Surface Optochemical Sensors

The objective of my research is to develop new surface optochemical sensors for studying cellular processes by investigating techniques to modify surface properties. The spectral characteristics of the modified surfaces and coatings are designed to show remarkable changes after interaction with analytes from biological fluids and cells. My studies focused on pancreatic cells and addressed the need for improved techniques to measure zinc release from pancreatic cells (chapter 3, 4) and to measure the metastasis potential of cancerous pancreatic cells (chapter 5). Chapter 3 describes the development of zinc sensing glass slides by conjugating a carboxylmodified ZnAF-2 to an amino functionalized glass surface. The sensor was used for the measurement of glucose-stimulated zinc ion release from cultured beta pancreatic cells with impact in diabetes research. In chapter 4 is described conjugation of the carboxyl-modified ZnAF-2 to antibody molecules (A2B5) that specifically recognize pancreatic cells. This enabled for the first time the use of targeted zinc sensors to monitor zinc release events from pancreatic cells. Chapter 5 describes development for the first time of a fluorescence sensor to measure the proteolysis activity of pancreatic cancer cells in microfluidic systems. The sensor was fabricated using a Layer by layer (LbL) deposition of polyelectrolyte. The sensor was based on Fluorescence Resonance Energy Transfer (FRET) between luminescent quantum dots (serve as donors) and rhodamine molecules (serve as acceptors) that are separated by multi-layers of polyelectrolytes. The microfluidic platform enables precise delivery of reactants to assemble the sensor and facilitate unique cellular assays of enzymatic activity and enzymatic expression on pancreatic cancer cells

El viaje de Nicolo dei Conti en los relatos de Pero Taflir y Poggio Bracciolini.

Sin resume

Mirabilis Oriens: fuentes y transmisión.

Sin resume

Innovative 3D Model of the Human Middle Ear in High Resolution with a Histological Microgrinding Method: A Feasibility Study and Comparison with μCT

Conclusion. The development of a histological 3D model of the tympanic cavity visualizes the exact microanatomy of the sound conduction organ and is therefore essential for finite elements simulations and surgical training. Objectives. So far, no accurate histological 3D model of the sound conduction system existed in literature. For 3D reconstruction of the very fine structures inside and outside the auditory ossicles, a method based on histological slices allows a more differential analysis of both hard and soft tissues and could thus be superior to μCT. Method. A complete temporal bone was embedded in epoxy resin and microground in distances of about 34 μm. After photodocumentation of every plane, a 3D reconstruction was performed by using the Computer Aided Design (CAD) program Rhinoceros 5®. For comparison, a μCT of the same specimen resulted in a 3D model of the calcified structures in the middle ear. Results. The histological 3D model gives an excellent overview to all anatomical soft and bony tissues of the human auditory ossicles. Specifically the fine blood vessel system and the exact dimension of cartilage areas inside the ossicles can be illustrated much more precisely than with μCT data. The present technique also allows the evaluation of the fine connecting ligaments inside the tympanic cavity

MEC-ConPaaS: An experimental single-board based mobile edge cloud

International audienceCloud infrastructures are extremely flexible and powerful, but their data centers are located very far from the end users. To address the limitations of these systems, many researchers are designing mobile edge clouds which complement traditional clouds with additional resources located in immediate proximity of the end users. However, currently there exists no open-source mobile edge cloud implementation which can easily be deployed over a campus or a city center to support real-world experimentations. We therefore present the design and implementation of MEC-ConPaaS, a mobile-edge cloud platform, which aims to support future research on edge cloud applications and middlewares. The system exploits single-board computers such as Raspberry Pis which are an order of magnitude cheaper than any server machine and much easier to setup in a distributed setting. We demonstrate that these devices are powerful enough to support real cloud applications, and to support further research on these topics

A survey of visualisation for live cell imaging

Live cell imaging is an important biomedical research paradigm for studying dynamic cellular behaviour. Although phenotypic data derived from images are difficult to explore and analyse, some researchers have successfully addressed this with visualisation. Nonetheless, visualisation methods for live cell imaging data have been reported in an ad hoc and fragmented fashion. This leads to a knowledge gap where it is difficult for biologists and visualisation developers to evaluate the advantages and disadvantages of different visualisation methods, and for visualisation researchers to gain an overview of existing work to identify research priorities. To address this gap, we survey existing visualisation methods for live cell imaging from a visualisation research perspective for the first time. Based on recent visualisation theory, we perform a structured qualitative analysis of visualisation methods that includes characterising the domain and data, abstracting tasks, and describing visual encoding and interaction design. Based on our survey, we identify and discuss research gaps that future work should address: the broad analytical context of live cell imaging; the importance of behavioural comparisons; links with dynamic data visualisation; the consequences of different data modalities; shortcomings in interactive support; and, in addition to analysis, the value of the presentation of phenotypic data and insights to other stakeholders

Surface Optochemical Sensors

The objective of my research is to develop new surface optochemical sensors for studying cellular processes by investigating techniques to modify surface properties. The spectral characteristics of the modified surfaces and coatings are designed to show remarkable changes after interaction with analytes from biological fluids and cells. My studies focused on pancreatic cells and addressed the need for improved techniques to measure zinc release from pancreatic cells (chapter 3, 4) and to measure the metastasis potential of cancerous pancreatic cells (chapter 5). Chapter 3 describes the development of zinc sensing glass slides by conjugating a carboxylmodified ZnAF-2 to an amino functionalized glass surface. The sensor was used for the measurement of glucose-stimulated zinc ion release from cultured beta pancreatic cells with impact in diabetes research. In chapter 4 is described conjugation of the carboxyl-modified ZnAF-2 to antibody molecules (A2B5) that specifically recognize pancreatic cells. This enabled for the first time the use of targeted zinc sensors to monitor zinc release events from pancreatic cells. Chapter 5 describes development for the first time of a fluorescence sensor to measure the proteolysis activity of pancreatic cancer cells in microfluidic systems. The sensor was fabricated using a Layer by layer (LbL) deposition of polyelectrolyte. The sensor was based on Fluorescence Resonance Energy Transfer (FRET) between luminescent quantum dots (serve as donors) and rhodamine molecules (serve as acceptors) that are separated by multi-layers of polyelectrolytes. The microfluidic platform enables precise delivery of reactants to assemble the sensor and facilitate unique cellular assays of enzymatic activity and enzymatic expression on pancreatic cancer cells