Introduction: Oral administration of a drug is the most common, ideal and preferred route of
administration. The main problem of oral drug formulations is their low bioavailability arises …

Background: Piroxicam is a non-steroidal anti-inflammatory drug belongs to BCS class II
drugs having poor solubility and is associated with a number of undesirable side-effects on …

In the present work a novel cyclosporine-loaded Eudragit S100 (pH-sensitive) nanoparticles-
laden contact lenses were designed to provide sustained release of cyclosporine at …

Technology Catalysts International reported in 2002 that approximately 35-40% of all new
chemical compounds suffer from poor aqueous solubility and present a major challenge to …

Objective: Self-microemulsifying drug delivery system (SMEDDS) and solid-SMEDDS of
telmisartan was aimed at overcoming the problems of poor solubility and bioavailability …

The current investigation was aimed to improve the solubility of poorly soluble drug,
cilostazol (CLZ). Self-nanoemulsifying drug delivery system (SNEDDS) composed of oil …

Solid‐self‐emulsifying drug delivery system (S‐SEDDS) of paclitaxel (Ptx) was developed
by the spray drying method with the purpose of improving the low bioavailability (BA) of Ptx …

Aim: Oral route has always been the favorite route of drug administration in many diseases
and till today it is the first way investigated in the development of new dosage forms. The …

Oral route is the easiest and most convenient route of drug administration, being non
invasive and cost effective, thereby leading worldwide drug delivery market. But major …

Lipid-based drug delivery systems are extensively reported in the literature for enhancing
drug solubility, permeability, and bioavailability. Selfnanoemulsifying drug delivery systems …