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 …

[PDF][PDF] Self-nano emulsifying drug delivery system for sertraline hydrochloride: design, preparation and characterization

HO Ammar, MM Ghorab, DM Mostafa… - International Journal of …, 2014 - academia.edu
Objective: Development and characterization of self-nanoemulsifying drug delivery system
for sertraline hydrochloride (SNEDDS). Methods: Solubility of sertraline hydrochloride in …

[PDF][PDF] Development and evaluation of a (SEDDS) self—emulsifying drug delivery system for darifenacin hydrobromide

N SreeHarsha, A Shariff, YA Shendkar… - Indian J. Pharm. Educ …, 2019 - ijper.org
Background: The formulation and development of new chemical entities has the major
challenge of low solubility. A fraction of newly manufactured drugs (40%) have poor …

[PDF][PDF] Solubility enhancement of satranidazole using self-emulsified drug delivery systems

NP Gurav, PM Dandagi, AP Gadad… - Indian J. Pharm. Educ …, 2016 - ijper.org
Background: Satranidazole is an antiprotozoal and antibacterial drug which falls under class
II drug as per biopharmaceutical classification systems having poor aqueous solubility. Aim …

Development, optimization and evaluation of losartan potassium loaded Self Emulsifying Drug Delivery System

N Kommana, K Bharti, DB Surekha, S Thokala… - Journal of Drug Delivery …, 2020 - Elsevier
In the current research work, losartan potassium (LP) loaded Self Emulsifying Drug Delivery
System (SEDDS) was formulated using various ratios of lipids, surfactants and co …

Enhanced dissolution of repaglinide: SMEDDS formulation and in-vitro evaluation

H Ponnaganti, K Abbulu - Research Journal of Pharmacy and …, 2014 - indianjournals.com
Repaglinide a BCS class II poorly water soluble drug was formulated into lipid drug delivery
system of self microemulsifying delivery system (SMEDDS). Surfactants and oil was selected …

A rundown through various methods used in the formulation of solid self-emulsifying drug delivery systems (S-SEDDS)

SRD Almeida, VK Tippavajhala - Aaps Pharmscitech, 2019 - Springer
The most common route of the drug administration is oral route despite the fact that most
drugs have low oral aqueous solubility and bioavailability especially for BCS class II and …

[引用][C] Development and evaluation of self emulsifying drug delivery of a poorly water soluble NSAID

SV Modi, NJ Patel - World J Pharm Pharm Sci, 2015

Formulation and statistical optimization of clozapine solid self emulsification system for improving the dissolution properties

R Pethani, K Dudhat, MM Soniwala… - Journal of Dispersion …, 2024 - Taylor & Francis
Clozapine is an atypical antipsychotic drug that exhibits low bioavailability (> 27%) due to
poor solubility and higher hepatic metabolism. The present investigation was aimed to …

A Review on Self-Micro Emulsifying Drug Delivery System: Evident to improve the oral bioavailability of hydrophobic drugs

DA Khairnar, AB Darekar… - Asian Journal of …, 2016 - indianjournals.com
The SMEDDS are the isotropic mixture of oil, surfactant and co-surfactant. SMEDDS solve
the problem of all BCS class of drug such as solubility, high molecular weight, pre systemic …