Preparation and characterization of lipid based nanosystems for topical delivery of quercetin

被引:110
作者
Bose, Sonali [1 ,2 ]
Michniak-Kohn, Bozena [1 ]
机构
[1] Rutgers State Univ, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
[2] Novartis Pharmaceut, Pharmaceut & Analyt Dev, E Hanover, NJ 07936 USA
关键词
Solid lipid nanoparticles; Nanostructured lipid carriers; Sonication; Physical stability; Solid lipid; Oleic acid; SKIN PENETRATION ENHANCERS; OLEIC-ACID; IN-VITRO; CONTROLLED-RELEASE; STRATUM-CORNEUM; CARRIERS NLC; TRANSDERMAL DELIVERY; PERMEATION ENHANCERS; NANOPARTICLES SLN; OXIDATIVE STRESS;
D O I
10.1016/j.ejps.2012.12.005
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The main objective of this study was to evaluate the potential of lipid nanosystems for topical delivery of the naturally occurring flavonoid quercetin. These lipid based nanosystems were manufactured using a solvent free probe ultrasonication process. Formulation factors such as the nature of the lipid (solid/combination of solid and liquid) in solid lipid nanoparticle (SLN) and nanostructured lipid carrier (NLC) systems and drug loading were evaluated to produce an optimum formulation with adequate physical stability for up to 14 weeks at 2-8 degrees C. The mean particle size of the optimized formulation was around 282 nm, with a zeta potential value of -36.57 +/- 2.67 mV, indicating the formation of a stable system. Release studies showed a biphasic release profile, characterized by an initial burst release followed by a more controlled release pattern from both SLN and NLC systems. The NLC system showed the highest improvement in topical delivery of quercetin manifested by the amount of quercetin retained in full thickness human skin, compared to a control formulation with similar composition and particle size in the micrometer range. This study demonstrated the feasibility of nanostructured lipid carrier systems for improved topical delivery of quercetin. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:442 / 452
页数:11
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