This study aimed to prepare a co-carrier-based solid dispersion (SD) of celecoxib (CXB) to
improve its dissolution and oral bioavailability. The CXB-loaded SD formulation was …

Cancer incidence worldwide is alarming and among the cancers that affect women ovarian
cancer is the most fatal. Many side effects are associated with conventional therapies and …

The authors aimed to create and characterise Cefpodoxime Proxetil (CDP) niosomes with
site-specific delivery in order to minimise disruptions in gastric disintegration and absorption …

Recent advances in the field of conversion of solid dispersions of poorly water-soluble drugs
in a wide range of hydrophilic or water-soluble carriers into solid dispersion tablets have …

The drugs of present use are lipophilic. Hence there is a need to surge the solubility of these
drugs. To encounter this necessity one of the approaches is the formulation of drugs in form …

Amorphous solid dispersion (ASD) has emerged to be an outstanding strategy among
multiple options available for improving solubility and consequently biological activity …

Ibrutinib is an anticancer drug, a Bruton's tyrosine kinase inhibitor with poor solubility in
aqueous media. This study reports on the study of the effectiveness of mesoporous carriers …

This study focuses on formulating and assessing an in-situ gastro-retentive gel for precise
delivery of verapamil hydrochloride to the stomach, aiming to extend its residence time and …

Context: Nanostructured lipid carriers can enhance skin penetration of active substances.
Coenzyme Q10 is a lipophilic antioxidant, that has poor skin penetration. This limitation is …

Most of the promising drugs in development channels are poorly water-soluble drugs which
limit formulation approaches, clinical application because of their low dissolution and …