Controlled release film forming systems in drug delivery: the potential for efficient drug delivery

TTD Tran, PHL Tran - Pharmaceutics, 2019 - mdpi.com
Despite many available approaches for transdermal drug delivery, patient compliance and
drug targeting at the desired concentration are still concerns for effective therapies. Precise …

Solid dispersions: a strategy for poorly aqueous soluble drugs and technology updates

MA Alam, R Ali, FI Al-Jenoobi… - Expert opinion on drug …, 2012 - Taylor & Francis
Introduction: Present article reviews solid dispersion (SD) technologies and other patented
inventions in the area of pharmaceutical SDs, which provide stable amorphous SDs. Areas …

The use of zein in the controlled release of poorly water-soluble drugs

PHL Tran, W Duan, BJ Lee, TTD Tran - International journal of …, 2019 - Elsevier
Although zein is a natural protein derived from corn, it has attracted much interest in
pharmaceutical and biomedical sciences. Recent remarkable investigations on the use of …

Controlled release systems containing solid dispersions: strategies and mechanisms

PHL Tran, TTD Tran, JB Park, BJ Lee - Pharmaceutical research, 2011 - Springer
In addition to a number of highly soluble drugs, most new chemical entities under
development are poorly water-soluble drugs generally characterized by an insufficient …

Molecular interactions in solid dispersions of poorly water-soluble drugs

TTD Tran, PHL Tran - Pharmaceutics, 2020 - mdpi.com
Physicochemical characterization is a crucial step for the successful development of solid
dispersions, including the determination of drug crystallinity and molecular interactions …

Coamorphous active pharmaceutical ingredient–small molecule mixtures: considerations in the choice of coformers for enhancing dissolution and oral bioavailability

A Newman, SM Reutzel-Edens, G Zografi - Journal of pharmaceutical …, 2018 - Elsevier
In the recent years, coamorphous systems, containing an active pharmaceutical ingredient
(API) and a small molecule coformer have appeared as alternatives to the use of either …

Improving physicochemical properties and pharmacological activities of ternary co-amorphous systems

X Fang, Y Hu, G Yang, W Shi, S Lu, Y Cao - European Journal of …, 2022 - Elsevier
The formation of co-amorphous by combining low molecular weight compounds with drugs
is a relatively new technology in the pharmaceutical field, which can significantly improve …

Formulation of aripiprazole-loaded pH-modulated solid dispersions via hot-melt extrusion technology: In vitro and in vivo studies

H McFall, S Sarabu, V Shankar, S Bandari… - International journal of …, 2019 - Elsevier
The objective of this study was to formulate aripiprazole (ARI)-loaded pH-modulated solid
dispersions (SD) to enhance solubility, dissolution, and bioavailability via hot-melt extrusion …

Impact of excipient interactions on drug bioavailability from solid dosage forms

R Panakanti, AS Narang - Pharmaceutical research, 2012 - Springer
Excipients are generally pharmacologically inert, but can interact with drugs in the dosage
form and the physiological factors at the site of absorption to affect the bioavailability of a …

Risk assessment and QbD based optimization of an Eprosartan mesylate nanosuspension: In-vitro characterization, PAMPA and in-vivo assessment

P Shekhawat, V Pokharkar - International journal of pharmaceutics, 2019 - Elsevier
Quality by design (QbD) principles were implemented to understand the product and
process variables of sonoprecipitation technique, for preparation of eprosartan mesylate …