Nanostructured lipid carrier versus solid lipid nanoparticles of simvastatin: Comparative analysis of characteristics, pharmacokinetics and tissue uptake
- 30 August 2011
- journal article
- research article
- Published by Elsevier BV in International Journal of Pharmaceutics
- Vol. 415 (1-2), 232-243
- https://doi.org/10.1016/j.ijpharm.2011.05.044
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Glyceryl Monooleate/Poloxamer 407 Cubic Nanoparticles as Oral Drug Delivery Systems: I. In Vitro Evaluation and Enhanced Oral Bioavailability of the Poorly Water-Soluble Drug SimvastatinAAPS PharmSciTech, 2009
- Enhancement of gastrointestinal absorption of quercetin by solid lipid nanoparticlesJournal of Controlled Release, 2009
- Formulation and In Vivo Evaluation of Self-Nanoemulsifying Granules for Oral Delivery of a Combination of Ezetimibe and SimvastatinDrug Development and Industrial Pharmacy, 2008
- The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugsInternational Journal of Pharmaceutics, 2004
- Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogsInternational Journal of Pharmaceutics, 2004
- Production and characterisation of mucoadhesive nanosuspensions for the formulation of bupravaquoneInternational Journal of Pharmaceutics, 2001
- In vitro–in vivo correlations for lipophilic, poorly water-soluble drugsEuropean Journal of Pharmaceutical Sciences, 2000
- Intestinal Permeation EnhancersJournal of Pharmaceutical Sciences, 2000
- Metabolism and Drug Interactions of 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Inhibitors in Transplant Patients: Are the Statins Mechanistically Similar?Pharmacology & Therapeutics, 1998
- Lipid-based vehicles for the oral delivery of poorly water soluble drugsAdvanced Drug Delivery Reviews, 1997