Recent trends of self-emulsifying drug delivery system for enhancing the oral bioavailability of poorly water-soluble drugs
P Tran, JS Park - Journal of Pharmaceutical Investigation, 2021 - Springer
Background The oral route is the most popular route for the clinical administration of drugs to
treat various diseases. Before a drug is absorbed into the blood circulation, it must undergo …
treat various diseases. Before a drug is absorbed into the blood circulation, it must undergo …
Design, development, and evaluation of spray dried flurbiprofen loaded sustained release polymeric nanoparticles using QBD approach to manage inflammation
Spray-dried Flurbiprofen (FLB) loaded polymeric nanoformulation using Eudragit L 100 and
Ethylcellulose. They were optimized and evaluated. This study determined drug release (%) …
Ethylcellulose. They were optimized and evaluated. This study determined drug release (%) …
Quality by design enabled development of oral self-nanoemulsifying drug delivery system of a novel calcimimetic cinacalcet HCl using a porous carrier: in vitro and in …
KC Panigrahi, CN Patra, MEB Rao - AAPS PharmSciTech, 2019 - Springer
In this present research, work quality by design-enabled development of cinacalcet HCl
(CH)-loaded solid self-nanoemulsifying drug delivery system (S-SNEDDS) was conducted …
(CH)-loaded solid self-nanoemulsifying drug delivery system (S-SNEDDS) was conducted …
Drug loading of tannic acid crosslinked hydroxyapatite/gelatin composites via spray dryer and kinetic studies
IB Gumus, E Kahraman, N Erdol-Aydin… - Drying …, 2023 - Taylor & Francis
The present study aims at studying the loading and release of 5-Fluorouracil (5-FU) drug
from hydroxyapatite/gelatin (HAp-GEL) composites. Composites were produced in the …
from hydroxyapatite/gelatin (HAp-GEL) composites. Composites were produced in the …
Formulation and evaluation of solid self-microemulsifying drug delivery system of chlorthalidone by spray drying technology
JK Madagul, DR Parakh, RS Kumar… - Drying …, 2017 - Taylor & Francis
The main objective of this study was to prepare a solid self-microemulsifying drug delivery
system (S-SMEDDS) by spray drying liquid SMEDDS with an inert solid carrier Aerosil 200 …
system (S-SMEDDS) by spray drying liquid SMEDDS with an inert solid carrier Aerosil 200 …
Development of self-microemulsifying drug delivery system of mebendazole by spray drying technology: characterization, in vitro and in vivo evaluation
In this study, a novel liquid self-microemulsifying drug delivery system (SMEDDS) containing
mebendazole was formulated and further developed into a solid form by a spray drying …
mebendazole was formulated and further developed into a solid form by a spray drying …
Application of factorial design approach in development and evaluation of self microemulsifying drug delivery system (SMEDDS) of mebendazole
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 …
natural or synthetic oils, surfactants and co-solvents/co-surfactants. Upon mild agitation …
[HTML][HTML] Development and Evaluation of a Solid Self-Microemulsifying Drug Delivery System Containing Cilostazol Using the Spray Drying Technique
M Patil, A Yadav, R Mogal, M Shaikh… - Biosciences …, 2024 - biotech-asia.org
A robust self-emulsifying formulation containing cilostazol was produced by mixing
hydrophilic surfactants with oil. Considering cilostazol's limited solubility and bioavailability …
hydrophilic surfactants with oil. Considering cilostazol's limited solubility and bioavailability …
Solid self nano-emulsifying system for the enhancement of dissolution and bioavailability of Prasugrel HCl: in vitro and in vivo studies
M Khanfar, S Al-Nimry, S Attar - Pharmaceutical Development and …, 2021 - Taylor & Francis
Abstract Prasugrel Hydrochloride (PHCl) is an antiplatelet drug. It is a class II drug with
variable bioavailability. The objective of this work was to enhance the solubility and hence …
variable bioavailability. The objective of this work was to enhance the solubility and hence …
Impact on HDL and LDL of Hyperlipidemic Rat Models: Designed Solid Self-Nanoemulsifying Drug Delivery Systems with Atorvastatin and Ezetimibe combination
AR Gardouh, AM Nasef, Y Mostafa… - Research Journal of …, 2022 - indianjournals.com
The main purpose of this study was to develop and evaluate solid self-nanoemulsifying drug
delivery systems (S-SNEDDs) of Atorvastatin/Ezetimibe combination to combine the …
delivery systems (S-SNEDDs) of Atorvastatin/Ezetimibe combination to combine the …