Electrically Controlled Drug Delivery from Graphene Oxide Nanocomposite Films

被引:319
作者
Weaver, Cassandra L. [1 ,2 ,3 ]
LaRosa, Jaclyn M. [1 ]
Luo, Xiliang [4 ]
Cui, Xinyan Tracy [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Ctr Neural Basis Cognit, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15260 USA
[4] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
graphene oxide; conducting polymers; drug delivery; controlled release; nanocomposites; CONTROLLED-RELEASE; NANO-GRAPHENE; IN-VIVO; POLYPYRROLE; NANOPARTICLES; NANOMATERIALS; EFFICIENCY; SYSTEMS;
D O I
10.1021/nn406223e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
On-demand, local delivery of drug molecules to target tissues provides a means for effective drug dosing while reducing the adverse effects of systemic drug delivery. This work explores an electrically controlled drug delivery nanocomposite composed of graphene oxide (GO) deposited inside a conducting polymer scaffold. The nanocomposite is loaded with an anti-inflammatory molecule, dexamethasone, and exhibits favorable electrical properties. In response to voltage stimulation, the nanocomposite releases drug with a linear release profile and a dosage that can be adjusted by altering the magnitude of stimulation. No drug passively diffuses from the composite in the absence of stimulation. In vitro cell culture experiments demonstrate that the released drug retains its bioactivity and that no toxic byproducts leach from the film during electrical stimulation. Decreasing the size and thickness of the GO nanosheets, by means of ultrasonication treatment prior to deposition into the nanocomposite, alters the film morphology, drug load, and release profile, creating an opportunity to fine-tune the properties of the drug delivery system to meet a variety of therapeutic needs. The high level of temporal control and dosage flexibility provided by the electrically controlled GO nanocomposite drug delivery platform make it an exciting candidate for on-demand drug delivery.
引用
收藏
页码:1834 / 1843
页数:10
相关论文
共 44 条
[1]   Biomimetic Delivery with Micro- and Nanoparticles [J].
Balmert, Stephen C. ;
Little, Steven R. .
ADVANCED MATERIALS, 2012, 24 (28) :3757-3778
[2]   Applications of carbon nanotubes in drug delivery [J].
Bianco, A ;
Kostarelos, K ;
Prato, M .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2005, 9 (06) :674-679
[3]   Graphene: Safe or Toxic? The Two Faces of the Medal [J].
Bianco, Alberto .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (19) :4986-4997
[4]   Controlled release of drug from folate-decorated and graphene mediated drug delivery system: Synthesis, loading efficiency, and drug release response [J].
Depan, D. ;
Shah, J. ;
Misra, R. D. K. .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2011, 31 (07) :1305-1312
[5]   The chemistry of graphene oxide [J].
Dreyer, Daniel R. ;
Park, Sungjin ;
Bielawski, Christopher W. ;
Ruoff, Rodney S. .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (01) :228-240
[6]   PREPARATION OF GRAPHITIC OXIDE [J].
HUMMERS, WS ;
OFFEMAN, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (06) :1339-1339
[7]   Guidance of stem cell fate on 2D patterned surfaces [J].
Kolind, Kristian ;
Leong, Kam W. ;
Besenbacher, Flemming ;
Foss, Morten .
BIOMATERIALS, 2012, 33 (28) :6626-6633
[8]   Polypyrrole as a model membrane for drug delivery [J].
Kontturi, K ;
Pentti, P ;
Sundholm, G .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 453 (1-2) :231-238
[9]   Small-scale systems for in vivo drug delivery [J].
LaVan, DA ;
McGuire, T ;
Langer, R .
NATURE BIOTECHNOLOGY, 2003, 21 (10) :1184-1191
[10]   Origin of Enhanced Stem Cell Growth and Differentiation on Graphene and Graphene Oxide [J].
Lee, Wong Cheng ;
Lim, Candy Haley Y. X. ;
Shi, Hui ;
Tang, Lena A. L. ;
Wang, Yu ;
Lim, Chwee Teck ;
Loh, Kian Ping .
ACS NANO, 2011, 5 (09) :7334-7341