Polymersomes: nature inspired nanometer sized compartments

被引:338
作者
LoPresti, Caterina [1 ]
Lomas, Hannah [1 ]
Massignani, Marzia [1 ]
Smart, Thomas [1 ]
Battaglia, Giuseppe [1 ]
机构
[1] Univ Sheffield, Dept Mat Engn, Kroto Res Inst, Sheffield S3 7HQ, S Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
BLOCK-COPOLYMER VESICLES; INFRARED-EMISSIVE POLYMERSOMES; MOLECULAR-WEIGHT DEPENDENCE; TRIBLOCK COPOLYMER; DIBLOCK COPOLYMER; BIODEGRADABLE POLYMERSOMES; GIANT VESICLES; IN-VIVO; RESPONSIVE VESICLES; DNA ENCAPSULATION;
D O I
10.1039/b818869f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Provided the right hydrophilic/hydrophobic balance can be achieved, amphiphilic block copolymers are able to assemble in water into membranes. These membranes can enclose forming spheres with an aqueous core. Such structures, known as polymer vesicles or polymersomes (from the Greek "-some'' = "body of''), have sizes that vary from tens to thousands of nanometers. The wholly synthetic nature of block copolymers affords control over parameters such as the molar mass and composition which ultimately determine the structure and properties of the species in solution. By varying the copolymer molecular mass it is possible to adjust the mechanical properties and permeability of the polymersomes, while the synthetic nature of copolymers allows the design of interfaces containing various biochemically-active functional groups. In particular, non-fouling and non-antigenic polymers have been combined with hydrophobic polymers in the design of biocompatible nano-carriers that are expected to exhibit very long circulation times. Stimulus-responsive block copolymers have also been used to exploit the possibility to trigger the disassembly of polymersomes in response to specific external stimuli such as pH, oxidative species, and enzyme degradation. Such bio-inspired 'bottom-up' supramolecular design principles offer outstanding advantages in engineering structures at a molecular level, using the same long-studied principles of biological molecules. Thanks to their unique properties, polymersomes have already been reported and studied as delivery systems for both drugs, genes, and image contrast agents as well as nanometer-sized reactors.
引用
收藏
页码:3576 / 3590
页数:15
相关论文
共 160 条
[1]   Self-porating polymersomes of PEG-PLA and PEG-PCL: hydrolysis-triggered controlled release vesicles [J].
Ahmed, F ;
Discher, DE .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (01) :37-53
[2]   Biodegradable polymersomes loaded with both paclitaxel and doxorubicin permeate and shrink tumors, inducing apoptosis in proportion to accumulated drug [J].
Ahmed, Fariyal ;
Pakunlu, Refika I. ;
Brannan, Aaron ;
Bates, Frank ;
Minko, Tamara ;
Discher, Dennis E. .
JOURNAL OF CONTROLLED RELEASE, 2006, 116 (02) :150-158
[3]   Shrinkage of a rapidly growing tumor by drug-loaded polymersomes: pH-triggered release through copolymer degradation [J].
Ahmed, Fariyal ;
Pakunlu, Refika I. ;
Srinivas, Goundla ;
Brannan, Aaron ;
Bates, Frank ;
Klein, Michael L. ;
Minko, Tamara ;
Discher, Dennis E. .
MOLECULAR PHARMACEUTICS, 2006, 3 (03) :340-350
[4]  
Alberts B., 2007, Molecular Biology of the Cell. (4th edition), Vfifth
[5]  
Alcantar NA, 2000, J BIOMED MATER RES, V51, P343, DOI 10.1002/1097-4636(20000905)51:3<343::AID-JBM7>3.0.CO
[6]  
2-D
[7]   LIPOSOME ELECTROFORMATION [J].
ANGELOVA, MI ;
DIMITROV, DS .
FARADAY DISCUSSIONS, 1986, 81 :303-+
[8]   Electromechanical limits of polymersomes [J].
Aranda-Espinoza, H ;
Bermudez, H ;
Bates, FS ;
Discher, DE .
PHYSICAL REVIEW LETTERS, 2001, 87 (20) :208301-1
[9]   Polymersome encapsulated hemoglobin: A novel type of oxygen carrier [J].
Arifin, DR ;
Palmer, AF .
BIOMACROMOLECULES, 2005, 6 (04) :2172-2181
[10]   Neuron-like tubular membranes made of diblock copolymer amphiphiles [J].
Battaglia, G ;
Ryan, AJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (13) :2052-2056