A one-pot strategy for biomimetic synthesis and self-assembly of gold nanoparticles

被引:22
|
作者
Wang, Yi [1 ]
Chen, Li Qiang [2 ]
Li, Yuan Fang [1 ]
Zhao, Xi Juan [1 ]
Peng, Li [2 ]
Huang, Cheng Zhi [1 ,3 ]
机构
[1] Southwest Univ, Coll Chem & Chem Engn, Educ Minist Key Lab Luminescence & Real Time Anal, Chongqing 400715, Peoples R China
[2] Southwest Univ, Coll Life Sci, Chongqing 400715, Peoples R China
[3] Southwest Univ, Coll Pharmaceut Sci, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
SHAPE-CONTROLLED SYNTHESIS; SILVER NANOPARTICLES; METAL NANOPARTICLES; OPTICAL-PROPERTIES; AQUEOUS-SOLUTION; DNA TEMPLATES; DEXTRAN; NANOSTRUCTURES; SURFACTANT; PROTEIN;
D O I
10.1088/0957-4484/21/30/305601
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A simple, one-pot and controllable strategy is reported in this contribution for biomimetic synthesis and self-assembly of gold nanoparticles (Au-NPs). It involves our synthesized polyaldehyde dextran (PAD), which has been proved to be a biomacromolecule with excellent biocompatibility and biodegradability, acting as both a reducing agent and a stabilizer. The morphology of the as-prepared Au-NP assemblies can be controlled by adjusting the reaction conditions, such as the concentration of aldehyde in PAD, the reaction time and the temperature. Investigations of the mechanism suggest that stabilizers may distribute on different crystal facets of NPs non-uniformly owing to the different binding forces, and dipole-dipole interaction of NPs could be the main driving force for the assembly of Au-NPs. In addition, intermolecular hydrogen bonding interaction of stabilizers could also act as a possible driving force. The excellent biocompatibility of the Au-NP assemblies makes them promising candidates for fabricating future optical nanodevices and application in biological systems.
引用
收藏
页数:8
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