Nearly 40% of new drug candidates exhibit low solubility in water, which is a challenge in
development of optimum oral solid dosage form in terms of formulation design and …

The aim of this study was to develop polyunsaturated fatty acid (PUFA) long chain glyceride
(LCG) enriched self-nanoemulsifying lipidic nanomicelles systems (SNELS) for augmenting …

Edaravone (EDR) is a well-recognized lipophilic free radical scavenger for diseases
including neurodegenerative disease, cardiovascular disease, and cancer. However, its oral …

The main objective of this study was to prepare a solid self-microemulsifying drug delivery
system (S-SMEDDS) by spray drying liquid SMEDDS with an inert solid carrier Aerosil 200 …

Over past many decades solubility had always been a major concern in leading to high
intrasubject/intersubject variability, lack of dose proportionality and ultimately low …

Carvedilol (CARV) is a widely used drug, which has shown low oral bioavailability. Lipid-
based drug delivery systems (LBDDS) appear as promising alternatives to overcome CARV …

Lipid based formulations (LBFs) are a promising formulation strategy for many poorly water-
soluble drugs and have been shown previously to enhance the oral exposure of CP …

The main objective of this study was to develop a pH gradient release pellet with self-
emulsifying drug delivery system (SEDDS), which could not only improve the oral …

It was the aim of this study to incorporate a model peptide bivalirudin in self-emulsifying drug
delivery system (SEDDS) and compare its storage stability with conventional aqueous …

The aim of study was to formulate self-microemulsifying drug delivery systems for modafinil.
It was also an objective to optimize formulation parameters and evaluate developed …