Scanning Probe Microscopy of Nanocomposite Membranes and Dynamic Organization

被引:6
作者
Montano, Gabriel A. [1 ]
Adams, Peter G. [1 ]
Xiao, Xiaoyin [2 ]
Goodwin, Peter M. [1 ]
机构
[1] Los Alamos Natl Lab, Ctr Integrated Nanotechnol, POB 1663, Los Alamos, NM 87545 USA
[2] Sandia Natl Labs, Albuquerque, NM 87185 USA
关键词
atomic force microscopy; programmable membrane-based nanocomposites; lipid bilayer assemblies; polymer membrane assemblies; nanotechnology; SUPPORTED LIPID-BILAYERS; ATOMIC-FORCE MICROSCOPY; PHOTOSYNTHETIC CORE COMPLEX; POLYMER BRUSHES; BLOCK-COPOLYMERS; 3-DIMENSIONAL STRUCTURES; PHOSPHOLIPID-MEMBRANES; CATIONIC NANOPARTICLES; DRUG-DELIVERY; PROTEINS;
D O I
10.1002/adfm.201203429
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanocomposite membrane assemblies are a class of materials that incorporate inorganic/organic nanoscale materials, such as fullerenes and gold nanoparticles or nanostructured materials with bio-inspired amphiphilic structures composed of molecules such as lipids or block copolymers. One of the intrigues of such materials is the potential to develop programmable membrane assemblies that mimic biological membrane complexity, dynamics and function. Due to the nanoscale nature of the assemblies, it becomes necessary to understand interactions between these materials with nanoscale resolution. Although many techniques are able to provide information as to the overall organization of membrane-based assemblies, only scanning probe microscopy (SPM) methods allow for a direct visualization of stochastic processes under environmentally relevant conditions. Here, an overview of nanocomposite membrane and thin film architecture investigations is presented with an emphasis on using in situ atomic force microscopy (AFM) in combination with fluorescence microscopy/spectroscopy techniques to understand organization and dynamics, in relation to activities and capabilities at the Center for Integrated Nanotechnologies.
引用
收藏
页码:2576 / 2591
页数:16
相关论文
共 122 条
[61]   Nanoscale protein patterning using self-assembled diblock copolymers [J].
Kumar, N ;
Hahm, JI .
LANGMUIR, 2005, 21 (15) :6652-6655
[62]   Activity study of self-assembled proteins on nanoscale diblock copolymer templates [J].
Kumar, Nitin ;
Parajuli, Omkar ;
Dorfman, Adam ;
Kipp, Dylan ;
Hahm, Jong-in .
LANGMUIR, 2007, 23 (14) :7416-7422
[63]   Reorganization of binary polymer brushes: Reversible switching of surface microstructures and nanomechanical properties [J].
Lemieux, M ;
Usov, D ;
Minko, S ;
Stamm, M ;
Shulha, H ;
Tsukruk, VV .
MACROMOLECULES, 2003, 36 (19) :7244-7255
[64]   Wide varieties of cationic nanoparticles induce defects in supported lipid bilayers [J].
Leroueil, Pascale R. ;
Berry, Stephanie A. ;
Duthie, Kristen ;
Han, Gang ;
Rotello, Vincent M. ;
McNerny, Daniel Q. ;
Baker, James R., Jr. ;
Orr, Bradford G. ;
Holl, Mark M. Banaszak .
NANO LETTERS, 2008, 8 (02) :420-424
[65]   Guided alignment and positioning of single DNA molecules by a structured contact line on a block copolymer surface [J].
Liu, G ;
Zhao, J .
LANGMUIR, 2006, 22 (07) :2923-2926
[66]  
Mangham A., 2007, ABSTR PAP AM CHEM S, V233
[67]   Probing Soft Matter with the Atomic Force Microscopies: Imaging and Force Spectroscopy [J].
McConney, Michael E. ;
Singamaneni, Srikanth ;
Tsukruk, Vladimir V. .
POLYMER REVIEWS, 2010, 50 (03) :235-286
[68]  
Minko S, 2001, MACROMOL RAPID COMM, V22, P206, DOI 10.1002/1521-3927(200102)22:3<206::AID-MARC206>3.0.CO
[69]  
2-#
[70]   Lipid nanoparticles:: recent advances [J].
Mueller, Rainer H. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :375-376