• Miss. Pranali Kumbhalkar
• Mr. Aslam Riyaz
• Mrs. Swati V Bodhankar
• Mr. Lokesh Mahajan
• Mr. Deepraj Tayade

Solubility of orally administered drug is major challenge of pharmaceutical industry as nearly 35-40% of newly launched drugs possess low aqueous solubility which leads to their poor dissolution and low bioavailability, resulting in high intra & inter subject variability & lack of dose proportionality. This can be increased by different methods like salt formation, solid dispersion and complex formation. Self-Emulsifying Drug Delivery System is gaining popularity for improving the solubility of lipophilic drugs. SEDDS are defined as isotropic mixtures of one or more hydrophilic solvents and co-solvents/surfactants that have a unique ability of forming fine oil-in-water (o/w) micro emulsions upon mild agitation followed by dilution in aqueous media, such as GI fluids. Present review provides an updated account of advancements in SEDDS with regard to its composition, evaluation, different dosage forms and newer techniques to convert liquid SEDDS to solid and also various applications.

Preparation and Evaluation of Solid-Self-Emulsifying Drug Delivery System Containing Olmesartan Medoxomil by using Capmul MCM-E8, Tween-80 and PEG 200

"Preparation and Evaluation of Solid-Self-Emulsifying Drug Delivery System Containing Olmesartan Medoxomil by using Capmul MCM-E8, Tween-80 and PEG 200", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.7, Issue 10, page no.2766-2780, October-2020, Available :http://www.jetir.org/papers/JETIR2010360.pdf

"Preparation and Evaluation of Solid-Self-Emulsifying Drug Delivery System Containing Olmesartan Medoxomil by using Capmul MCM-E8, Tween-80 and PEG 200", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.7, Issue 10, page no. pp2766-2780, October-2020, Available at : http://www.jetir.org/papers/JETIR2010360.pdf