Development of self-nanoemulsifying drug delivery system for oral bioavailability enhancement of valsartan in beagle dogs

Z Li, W Zhang, Y Gao, R Xiang, Y Liu, M Hu… - Drug delivery and …, 2017 - Springer
Valsartan, an angiotensin II receptor antagonist, is widely used to treat high blood pressure
in the clinical setting. However, its poor water solubility results in the low oral bioavailability …

Formulation, characterization and in vivo evaluation of self-nanoemulsifying drug delivery system for oral delivery of valsartan

M Chopra, UY Nayak, A Kumar Gurram… - Current …, 2014 - ingentaconnect.com
Valsartan is an effective, highly selective and orally active antihypertensive exhibiting low
aqueous solubility and poor dissolution that limit its absorption resulting in low …

Development, optimization, and characterization of solid self-nanoemulsifying drug delivery systems of valsartan using porous carriers

S Beg, S Swain, HP Singh, CN Patra, MEB Rao - Aaps Pharmscitech, 2012 - Springer
The present studies entail formulation development of novel solid self-nanoemulsifying drug
delivery systems (S-SNEDDS) of valsartan with improved oral bioavailability, and evaluation …

[PDF][PDF] Self-nanoemulsifying drug delivery systems of Valsartan: preparation and in-vitro characterization

PS Rajinikanth, NW Keat, S Garg - International journal of drug delivery, 2012 - core.ac.uk
The main objective this study is to prepare and evaluate the selfnanoemulsifying drug
delivery (SNEDDS) system in order to achieve a better dissolution rate of a poorly water …

[PDF][PDF] Enhancement of solubility and oral bioavailability of poorly soluble drug valsartan by novel solid self emulsifying drug delivery system

BU Sri, YI Muzib, D Bhikshapathi, R Sravani - Int. J. Drug Deliv, 2015 - core.ac.uk
The main objective of present work was to prepare a solid SEDDS for enhancement of oral
bioavailability of Valsartan, poorly water soluble drug. The solubility of the drug was …

Design and optimization of candesartan loaded self-nanoemulsifying drug delivery system for improving its dissolution rate and pharmacodynamic potential

R Verma, D Kaushik - Drug Delivery, 2020 - Taylor & Francis
During the last decades, much attention has been focused on SNEDDS approach to resolve
concerns of BCS II class drugs with accentuation on upgrading the solubility and …

[PDF][PDF] The effect of converting liquid valsartan SNEDDS into solid SNEDDS using different solid carriers on its performance

M Yasser, S Gad, M El-sayed, M Ghorab - Int J Bio Pharm Res, 2013 - researchgate.net
Valsartan is an angiotensin converting enzyme inhibitor which is poorly soluble in water,
which leads to low oral bioavailability (19-25%). For this reason, the study target was to …

Enhanced oral bioavailability of valsartan using a polymer-based supersaturable self-microemulsifying drug delivery system

DW Yeom, BR Chae, HY Son, JH Kim… - International Journal …, 2017 - Taylor & Francis
A novel, supersaturable self-microemulsifying drug delivery system (S-SMEDDS) was
successfully formulated to enhance the dissolution and oral absorption of valsartan (VST), a …

Preparation and evaluation of a lipid-based drug delivery system to ımprove valsartan oral bioavailability: pharmacokinetic and pharmacodynamic analysis

E Gülmezoğlu, G Yıldız Türkyılmaz… - Drug Development and …, 2022 - Taylor & Francis
Antihypertensive treatment reduces the risk of cardiovascular complications in patients with
high mortality with hypertension. Valsartan is highly selective antihypertensive that is rapidly …

Formulation and in-vitro characterization of Self Nano-emulsifying Drug Delivery System (SNEDDS) for enhanced solubility of candesartan cilexetil

D Elsegaie, M Teaima, MI Tadrous… - Research Journal of …, 2019 - indianjournals.com
Candesartan cilexetil is the prodrug of candesartan, a selective angiotensin II receptor
antagonist, used in the management of hypertension and heart failure. It is characterized by …