The preparation of polypyrrole surfaces in the presence of mesoporous silica nanoparticles and their biomedical applications

被引:36
作者
Cho, Youngnam [1 ]
Ben Borgens, Richard [1 ,2 ]
机构
[1] Purdue Univ, Ctr Paralysis Res, Sch Vet Med, W Lafayette, IN 47907 USA
[2] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
关键词
ELECTRICALLY CONDUCTING POLYMER; DRUG-DELIVERY; NEURITE EXTENSION; CELL SCAFFOLDS; COMPOSITE; RELEASE; ENVIRONMENTS; PARTICLES; GROWTH; ARRAYS;
D O I
10.1088/0957-4484/21/20/205102
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
The deposition of carboxylic acid-terminated conducting polymer into two- or three-dimensional structures made up of colloidal particles has been successfully completed. This was accomplished using electrochemical deposition of ordered arrays of mesoporous silica nanoparticles (MSNs) as a template. Subsequent removal of the template yielded a porous polypyrrole surface. The co-polymerization of pyrrole with carboxylic acid-terminated pyrrole derivatives overcame the limitations of a lack of reactive functional groups-by facilitating the direct coupling of the film with biomolecules or drugs on the surface. Such Ppy films were characterized by several techniques: (1) scanning electron microscope (SEM) to evaluate surface topography, (2) x-ray photoelectron spectroscopy (XPS) to assess the chemical composition of the films, (3) four-point probe to measure the conductivity, and cyclic voltammogram to observe surface electroactivity. To assay the biological effectiveness of this preparation, we used phase-contrast light microscopy to compare neurite outgrowth from PC 12 cells grown on Ppy films in the presence and absence of electrical stimulation. These electrically functional, biocompatible composites show promise as novel neural implants that would deliver specific biologically active molecules in a highly localized manner to damaged or otherwise vulnerable cells such as found in the nervous system.
引用
收藏
页数:9
相关论文
共 43 条
[1]
Conducting-polymer nanotubes for controlled drug release [J].
Abidian, MR ;
Kim, DH ;
Martin, DC .
ADVANCED MATERIALS, 2006, 18 (04) :405-+
[2]
Influences of material characteristics on ibuprofen drug loading and release profiles from ordered micro- and mesoporous silica matrices [J].
Andersson, J ;
Rosenholm, J ;
Areva, S ;
Lindén, M .
CHEMISTRY OF MATERIALS, 2004, 16 (21) :4160-4167
[3]
Development of magnetic nanostructured silica-based materials as potential vectors for drug-delivery applications [J].
Arruebo, M ;
Galán, M ;
Navascués, N ;
Téllez, C ;
Marquina, C ;
Ibarra, MR ;
Santamaría, J .
CHEMISTRY OF MATERIALS, 2006, 18 (07) :1911-1919
[4]
Honeycomb-structured porous films from polypyrrole-containing block copolymers prepared via RAFT polymerization as a scaffold for cell growth [J].
Beattie, D ;
Wong, KH ;
Williams, C ;
Poole-Warren, LA ;
Davis, TP ;
Barner-Kowollik, C ;
Stenzel, MH .
BIOMACROMOLECULES, 2006, 7 (04) :1072-1082
[5]
Simultaneous application of two neurotrophic factors after spinal cord injury [J].
Bohnert, Debra M. ;
Purvines, Scott ;
Shapiro, Scott ;
Borgens, Richard B. .
JOURNAL OF NEUROTRAUMA, 2007, 24 (05) :846-863
[6]
Functionalized mesoporous silica nanoparticle-based drug delivery system to rescue acrolein-mediated cell death [J].
Cho, Youngnam ;
Shi, Riyi ;
Borgens, Richard B. ;
Ivanisevic, Albena .
NANOMEDICINE, 2008, 3 (04) :507-519
[7]
A mesoporous silica nanosphere-based drug delivery system using an electrically conducting polymer [J].
Cho, Youngnam ;
Shi, Riyi ;
Ivanisevic, Albena ;
Ben Borgens, Richard .
NANOTECHNOLOGY, 2009, 20 (27)
[8]
The effect of surface charge on the uptake and biological function of mesoporous silica nanoparticles 3T3-L1 cells and human mesenchymal stem cells [J].
Chung, Tsai-Hua ;
Wu, Si-Han ;
Yao, Ming ;
Lu, Chen-Wen ;
Lin, Yu-Shen ;
Hung, Yann ;
Mou, Chung-Yuan ;
Chen, Yao-Chang ;
Huang, Dong-Ming .
BIOMATERIALS, 2007, 28 (19) :2959-2966
[9]
Collier JH, 2000, J BIOMED MATER RES, V50, P574, DOI 10.1002/(SICI)1097-4636(20000615)50:4<574::AID-JBM13>3.0.CO
[10]
2-I