Solid dispersions have achieved significant interest as an effective means of enhancing the
dissolution rate and thus the bioavailability of a range of weakly water‐soluble drugs. Solid …

Introduction Infections caused by parasitic flatworms impose a considerable worldwide
health burden. Recently, World Health Organization launched its roadmap for neglected …

Introduction Self-emulsifying drug delivery systems (SEDDS) are a promising strategy to
improve the oral bioavailability of poorly water-soluble drugs (PWSD). However, poor drug …

The low and variable oral bioavailability of poorly water soluble drugs remains a major
concern for the pharmaceutical industry. Spray congealing is an emerging technology for the …

To date, the treatment for cysticercosis and neurocysticercosis consists of a single oral
intake of praziquantel (5–10 mg/kg), which since it is only available as tablets, hinders its …

In the last decades, Green Chemistry has been gaining widespread attention within the
pharmaceutical field. It is thus very important to bring more sustainable approaches into the …

The development of medicines designed for children can be challenging since this distinct
patient population requires specific needs. A formulation designed for paediatric patients …

Because of the rapid development of nanotechnologies, materials, in particular, solid
dispersions (SDs), which are actively introduced into the life of modern man, have been …

This paper aims to evaluate the product contamination by elemental impurities during the
mechanochemical synthesis of praziquantel (PZQ) co-crystal, polymeric dispersion and …

This review aims to provide an overview of studies that address the use, in therapeutic
applications, of solid dispersions (SDs) with biological activities in vitro and/or in vivo mainly …