Abstract

We studied the quantum dot-liposome complex (QLC), which is the giant unilamellar vesicle with quantum dots (QDs) incorporated in its lipid bilayer. A spin coating method in conjunction with the electroformation technique yielded vesicles with highly homogeneous unilamellar structure. We observed QD size dependence of the QLC formation: QLCs form with blue, green and yellow-emission QD (core radius ~1.05 nm, 1.25 nm and 1.65 nm) but not with red-emission QD (core radius ~2.5 nm). In order to explain this size dependence, we made a simple model explaining the QD size effect on QLC formation in terms of the molecular packing parameter and the lipid conformational change. This model predicts that QDs below a certain critical size (radius ≈ 1.8 nm) can stably reside in a lipid bilayer of 4 - 5 nm in thickness for Egg-PC lipids. This is consistent with our previous experimental results. In the case of red-emission QD, QD-aggregations are only observed on the fluorescent microscopy instead of QLC. We expected that the reduction of packing parameter (P) would lead to the change of specific QD radius. This prediction could be verified by our experimental observation of the shift of the specific QD size by mixing DOPG.

Highlights

  • Labeling biomolecules and cells with organic fluorophores are representative tools for studying the underlying complex interactions and the dynamics in metabolic processes in various time and length scales

  • We studied the stability problem of quantum dots (QDs) inside the lipid bilayer depending on the size of QD as shown Figure 1 and experimentally proposed quantum dot-liposome complex (QLC), which are GUVs (Giant Unilamellar Vesicles) with QDs below critical QD size loaded into the DOPC lipid bilayer

  • We proposed a simple model to describe the stability of QDs embedded in lipid bilayer in terms of molecular packing parameter and the conformational change of the lipid chain

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Summary

Introduction

Labeling biomolecules and cells with organic fluorophores are representative tools for studying the underlying complex interactions and the dynamics in metabolic processes in various time and length scales. These organic fluorophores have been gradually replaced by nano-size semiconductor nanocrystals [1] such as quantum dots (QDs). One good example is QLC (Quantum dot-Liposome Complex) which is a giant unilamellar vesicle with QDs incorporated in the lipid bilayer [12] [13] [14] [15].

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