[PDF][PDF] Formulation and in vitro evaluation of solid-self-emulsifying drug delivery system (SEDDS) of glibenclamide
M Saifee, S Zarekar, VU Rao, Z Zaheer… - Am J Adv Drug …, 2013 - academia.edu
Aim of present study was to develop solid self micro emulsifying drug delivery system (S-
SEDDS) with Aerosil 200 for enhancement of dissolution rate of model drug Glibenclamide …
SEDDS) with Aerosil 200 for enhancement of dissolution rate of model drug Glibenclamide …
Formulation and development of solid self micro-emulsifying drug delivery system (S-SMEDDS) containing chlorthalidone for improvement of dissolution
PV Dangre, RM Gilhotra, SN Dhole - Journal of pharmaceutical …, 2016 - Springer
The objective of the present study was to develop a self micro-emulsifying drug delivery
system (SMEDDS) of chlorthalidone (CTD) to improve its solubility and dissolution. CTD is a …
system (SMEDDS) of chlorthalidone (CTD) to improve its solubility and dissolution. CTD is a …
Development and characterization of solid self-emulsifying drug delivery system containing nateglinide
V Suvarna - Asian Journal of Pharmaceutics (AJP), 2017 - asiapharmaceutics.info
Introduction: To develop self-emulsifying drug delivery system (SEDDS) of nateglinide to
convert it into solid SEDDS (S-SEDDS) aerosil-200 as adsorbent. Materials and Methods …
convert it into solid SEDDS (S-SEDDS) aerosil-200 as adsorbent. Materials and Methods …
Development, evaluation and optimization of solid self emulsifying drug delivery system (s-sedds) of lercanidipine hydrochloride
P Bhargavi, A Naha, S Kannan… - Research Journal of …, 2020 - indianjournals.com
The objective of the study is to formulate Solid Self Emulsifying Drug Delivery System
(SEDDS) for improvement of solubility and dissolution of poorly water-soluble drug …
(SEDDS) for improvement of solubility and dissolution of poorly water-soluble drug …
[PDF][PDF] Formulation and evaluation of solid self micro emulsifying drug delivery system using aerosil 200 as solid carrier
DA Bhagwat, JID Souza - International current pharmaceutical …, 2012 - researchgate.net
Improvement of bio-availability of poorly water soluble drugs presents one of the furthermost
challenge in drug formulations. One of the most admired and commercially viable …
challenge in drug formulations. One of the most admired and commercially viable …
[PDF][PDF] Development of solid self micro emulsifying drug delivery system with neusilin US2 for enhanced dissolution rate of telmisartan
A Bhagwat Durgacharan, I D'Souza John - Int J Drug Dev Res, 2012 - researchgate.net
Aim of present study was to develop solid self micro emulsifying drug delivery system (S-
SMEDDS) with Neusilin US2 for enhancement of dissolution rate of Telmisartan (TEL) …
SMEDDS) with Neusilin US2 for enhancement of dissolution rate of Telmisartan (TEL) …
Glibenclamide-loaded self-nanoemulsifying drug delivery system: development and characterization
SK Singh, PR Prasad Verma… - Drug development and …, 2010 - Taylor & Francis
Objective: To develop and characterize self-nanoemulsifying drug delivery system
(SNEDDS) of the poorly water-soluble drug, glibenclamide (GBD). Methods: Solubility of …
(SNEDDS) of the poorly water-soluble drug, glibenclamide (GBD). Methods: Solubility of …
Formulation and evaluation of solid self-microemulsifying drug delivery system of chlorthalidone by spray drying technology
JK Madagul, DR Parakh, RS Kumar… - Drying technology, 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 …
[PDF][PDF] Formulation and evaluation of solid self-emulsifying drug delivery system of Gliclazide
SR Deshmukh, SS Bakhle, KP Upadhye… - Int J Pharm Pharm …, 2016 - academia.edu
Objective: Gliclazide (GCZ) is a widely prescribed anti-diabetic drug belongs to class IΙ
under BCS and exhibit low and variable oral bioavailability due to its poor aqueous …
under BCS and exhibit low and variable oral bioavailability due to its poor aqueous …
Self emulsifying drug delivery system for enhanced solubility and dissolution of glipizide
AG Agrawal, A Kumar, PS Gide - Colloids and Surfaces B: Biointerfaces, 2015 - Elsevier
The aim of this study was to develop self emulsifying drug delivery systems (SEDDS) of
glipizide and to convert it into solid SEDDS (S-SEDDS) using Syloid® 244 FP as adsorbent …
glipizide and to convert it into solid SEDDS (S-SEDDS) using Syloid® 244 FP as adsorbent …