This thesis investigates the biopharmaceutical knowledge of different liposomal formulations
using two different phosphatidylcholines (EPC and S 90) in the presence and absence of …

The main purpose of this study was to evaluate oral bioavailability of the poorly water-
soluble drug fenofibrate when liposomes containing a bile salt were used as oral drug …

Despite the enormous amount of effort spent during the past 44 years (greater than 114,000
scientific publications) and the well-formed consensus within the scientific community about …

The performance of four different lipid-based (Tween 80–Captex 200P, Tween 80–Capmul
MCM, Tween 80–Caprol 3GO and Tween 80–soybean oil) and one commercially available …

Liposomes due to their biphasic characteristic and diversity in design, composition and
construction, offer a dynamic and adaptable technology for enhancing drug solubility …

Lipid matrix particles (LMP) may be used as better carriers for poorly water-soluble drugs
than liquid lipid carriers because of reduced drug mobilization in the formulations. However …

The aim of this study was to examine the encapsulation of flurbiprofen in to liposomes and
further to achieve sustained as well as controlled release pattern of flurbiprofen from multi …

The present study investigated the utility of in vitro lipolysis performance indicators drug
solubilization and maximum supersaturation ratio (SR M) for their predictive use for the in …

The solubilizing properties of lipid-based formulations (LBFs) can change dramatically
following dispersion and digestion of the formulation components. This study investigated …

Using lipid-based drug delivery systems (LbDDS) is an efficient strategy to enhance the low
oral bioavailability of poorly water-soluble drugs. Here the oral absorption of fenofibrate (FF) …