Preparation and Optimization of Nanoemulsions for targeting DrugDelivery

Nanoemulsions have appeared as a novel drug delivery system which allows sustained or controlled release of drug, biological active ingredient and genetic material. Nanoemulsion is a dispersion consisting of oil, surfactant and an aqueous phase, which is a isotropically clear and thermo-dynamically or kinetically stable liquid solution, usually with droplet diameter within the range of 10-500nm. Although interest in nano-emulsions was developed for more than two decades now, mainly for nanoparticle preparation, it is in the last few years that direct applications of nano-emulsions in consumer products are being developed, mainly in pharmacy and cosmetics. These recent applications have made that studies on optimization methods for nano-emulsion preparation be a requirement. The design of effective formulations for drugs has long been a major task, because drug efficacy can severely limited by instability or poor solubility in the vehicle. Nanoemulsion is being applied to enhance the solubility and bioavailability of water insoluble drugs. The nanosized droplets leading to an enormous increase in interfacial areas associated with nanoemulsion would influence the transport properties of the drug [1, 2]. Recently, there has been a considerable attraction for this formulation, for the delivery of hydrophilic as well as hydrophobic drug as drug carriers because of its improved drug solubilization capacity, long shelf life, ease of preparation and improvement of bioavailability of drugs. This review is focused on the most recent literature on developments of nano-emulsions as final application products and on the optimization of their preparation.

[1]  F. Ahmad,et al.  Investigation of Nanoemulsion System for Transdermal Delivery of Domperidone: Ex-vivo and in vivo Studies , 2008 .

[2]  Kamalinder K. Singh,et al.  Formulation, antimalarial activity and biodistribution of oral lipid nanoemulsion of primaquine. , 2008, International journal of pharmaceutics.

[3]  S. Adachi,et al.  Continuous preparation of O/W nano-emulsion by the treatment of a coarse emulsion under subcritical water conditions , 2007 .

[4]  Gaoyong Zhang,et al.  Oil-in-water nanoemulsions for pesticide formulations. , 2007, Journal of colloid and interface science.

[5]  Sushma Talegaonkar,et al.  Development and bioavailability assessment of ramipril nanoemulsion formulation. , 2007, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[6]  Jian Xu,et al.  Formation and stability of paraffin oil-in-water nano-emulsions prepared by the emulsion inversion point method. , 2006, Journal of colloid and interface science.

[7]  C. Solans,et al.  Optimization of nano-emulsion preparation by low-energy methods in an ionic surfactant system. , 2006, Langmuir : the ACS journal of surfaces and colloids.

[8]  S. Sajjadi Nanoemulsion formation by phase inversion emulsification: on the nature of inversion. , 2006, Langmuir : the ACS journal of surfaces and colloids.

[9]  U. Olsson,et al.  Oil/water droplet formation by temperature change in the water/c(16)e(6)/mineral oil system. , 2006, Langmuir : the ACS journal of surfaces and colloids.

[10]  Kuniaki Tanaka,et al.  Formation and Charaterization of Submicrometer Oil-in-Water (O/W) Emulsions, Using High-Energy Emulsification , 2006 .

[11]  Jordi Esquena,et al.  The influence of surfactant mixing ratio on nano-emulsion formation by the pit method. , 2005, Journal of colloid and interface science.

[12]  M. Khan,et al.  Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate. , 2004, International journal of pharmaceutics.

[13]  I. Capek Degradation of kinetically-stable o/w emulsions. , 2004, Advances in colloid and interface science.

[14]  C. Solans,et al.  Nano-Emulsions: Formation, Properties, and Applications , 2003 .

[15]  M. Lawrence,et al.  Microemulsion-based media as novel drug delivery systems , 2000 .

[16]  P. Thoren,et al.  Triglyceride-based microemulsion for intravenous administration of sparingly soluble substances. , 1998, Journal of pharmaceutical sciences.

[17]  I. Lifshitz,et al.  The kinetics of precipitation from supersaturated solid solutions , 1961 .