Liposome-based nanocapsules

被引:48
作者
Ruysschaert, T
Germain, M
Gomes, JFPD
Fournier, D
Sukhorukov, GB
Meier, W
Winterhalter, M [1 ]
机构
[1] CNRS, UMR 5089, Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
[2] Univ Porto, P-4100 Oporto, Portugal
[3] Max Planck Inst Colloids & Interfaces, D-14476 Golm, Germany
[4] Univ Basel, CH-4056 Basel, Switzerland
[5] Int Univ Bremen, D-28726 Bremen, Germany
关键词
biosensor; nanocapsules; polymer network; stabilized liposomes;
D O I
10.1109/TNB.2004.824273
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we present three different types of mechanically stable nanometer-sized hollow capsules. The common point of the currently developed systems in our laboratory is that they are liposome based. Biomolecules can be used to functionalize lipid vesicles to create a new type of intelligent material. For example, insertion of membrane channels into the capsule wall can modify the permeability. Covalent binding of antibodies allows targeting of the capsule to specific sites. Liposomes loaded with enzymes may provide an optimal environment for them with respect to the maximal turnover and may stabilize the enzyme. However, the main drawback of liposomes is their instability in biological media as well as their sensitivity to many external parameters such as temperature or osmotic pressure. To increase their stability we follow different strategies: 1) polymerize a two-dimensional network in the hydrophobic core of the membrane; 2) coat the liposome with a polyelectrolyte shell; or 3) add surface active polymers to form mixed vesicular structures.
引用
收藏
页码:49 / 55
页数:7
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