[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 …

Pharmaceutical dispersion techniques for dissolution and bioavailability enhancement of poorly water-soluble drugs

X Zhang, H Xing, Y Zhao, Z Ma - Pharmaceutics, 2018 - mdpi.com
Over the past decades, a large number of drugs as well as drug candidates with poor
dissolution characteristics have been witnessed, which invokes great interest in enabling …

Microwave-induced in situ amorphization: A new strategy for tackling the stability issue of amorphous solid dispersions

W Qiang, K Löbmann, CP McCoy, GP Andrews… - Pharmaceutics, 2020 - mdpi.com
The thermodynamically unstable nature of amorphous drugs has led to a persistent stability
issue of amorphous solid dispersions (ASDs). Lately, microwave-induced in situ …

Amorphization within the tablet: Using microwave irradiation to form a glass solution in situ

M Doreth, MA Hussein, PA Priemel, H Grohganz… - International Journal of …, 2017 - Elsevier
In situ amorphization is a concept that allows to amorphize a given drug in its final dosage
form right before administration. Hence, this approach can potentially be used to circumvent …

Quantification of microwave-induced amorphization of celecoxib in PVP tablets using transmission Raman spectroscopy

M Edinger, MM Knopp, H Kerdoncuff… - European Journal of …, 2018 - Elsevier
In this study, the influence of drug load on the microwave-induced amorphization of
celecoxib (CCX) in polyvinylpyrrolidone (PVP) tablets was investigated using quantitative …

Increased bioavailability of efonidipine hydrochloride nanosuspensions by the wet-milling method

S Huang, Q Zhang, H Li, Y Sun, G Cheng, M Zou… - European Journal of …, 2018 - Elsevier
The aim of this study was to improve the oral bioavailability of a practically insoluble drug,
efonidipine hydrochloride (EFH), by agglomeration in acid solution/gastric fluid. The EFH …

RP-HPLC method development and validation for the quantification of Efonidipine hydrochloride in HME processed solid dispersions

AS Rajput, DK Jha, S Gurram, DS Shah… - Future Journal of …, 2020 - Springer
Background Efonidipine hydrochloride (EFO) is a poorly water-soluble drug and, hence, has
poor bioavailability. Solid dispersions (SDs) of EFO using Eudragit EPO were prepared …

Improved drug transfer into brain tissue via the “nose-to-brain” approach using suspension or powder formulations based on the amorphous solid dispersion …

S Suwabe, T Tagami, K Ogawa, T Ozeki - European Journal of …, 2023 - Elsevier
Intranasal administration has attracted increasing attention as a drug delivery approach
based on nose-to-brain drug delivery from the nasal cavity to brain tissue directly, bypassing …

Effect of preparation method on the surface properties and UV imaging of indomethacin solid dispersions

K Asare-Addo, M Alshafiee, K Walton, A Ward… - European Journal of …, 2019 - Elsevier
This work explores the use of UV imaging in solid dispersion systems. Solid dispersions are
one of the common strategies used in improving the dissolution of poorly soluble drugs …

In Vitro-In Vivo Correlation for Solid Dispersion of a Poorly Water-Soluble Drug Efonidipine Hydrochloride

X Cheng, J Gao, J Li, G Cheng, M Zou, H Piao - AAPS PharmSciTech, 2020 - Springer
The aim of this present study was to investigate the ability of different dissolution methods to
predict the in vivo performance of efonidipine hydrochloride (EFH). The solid dispersions of …