Multifunctional DNA Nanomaterials for Biomedical Applications

被引:18
|
作者
Tam, Dick Yan [1 ,2 ]
Lo, Pik Kwan [1 ,2 ]
机构
[1] City Univ Hong Kong, Dept Biol & Chem, Kowloon, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Shenzhen Key Lab Biochip Res, Shenzhen 518057, Peoples R China
基金
美国国家科学基金会;
关键词
NUCLEIC-ACID JUNCTIONS; SINGLE-STRANDED-DNA; INTRACELLULAR DELIVERY; ORIGAMI NANOSTRUCTURES; CRYSTAL-STRUCTURE; BINDING AFFINITY; BLOCK-COPOLYMERS; CELLULAR UPTAKE; PROTEIN ARRAYS; PH CHANGES;
D O I
10.1155/2015/765492
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The rapidly emerging DNA nanotechnology began with pioneer Seeman's hypothesis that DNA not only can carry genetic information but also can be used as molecular organizer to create well-designed and controllable nanomaterials for applications in materials science, nanotechnology, and biology. DNA-based self-assembly represents a versatile system for nanoscale construction due to the well-characterized conformation of DNA and its predictability in the formation of base pairs. The structural features of nucleic acids form the basis of constructing a wide variety of DNA nanoarchitectures with well-defined shapes and sizes, in addition to controllable permeability and flexibility. More importantly, self-assembled DNA nanostructures can be easily functionalized to construct artificial functional systems with nanometer scale precision for multipurposes. Apparently scientists envision artificial DNA-based nanostructures as tool for drug loading and in vivo targeted delivery because of their abilities in selective encapsulation and stimuli-triggered release of cargo. Herein, we summarize the strategies of creating multidimensional self-assembled DNA nanoarchitectures and review studies investigating their stability, toxicity, delivery efficiency, loading, and control release of cargos in addition to their site-specific targeting and delivery of drug or cargo molecules to cellular systems.
引用
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页数:21
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