The analysis of low abundant biological molecules is often challenging due to their chemical properties, low concentration and limited sample volumes. Neuropeptides are one group of molecules that fits these criteria. Neuropeptides also play an important role in biological functions, which makes them extra interesting to analyze. A classic chemical analysis involves sampling, sample preparation, separation and detection. In this thesis, an enhanced solid supported microdialysis method was developed and used as a combined sampling- and preparation technique. In general, significantly increased extraction efficiency was obtained for all studied peptides. To be able to control the small sample volumes and to minimize the loss of neuropeptides because of unwanted adsorption onto surfaces, the subsequent analysis steps were miniaturized to a micro total analysis system (µ-TAS), which allowed sample pre-treatment, injection, separation, manipulation and detection. In order to incorporate these analysis functions to a microchip, a novel microfabrication protocol was developed. This method facilitated three-dimensional structures to be fabricated without the need of clean room facilities. The sample pre-treatment step was carried out by solid phase extraction from beads packed in the microchip. Femtomole levels of neuropeptides were detected from samples possessing the same properties as microdialysates. The developed injection system made it possible to conduct injections from a liquid chromatographic separation into a capillary electrophoresis channel, which facilitated for advanced multidimensional separations. An electrochemical sample manipulation system was also developed. In the last part, different electrospray emitter tip designs made directly from the edge of the microchip substrate were developed and evaluated. The emitters were proven to be comparable with conventional, capillary based emitters in stability, durability and dynamic flow range. Although additional developments remain, the analysis steps described in this thesis open a door to an integrated, on-line µ-TAS for neuropeptides analysis in complex biological samples.

Advances in life science require knowledge of active molecules in complex biological systems. These molecules are often only present for a certain time and at limited concentrations. Integrated micro-analytical tools for sampling, separation and mass spectrometric (MS) detection would meet these requests and are therefore continuously gaining interest. An on-line coupling of analytical functions provides shorter analysis time and less manual sample handling. In this thesis, improved compatibility of microdialysis sampling and multidimensional separations coupled to MS detection are developed and discussed. Microdialysis was used in vitro for determination of the non-protein bound fraction of the drug ropivacaine. The sampling unit was coupled on-line to capillary column liquid chromatography (LC) followed by ultraviolet or MS detection. For MS detection, the system was extended with a desalting step and an addition of internal standard. A method for MS screening of microdialysates, collected in vivo, was also developed. The method involved sampling and measurements of the chemical pattern of molecules that generally are ignored in clinical investigations. Chemometric tools were used to extract the relevant information and to compare samples from stimulated and control tissues. Complex samples often require separation in more than one dimension. On-line interfaces for sample transfer between LC and capillary electrophoresis (CE) were developed in soft poly(dimethylsiloxane) (PDMS). MS detection in the LC-CE system was optimised on frequent sampling of the CE peak or on high resolution in mass spectra using time-of-flight (TOF)MS or Fourier transform ion cyclotron resonance (FTICR)MS, respectively. Aspects on electrode positioning in the LC-CE interface led to development of an on-column CE electrode. A successful method for deactivation of the PDMS surface using a polyamine polymer was also developed. The systems were evaluated using peptides and proteins, molecules that are gaining increased attention in bioscience, and consequently also in chemical analysis.

As aves marinhas são sensíveis às alterações em todos os níveis tróficos, decorrentes de variações na disponibilidade de presas e contaminação por alguns compostos, capazes de se acumular nos tecidos dos organismos e magnificar-se através da cadeia trófica. As ilhas oceânicas brasileiras abrigam importantes colônias reprodutivas de aves marinhas e, apesar de serem consideradas locais remotos, estão sujeitas à contaminação decorrente de atividades humanas. Este trabalho avaliou a presença de poluentes orgânicos persistentes (POPs) em sangue, uma matriz não-destrutiva, de seis espécies de aves marinhas no Arquipélago de São Pedro e São Paulo e na Ilha da Trindade, que possibilita o monitoramento destes indivíduos ao longo dos anos. Os resultados indicaram que os principais POPs detectados no sangue (em ng g-1 de massa úmida) foram PCBs (0,05 a 55,09), DDTs (0,01 a 17,36) e Mirex (0,01 a 5,53). A migração influenciou nos altos níveis de POPs encontrados em Pterodroma arminjoniana e a massa (g) média dos indivíduos apresentou uma forte correlação negativa com as concentrações dos compostos predominantes no sangue. O sexo das aves não contribuiu significativamente nas concentrações de POPs em espécies monotípicas, exceto para a espécie Sula leucogaster que apresenta dimorfismo sexual acentuado. O comportamento alimentar, avaliado através da análise de isótopos estáveis de carbono e de nitrogênio (δ13C e δ15N), bem como as condições biológicas de cada animal contribuíram para explicar as variações nos perfis de contaminação entre as diferentes espécies. No geral, observou-se que as concentrações de POPS nos dois locais apresentaram valores baixos e similares sugerindo a via atmosférica como principal mecanismo de entrada desses contaminantes para estas regiões. Os resultados inéditos de POPs em sangue das aves marinhas nas duas mais recentes unidades de conservação marinhas criadas no Brasil, podem contribuir como referência para o monitoramento desses compostos em longo-prazo nessas regiões. / Seabirds are sensitive to changes at all trophic levels, due to variations in prey availability and contamination by some compounds, which can be accumulated in the tissues of organisms and to be magnified through the trophic chain. The Brazilian oceanic islands harbor important seabird breeding colonies and, although they are considered remote sites, they are subject to contamination from human activities. This work evaluated the presence of Persistent Organic Pollutants (POPs) in blood, a non-destructive matrix, of six species of seabirds in the São Pedro and São Paulo Archipelago (SPSPA) and Trindade Island (TI), that allows the monitoring of these individuals over the years. The results indicated that the major POPs detected in blood (ng g-1 in wet weight) were PCBs (0.05 to 55.09), DDTs (0.01 to 17.36) and Mirex (0.01 to 5,53). Migration influenced the high levels of POPs found in Pterodroma arminjoniana and the mean mass (g) of the individuals drove a strong negative correlation with the concentrations of the predominant compounds in the blood. The gender of the individuals did not contribute significantly to the concentrations of POPs in monotypic species, except for the species Sula leucogaster that presents marked sexual dimorphism. The feeding behavior was evaluated through the analysis of stable isotopes of carbon and nitrogen (δ13C and δ15N) as well as the biological conditions of each animal contributed to explain the variations in the contamination profiles between the different species. In general, we observed that POPS concentrations at both sites presented low and similar values suggesting the atmospheric transport as the main input mechanism of these compounds for these regions. The unpublished results of POPs, in blood of seabirds from the two most recent marine conservation units created in Brazil, can contribute as reference values for their long-term monitoring in those regions.

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Modern separation and spectrometric techniques for biological sample lipidom investigation Due recent progress in field of mass spectrometry the lipidomics, part of metabolomics, is increasing its importance for broad fields of biological study. The aim of this study is to test the lipid extraction techniques and to optimize the preseparation and separation of lipids suitable for mass spectrometry detection. The fragmentation patterns of four, the most abundant lipid classes of glycerolipids (PC, PE, TG, DG), were acquired for the proposed system. These patterns were compared with literature. The most appropriate method for extraction was declared technique according Folch based on methanol and chloroform solution. The preseparation due SPE method is very useful tool for lipid determination. The optimized were focused to reach higher recovery especially in polar lipid fraction. Proposed HPLC system is based on methanol with ammonium buffer, water and isopropanol. The testing was done on three columns with different type of sorbents (Gemini, Syncronis and Kinetex). The separation was evaluated according mass spectrometer response, shape and wide of particular analytes peaks. Composition contains 20% of water was determinate as the best and also the best separation was achieved by Kinetex column. The proposed...