Wydallis, John B., authorHenry, Charles S., advisorVan Orden, Alan, committee memberBarisas, B. George, committee memberMcNaughton, Brian R., committee memberDandy, David S., committee member2016-08-182016-08-182016http://hdl.handle.net/10217/176594Distribution of molecules over space and time drive a multitude of macroscopic and microscopic biological processes. There is a need to design novel imaging techniques that can map molecular distributions with spatiotemporal resolution. In this thesis, new electrochemical approaches to provide spatiotemporal imaging are presented. The bulk of this work utilizes high-density platinum micro-electrode arrays fabricated using complementary metal oxide semiconductor (CMOS) fabrication techniques as well as microfluidics and carbon-based electrodes fabricated using soft lithography fabrication techniques. The systems described in this dissertation focus on quantification of biologically relevant neurotransmitters, mainly catecholamines and nitric oxide with concentration ranges from nM to mM. The pitch, or resolution between two "pixels" of electrochemical data, was 250 µm for microfluidic based sampling methods and 12.5 µm for the CMOS based sensors. Descriptions of fabrication methods for the carbon based electrodes and CMOS electrodes are described in this work. Finally, potential future directions of this technology is discussed in the final chapter.born digitaldoctoral dissertationsengCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.CMOSelectrode arraysoptical profilometryelectrochemical imagingchemical gradientsmicrofluidicsDevelopment of electrochemical imaging methods using micro-electrode arrays and microfluidic networksText