Meniscus-Directed Assembly of Biologically Active Coatings of Cells, Microparticles, and Nanoparticles

dc.contributor.advisorOrlin Velev, Committee Chairen_US
dc.contributor.advisorAnne Lazarides, Committee Memberen_US
dc.contributor.advisorJan Genzer, Committee Memberen_US
dc.contributor.advisorChristine Grant, Committee Memberen_US
dc.contributor.advisorCarol Hall, Committee Memberen_US
dc.contributor.authorStamm, Lindsey Brooks Jerrimen_US
dc.date.accessioned2010-04-02T18:31:56Z
dc.date.available2010-04-02T18:31:56Z
dc.date.issued2009-04-23en_US
dc.degree.disciplineChemical Engineeringen_US
dc.degree.leveldissertationen_US
dc.degree.namePhDen_US
dc.description.abstractConvective assembly principles and techniques were used in two complementary studies for depositing close packed yeast-coated surfaces and gold nanoparticle wires. Convective assembly at high volume fraction was used for the rapid deposition of uniform, close-packed coatings of Saccharomyces cerevisiae onto glass slides. A computational model was developed to calculate the thickness profiles of such coatings for various experimental conditions. Both experimentation and numerical simulations demonstrated that the deposition process is strongly affected by the presence of sedimentation. The deposition device was inclined to increase the uniformity of the coatings by causing the cells to sediment toward the three-phase contact line. In accordance with the simulation, the experiments showed that both increasing the angle of the device and decreasing the angle between the slides increased the uniformity of the deposited coatings. Finally, the “convective-sedimentation†assembly method was used to deposit composite coatings of live cells and large latex particles as an example of biologically active composite coatings. These coatings were allowed to proliferate and demonstrate a proof-of-concept of a self-cleaning surface. Two methods were developed for the deposition of micro- and nanoparticles into linear assemblies that could be used in biosensors and biomaterials. In capillary-guided deposition, a capillary is withdrawn across a wettable substrate, resulting in the assembly of a particle line. We characterized the effects of particle concentration and withdrawal speed and correlated them to structure of the deposited assemblies. The particles are assembled into one of three different structures, depending on the particle volume fraction and deposition speed. We demonstrate that the metallic nanoparticle lines are Ohmically conductive. Using wedge-templated deposition, linear assemblies were deposited from sessile droplets on moderately hydrophobic surfaces. The particles convectively assemble at the freely-receding three-phase contact line and are pulled into a line against the wedge. The deposited lines can be long and narrow with a few breaks or significantly wider and shorter but unbroken. These methods could be used for engineered patterning of nanoparticle structures on surfaces.en_US
dc.identifier.otheretd-03242009-121746en_US
dc.identifier.urihttp://www.lib.ncsu.edu/resolver/1840.16/3552
dc.rightsI hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dis sertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to NC State University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.en_US
dc.subjectnanoparticleen_US
dc.subjectcell coatingen_US
dc.subjectcolloiden_US
dc.titleMeniscus-Directed Assembly of Biologically Active Coatings of Cells, Microparticles, and Nanoparticlesen_US

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