Related references
Note: Only part of the references are listed.Formation of physically stable amorphous phase of ibuprofen by solid state milling with kaolin
Subrata Mallick et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2008)
Current perspectives of solubilization: Potential for improved bioavailability
Subrata Mallick et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2007)
Interaction characteristics and thermodynamic behaviour of gatifloxacin by aluminium hydroxide
Subrata Mallick et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2007)
Interaction of naproxen with ionic cyclodextrins in aqueous solution and in the solid state
P Mura et al.
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS (2005)
Solid-state characterization and dissolution properties of naproxen-arginine-hydroxypropyl-beta-cyclodextrin ternary system
P Mura et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2005)
Celecoxib-cyclodextrin systems: Characterization and evaluation of in vitro and in vivo advantage
MS Nagarsenker et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2005)
Dissolution rate enhancement by adsorption of poorly soluble drugs on hydrophilic silica aerogels
I Smirnova et al.
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY (2004)
Comparison of the effect of chitosan and polyvinylpyrrolidone on dissolution properties and analgesic effect of naproxen
N Zerrouk et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2004)
Characterization of the mechanism of interaction in ibuprofen-Eudragit RL100 (R) coevaporates
R Pignatello et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2004)
Characterization of ibuproxam binary and ternary dispersions with hydrophilic carriers
M Cirri et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2004)
Formation of physically stable amorphous drugs by milling with neusilin
MK Gupta et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2003)
Enhancement of dehydroepiandrosterone solubility and bioavailability by ternary complexation with alpha-cyclodextrin and glycine
PC Mora et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2003)
Quantitative biopharmaceutics classification system: The central role of dose/solubility ratio
E Rinaki et al.
PHARMACEUTICAL RESEARCH (2003)
Enhanced drug dissolution using evaporative precipitation into aqueous solution
M Sarkari et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2002)
Stabilization of amorphous indomethacin by co-grinding in a ternary mixture
T Watanabe et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2002)
Influence of alkali metal counterions on the glass transition temperature of amorphous indomethacin salts
P Tong et al.
PHARMACEUTICAL RESEARCH (2002)
Improvement of solubility and oral bioavailability of a poorly water-soluble drug, TAS-301, by its melt-adsorption on a porous calcium silicate
M Kinoshita et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2002)
Cryogenic grinding of indomethacin polymorphs and solvates: Assessment of amorphous phase formation and amorphous phase physical stability
KJ Crowley et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2002)
Processing of carbamazepine PEG 4000 solid dispersions with supercritical carbon dioxide: preparation, characterisation, and in vitro dissolution
M Moneghini et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2001)
Detoxification of endotoxin by aluminum hydroxide adjuvant
Y Shi et al.
VACCINE (2001)
Enhanced drug dissolution and bulk properties of solid dispersions granulated with a surface adsorbent
MK Gupta et al.
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY (2001)
Improving drug solubility for oral delivery using solid dispersions
C Leuner et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2000)