Recent advances in self-emulsifying drug delivery systems (SEDDS)

B Singh, S Beg, RK Khurana… - Critical Reviews™ in …, 2014 - dl.begellhouse.com
One of the biggest challenges confronting the contemporary drug delivery science today is
to improve on the oral bioavailability of a vast number of drugs exhibiting poor and …

Novel solid self-nanoemulsifying drug delivery system (S-SNEDDS) for oral delivery of olmesartan medoxomil: design, formulation, pharmacokinetic and …

A Nasr, A Gardouh, M Ghorab - Pharmaceutics, 2016 - mdpi.com
The main purpose of this study was to develop a solid self-nanoemulsifying drug delivery
system (S-SNEDDS) of Olmesartan (OLM) for enhancement of its solubility and dissolution …

[PDF][PDF] Nanosuspension as Promising and Potential Drug Delivery: A Review. 2020

H Chinthaginjala, H Abdul… - Int J Life Sci …, 2020 - pdfs.semanticscholar.org
In the last decade, nanosuspensions have gained considerable interest as a method for
formulating poorly soluble drugs. Because of their cost-effectiveness and technological …

The role of coatings and plasticizers compatibility in stability of advanced gastro-resistant self-emulsifying pellets designed for the delivery of volatile compounds: A …

J Macku, J Vyslouzil, J Muselik, M Pavelkova… - Journal of Drug Delivery …, 2024 - Elsevier
The gastro-resistant behaviour of solid self-emulsifying drug delivery systems (S-SEDDS)
represents a significant and innovative advancement in delivering poorly soluble drugs. Due …

Development and Characterization of Novel Solid Self Nanoemulsifying Drug Delivery System of Fimasartan

R Suthar, A Solanki, R Palva, P Prajapati… - Journal of …, 2025 - Springer
Purpose The objective of the present study was to prepare a solid self-nano emulsifying
drug delivery system (S-SNEDDS) of Fimasartan Potassium Trihydrate (FPT), a poorly water …

Design and development of an in situ synthesized layered double hydroxide structure of Fe-induced hydroxyapatite for drug carriers

A Manna, S Pramanik, A Tripathy, Z Radzi, A Moradi… - RSC …, 2016 - pubs.rsc.org
Iron (Fe)-induced hydroxyapatite (HA) layered double hydroxides (LDH) with different
concentrations of Fe (FH95 and FH85) were prepared by a novel in situ coprecipitation …

[PDF][PDF] Spray dried lactose based proniosomes as stable provesicular drug delivery carriers: Screening, formulation, and physicochemical characterization

A Nasr, M Qushawy, S Swidan - Int. J. Appl. Pharm, 2018 - academia.edu
Objective: In the present investigation efforts were considered to optimize the different
conditions for the preparation of spray dried lactose based proniosomes. The aim of this …

[PDF][PDF] Pharmacokinetic and pharmacodynamic interaction between aceclofenac and rosiglitazone in rats

R Sathish, J Anbu, A ANJANA, KFHN AHAMED… - metabolism, 2012 - Citeseer
The present study was carried out to investigate the pharmacokinetics and
pharmacodynamic interaction of Aceclofenac and Rosiglitazone alone and their …

Development of Drug-Loaded Solid Self-Emulsifying System Based Orally Disintegrating Tablets for the Effectual Oral Delivery of Deferasirox.

P Sable, S LAHOTI… - Indian Journal of …, 2023 - search.ebscohost.com
Deferasirox is an iron chelator used in the treatment of iron overload. It shows good oral
bioavailability of 70% but is plagued with various side effects that could be addressed if the …

[PDF][PDF] An Approach to Enhance the Solubility and Bioavailability of Poorly Water Soluble Drug Aceclofenac by Self-Emulsifying Technique Using Natural Oil

G Aswini, A Sapkota - researchgate.net
Self-emulsifying drug delivery system (SEDDS) is an isotropic mixture of drug, oil, surfactant
and co-surfactant which spontaneously forms emulsion in aqueous environment under …