Document Type
Dissertation
Degree
Doctor of Philosophy (PhD)
Major/Program
Biomedical Engineering
First Advisor's Name
Chenzhong Li
First Advisor's Committee Title
Committee Chair
Second Advisor's Name
Ranu Jung
Second Advisor's Committee Title
Committee Member
Third Advisor's Name
Shekhar Bhansali
Third Advisor's Committee Title
Committee Member
Fourth Advisor's Name
Wei-Chiang Lin
Fourth Advisor's Committee Title
Committee Member
Fifth Advisor's Name
Sharan Ramaswamy
Fifth Advisor's Committee Title
Committee Member
Keywords
Nanotoxicity, Electrochemistry, Single Cell, Cell Electronics, Dielectrophoresis, Bio-MEMS, Nanotechnology
Date of Defense
12-11-2014
Abstract
Increasing useof nanomaterials in consumer products and biomedical applications creates the possibilities of intentional/unintentional exposure to humans and the environment. Beyond the physiological limit, the nanomaterialexposure to humans can induce toxicity. It is difficult to define toxicity of nanoparticles on humans as it varies by nanomaterialcomposition, size, surface properties and the target organ/cell line. Traditional tests for nanomaterialtoxicity assessment are mostly based on bulk-colorimetric assays. In many studies, nanomaterials have found to interfere with assay-dye to produce false results and usually require several hours or days to collect results. Therefore, there is a clear need for alternative tools that can provide accurate, rapid, and sensitive measure of initial nanomaterialscreening. Recent advancement in single cell studies has suggested discovering cell properties not found earlier in traditional bulk assays. A complex phenomenon, like nanotoxicity, may become clearer when studied at the single cell level, including with small colonies of cells. Advances in lab-on-a-chip techniques have played a significant role in drug discoveries and biosensor applications, however, rarely explored for nanomaterialtoxicity assessment. We presented such cell-integrated chip-based approach that provided quantitative and rapid response of cellhealth, through electrochemical measurements. Moreover, the novel design of the device presented in this study was capable of capturing and analyzing the cells at a single cell and small cell-population level. We examined the change in exocytosis (i.e. neurotransmitterrelease) properties of a single PC12 cell, when exposed to CuOand TiO2 nanoparticles. We found both nanomaterials to interfere with the cell exocytosis function. We also studied the whole-cell response of a single-cell and a small cell-population simultaneously in real-time for the first time. The presented study can be a reference to the future research in the direction of nanotoxicity assessment to develop miniature, simple, and cost-effective tool for fast, quantitative measurements at high throughput level. The designed lab-on-a-chip device and measurement techniques utilized in the present work can be applied for the assessment of othernanoparticles' toxicity, as well.
Identifier
FI15032160
Recommended Citation
Shah, Pratikkumar, "Development of a Lab-on-a-Chip Device for Rapid Nanotoxicity Assessment In Vitro" (2014). FIU Electronic Theses and Dissertations. 1834.
https://digitalcommons.fiu.edu/etd/1834
Included in
Analytical Chemistry Commons, Bioelectrical and Neuroengineering Commons, Biomedical Devices and Instrumentation Commons, Electronic Devices and Semiconductor Manufacturing Commons, Molecular, Cellular, and Tissue Engineering Commons, Nanotechnology Fabrication Commons
Rights Statement
In Copyright. URI: http://rightsstatements.org/vocab/InC/1.0/
This Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).