Application of surfactants in solid dispersion technology for improving solubility of poorly water soluble drugs
SP Chaudhari, RP Dugar - Journal of drug delivery science and technology, 2017 - Elsevier
Discovery of several poorly water soluble drugs in the past decade has led to the constant
need of developing a novel dosage form which increases the solubility of these drug. They …
need of developing a novel dosage form which increases the solubility of these drug. They …
Solid dispersions containing ursolic acid in Poloxamer 407 and PEG 6000: A comparative study of fusion and solvent methods
JO Eloy, JM Marchetti - Powder technology, 2014 - Elsevier
Ursolic acid is a molecule with several therapeutic applications not yet commercially
explored because of its bioavailability-limiting water insolubility. To avoid this drawback …
explored because of its bioavailability-limiting water insolubility. To avoid this drawback …
Solubility measurement and various solubility parameters of glipizide in different neat solvents
Glipizide (GLZ) is an oral hypoglycemic agent, which is a weakly aqueous soluble drug. The
solubility values of GLZ in various neat solvents are scarce in the literature. Hence, the …
solubility values of GLZ in various neat solvents are scarce in the literature. Hence, the …
[PDF][PDF] Solid dispersion-a approach to enhance the dissolution rate of poorly water soluble drugs
D Bhowmik, G Harish, S Duraivel, BP Kumar… - The pharma …, 2013 - academia.edu
In recent years, the formulation of poorly soluble compounds presented interesting
challenges for formulation scientists in the pharmaceutical industry. Up to 40% of new …
challenges for formulation scientists in the pharmaceutical industry. Up to 40% of new …
Development and physicochemical characterization of solid dispersions containing praziquantel for the treatment of schistosomiasis
PR Dametto, AC Dametto, L Polese, CA Ribeiro… - Journal of Thermal …, 2017 - Springer
Praziquantel (PZQ) is an anthelminthic agent active against parasitic flatworms of the
Schistosoma type and the most important drug for the treatment and morbidity control of …
Schistosoma type and the most important drug for the treatment and morbidity control of …
[PDF][PDF] Preparation and in vitro characterization of a non-effervescent floating drug delivery system for poorly soluble drug, glipizide
VS Meka, S Pillai, SR Dharmalingham, R Sheshala… - Acta Pol. Pharm, 2015 - ptfarm.pl
The aim of the present study was to formulate a non-effervescent floating drug delivery
system of glipizide, a poorly water soluble drug. The solubility of glipizide was initially …
system of glipizide, a poorly water soluble drug. The solubility of glipizide was initially …
Formulation and evaluation of solid dispersion of glipizide for solubility and dissolution rate enhancement
A Gupta, MK Kataria, A Bilandi - International Journal of Pharmaceutics …, 2014 - neliti.com
The poor solubility of drug substances in water and their low dissolution rate in aqueous GIT
fluid often leads toinsufficient bioavailability. Glipizide is a class-II antidiabetic drug which is …
fluid often leads toinsufficient bioavailability. Glipizide is a class-II antidiabetic drug which is …
[PDF][PDF] Solubility enhancement of olmesartan by utilization of solid dispersion and complexation techniques
T El-nawawy, AM Swailem, D Ghorab… - Int. J. Novel Drug Deliv …, 2012 - Citeseer
Objective: The aim of the present study was to enhance the dissolution of poorly-water
soluble Olmesartan medoxomil by solid dispersion preparation and formation of inclusion …
soluble Olmesartan medoxomil by solid dispersion preparation and formation of inclusion …
Formulation and evaluation of diacerein solid dispersion for solubility and dissolution rate enhancement
SS Chitlange, GR Pawbake, SV Pandkar… - Research Journal of …, 2011 - indianjournals.com
Solubility is an important physicochemical factor affecting absorption of drug and its
therapeutic effectiveness. Diacerein (DIA) is a poorly water-soluble anti-inflammatory …
therapeutic effectiveness. Diacerein (DIA) is a poorly water-soluble anti-inflammatory …
[PDF][PDF] A factorial study on the effects of Hpβ cyclodextrin, PVP K30 and SLS on the solubility and dissolution rate of efavirenz
KPR Chowdary, A Naresh - Int J App Bio Pharm Technol, 2010 - Citeseer
The objective of the study is to evaluate the individual main effects and combined (or
interaction) effects of Hydroxy propyl β cyclodextrin (HPβCD), poly vinyl pyrrolidone (PVP …
interaction) effects of Hydroxy propyl β cyclodextrin (HPβCD), poly vinyl pyrrolidone (PVP …