Este trabalho de doutorado apresenta o desenvolvimento de novas tecnologias para fabricação de microsistemas analíticos e detecção eletroquímica. Primeiramente, a poliuretana elastomérica, derivada de uma fonte renovável, o óleo de mamona, foi utilizada como um novo e alternativo material para fabricação de microdispositivos. Foram avaliadas as características físicas dos microcanais formados por moldagem, a compatibilidade química com solventes e eletrólitos, as características de superfície através dos ângulos de contato, o EOF em diferentes pHs e a performance analítica em experimentos de eletroforese com detecção eletroquímica. A segunda parte do trabalho apresenta o desenvolvimento de um método para a determinação simultânea de azo-corantes comumente usados na indústria alimentícia. Amaranto, amarelo crepúsculo FCF, amarelo sólido AB, ponceu 4R e vermelho 2G, foram separados e quantificados através de eletroforese em microdispositivos com detecção eletroquímica. Foram estudados e otimizados vários parâmetros que influenciaram a separação eletroforética e detecção eletroquímica, em experimentos realizados usando microdispositivos de vidro e eletrodo de trabalho de carbono vítreo. Finalmente, a terceira parte desse trabalho apresenta o uso das propriedades magnéticas e eletrocatalíticas de nanofios de níquel no desenvolvimento de um detector adaptativo magneticamente modulável para eletroforese em microdispositivos. / The development of microfluidic analytical systems has witnessed an explosive growth during the last 15 years. Particular attention has been given to microchip electrophoresis because of their fast and efficient separation capabilities. Electrochemistry detection offers considerable promise for such microfluidic systems, with features that include remarkable sensitivity, inherent miniaturization and portability, low cost, and high compatibility with microfabrication technologies. This thesis shows the development of new fabrication technologies for miniaturized analytical systems with electrochemical detection and it is presented in four chapters, Chapter I shows an introductory view of the main aspects related to miniaturization of analytical systems and amperometric detection configurations commonly coupled to microchip electrophoresis. In Chapter II, the use of elastomeric polyurethane (PU), derived from castor oil (CO) biosource, as a new material for fabrication of microfluidic devices by rapid prototyping is presented. Including the irreversible sealing step, PU microchips were fabricated in less than 1 h by casting PU resin directly on the positive high-relief molds fabricated by standard photolithography and nickel electrodeposition. Physical characterization of microchannels was performed by scanning electron microscopy (SEM) and profilometry. Polymer surface was characterized using contact angle measurements and the results showed that the hydrophilicity of the PU surface increases after oxygen plasma treatment. The polymer surface demonstrated the capability of generating an electroosmotic flow (EOF) of 2.6 × 10-4 cm2 V-1 s-1 at pH 7 in the cathode direction, which was characterized by current monitoring method at different pH values. The compatibility of PU with a wide range of solvents and electrolytes was tested by determining its degree of swelling over a 24 h period of contact. The performance of microfluidic systems fabricated using this new material was evaluated by fabricating miniaturized capillary electrophoresis systems. We used catecholamines as model analytes that were separated in aqueous solutions and detected with end-channel amperometric detection. In Chapter III, a method based on microchip electrophoresis with electrochemical detection has been developed for the simultaneous determination of Yellow AB, Red 2G, Sunset Yellow, Ponceu 4R, and Amaranth which are azo-dyes frequently added to foodstuffs. Factors affecting both separation and detection processes were examined and optimized, with best performance achieved by using a 10 mM phosphate buffer (pH 11) as running buffer and applying a voltage of 2500 V both in the separation and in the electrokinetic injection (duration 4 s). Under these optimal conditions, the target dye analytes could be separated and detected within 300 s by applying a detection potential of -1,0 V (vs. Ag/AgCl) to the glassy carbon (GC) working electrode. The recorded peaks were characterized by a good repeatability (RSD = 1,8 - 3,2%), high sensitivity, and a wide linear range. Detection limits of 3.8, 3.4, 3.6, 9.1, 15.1 ?M were obtained for Yellow AB, Red 2G, Sunset Yellow, Ponceu 4R, and Amaranth, respectively. Fast, sensitive, and selective response makes the new microchip protocol very attractive for the quantitative analysis of commercial soft drinks and candies Finally, in Chapter IV, we demonstrate for the first time the use of adaptive functional nickel nanowires for switching on demand operation of microfluidic devices. Controlled reversible magnetic positioning and orientation of these nanowires at the microchannel outlet offers modulation of the detection and separation processes, respectively. The former facilitates switching between active and passive detection states to allow the microchip to be periodically activated to perform a measurement and reset it to the passive (\"off\") state between measurements. Fine magnetic tuning of the separation process (post channel broadening of the analyte zone) is achieved by reversibly modulating the nanowire orientation (i.e., detector alignment) at the channel outlet. The concept can be extended to other microchip functions and stimuli-responsive materials and holds great promise for regulating the operation of microfluidic devices in reaction to specific needs or unforeseen scenarios.

Abstract The subject of this thesis is flow imaging by methods based on the nuclear magnetic resonance (NMR) phenomenon. The thesis consists of three related topics: In the first one the feasibility of measuring velocity maps and distributions inside a microfluidic device by pulsed field gradient (PFG) NMR has been demonstrated. The second topic was to investigate microfluidic gas flow using a combination of a special detection technique and a powerful signal enhancement method. The third topic is related to the unambiguous determination of velocities under challenging experimental conditions and introduces a new, improved velocity imaging sequence. In the first part, well established imaging methods have been used to study water flow inside a micromixer. A surface coil matching the region of interest of the mixer was home built and used in the measurements in order to gain a better signal-to-noise ratio. Velocities inside the mixer have been measured by phase-encoding velocity, with unprecedented spatial resolution. Two dimensional NMR imaging and velocity maps revealed clogging and different manufacturing qualities of the mixers. In addition to the velocity maps, which display an average velocity for spins within one pixel, complete velocity distributions (so called average propagators) were measured. It was found that in the absence of spatial resolution in the third dimension, the propagator data can provide valuable insight to the flow system by revealing overlapping flow passages. The next topic was gas flow inside a microfluidic device. It was investigated by time-of-flight flow imaging. The measurement of the weak gas signal was enabled by the use of two signal enhancement techniques: remote detection NMR and parahydrogen induced polarization (PHIP). The results demonstrate that a very significant signal enhancement can be achieved by this technique. In the future it may enable the investigation of interesting chemical reactions inside microreactors. The third and last topic of the thesis deals with measuring flow by the so called multiecho sequences. When multiecho sequences are used in combination with phase encoding velocity, an error may be introduced: the multiecho sequence may produce a cumulative error to the phase of the magnetization, if it is sensitive to RF pulse imperfections. The problem has been elaborately explained and various solutions discussed, among the newly proposed one. Experimental results demonstrate the performance of the new velocity imaging sequence and show that the new sequence enables the unambiguous determination of velocities even in challenging experimental conditions resulting from inhomogeneous radio frequency fields of the measurement coils.

Microfluidic flow devices coupled with quantitative Raman spectroscopy are able to provide a deep insight into the reaction mechanism and kinetics of electrocatalytic reactions. With a microfluidic flow device made with glass microscope slides and polymer building blocks, the feasibility of this technique was examined by methanol electrooxidation reaction with a Pt working electrode. Pre-calibration of the Raman peak area was done with solutions of known concentrations of methanol and its major oxidation product, i.e., formate, which enabled the time-dependent Raman spectra taken during the reaction to be converted to time-dependent concentrations. These were interpreted in terms of a model with one-dimensional convection and the reaction kinetics. An improved version of this technique was then applied to a comparative study of different alcohols with Ni-based electrodes. This showed the production of formate as the major product from the oxidation of alcohols with vicinal OH groups, leading to the discovery that C-C bond dissociation is a major reaction pathway for vicinal diols and triols if Ni electrocatalysts are used. It is also suggested that the cleavage of C-C bonds is the rate-determining step. The potential use of printed circuit boards (PCB) in the next generation of a novel microfluidic device was explored, as PCB have advantages over regular electrochemical microfluidic substrates, such as simpler electrode fabrication strategies, more wiring layers, and customization of size and shape of electrodes. Pretreatments and electrodeposition protocols of nickel, silver, palladium and platinum on PCB were successfully developed, together with four types of PCB-based microfluidic devices designed with an open-source PCB design software. This work establishes a new electrochemical microfluidic platform for online and in-situ monitoring of electrocatalytic reactions, which can quickly determine the reaction mechanism and kinetics. / Graduate

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Protecting drinking water supplies from pathogens such as Cryptosporidium parvum is a major concern for water treatment plants worldwide. The sensitivity and specificity of current detection methods are largely determined by the effectiveness of the concentration and separation methods used. In this study, disposable microfluidic micromixers were fabricated to effectively isolate Cryptosporidium parvum Oocysts from water samples, while allowing direct observation of Oocysts captured in the device using high quality immunofluorescence microscopy. In parallel, quantitative analysis of the capture yield was carried out by analyzing the waste from the microfluidics outlet with an Imaging Flow Cytometer. At the optimal flow rate, capture efficiencies higher than 95% were achieved in spiked samples, suggesting that scaled microfluidic isolation and detection of Cryptosporidium parvum will provide a faster and more efficient detection method for Cryptosporidium compared to other available laboratory-scale technologies.

Cyanobacteria, also known as blue-green algae for a long time, are the most ancient and problematic bloom-forming phylum on earth. An alert levels framework has been established by World Health Organization(WHO) to prevent the potential harmful cyanobacterial blooms. Normally, low cyanobacteria levels are found in surface water. 2000 cyanobacterial cells/mL and 100,000 cyanobacterial cells/mL are established for WHO Alert Level 1 and 2, respectively. However, eutrophication, climate change and other factors may promote the spread of cyanobacteria and increase the occurrence of harmful cyanobacterial blooms in water on a global scale. Hence, a rapid real time cyanobacteiral monitoring system is required to protect public health from the cyanotoxins produced by toxic cyanobacterial species. Current methods to control or prevent the development of harmful cyanobacterial blooms are either expensive, time consuming or not effective in the long term. The best method to control the blooms is to prevent the formation of the blooms at the very beginning. Although emerging advanced autofluorescence-based sensors, imaging flow cytometry applications, and remote sensing have been utilized for rapid real-time enumeration and classification of cyanobacteria, the need to accurately monitor low-level cyanobacterial species in water remains unsolved. Microflow cytometry has been employed as a functional cell analysis technique in past decades, and it can provide real-time, accurate results. The autofluorescence of cyanobacterial pigments can be used for determination and counting of cyanobacterial density in water. A pre-concentration system of an automated cyanobacterial concentration and recovery system (ACCRS) based on tangential flow filtration and back-flushing technique was applied to reduce the sample assay volume and increase the concentration of target cells for further cell capture and detection. In this project, a microflow cytometry platform with a microfluidic device and an automated pre-concentration system was established to monitor cyanobacteria and provide early warning alerts for potential harmful blooms. In this work, quantification of low-level cyanobacterial samples (∼ 5 cyanobacterial cells/mL) in water has been achieved by using a microflow cytometer together with a pre-concentration system (ACCRS). Meanwhile, this platform can also provide early warning alerts for potential harmful cyanobacterial blooms at least 15 days earlier before reaching WHO Alert Level 1. Results have shown that this platform can be applied for rapid determination of cyanobacteria and early warning alerts can be triggered for authorities to protect the public and the environment. / Thesis / Doctor of Engineering (DEng) / Harmful cyanobacterial blooms have been a rising risk to the public heath across the world in recent decades. Alert levels of cyanobacteria in water has also been established. In this case, a rapid on-side monitoring system for cyanobacteria is required. In this thesis, a microflow cytometer platform combined with a bacterial concentration and recovery system was built to quickly monitor the relatively low level of cyanobacteria for early warning alerts. A pre-enrichment system based on tangential flow filtration and back-flushing technique was applied to increase the concentration levels of microbial samples and a microfluidic device capable of collecting phycocyanin fluorescence was designed to count cyanobacterial cells. The limit of quantification for cyanobacterial concentration based on the microflow cytometry platform was as low as ∼ 5 cells/mL. We can claim that the microflow cytometry platform can provide useful early warning alerts for the decision-makers to control the potential harmful cyanobacterial blooms at the very early stage and protect the aquatic animals and public health.

Surface science is a multidisciplinary subject which affects us on a daily basis. Surfaces are of particular interest because the chemical bonding and atomic structure is different at the surface compared to the bulk properties of a material. This interface is of great significance because it is where charge exchange, or new chemical bonds occur. One essential aspect of surface science is surface wettability, which can be harnessed to produce self-cleaning surfaces. This very lucrative notion, where surfaces with low adhesion to liquids, can result in quick and autonomous shedding, has inspired a multitude of device fabrication and implementation. Over the past decade, several self-cleaning surfaces have been fabricated from superhydrophobic surfaces, which depends on a stable interface between solid, liquid and gas. These surfaces, however, are restricted in their applications and fail to operate upon mechanical damage or nonhomogeneous fabrication processes. Recent advances in wettability science have produced omniphobic lubricant-infused surfaces (OLIS). These surfaces are created by tethering a liquid to a surface, providing a stable liquid interface, which results in excellent aqueous and organic liquid repellency, and high robustness toward physical damage. This thesis will encompass an overview of the classical models for surface wettability, new models for liquid mobility, the criteria required to obtain OLIS, as well as some of the biomedical engineering applications fabricated from this technology. Herein, a novel manufacturing process was developed to produce smooth channeled polymeric microfluidic devices from rough 3D printed molds. Additionally, we integrated OLIS technology with electroconductive sensors to create high surface area electroactive material with self-cleaning properties, ideal to combat non-specific adhesion of biomolecules. Furthermore, our fabrication methods are inexpensive and have the potential to be easily integrated into manufacturing processes to create highly functional microfluidic devices, optimal for lab-on-chip diagnostic platforms. / Thesis / Master of Applied Science (MASc) / Recent advances in wettability science have produced omniphobic lubricant-infused surfaces (OLIS) inspired by the Nepenthes pitcher plant. These surfaces are created by tethering a liquid to a surface, providing a stable liquid interface, which results in excellent aqueous and organic liquid repellency, as well high robustness toward physical damage and high pressure dispensing scenarios. The motivation for this thesis is to expand on the applications for OLIS devices. Herein, a novel manufacturing process was developed to produce smooth channeled polymeric microfluidic devices from rough 3D printed molds. Additionally, we integrated OLIS technology with electroconductive sensors to create high surface area electroactive material with self-cleaning properties, ideal to combat non-specific adhesion of biomolecules.

Orientador: Mônica Alonso Cotta / Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Física Gleb Wataghin / Made available in DSpace on 2018-09-02T02:33:05Z (GMT). No. of bitstreams: 1 Monteiro_MoniellenPires_D.pdf: 5193520 bytes, checksum: fab290a9074ae3dd188d4ebb636ff0e7 (MD5) Previous issue date: 2017 / Resumo: Nesta tese investigamos processos de adesão da Xylella fastidiosa, bactéria gram-negativa, fitopatógena, que forma biofilmes no xilema de plantas. O trabalho teve como objetivos entender alguns aspectos do processo de adesão bacteriana e do mecanismo de transporte de células e biofilmes em sistemas que simulam os vasos do xilema. Consideramos em particular as estratégias utilizadas pela X.fastidiosa para aderir à superfície, dentre elas, a secreção de substâncias poliméricas extracelulares (EPS), a presença de adesinas fimbriais (pili) e afimbriais (XadA1) e moléculas sinalizadoras de detecção de quórum (relacionadas à formação de agregados). Como ponto de partida quantificamos as propriedades elásticas do sistema composto pelo EPS e células bacterianas, em diferentes tempos de cultivo bacteriano. Para isso utilizamos medidas de espectroscopia de força e Raman confocal durante os estágios iniciais de adesão celular e formação de agregados. Mostramos que a rigidez do sistema célula/EPS diminui progressivamente com o aumento do tempo de crescimento bacteriano. Verificamos que existe uma mudança no valor de rigidez em diferentes partes da célula, região polar e corpo bacteriano; os menores valores de rigidez encontrados no polo sugerem uma resposta mecânica mais flexível nesta região, associada com o ponto de adesão inicial da célula à superfície. No estudo de adesão e mobilidade da X.fastidiosa, utilizamos dispositivos microfluídicos modificados quimicamente, via funcionalização de superfície (em microcanais Polidimetilsiloxano/vidro) e via introdução de molécula de detecção de quórum (em microcanais impressos em poliácido láctico), para tornar o ambiente mais próximo ao do xilema da planta. Foram feitas funcionalizações de superfície com uma celulose sintética, simulando a composição química dos vasos do xilema (majoritariamente composto por celulose), e com a adesina XadA1, e observamos os efeitos sobre a adesão, crescimento e mobilidade celular. Verificamos que a adesina XadA1 aumenta a densidade bacteriana se comparada às demais superficies, além de aumentar a força de adesão bacteriana à superfície. Quanto a inserção de molécula sinalizadora, observamos que a presença destas moléculas no cultivo bacteriano aumenta a densidade celular e altera a forma de pequenos agregados / Abstract: In this thesis we investigated the adhesion processes of Xylella fastidiosa, a gram-negative, phytopathogenic bacterium that forms biofilms in the xylem of plants. The objective of this work was the understanding of several aspects of the bacterial adhesion process, as well as the mechanism of cell and biofilm transport in systems that simulate xylem vessels. In particular, we considered the strategies used by X.fastidiosa to adhere to a surface; among them, the secretion of extracellular polymeric substances (EPS), the presence of fimbrial (pili) and afimbrial (XadA1) adhesins and quorum detection molecules (related to cluster formation). As a starting point we quantified the elastic properties of the system composed of EPS and bacterial cells, at different times of bacterial culture. For this purpose, we used force spectroscopy and confocal Raman measurements during the initial stages of cell adhesion and cluster formation. We have shown that stiffness decreases progressively with increasing bacterial growth time. We observed that stiffness values varied along different parts of the cell, polar region and bacterial body. The lower stiffness values found at the pole suggest a more flexible mechanical response in this region, associated with the initial adhesion point of the cell to the surface. For the investigation on X.fastidiosa adhesion and mobility, we used chemically modified microfluidic devices via surface functionalization (in Polydimethylsiloxane / glass microchannels) and via the introduction of a quorum detection molecule (in microchannels printed on polylactic acid) to make the environment more closely resemble the plant xylem. Surface functionalizations were performed with a synthetic cellulose, simulating the chemical composition of xylem vessels (mainly composed of cellulose), and the XadA1 adhesin, and we observed the effects on cell adhesion, growth and mobility. Our results showed that immobilized XadA1 increased the bacterial density when compared to other surfaces studied; furthermore, it increased the bacterial adhesion force to the surface. Regarding the addition of the signaling molecules, we observed that their presence in the bacterial culture increases cell density and changes the shape of small clusters / Doutorado / Física / Doutora em Ciências / 2010/51748-7 / 479486/2012-3 / FAPESP / CNPQ

Woven textile fabrics were designed and constructed from hydrophilic and hydrophobic spun yarns to give planar substrates containing amphiphilic microchannels with defined orientations and locations. Polypropylene fibers were spun to give hydrophobic yarns, and the hydrophilic yarns were spun from a poly(ethylene terephthalate) copolyester. Water wicking rates into the fabrics were measured by video microscopy and longitudinal wicking tests from single drops and from reservoirs. Intra-yarn microchannels in the hydrophilic polyester yarns were shown to selectively transport aqueous fluids, with the flow path governed by the placement of the hydrophilic yarns in the fabric. Simultaneous wicking of an aqueous and hydrocarbon fluid into the hydrophilic and hydrophobic microchannels of an amphiphilic fabric was successfully demonstrated. The high degree of interfacial contact and micron-scale diffusion lengths of such co-flowing immiscible fluid streams inside amphiphilic fabrics suggest potential applications as highly scalable and affordable microcontactors for industrial liquid-liquid extractions. The efficiency of liquid-liquid extractions carried out with the amphiphilic fabrics was evaluated. Solvent extraction efficiencies were shown to reach up to ~98%.