Mixture experiment methods in the development and optimization of microemulsion formulations.

[1]  K. A. Khan The concept of dissolution efficiency , 1975, The Journal of pharmacy and pharmacology.

[2]  J. Cornell,et al.  Experiments with Mixtures , 1992 .

[3]  H. Blume,et al.  Pharmaceutical Quality of Glibenclamide Products A Multinational Postmarket Comparative Study , 1993 .

[4]  B. Müller,et al.  Deactivation of amorphous glibenclamide during dissolution , 1996 .

[5]  A. Mitrevej,et al.  Effect of Grinding of β-Cyclodextrin and Glibenclamide on Tablet Properties. Part I. in vitro , 1996 .

[6]  S. P. Moulik,et al.  Structure, dynamics and transport properties of microemulsions , 1998 .

[7]  Roger Phan-Tan-Luu,et al.  Pharmaceutical Experimental Design , 1998 .

[8]  D Vojnovic,et al.  Experimental design for a pharmaceutical formulation: optimisation and robustness. , 1998, Journal of pharmaceutical and biomedical analysis.

[9]  M. Lawrence,et al.  Nonionic oil-in-water microemulsions: the effect of oil type on phase behaviour. , 2000, International journal of pharmaceutics.

[10]  S. Benita,et al.  Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs. , 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[11]  S. Chi,et al.  Transdermal delivery of ketoprofen using microemulsions. , 2001, International journal of pharmaceutics.

[12]  Koji Takahashi,et al.  Microemulsion formulation for enhanced absorption of poorly soluble drugs. I. Prescription design. , 2002, Journal of controlled release : official journal of the Controlled Release Society.

[13]  Richard G. Brereton,et al.  Chemometrics: Data Analysis for the Laboratory and Chemical Plant , 2003 .

[14]  P. Mura,et al.  Development and Evaluation of Glyburide Fast Dissolving Tablets Using Solid Dispersion Technique , 2004, Drug development and industrial pharmacy.

[15]  Subhabrata Ray,et al.  Formulation design of self-microemulsifying drug delivery systems for improved oral bioavailability of celecoxib. , 2004, Biological & pharmaceutical bulletin.

[16]  P. Constantinides,et al.  Lipid Microemulsions for Improving Drug Dissolution and Oral Absorption: Physical and Biopharmaceutical Aspects , 1995, Pharmaceutical Research.

[17]  N. Najib,et al.  In Vitro and In Vivo Evaluation of Glibenclamide in Solid Dispersion Systems , 2004, Drug development and industrial pharmacy.

[18]  Ping Gao,et al.  Application of a Mixture Experimental Design in the Optimization of a Self‐Emulsifying Formulation with a High Drug Load , 2005, Pharmaceutical development and technology.

[19]  S. Furlanetto,et al.  Mixture design in the optimization of a microemulsion system for the electrokinetic chromatographic determination of ketorolac and its impurities: Method development and validation , 2006, Electrophoresis.

[20]  Wei Wu,et al.  Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system. , 2006, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[21]  R. Holm,et al.  Optimization of Self-Microemulsifying Drug Delivery Systems (SMEDDS) Using a D-Optimal Design and the Desirability Function , 2006, Drug development and industrial pharmacy.

[22]  Paola Mura,et al.  Fast-Dissolving Tablets of Glyburide Based on Ternary Solid Dispersions with PEG 6000 and Surfactants , 2007, Drug delivery.