Objective: The present study involves the development of SNEDDS employing essential oils
for enhancing biopharmaceutical performance. Methods: Preliminary investigations …

The objectives of the present studies were to develop the systematically optimized
selfnanoemulsifying drug delivery systems (SNEDDS) of valsartan employing the holistic …

The aim of this work was to enhance dissolution rate and oral bioavailability of repaglinide.
This was achieved by development of liquisolid tablet with the liquid component being self …

The main objective of this study was to compare the powder property, dissolution and
bioavailability of 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol (PLAG)-loaded self-emulsifying …

The aim of the present study was to formulate and optimize nanostructured lipid carriers
(NLC) to enhance oral bioavailability of telmisartan.“Box-Behnken design (3-factor, 3-level)” …

The novel self-nanoemulsifying self-nanosuspension (SNESNS) combines the advantages
of two efficient solubilization technologies; the nanoemulsion and the nanosuspension. The …

The present investigation was aimed to formulate self-nanoemulsifying granules (SNEGs) of
poorly water soluble drug, Olmesartan Medoxomil (OLM) to improve its solubility and oral …

The objective of this study was to develop and optimise self-nanoemulsifying drug delivery
system (SNEDDS) of atorvastatin calcium (ATC) for improving dissolution rate and …

Objective The aim of this study was to investigate the in vitro and in vivo performance of self-
nanoemulsifying drug delivery systems (SNEDDSs) of talinolol (TAL), a poorly water-soluble …

In the present investigation, improved release telmisartan liquisolid tablets were formulated
using Avicel Ph 102 and Aerosil 200 as the carrier and coating material respectively …