Stability and physicochemical characterization of novel milk-based oral formulations.

[1]  P. Macheras,et al.  Novel milk-based oral formulations: proof of concept. , 2010, International journal of pharmaceutics.

[2]  P. Wolschann,et al.  Density functional calculations on meloxicam-beta-cyclodextrin inclusion complexes. , 2009, International journal of pharmaceutics.

[3]  C. Pouton,et al.  Design of lipid-based formulations for oral administration of poorly water-soluble drugs: precipitation of drug after dispersion of formulations in aqueous solution. , 2009, Journal of pharmaceutical sciences.

[4]  Jing Li,et al.  Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent. , 2009, Journal of pharmaceutical sciences.

[5]  M. Yeh,et al.  Improving Tenoxicam Solubility and Bioavailability by Cosolvent System , 2009, AAPS PharmSciTech.

[6]  Anette Müllertz,et al.  Lipid-based Formulations for Danazol Containing a Digestible Surfactant, Labrafil M2125CS: In Vivo Bioavailability and Dynamic In Vitro Lipolysis , 2008, Pharmaceutical Research.

[7]  S. Mutalik,et al.  Enhancement of dissolution rate and bioavailability of aceclofenac: a chitosan-based solvent change approach. , 2008, International journal of pharmaceutics.

[8]  Sonu Bhatia,et al.  Solubility enhancement of cox-2 inhibitors using various solvent systems , 2003, AAPS PharmSciTech.

[9]  C. Porter,et al.  Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs , 2007, Nature Reviews Drug Discovery.

[10]  Jörg Breitkreutz,et al.  Paediatric and geriatric drug delivery , 2007, Expert opinion on drug delivery.

[11]  D. Hauss.  ORAL LIPID-BASED FORMULATIONS : BRIDGING THE GAP BETWEEN KNOWLEDGE AND KNOW-HOW , 2007 .

[12]  N. Rasenack,et al.  Dissolution Rate Enhancement by in Situ Micronization of Poorly Water-Soluble Drugs , 2002, Pharmaceutical Research.

[13]  Joachim Grevel,et al.  Improved Dose Linearity of Cyclosporine Pharmacokinetics from a Microemulsion Formulation , 1994, Pharmaceutical Research.

[14]  Joachim Grevel,et al.  Influence of a Fat-Rich Meal on the Pharmacokinetics of a New Oral Formulation of Cyclosporine in a Crossover Comparison with the Market Formulation , 2004, Pharmaceutical Research.

[15]  K. Johnston,et al.  Spray freezing into liquid (SFL) particle engineering technology to enhance dissolution of poorly water soluble drugs: organic solvent versus organic/aqueous co-solvent systems. , 2003, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[16]  N. Rasenack,et al.  Microcrystals for dissolution rate enhancement of poorly water-soluble drugs. , 2003, International journal of pharmaceutics.

[17]  K. Johnston,et al.  Micronized powders of a poorly water soluble drug produced by a spray-freezing into liquid-emulsion process. , 2003, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[18]  K. Johnston,et al.  Physical Stability of Micronized Powders Produced by Spray-Freezing into Liquid (SFL) to Enhance the Dissolution of an Insoluble Drug , 2003, Pharmaceutical development and technology.

[19]  N. Rasenack,et al.  Micronization of anti-inflammatory drugs for pulmonary delivery by a controlled crystallization process. , 2003, Journal of pharmaceutical sciences.

[20]  S. Santoyo,et al.  Study of the Complexation Behavior of Tenoxicam with Cyclodextrins in Solution: Improved Solubility and Percutaneous Permeability , 2002, Drug development and industrial pharmacy.

[21]  M. Michalski,et al.  Apparent ζ-potential as a tool to assess mechanical damages to the milk fat globule membrane , 2002 .

[22]  Brian J. Wright,et al.  Addition of Polarization and Diffuse Functions to the LANL2DZ Basis Set for P-Block Elements , 2001 .

[23]  C. Pouton,et al.  Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems. , 2000, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[24]  Brahma N. Singh.  Effects of Food on Clinical Pharmacokinetics , 1999, Clinical pharmacokinetics.

[25]  Colin W. Pouton,et al.  Formulation of self-emulsifying drug delivery systems , 1997 .

[26]  W. Charman,et al.  Lipid-based vehicles for the oral delivery of poorly water soluble drugs , 1997 .

[27]  Hans W. Horn,et al.  Fully optimized contracted Gaussian basis sets for atoms Li to Kr , 1992 .

[28]  S. Fowler,et al.  Spectrofluorometric studies of the lipid probe, nile red. , 1985, Journal of lipid research.

[29]  I. W. Levin,et al.  Effects of anesthetic and nonanesthetic steroids on dipalmitoylphosphatidylcholine liposomes: a calorimetric and Raman spectroscopic investigation. , 1984, Biochemistry.

[30]  Pieter Walstra,et al.  Dairy chemistry and physics , 1984 .

[31]  R. G. Snyder,et al.  Carbon-hydrogen stretching modes and the structure of n-alkyl chains. 2. Long, all-trans chains , 1984 .

[32]  R. G. Snyder,et al.  C-H stretching modes and the structure of n-alkyl chains. II: Long, all-trans chains , 1984 .

[33]  G. Forrest.  Raman spectroscopy of the milk globule membrane and triglycerides , 1978 .

[34]  R. G. Crounse,et al.  Fluorescence Assay in Biology and Medicine , 1963 .

[35]  E. Jack,et al.  The Electrokinetic Potential of Milk Fat , 1937 .