4.1 Review

NANOEMULSIONS AS PARENTERAL DRUG DELIVERY SYSTEMS

Journal

QUIMICA NOVA
Volume 35, Issue 9, Pages 1827-1840

Publisher

SOC BRASILEIRA QUIMICA
DOI: 10.1590/S0100-40422012000900023

Keywords

emulsion; parenteral; drug

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NANOEMULSIONS AS PARENTERAL DRUG DELIVERY SYSTEMS. Lipid nanoemulsions have recently been proposed as parenteral delivery systems for poorly-soluble drugs. These systems consist of nanoscale oil/water dispersions stabilized by an appropriate surfactant system in which the drug is incorporated into the oil core and/or adsorbed at the interface. This article reviews technological aspects of such nanosystems, including their composition, preparation methods, and physicochemical properties. From this review, it was possible to identify five groups of nanoemulsions based on their composition. Biopharmaceutical aspects of formulations containing some commercially available drugs (diazepam, propofol, dexamethasone, etomidate, flurbiprofen and prostaglandin E1) were then discussed.

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