Over the last few decades, polymers have been extensively used as pharmaceutical
excipients in drug delivery systems. Pharmaceutical polymers evolved from being simply …

Co amorphous systems are supersaturated drug delivery systems which offer a basic
platform for delivery of multicomponent adducts (combination of more than one active …

The main objective of this investigation was to develop an in vitro–in vivo correlation (IVIVC)
for immediate release candesartan cilexetil formulations by designing an in vitro dissolution …

This study aimed to improve dissolution rate of valsartan in an acidic environment and
consequently its oral bioavailability by solid dispersion formulation. Valsartan was selected …

The intent of the current work is to study the effect of polyethylene glycol 8000 and
polyethylene glycol 10000 as hydrophilic carriers on dissolution behaviour of flurbiprofen. In …

Purpose The present study aimed to improve the dissolution properties of nateglinide, an
anionic drug with poor water solubility and a high log P value, which results in decreased …

Abstract Valsartan (VAL) and Hydrochlorothiazide (HCTZ) as a fixed-dose combination are
widely used for the management of hypertension. To enhance the dissolution and oral …

Valsartan is an antihypertensive drug used primarily orally, however, due to its hydrophobic
nature it has got low bio-availability thus requiring higher dosage/frequency and causing …

Valsartan (VST) is a poorly water-soluble antihypertensive drug. The aim of this study was to
prepare, characterize, and evaluate a new salt of VST using choline (CHN) as a counter …

Materials and Methods: SSDs and physical mixtures (PMs) were prepared using various
ratios of hydrophilic carriers (polyethylene glycol 4000, polyethylene glycol 6000, and …