[HTML][HTML] Fundamental aspects of solid dispersion technology for poorly soluble drugs

Y Huang, WG Dai - Acta Pharmaceutica Sinica B, 2014 - Elsevier
The solid dispersion has become an established solubilization technology for poorly water
soluble drugs. Since a solid dispersion is basically a drug–polymer two-component system …

[HTML][HTML] Drugs repurposed: An advanced step towards the treatment of breast cancer and associated challenges

JA Malik, S Ahmed, B Jan, O Bender… - Biomedicine & …, 2022 - Elsevier
Breast cancer (BC) is mostly observed in women and is responsible for huge mortality in
women subjects globally. Due to the continued development of drug resistance and other …

Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs

T Vasconcelos, B Sarmento, P Costa - Drug discovery today, 2007 - Elsevier
Solid dispersions are one of the most promising strategies to improve the oral bioavailability
of poorly water soluble drugs. By reducing drug particle size to the absolute minimum, and …

Liquid antisolvent precipitation and stabilization of nanoparticles of poorly water soluble drugs in aqueous suspensions: Recent developments and future perspective

AA Thorat, SV Dalvi - Chemical Engineering Journal, 2012 - Elsevier
The liquid antisolvent (LAS) precipitation process for production of ultra-fine particles has
been widely researched for a last few decades. In LAS process, precipitation of solute is …

Drug–excipient compatibility screening—role of thermoanalytical and spectroscopic techniques

R Chadha, S Bhandari - Journal of pharmaceutical and biomedical …, 2014 - Elsevier
Estimation of drug–excipient interactions is a crucial step in preformulation studies of drug
development to achieve consistent stability, bioavailability and manufacturability of solid …

Chitosan nanoparticles loaded with dorzolamide and pramipexole

S Papadimitriou, D Bikiaris, K Avgoustakis… - Carbohydrate …, 2008 - Elsevier
Chitosan (CS) nanoparticles of dorzolamide hydrochloride (Dorzo) and pramipexole
hydrochloride (Prami) were prepared by the ionic gelation method and their in vitro …

Solid-state analysis of amorphous solid dispersions: Why DSC and XRPD may not be regarded as stand-alone techniques

S Dedroog, T Pas, B Vergauwen, C Huygens… - … of Pharmaceutical and …, 2020 - Elsevier
Amorphous solid dispersions (ASDs) are single-phase amorphous systems, where drug
molecules are molecularly dispersed (dissolved) in a polymer matrix. The molecular …

Solid dispersions, part I: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs

DN Bikiaris - Expert opinion on drug delivery, 2011 - Taylor & Francis
Introduction: In recent years, the number of active pharmaceutical ingredients with high
therapeutic impact, but very low water solubility, has increased significantly. Thus, a great …

Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size …

E Karavas, E Georgarakis, MP Sigalas… - European journal of …, 2007 - Elsevier
In the present study the release mechanism of the sparingly water-soluble drug felodipine
(FELO) from particulate solid dispersions in PVP or PEG was investigated. FT-IR data …

A review on current nanomaterials and their drug conjugate for targeted breast cancer treatment

JJ Lee, L Saiful Yazan… - International journal of …, 2017 - Taylor & Francis
Breast cancer is the most common malignancy worldwide, especially among women, with
substantial after-treatment effects. The survival rates of breast cancer have decreased over …