Quality by design: Understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box–Behnken design and desirability function
- 6 March 2007
- journal article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 332 (1-2), 55-63
- https://doi.org/10.1016/j.ijpharm.2006.09.060
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Optimisation and characterisation of bioadhesive controlled release tetracycline microspheresInternational Journal of Pharmaceutics, 2005
- pH-sensitive nanoparticles for improving the oral bioavailability of cyclosporine AInternational Journal of Pharmaceutics, 2004
- Cyclosporine-loaded polycaprolactone nanoparticles: immunosuppression and nephrotoxicity in ratsEuropean Journal of Pharmaceutical Sciences, 2001
- Formulation and physical characterization of water-in-oil microemulsions containing long- versus medium-chain glyceridesInternational Journal of Pharmaceutics, 1997
- Factors Affecting the Efficiency of a Self-Emulsifying Oral Delivery SystemDrug Development and Industrial Pharmacy, 1997
- An investigation into physical and chemical properties of semi-solid self-emulsifying systems for hard gelatin capsulesInternational Journal of Pharmaceutics, 1996
- CyclosporinDrugs, 1995
- Self-emulsifying drug delivery systems (SEDDS) with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugsInternational Journal of Pharmaceutics, 1994
- Intraindividual variability in the relative systemic availability of cyclosporin after oral dosingEuropean Journal of Clinical Pharmacology, 1988
- Some New Three Level Designs for the Study of Quantitative VariablesTechnometrics, 1960