[PDF][PDF] Solid Dispersion: Methods and Polymers to increase the solubility of poorly soluble drugs

LA Nikghalb, G Singh, G Singh… - Journal of Applied …, 2012 - japsonline.com
The solubility behaviour of drugs remains one of the most exigent aspects in formulation
development. These days, the number of new chemical entities has dramatically increased …

[HTML][HTML] Development and characterization of an atorvastatin solid dispersion formulation using skimmed milk for improved oral bioavailability

A Choudhary, AC Rana, G Aggarwal, V Kumar… - … Pharmaceutica Sinica B, 2012 - Elsevier
Atorvastatin has low aqueous solubility resulting in low oral bioavailability (12%) and thus
presents a challenge in formulating a suitable dosage form. To improve the aqueous …

[图书][B] Thin layer chromatography in drug analysis

L Komsta, M Waksmundzka-Hajnos, J Sherma - 2013 - books.google.com
Used routinely in drug control laboratories, forensic laboratories, and as a research tool, thin
layer chromatography (TLC) plays an important role in pharmaceutical drug analyses. It …

Amino acids as co-amorphous excipients for tackling the poor aqueous solubility of valsartan

Y Huang, Q Zhang, JR Wang, KL Lin… - Pharmaceutical …, 2017 - Taylor & Francis
Co-amorphization has recently been shown to be a promising approach for stabilizing
amorphous drugs and improving the dissolution rate of poorly water-soluble drugs. In this …

Optimization of valsartan encapsulation in biodegradables polyesters using Box-Behnken design

O Sadoun, F Rezgui, C G'Sell - Materials science and engineering: C, 2018 - Elsevier
The aim of this study was to encapsulate an antihypertensive drug (valsartan) within
polyester microparticles, namely constituted of poly (lactic acid)(PLA) and poly (ε …

Recent research on formulation development of BCS class II drugs–A review

KPR Chowdary - … Research Journal of Pharmaceutical and Applied …, 2013 - scienztech.org
BCS class II drugs pose challenging problems in their pharmaceutical product development
process because of their low solubility and dissolution rates. They require enhancement in …

[HTML][HTML] Design and physico-mechanical evaluation of fast-dissolving valsartan polymeric drug delivery system by electrospinning method

M Mohammadreza, P Iraji, Z Mahmoudi… - Iranian Journal of …, 2021 - ncbi.nlm.nih.gov
Objective (s): Chronic hypertension is a pervasive morbidity and the leading risk factor for
cardiovascular diseases. Valsartan, as an antihypertensive drug, has low solubility and …

Dissolution-enhancing mechanism of alkalizers in poloxamer-based solid dispersions and physical mixtures containing poorly water-soluble valsartan

NS Ha, TTD Tran, PHL Tran, JB Park… - Chemical and …, 2011 - jstage.jst.go.jp
The purpose of this study was to investigate the effects of alkalizers in dissolution rate and
crystal structure of valsartan (VAL) in Poloxamer 407 (POX)-based solid dispersions (SD) …

Effects of solvents and crystallization conditions on the polymorphic behaviors and dissolution rates of valsartan

TTD Tran, PHL Tran, JB Park, BJ Lee - Archives of pharmacal research, 2012 - Springer
For the quality evaluation of raw materials, the influence of various types of solvents on the
polymorphic crystallization behaviors and dissolution rates of two sources of valsartan (VAL) …

[PDF][PDF] Formulation optimization and evaluation of nanostructured lipid carriers containing valsartan

RJ Patel, ZP Patel - International journal of pharmaceutical …, 2013 - researchgate.net
Nanostructured lipid carriers (NLCs), a lipid based colloidal carrier system, offer many
advantages such as increase the solubility, improves the bioavailability and therapeutic …