Self assembly of amphiphilic C60 fullerene derivatives into nanoscale supramolecular structures

被引:41
作者
Partha R. [1 ]
Lackey M. [1 ]
Hirsch A. [2 ]
Casscells S.W. [1 ]
Conyers J.L. [1 ]
机构
[1] Department of Internal Medicine, The University of Texas Health Science Center, Houston, Houston, TX 77030
[2] Institut für Organische Chemie der Friedrich Alexander, Universität Erlangen-Nürnberg, D-91054 Erlangen
关键词
Fullerene; Dynamic Light Scattering; Dynamic Light Scattering; Multilamellar Vesicle; Spherical Vesicle;
D O I
10.1186/1477-3155-5-6
中图分类号
学科分类号
摘要
Background: The amphiphilic fullerene monomer (AF-1) consists of a "buckyball" cage to which a Newkome-like dendrimer unit and five lipophilic C12 chains positioned octahedrally to the dendrimer unit are attached. In this study, we report a novel fullerene-based liposome termed 'buckysome' that is water soluble and forms stable spherical nanometer sized vesicles. Cryogenic electron microscopy (Cryo-EM), transmission electron microscopy (TEM), and dynamic light scattering (DLS) studies were used to characterize the different supra-molecular structures readily formed from the fullerene monomers under varying pH, aqueous solvents, and preparative conditions. Results: Electron microscopy results indicate the formation of bilayer membranes with a width of ∼6.5 nm, consistent with previously reported molecular dynamics simulations. Cryo-EM indicates the formation of large (400 nm diameter) multilamellar, liposome-like vesicles and unilamellar vesicles in the size range of 50-150 nm diameter. In addition, complex networks of cylindrical, tube-like aggregates with varying lengths and packing densities were observed. Under controlled experimental conditions, high concentrations of spherical vesicles could be formed. In vitro results suggest that these supra-molecular structures impose little to no toxicity. Cytotoxicity of 10-200 μM buckysomes were assessed in various cell lines. Ongoing studies are aimed at understanding cellular internalization of these nanoparticle aggregates. Conclusion: In this current study, we have designed a core platform based on a novel amphiphilic fullerene nanostructure, which readily assembles into supra-molecular structures. This delivery vector might provide promising features such as ease of preparation, long-term stability and controlled release. © 2007 Partha et al; licensee BioMed Central Ltd.
引用
收藏
相关论文
共 41 条
[1]  
Ferrari M., Cancer nanotechnology: Opportunities and challenges, Nat Rev Cancer, 5, pp. 161-171, (2005)
[2]  
Torchilin V.P., Multifunctional nanocarriers, Adv Drug Deliv Rev, 58, pp. 1532-1555, (2006)
[3]  
Liposomes As Drug Carriers, (1988)
[4]  
Pharmaceutical Particulate Carriers, (1993)
[5]  
Joester D., Losson M., Pugin R., Heinzelmann H., Walter E., Merkle H.P., Diederich F., Amphiphilic dendrimers: Novel self-assembling vectors for efficient gene delivery, Angew Chem Int Ed Engl, 42, pp. 1486-1490, (2003)
[6]  
Portney N.G., Ozkan M., Nano-oncology: Drug delivery, imaging, and sensing, Anal Bioanal Chem, 384, pp. 620-630, (2006)
[7]  
Klumpp C., Kostarelos K., Prato M., Bianco A., Functionalized carbon nanotubes as emerging nanovectors for the delivery of therapeutics, Biochim Biophys Acta, 1758, pp. 404-412, (2006)
[8]  
Barratt G., Colloidal drug carriers: Achievements and perspectives, Cell Mol Life Sci, 60, pp. 21-37, (2003)
[9]  
Freeman A.I., Mayhew E., Targeted drug delivery, Cancer, 58, pp. 573-583, (1986)
[10]  
Seltzer S.E., The role of liposomes in diagnostic imaging, Radiology, 171, pp. 19-21, (1989)