[HTML][HTML] Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems

BJ Boyd, CAS Bergström, Z Vinarov, M Kuentz… - European Journal of …, 2019 - Elsevier
Poorly water-soluble drugs continue to be a problematic, yet important class of
pharmaceutical compounds for treatment of a wide range of diseases. Their prevalence in …

Supersaturating drug delivery systems: the potential of co-amorphous drug formulations

R Laitinen, K Löbmann, H Grohganz, P Priemel… - International Journal of …, 2017 - Elsevier
Amorphous solid dispersions (ASDs) are probably the most common and important
supersaturating drug delivery systems for the formulation of poorly water-soluble …

Amorphous solid dispersions and the contribution of nanoparticles to in vitro dissolution and in vivo testing: Niclosamide as a case study

MO Jara, ZN Warnken, RO Williams III - Pharmaceutics, 2021 - mdpi.com
We developed an amorphous solid dispersion (ASD) of the poorly water-soluble molecule
niclosamide that achieved a more than two-fold increase in bioavailability. Notably, this …

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 …

In vitro methods to assess drug precipitation in the fasted small intestine – a PEARRL review

PJ O'Dwyer, C Litou, KJ Box… - Journal of Pharmacy …, 2019 - academic.oup.com
Objectives Drug precipitation in vivo poses a significant challenge for the pharmaceutical
industry. During the drug development process, the impact of drug supersaturation or …

Interplay of supersaturation and solubilization: lack of correlation between concentration-based supersaturation measurements and membrane transport rates in …

A Elkhabaz, DE Moseson, J Brouwers… - Molecular …, 2019 - ACS Publications
Supersaturating formulations are increasingly being used to improve the absorption of orally
administered poorly water-soluble drugs. To better predict outcomes in vivo, we must be …

Influence of drug–polymer interactions on dissolution of thermodynamically highly unstable cocrystal

MS Jasani, DP Kale, IP Singh… - Molecular …, 2018 - ACS Publications
Solubility advantage of thermodynamically highly unstable cocrystals, which undergo
solution-mediated phase transformation (SMPT) in less than 1 min, does not translate to …

Kinetic solubility improvement and influence of polymers on controlled supersaturation of itraconazole-succinic acid nano-co-crystals

Z Huang, S Staufenbiel, R Bodmeier - International Journal of …, 2022 - Elsevier
Nano-co-crystals enhance the solubility and dissolution rate of poorly soluble drugs. The
objective of this study was to obtain a better understanding of the dissolution process of …

Combination of co-crystal and nanocrystal techniques to improve the solubility and dissolution rate of poorly soluble drugs

Z Huang, S Staufenbiel, R Bodmeier - Pharmaceutical research, 2022 - Springer
Purpose Solubility and dissolution rate are essential for the oral absorption and
bioavailability of poorly soluble drugs. The aim of this study was to prepare nano-co-crystals …

The influence of polymers on the supersaturation potential of poor and good glass formers

LI Blaabjerg, H Grohganz, E Lindenberg, K Löbmann… - Pharmaceutics, 2018 - mdpi.com
The increasing number of poorly water-soluble drug candidates in pharmaceutical
development is a major challenge. Enabling techniques such as amorphization of the …