Electronic Theses and Dissertations
Identifier
669
Date
2012
Document Type
Thesis
Degree Name
Master of Science
Major
Physics
Concentration
Materials Science
Committee Chair
Lam Yu
Committee Member
Firouzeh Sabri
Committee Member
Sanjay Mishra
Abstract
Graphene and graphene oxide (GO) are two-dimensional nanomaterials with promising biomedical application potential, including drug and gene delivery, bio-imaging, and photothermal therapy. However, the nature of interactions between these materials and cells is poorly understood. Here, cell surface adhesion, subcellular localization, and size-dependent uptake are investigated in C2C12 cells using bovine serum albumin (BSA)-functionalized GO. Small BSA-GO nanosheets enter cells through clathrin-mediated endocytosis (CME), while large nanosheets enter cells through both CME and phagocytosis. Cytotoxicity is minimal. AFM-based size/thickness characterization of BSA-GO is performed in a systematic fashion, and a practical protocol for such analysis is presented. Size-dependent uptake results provide needed information about fundamental cellular interactions between cells and two-dimensional nanomaterials and will be useful in future biomedical and toxicological studies. BSA-functionalized GO is employed as a model system for quantifying surface charge distribution in biologically-relevant materials, and preliminary surface potential measurements by Kelvin probe force microscopy are presented.
Library Comment
Dissertation or thesis originally submitted to the local University of Memphis Electronic Theses & dissertation (ETD) Repository.
Recommended Citation
Gilbertson, Ben, "Cellular Uptake of Protein-Coated Graphene Oxide Nanosheets: Characterization, Mechanisms, Size-Dependence, and the Role of Surface Charge" (2012). Electronic Theses and Dissertations. 552.
https://digitalcommons.memphis.edu/etd/552
Comments
Data is provided by the student.