ARTICLE;
CHEMICAL COMPOSITION;
CHEMICAL PHENOMENA;
CONTROLLED STUDY;
DRUG DOSAGE FORM;
DRUG DOSAGE FORM COMPARISON;
DRUG RELEASE;
DRUG SOLUBILITY;
EXPERIMENTAL DESIGN;
FASTED STATE CONDITION;
IN VITRO STUDY;
MESOPOROUS SILICA BASED DOSAGE FORM;
PARACHUTE EFFECT;
PROCESS OPTIMIZATION;
SIMULATION;
SPRING EFFECT;
TIME SERIES ANALYSIS;
TRANSFER MODEL EXPERIMENT;
ANALOGS AND DERIVATIVES;
CHEMICAL MODEL;
CHEMISTRY;
COMPARATIVE STUDY;
DELAYED RELEASE FORMULATION;
DIET RESTRICTION;
DRUG FORMULATION;
INTESTINAL SECRETIONS;
KINETICS;
PARTICLE SIZE;
PHARMACEUTICS;
POROSITY;
PROCEDURES;
SOLUBILITY;
STOMACH JUICE;
Evaluation of the dissolution behaviour of novel fenofibrate silica formulations in preprandial biorelevant media AAPS Poster M1189
Fei Y, et al. Evaluation of the dissolution behaviour of novel fenofibrate silica formulations in preprandial biorelevant media AAPS Poster M1189, AAPS Annual Meeting, San Antonio, Texas 2013.
Predicting the oral absorption of a poorly soluble, poorly permeable weak base using biorelevant dissolution and transfer models coupled with a physiologically based pharmacokinetic model
Wagner C, et al. Predicting the oral absorption of a poorly soluble, poorly permeable weak base using biorelevant dissolution and transfer models coupled with a physiologically based pharmacokinetic model. EJPB 2012; 82: 127-138.
Precipitation in the small intestine may play a more important role in the absorption of poorly soluble weak bases: Case example nelfinavir
Shono Y, et al. Precipitation in the small intestine may play a more important role in the absorption of poorly soluble weak bases: case example nelfinavir. EJPB 2011; 79: 349-356.
Prediction of oral absorption of cinnarizine - A highly supersaturating poorly soluble weak base with borderline permeability
Berlin M, et al. Prediction of oral absorption of cinnarizine-a highly supersaturating poorly soluble weak base with borderline permeability. Eur J Pharm Biopharm 2014; 88: 795-806.
Synthesis based on the wet impregnation method and characterization of iron and iron oxide-silica nanocomposites
Alcalá M, Real M,. Synthesis based on the wet impregnation method and characterization of iron and iron oxide-silica nanocomposites. Solid State Ionics 2006; 177: 955-960.
Biorelevant in vitro dissolution testing of micronized or nanosized products of fenofibrate with a view to predicting plasma profiles
Jünemann D, et al. Biorelevant in vitro dissolution testing of micronized or nanosized products of fenofibrate with a view to predicting plasma profiles. Eur J Pharm Biopharm 2011; 77: 257-264.
Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds
Vertzoni M, et al. Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds. Eur J Pharm Biopharm 2005; 60: 413-417.
List of generally regarded as safe ingredients, US-HHS FDA. (accessed 18 February, 2015) http://www.accessdata.fda.gov/scripts/fdcc/index.cfm?set=SCOGS&sort=Sortsubstance&order=ASC&startrow=251&type=basic&search=.
