Recent developments in self-microemulsifying drug delivery system: an overview

D Kaushik - Asian Journal of Pharmaceutics (AJP), 2019 - asiapharmaceutics.info
Self-microemulsifying drug delivery system (SMEDDS) has emerged as a distinctive
approach for the improvement of low bioavailability, high intra-and inter-subject …

Self-micro emulsifying drug delivery system: an approach for enhancement of bioavailability of poorly water soluble drugs

VR Potphode, AS Deshmukh… - Asian Journal of …, 2016 - indianjournals.com
The improvement of oral bioavailability of poorly water soluble drug can be considered as
one of the greatest challenges in drug formulation. In recent years today, up to 90% of all …

Development, optimization, characterization and impact of in vitro lipolysis on drug release of telmisartan loaded SMEDDS

R Verma, D Kaushik - Drug Delivery Letters, 2019 - ingentaconnect.com
Objective: The objective of the current research is systematic optimization and development
of microemulsion preconcentrates to get better solubility that results in improvement of oral …

Quality based design approach for improving oral bioavailability of valsartan loaded SMEDDS and study of impact of lipolysis on the drug diffusion

R Verma, V Mittal, D Kaushik - Drug Delivery Letters, 2018 - ingentaconnect.com
Background and Objective: In the present investigation, we have developed, optimized and
evaluated a self-micro emulsifying drug delivery system (SMEDDS) of an anti-hypertensive …

[PDF][PDF] Self-microemulsifying drug delivery system: A vital approach for bioavailability enhancement

R Verma, V Mittal, D Kaushik - Int. J. ChemTech Res, 2017 - researchgate.net
In modern drug discovery techniques, about 40% of active moieties exhibit poorly water
soluble which and present a major challenge to modern drug delivery system results in low …

Application of factorial design approach in development and evaluation of self microemulsifying drug delivery system (SMEDDS) of mebendazole

DR Parakh, MP Patil, SS Sonawane… - Journal of …, 2017 - Springer
Self microemulsifying drug delivery systems (SMEDDS) are defined as isotropic mixtures of
natural or synthetic oils, surfactants and co-solvents/co-surfactants. Upon mild agitation …

Advanced delivery of poorly water soluble drug atorvastatin by lipid based formulation

AS Deshmukh, VR Mahajan - Asian journal of pharmaceutical research …, 2015 - ajprd.com
Atorvastatin Calcium used to lower cholesterol level in plasma of body by competitive
inhibiting HMG-CoA reductase, the rate determining enzyme in cholesterol biosynthesis via …

Application of D-optimal Mixture Design for Development and Optimization of Olmesartan Medoxomil Loaded SMEDDS

N Gahlawat, R Verma, D Kaushik - Current Drug Therapy, 2020 - ingentaconnect.com
Background: Olmesartan medoxomil is an angiotensin II receptor blocker antihypertensive
drug, which has low oral bioavailability because of poor aqueous solubility. Objective: The …

[PDF][PDF] Development of Aceclofenac Solid Self-Emulsifying Drug Delivery Systems

S Aashritha, B Srivastava, P Sneha… - International Journal of …, 2022 - academia.edu
Self-Micro-Emulsifying drug delivery system is the latest and innovative approaches have
been interested in signi icant interest like an effective means for improving solubility …

[PDF][PDF] FORMULATION AND CHARAC TERIZATION OF SOLID LIPID NANOPARTICLES OF QUETIAPINE FUMARATE TO IMPROVE SOLUBILITY

MY Gaikwad, AS Deshmukh, VR Mahajan - 2019 - researchgate.net
Quetiapine fumarate is an antipsychotic drug with plasma half-life 6 hr. and having poor oral
bioavailability (9%) because of first pass metabolism. The aim of the present study was to …