbal, B Mitra, U Jain, Y Gong, A Agrawal… - … Pharmaceutica Sinica B, 2021 - Elsevier
Amorphous solid dispersions (ASDs) are popular for enhancing the solubility and
bioavailability of poorly water-soluble drugs. Various approaches have been employed to …

Strategies to address low drug solubility in discovery and development

HD Williams, NL Trevaskis, SA Charman… - Pharmacological …, 2013 - ASPET
Drugs with low water solubility are predisposed to low and variable oral bioavailability and,
therefore, to variability in clinical response. Despite significant efforts to “design in” …

Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: formulation and process considerations

A Paudel, ZA Worku, J Meeus, S Guns… - International journal of …, 2013 - Elsevier
Spray drying is an efficient technology for solid dispersion manufacturing since it allows
extreme rapid solvent evaporation leading to fast transformation of an API-carrier solution to …

The use of amorphous solid dispersions: A formulation strategy to overcome poor solubility and dissolution rate

G Van den Mooter - Drug Discovery Today: Technologies, 2012 - Elsevier
The use of amorphous solid dispersions is an interesting strategy to increase the
bioavailability of poorly soluble drugs by improving their rate and extent of dissolution. Lack …

Evaluation of amorphous solid dispersion properties using thermal analysis techniques

JA Baird, LS Taylor - Advanced drug delivery reviews, 2012 - Elsevier
Amorphous solid dispersions are an increasingly important formulation approach to improve
the dissolution rate and apparent solubility of poorly water soluble compounds. Due to their …

Amorphous solid dispersions: utilization and challenges in drug discovery and development

Y He, C Ho - Journal of pharmaceutical sciences, 2015 - Elsevier
Amorphous solid dispersion (ASD) can accelerate a project by improving dissolution rate
and solubility, offering dose escalation flexibility and excipient acceptance for toxicology …

In vivo methods for drug absorption–comparative physiologies, model selection, correlations with in vitro methods (IVIVC), and applications for formulation/API …

E Sjögren, B Abrahamsson, P Augustijns… - European Journal of …, 2014 - Elsevier
This review summarizes the current knowledge on anatomy and physiology of the human
gastrointestinal tract in comparison with that of common laboratory animals (dog, pig, rat and …

Modification of physicochemical characteristics of active pharmaceutical ingredients and application of supersaturatable dosage forms for improving bioavailability of …

K Kawakami - Advanced drug delivery reviews, 2012 - Elsevier
New chemical entities are required to possess physicochemical characteristics that result in
acceptable oral absorption. However, many promising candidates need physicochemical …

pH-sensitive polymeric nanoparticles to improve oral bioavailability of peptide/protein drugs and poorly water-soluble drugs

XQ Wang, Q Zhang - European Journal of Pharmaceutics and …, 2012 - Elsevier
pH-sensitive polymeric nanoparticles are promising for oral drug delivery, especially for
peptide/protein drugs and poorly water-soluble medicines. This review describes current …

Taste masking of paracetamol by hot-melt extrusion: an in vitro and in vivo evaluation

M Maniruzzaman, JS Boateng, M Bonnefille… - European Journal of …, 2012 - Elsevier
The purpose of this study was the in vitro and in vivo evaluation of the masking efficiency of
hot melt extruded paracetamol (PMOL) formulations. Extruded granules containing high …