50 resultados para Willman, Elvira


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Understanding how the brain works has been one of the greatest goals of mankind. This desire fuels the scientific community to pursue novel techniques able to acquire the complex information produced by the brain at any given moment. The Electrocorticography (ECoG) is one of those techniques. By placing conductive electrodes over the dura, or directly over the cortex, and measuring the electric potential variation, one can acquire information regarding the activation of those areas. In this work, transparent ECoGs, (TrECoGs) are fabricated through thin film deposition of the Transparent Conductive Oxides (TCOs) Indium-Zinc-Oxide (IZO) and Gallium-Zinc-Oxide (GZO). Five distinct devices have been fabricated via shadow masking and photolithography. The data acquired and presented in this work validates the TrECoGs fabricated as efficient devices for recording brain activity. The best results were obtained for the GZO- based TrECoG, which presented an average impedance of 36 kΩ at 1 kHz for 500 μm diameter electrodes, a transmittance close to 90% for the visible spectrum and a clear capability to detect brain signal variations. The IZO based devices also presented high transmittance levels (90%), but with higher impedances, which ranged from 40 kΩ to 100 kΩ.

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A malária é uma doença infeciosa transmitida através da picada de um mosquito fêmea Anopheles infetado com o parasita protozoário do género Plasmodium (P.), sendo o P. falciparum a espécie mais mortal. É responsável pela morte de milhares de pessoas por ano, nomeadamente nos países em vias desenvolvimento, países esses que não detêm as condições necessárias para a prática da microscopia ótica em larga escala, que continua nos dias de hoje a ser a técnica de eleição para o diagnóstico da doença. A conceção de testes de baixo custo e de fácil utilização tais como os testes de diagnóstico rápido (TDR) são uma mais-valia no diagnóstico deste tipo de doenças. A presente dissertação centra-se no desenvolvimento de um TDR num formato competitivo, baseado em nanopartículas de ouro (AuNP) funcionalizadas com ácido mercaptoundecanoico (MUA) ou com o pentapétido Cys-Ala-Leu-Asn-Asn (CALNN) e conjugadas com um anticorpo monoclonal anti-PfHRP2 que reconhece especificamente a proteína rica em histidina 2 produzida pelo P. falciparum (PfHRP2). Para isso, utilizou-se uma tecnologia inovadora na conceção do TDR, a tecnologia lab on paper, que utiliza o papel Whatman nº1. Os estudos de estabilidade de AuNP funcionalizadas com citrato de sódio, MUA ou CALNN por variação da força iónica e pH do meio mostraram que o pentapéptido CALNN é o agente de revestimento mais resistente a oscilações de força iónica, comparativamente com o citrato de sódio e o MUA e que apenas as AuNP revestidas com citrato de sódio atingiram o ponto de agregação ao pKa da molécula de revestimento. Os principais resultados obtidos aquando do desenvolvimento do TDR revelaram que o valor de diluição ótima de anticorpo anti-IgG (solução mãe a 11 mg.mL-1) imobilizado na linha de controlo é de 1:40 e 1:90, utilizando para deteção os bionanoconjugados AuNP-MUA-Anticorpo e AuNP-CALNN-Anticorpo, respetivamente. Com a aplicação da solução AuNP-CALNN-Anticorpo visualizou-se o aparecimento de cor vermelha na linha de teste, o que demonstra a deteção do antigénio pelos bionanoconjugados. A deteção ocorreu com a aplicação de 2,5 μL de PfHRP2 a 1,5 mg.mL-1. Numa análise global após a aplicação de culturas de sangue não infetadas ou infetadas com o parasita da malária, obteve-se cor na linha de controlo com uma diluição de 1:20 do anticorpo anti-IgG imobilizado. Em relação à linha de teste, na presença de culturas não infetadas, obteve-se sinal na mesma aplicando bionanoconjugados AuNP-MUA-Anticorpo e 2,5 μL de PfHRP2 a 2,6 mg.ml-1.

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Fully comprehending brain function, as the scale of neural networks, will only be possi-ble with the development of tools by micro and nanofabrication. Regarding specifically silicon microelectrodes arrays, a significant improvement in long-term performance of these implants is essential. This project aims to create a silicon microelectrode coating that provides high-quality electrical recordings, while limiting the inflammatory response of chronic implants. To this purpose, a combined chitosan and gold nanoparticles coating was produced allied with electrodes modification by electrodeposition with PEDOT/PSS in order to reduce the im-pedance at 1kHz. Using a dip-coating mechanism, the silicon probe was coated and then charac-terized both morphologically and electrochemically, with focus on the stability of post-surgery performance in anesthetized rodents. Since not only the inflammatory response analysis is vital, the electrodes recording degradation over time was also studied. The produced film presented a thickness of approximately 50 μm that led to an increase of impedance of less than 20 kΩ in average. On a 3 week chronic implant, the impedance in-crease on the coated probe was of 641 kΩ, compared with 2.4 MΩ obtained for the uncoated probe. The inflammatory response was also significantly reduced due to the biocompatible film as proved by histological tests.

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The unique proprieties exhibited by nanoscale particles compared to their macro size counterparts allow for the creation of novel neural activity manipula-tion procedures. In this sense, gold nanoparticles (AuNPs) can be used to stimu-late the electrical activity of neuron by converting light into heat. During this dissertation, AuNPs are synthesized by the citrate reduction method, resulting in a hydrodynamic diameter of approximately 16 nm and an absorbance peak of 530 nm. A system to control a 532 nm laser and measure the temperature variation was custom built from scratch specifically for this project. Temperature is then measured with recourse to a thermocouple and through changes in impedance. The built system had in consideration the necessities pre-sented by in vivo tests. Trials were performed by measuring the temperature rise of colloidal AuNP solutions, having the temperature variation reached a maximum of ap-proximately 18 ºC relative to control trials; successfully showing that light is ef-fectively transduced into heat when AuNPs are present. This novel approach enables an alternative to optogenetics, which require the animal to be genetically modified in order to allow neuron stimulation.