Encapsulation of bilayer vesicles by self-assembly

Vesicles of lipid bilayers have been investigated as drug-delivery vehicles for almost 20 years 1-8 . The vesicles’ interior space is separated from the surrounding solution because small molecules have only limited permeability through the bilayer. Single-walled (unilamellar) vesicles are made by a...

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Bibliographic Details
Published in:Nature (London) 1997-05, Vol.387 (6628), p.61-64
Main Authors: Walker, Scott A, Kennedy, Michael T, Zasadzinski, Joseph A
Format: Article
Language:English
Subjects:
Artificial membranes and reconstituted systems
Bacterial Proteins
Biochemistry
Biological and medical sciences
Biology
Biotin
Calcium
Dialysis
Drug Delivery Systems
Freeze Fracturing
Fundamental and applied biological sciences. Psychology
General pharmacology
Humanities and Social Sciences
letter
Lipid Bilayers - chemistry
Liposomes
Medical sciences
Membrane physicochemistry
Microscopy, Electron
Molecular biophysics
multidisciplinary
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Science
Science (multidisciplinary)
Streptavidin
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Summary:Vesicles of lipid bilayers have been investigated as drug-delivery vehicles for almost 20 years 1-8 . The vesicles’ interior space is separated from the surrounding solution because small molecules have only limited permeability through the bilayer. Single-walled (unilamellar) vesicles are made by a variety of non-equilibrium techniques, including mechanical disruption of lamellar phases by sonication or extrusion through filters, or chemical disruption by detergent dialysis or solvent removal 5 . These techniques do not, however, allow the encapsulation of a specific volume, nor can they be used to encapsulate other vesicles. Here we show that molecular-recognition processes mediated by lipophilic receptors and substrates (here the biotin–streptavidin complex) 9 can be used to produce a multicompartmental aggregate of tethered vesicles encapsulated within a large bilayer vesicle. We can these encapsulated aggregates vesosomes. Encapsulation is achieved by unrolling bilayers from cochleate cylinders 5,10-12 which are tethered to the aggregate by biotin–streptavidin coupling. These compartmentalized vesosomes could provide vehicles for multicomponent or multifunctional drug delivery 2-4,6 ;in particular, the encapsulating membrane could significantly modify permeation properties, or could be used to enhance the biocompatibility of the system.
ISSN:0028-0836
1476-4687
DOI:10.1038/387061a0