Stable polymethacrylate nanocapsules from ultraviolet light-induced template radical polymerization of unilamellar liposomes

被引:46
作者
da Silva Gomes, Joana Filipa Pereira [1 ]
Sonnen, Andreas F-P.
Kronenberger, Astrid
Fritz, Juergen
Neto Coelho, Manuel Alvaro
Fournier, Didier
Fournier-Noel, Clara
Mauzac, Monique
Winterhalter, Mathias
机构
[1] CNRS, Inst Pharmacol & Biol Struct, UMR5089, F-31077 Toulouse, France
[2] Int Jacobs Univ Bremen, D-28759 Bremen, Germany
[3] Univ Porto, Fac Engn, Lab Engn Proc Ambiente & Energia, P-4100 Oporto, Portugal
[4] Univ Oxford, Div Struct Biol, Oxford OX3 7BN, England
[5] UPS, CNRS, UMR5623, Lab Interact Mol & React Chim & Photochim, Toulouse, France
基金
英国惠康基金;
关键词
D O I
10.1021/la0613575
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We employed UV-induced template polymerization to create hollow nanometer-sized polymer capsules. Homogeneous, unilamellar liposomes served as a two-dimensional template for the cross-linking of either butyl methacrylate or hydroxyethyl methacrylate with the bifunctional ethyleneglycol dimethacrylate. Different molar ratios of lipid/hydrophobic monomer/bifunctional monomer/photoinitiator were tested and dynamic light scattering revealed negligible changes of size at a defined molar ratio of 2/1/10/20, respectively. Cryo-transmission electron microscopy provided clear evidence that incorporation of the methacrylate monomers into and polymerization in the hydrophobic bilayer phase does not disrupt vesicle integrity. Moreover, after solubilization of the lipids, the polymethacrylate nanocapsules were stable at conditions needed for negative staining and could be visualized by atomic force microscopy. In contrast to previous findings, the nanocapsule size and shape did not change considerably after removal of the template phase, and the size distribution remained strictly monomodal. The employed method is not only an advance to fortify liposomes, but the nanocapsules themselves can be functionalized.
引用
收藏
页码:7755 / 7759
页数:5
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