Preliminary tests in the field of drug storage and release of composite materials known as
liposils were described. These silica-based particles were obtained via liposome templating …

Polylactic acid (PLA-l) microspheres were prepared as a biodegradable polymeric carrier for
a non-steroidal anti-inflammatory drug, nimesulide. The preparation of this system was …

A novel liposome‐in‐microsphere (LIM) formulation has been created comprising drug‐
loaded liposomes within pH responsive Eudragit S100 microspheres. The liposomes …

Numerous amorphous solid dispersion (ASD) formulations of celecoxib (CEL) have been
attempted for enhancing the solubility, dissolution rate, and in vivo pharmacokinetics via …

The encapsulation of liquids and semi-solids provides solutions for convenient delivery
through improved oral absorption of poorly water-soluble drugs. In addition, low dose …

Background: Raloxifene, a second-generation selective estrogen receptor modulator
(SERM) used to prevent osteoporosis in postmenopausal women is administered orally in …

Lipid nanoparticles based on solid matrix have emerged as potential drug carriers to
improve gastrointestinal (GI) absorption and oral bioavailability of several drugs, especially …

Drug delivery of poorly soluble drugs in form amorphous solid dispersions (ASDs) is an
appealing method to increase in vivo bioavailability. For rational formulation design, a …

More than 40% of active compounds identified through screening of combinatorial libraries
are poorly water-soluble, rendering them unsuitable for further drug development because …

This review details the properties of solid lipid microparticles (SLMs): a promising drug
carrier system that has been until now rather unexploited. First, the advantages of SLMs …