Quantitative characterization of the lipid encapsulation of quantum dots for biomedical applications
Abstract
The water solubilization of nanoparticles is key for many applications in biomedicine. Despite the importance of surface functionalization, progress has been largely empirical and very few systematic studies have been performed. Here we report on the water solubilization of quantum dots using lipid encapsulation. We systematically evaluate the monodispersity, zeta potential, stability, and quantum yield for quantum dots encapsulated with single and double acyl–chain lipids, pegylated double acyl–chain lipids, and single alkyl–chain surfactant molecules with charged head groups. We show that charged surfactants and pegylated lipids are important to obtain monodisperse suspensions with high yield and excellent long-term stability.
Graphical Abstract
Lipid encapsulation is a biomimetic approach to water solubilization of nanoparticles that takes advantage of hydrophobic interactions to drive formation of an outer leaflet. The physicochemical properties of lipid-encapsulated nanoparticles, such as monodispersity, zeta potential, stability, and quantum yield, can be optimized by varying the composition of the lipid layer through combinations of single- and double–acyl chain lipids, pegylated double–acyl chain lipids, and single–alkyl chain surfactant molecules with charged head groups.
Key words: Quantum dots, Lipids, Surface functionalization, Biomedicine, Solubilization
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The authors acknowledge support from the National Institutes of Health (U54CA151838) and the National Science Foundation (NSF) (CHE-0905869). J.F.G. acknowledges support from the NSF Integrative Graduate Education and Research Traineeship program. A.W. acknowledges support from the Institute for NanoBioTechnology Research Experience for Undergraduates program at Johns Hopkins University.
PII: S1549-9634(11)00597-1
doi:10.1016/j.nano.2011.12.002
© 2011 Elsevier Inc. All rights reserved.

