Related references
Note: Only part of the references are listed.Design and Characterization of Nanocrystal Formulations Containing Ezetimibe
Tugba Gulsun et al.
CHEMICAL & PHARMACEUTICAL BULLETIN (2011)
Universal wet-milling technique to prepare oral nanosuspension focused on discovery and preclinical animal studies - Development of particle design
Toshiyuki Niwa et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2011)
Novel crystalline solid dispersion of tranilast with high photostability and improved oral bioavailability
Yohei Kawabata et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Spray Drying Technique. I: Hardware and Process Parameters
Krzysztof Cal et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Spray Drying Technique: II. Current Applications in Pharmaceutical Technology
Krzysztof Sollohub et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Nanoparticulation of Poorly Water Soluble Drugs Using a Wet-Mill Process and Physicochemical Properties of the Nanopowders
Yusuke Tanaka et al.
CHEMICAL & PHARMACEUTICAL BULLETIN (2009)
Spray drying from complex solvent systems broadens the applicability of Kollicoat IR as a carrier in the formulation of solid dispersions
Sandrien Janssens et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2009)
Morphology and surface states of colloidal probucol nanoparticles evaluated by atomic force microscopy
Kunikazu Moribe et al.
CHEMICAL & PHARMACEUTICAL BULLETIN (2008)
Drying of crystalline drug nanosuspensions - The importance of surface hydrophobicity on dissolution behavior upon redispersion
Bernard Van Eerdenbrugh et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2008)
Alternative matrix formers for nanosuspension solidification: Dissolution performance and X-ray microanalysis as an evaluation tool for powder dispersion
Bernard Van Eerdenbrugh et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2008)
Formation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture
Adchara Pongpeerapat et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)
Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An Overview
Dwayne T. Friesen et al.
MOLECULAR PHARMACEUTICS (2008)
Drug Nanoparticles: Formulating Poorly Water-Soluble Compounds
Elaine M. Merisko-Liversidge et al.
TOXICOLOGIC PATHOLOGY (2008)
The utility of cyclodextrins for enhancing oral bioavailability
Rebecca L. Carrier et al.
JOURNAL OF CONTROLLED RELEASE (2007)
In vitro and in vivo evaluation of a fast-disintegrating lyophilized dry emulsion tablet containing griseofulvin
Iman Saad Ahmed et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2007)
Cyclodextrins as pharmaccutical solubilizers
Marcus E. Brewster et al.
ADVANCED DRUG DELIVERY REVIEWS (2007)
Characterization of physico-chemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media milling
B. Van Eerdenbrugh et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2007)
Application of nanoparticles in oral delivery of immediate release formulations
Filippos Kesisoglou et al.
CURRENT NANOSCIENCE (2007)
Preparation of redispersible dry nanocapsules by means of spray-drying:: Development and characterisation
Patrice Tewa-Tayne et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2007)
Preparation and in vitro/in vivo evaluation of nano-sized crystals for dissolution rate enhancement of ucb-35440-3, a highly dosed poorly water-soluble weak base
J. Hecq et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2006)
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
RN Gursoy et al.
BIOMEDICINE & PHARMACOTHERAPY (2004)
Nanosizing: a formulation approach for poorly-water-soluble compounds
E Merisko-Liversidge et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2003)
Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules
MK Gupta et al.
PHARMACEUTICAL RESEARCH (2002)
Production and characterization of a budesonide nanosuspension for pulmonary administration
C Jacobs et al.
PHARMACEUTICAL RESEARCH (2002)
Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
CW Pouton
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2000)
Drug-like properties and the causes of poor solubility and poor permeability
CA Lipinski
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS (2000)
Share Paper
