Biomimetic nanoparticles: preparation, characterization and biomedical applications

被引:0
|
作者
Carmona-Ribeiro, Ana Maria [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, Biocolloids Lab, BR-05513970 Sao Paulo, Brazil
来源
基金
巴西圣保罗研究基金会;
关键词
cationic lipid; phospholipids; bilayer fragments; vesicles; silica; polymeric particles; antigens; novel cationic immunoadjuvants; drugs; AMPHOTERICIN-B FORMULATION; SUPPORTED LIPID-BILAYERS; COLLOID STABILITY; CATIONIC VESICLES; DIOCTADECYLDIMETHYLAMMONIUM CHLORIDE; COMPETITIVE ADSORPTION; PHYSICAL-CHEMISTRY; SYNTHETIC LIPIDS; SURFACE-CHARGE; PARTICLE-SIZE;
D O I
暂无
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Mimicking nature is a powerful approach for developing novel lipid-based devices for drug and vaccine delivery. In this review, biomimetic assemblies based on natural or synthetic lipids by themselves or associated to silica, latex or drug particles will be discussed. In water, self-assembly of lipid molecules into supramolecular structures is fairly well understood. However, their self-assembly on a solid surface or at an interface remains poorly understood. In certain cases, hydrophobic drug granules can be dispersed in aqueous solution via lipid adsorption surrounding the drug particles as nanocapsules. In other instances, hydrophobic drug molecules attach as monomers to borders of lipid bilayer fragments providing drug formulations that are effective in vivo at low drug-to-lipid-molar ratio. Cationic biomimetic particles offer suitable interfacial environment for adsorption, presentation and targeting of biomolecules in vivo. Thereby antigens can effectively be presented by tailored biomimetic particles for development of vaccines over a range of defined and controllable particle sizes. Biomolecular recognition between receptor and ligand can be reconstituted by means of receptor immobilization into supported lipidic bilayers allowing isolation and characterization of signal transduction steps.
引用
收藏
页码:249 / 259
页数:11
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