Innovations in thermal processing: hot-melt extrusion and KinetiSol® dispersing

DK Tan, DA Davis Jr, DA Miller, RO Williams III… - Aaps Pharmscitech, 2020 - Springer
Thermal processing has gained much interest in the pharmaceutical industry, particularly for
the enhancement of solubility, bioavailability, and dissolution of active pharmaceutical …

Approaches to increase mechanistic understanding and aid in the selection of precipitation inhibitors for supersaturating formulations–a PEARRL review

DJ Price, F Ditzinger, NJ Koehl… - Journal of Pharmacy …, 2019 - academic.oup.com
Objectives Supersaturating formulations hold great promise for delivery of poorly soluble
active pharmaceutical ingredients (APIs). To profit from supersaturating formulations …

Biopharmaceutical understanding of excipient variability on drug apparent solubility based on drug physicochemical properties. Case study: Superdisintegrants

P Zarmpi, T Flanagan, E Meehan, J Mann, N Fotaki - The AAPS Journal, 2020 - Springer
The presence of different excipient types/brands in solid oral dosage forms may affect
product performance and drug bioavailability. Understanding the biopharmaceutical …

Supersaturation and Precipitation Applicated in Drug Delivery Systems: Development Strategies and Evaluation Approaches

Y Gan, JPA Baak, T Chen, H Ye, W Liao, H Lv, C Wen… - Molecules, 2023 - mdpi.com
Supersaturation is a promising strategy to improve gastrointestinal absorption of poorly
water-soluble drugs. Supersaturation is a metastable state and therefore dissolved drugs …

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 …

[HTML][HTML] Stability Studies of Amorphous Ibrutinib Prepared Using the Quench-Cooling Method and Its Dispersions with Soluplus®

I Mucha, B Karolewicz, A Górniak - Polymers, 2024 - mdpi.com
The successful development of an amorphous form of a drug demands the use of process
conditions and materials that reduce their thermodynamic instability. For the first time, we …

Application of a refined developability classification system

J Rosenberger, J Butler, U Muenster… - Journal of Pharmaceutical …, 2019 - Elsevier
Abstract In 2010, the Developability Classification System was proposed as an extension of
the Biopharmaceutics Classification System to align the classification system with the need …

Calculation of drug-polymer mixing enthalpy as a new screening method of precipitation inhibitors for supersaturating pharmaceutical formulations

DJ Price, A Nair, M Kuentz, J Dressman… - European Journal of …, 2019 - Elsevier
Supersaturating formulations are widely used to improve the oral bioavailability of poorly
soluble drugs. However, supersaturated solutions are thermodynamically unstable and such …

[PDF][PDF] Formulation and characterization of lafutidine nanosuspension for oral drug delivery system

NM Dawood, SN Abdal-Hamid - Int J App Pharm, 2018 - researchgate.net
Objective: The objective of this study was to prepare nanosuspension of a practical water
insoluble antiulcer drug which is lafutidine to enhance the solubility, dissolution rate with …

[PDF][PDF] Formulation and in vitro evaluation of amlodipine gastroretentive floating tablets using a combination of hydrophilic and hydrophobic polymers

AT Alhamdany, AK Abbas - Int J App Pharm, 2018 - academia.edu
Objective: The aim of this study was to formulate a developed floating tablet of amlodipine
using different concentrations and types of hydrophilic and hydrophobic polymers to be …