Per- and polyfluoroalkyl substances (PFASs) are man-made fluorinated compounds that havebeen detected in humans, the environment, and wildlife. The strong C-F bonds contribute tothe high thermal stability of some PFASs and make them extremely resistant to degradationunder normal environmental conditions. The commonly studied classes of PFASs areperfluoroalkyl carboxylic acids and perfluoroalkyl sulfonic acids. Though the phase-out ofperfluorooctane sulfonic acid and perfluorooctanoic acid for some time, they were the mostfrequent compounds measured and detected in biota.In this study, the total oxidisable precursor (TOP) assay, which is a method used to indirectlymeasure and estimate PFAS precursors, was evaluated. Different parameters were studied tounderstand their effects on oxidation of precursor compounds following TOP assay method(e.g., oxidation rate, pH of the oxidation solution and different washing steps during solidphaseextraction)The results from this experiment showed that the target precursors were oxidised and part ofthe proportion of the compounds formed ranged from 37 to 100% (molar ratio). Whenperforming TOP assay, it was shown that some precursors oxidised before 0.5 h while otherprecursors were oxidised after 4 hours. However, it was still unknown what products wereformed when some precursors were oxidised e.g., 7:3 fluorotelomer carboxylic acid (7:3-FTCA) and 10:2 fluorotelomer unsaturated carboxylic acid (10:2- FTUCA) because of animbalance of precursors to degradation products (molar to molar ratio).When the washing steps for solid-phase extraction were evaluated for potential losses ofprecursors, it could be seen that the ammonium acetate and the 20% methanol in Milli-Q waterled to the loss of some precursors. These results showed precautions were needed wheninterpreting the results using TOP assay.

Coffee contains many antioxidants including purpurogallin, which is a hydrophobic phenolic antioxidant that is difficult to measure with reported methods. A method combining solid-phase extraction and liquid chromatography–mass spectrometry was developed to detect and quantify purpurogallin in brewed beverages, including coffee. For beverage preparation, water extraction was adopted for improved correlation with moka pot brewing. Purpurogallin was detected in all commercial coffee samples, and its content in ground coffees ranged from 455-630 ng/g dry weight. Purpurogallin was only detected in two English breakfast tea samples (335-360 ng/g dry weight) and was not detected in any cocoa sample. Antioxidant activity, total phenolic content, and phenolic profile of coffees with different degrees of roasting were determined and analyzed. The developed methodology was then further improved, and coffees with different roasting degrees were analyzed for their antioxidant activity, total phenolic content, and phenolic profile. The antioxidant activity ranged from 63.9-92.0 mg Trolox equivalents per gram of coffee (dry weight), and the total phenolic content ranged from 36.0-57.7 mg gallic acid equivalents per gram of coffee (dry weight). However, the total phenolic content was not correlated with the roasting degree (p > 0.05). When the roasting degree increases, chlorogenic acid decreases drastically, but shikimic acid, caffeic acid, gallic acid, pyrogallol, and purpurogallin increase correspondingly. The results suggest that purpurogallin is a common antioxidant in roasted coffees, and an increase in roasting degree will not only lead to dramatic breakdown of chlorogenic acid, but also promote significant formation of other phenolic compounds that can provide antioxidant activity.

Ce mémoire de maîtrise présente, en trois parties, les différents rôles de la "tension eschatologique" dans la vie spirituelle chrétienne selon Spe Salvi, deuxième encyclique de Benoît XVI. Dans un premier temps, ce travail en théologie spirituelle présente les résultats d’une recherche exploratrice du contenu argumentatif de l’encyclique en mettant en évidence les rôles de l’espérance chrétienne dans la vie spirituelle, l’authenticité de ces rôles étant vérifiée à l’aide d’une définition reconnue de la vie spirituelle. Dans un deuxième temps est proposée une herméneutique de ces résultats selon le critère de "tension eschatologique" puisé à même l’encyclique. Les deuxième et troisième parties proposent une analyse comparative des résultats obtenus avec deux corpus concernant l’eschatologie: d’une part différents écrits de Joseph Ratzinger et, d’autre part, les grandes lignes de la doctrine de Jürgen Moltmann. Comme application et confirmation des résultats de la recherche, la conclusion met brièvement en évidence d’éventuelles conséquences doctrinales et pastorales.

Topical inquiries for the Swedish Defence Research Agency (FOI) include analysis of explosive substances in different sample types. Research into explosives in complex matrixes can provide an analytical support function for forensic investigation i.e. tools for areas such as finding bomb factories, identification and risk analysis of home-made explosives (HME) and improvised explosive devices (IED) as well as preventive measures against maliciously intended use of explosives. Additionally, the research may lay the groundwork for indications of health- and environmental hazards. Utilizing state-of-the-art equipment and years of extensive expertise, FOI is able to carry out these types of research tasks to provide security and sustainability for society. The aim of this thesis project is to establish and validate developed methods for collecting, extracting, separating, and detecting trace amounts of explosives in various bodies of water using a solid-phase extraction (SPE) robot and a high-resolution (HR) mass spectrometer (MS) connected to an ultra-high-performance liquid chromatograph (UHPLC). Particular areas of interest include locations in the Stockholm archipelago where experimental detonations of explosives have taken place. Overall, UHPLC-HRMS analysis provides a powerful tool for analyzing explosives in complex matrixes with unambiguous and reliable measurement data. The compounds of investigation were hexogen (RDX), octogen (HMX), pentyl (PETN), and trotyl (TNT). To summarize, during the course of the thesis, trace amounts of some explosives were detected and quantified in various bodies of water. Furthermore, the applied method for the project was successful in qualitatively and quantitatively analyze the compounds of interest with limit of detection ranging between 0.33–11 μg/L (ppb) in various water sources.

Per- and polyfluoroalkyl substances (PFAS) are organic synthetic compounds used in several industries because of their unique properties and thermal and chemical stability. Perfluorooctanesulfonic acid (PFOS) and perfluorooctaonic acid (PFOA) are two of the most prominent PFAS that are undegradable and accumulate in nature. To study the impact of PFOS and PFOA on the liver in a controlled environment, organoids can be used. A sensitive and selective LC-MS/MS method for individual and simultaneous analysis of PFOS and PFOA in liver organoid media and equipment used in organoid analyses was developed. For detection of low concentrations, ability to analyse complex organoid samples, and limit background contamination, a solid phase extraction (SPE) column, automatic filter (AFFL) and a trap column was included. The AFFL-SPE-LC-MS/MS was optimised efficiently through Design of Experiment (DoE) regarding the loading phase in the LC and six MS parameters for PFOS and PFOA. Validation was controlled against Eurachem’s guideline showing high sensitivity, detecting LOD at 6 pg/mL. The method demonstrated high repeatability with an RSD below 8 % for most samples. Simultaneous analysis of PFOS and PFOA demonstrated high selectivity. Nevertheless, the method showed low intermediate precision and varying reliability, as well as persistent background contamination limiting detection of lower concentrations. The method was fit for purpose and allowed rapid analysis of PFOS and PFOA in organoid media and equipment used in organoid analyses. Result from studies of PFAS in liver organoids through analysis with this method can aid in understanding the connection between PFAS and metabolic diseases. / Populärvetenskaplig sammanfattning Per- och polyfluorerade alkylsubstanser (PFAS) är en grupp av människoskapta, syntetiska ämnen med unika egenskaper. Dessa egenskaper gör att de är olja- och vattenavvisande, och har många applikationsområden. De finns i textiler, livsmedelsförpackningar, brandsläckningsskum och andra industriprodukter. De är väldigt termiskt och kemisk stabila, vilket gör att de inte bryts ner och därmed ackumulerar i miljön. Flera studier har också visat koppling mellan PFAS och många kroniska sjukdomar, som hormonstörningar, cancer, immunsuppression och metabolt associerad fettlever (MAFLD, tidigare nonalkoholisk fettlever (NAFLD)). Kopplingen mellan MAFLD och PFAS har fått mycket uppmärksamhet då levern har visats sig vara ett målorgan för PFAS. Eftersom PFAS är ihärdiga, har ett komplicerat spridningsbeteende och ackumulerar i naturen är det svårt att studera kopplingen mellan MAFLD och PFAS i en kontrollerad miljö. För att studera effekten av PFAS kan man använda organoider, laboratorieodlade 3D modeller gjord från stamceller för att imitera ett äkta organ.    Någon av de mest omtalade PFAS ämnen är perfluoroktansyra (PFOA) och perfluoroktansulfonat (PFOS), vilket är fokus för detta arbete. Leverorganoiderna kan utsättas för PFOS och PFOA, och mediet de ligger i kan extraheras och studeras med konventionella analytiska metoder för att få en bild av hur PFAS påverkar levern. I detta arbete vill analysen ske via vätskekromatografi med masspektrometri som detektion (LC-MS/MS). Med LC-MS/MS separeras den studerade molekylen, analyten från lösningen baserat på dess kemiska egenskaper. Analyten detekteras baserat på dess massa, mer bestämd massa/laddning-fördelningen (m/z). För att anpassa LC-MS metoden till injektion av komplexa organoidprover inkluderades ett automatiskt filter (AFFL) samt ett extra automatiskt separationssteg med en kolonn med fastfasextraktion (SPE). I övrigt ger SPE möjligheten att små mängder PFAS kan uppkoncentreras och fokuseras på kolonnen, vilket ger en sensitiv metod som kan detektera låga koncentrationer. SPE och AFFL implementerades båda för att bättre kunna separera och detektera PFOS och PFOA från andra ämnen, samt filtrera bort föroreningar och stora molekyler som kan skada LC-MS/MS instrumentet i längden. Då PFAS hopar upp sig i vår omgivning, visade det sig att kontamination av PFAS från systemet blev en utmaning under metodutvecklingen. Därför implementerades PFAS fritt utstyr, samt en extra kolonn för att fånga PFAS från systemet och på så sätt minska bakgrundskontaminationen som detekterades.    AFFL-SPE-LC-MS/MS metoden optimerades via en maskininlärningsbaserad optimeringsmetod baserad på parametrar i LC och MS. Metoden baserar sig på att, med tre värden för varje parameter, uppger programmet ett antal experiment som måste utföras för att kunna beräkna ett optimalt värde för varje parameter. Med resultatet från experimenten kan modellen matematiskt, genom en Bayes baserat Gaussian modell, uppskatta optimala värden för metoden. På så sätt kunde metoden optimeras systematiskt och tidseffektivt.    Innan rutinanvändning måste den optimerade metoden valideras. Validering blev gjord genom at följa Eurachem’s riktlinjer. Metoden visade hög repeterbarhet, selektivitet och riktighet. Den har hög sensitivitet, och kan detektera låga mängder, men bakgrundskontaminationen kunde inte elimineras totalt, och gör att man måste korrigera för detta i rutinanalyser. Komplexiteten av AFFL-SPE-LC-MS/MS med flera kolonner och filter gjorde att metoden visade låg robusthet och behövde justeras ofta. AFFL-SPE-LC-MS/MS metoden gör det möjligt att snabbt studera PFOS och PFOA i leverorganoider och utstyr använt i organoidanalyser, och kan bidra i forskningen för att bättre förstå hur PFAS påverkar levern. / Health Effects of Persistent Organic Pollutants

Per- and polyfluoroalkyl substances (PFASs) are a group of artificial chemicals which have been used in a wide area of applications such as surface protection agents in cloths and different industrial applications. It has been found that PFASs are potentially toxic and are frequently found in the environment due to their persistent and mobile properties. Effluents from wastewater treatment plants (WWTPs) have been identified as an important point source of PFASs. Bark, by-product from the paper and wood industry, is a low-cost adsorbent and has the potential to be used as a filter material for PFASs in WWTPs. In this study, the removal of PFASs in wastewater has been investigated using granulated active carbon (GAC) (n = 2) and bark (n = 2) in a pilot scale experiment at Kungsängsverket, Uppsala over a period of five weeks. The specific objects included: i) investigate the influence of flow-rate (10, 30 40 and 60 Ld-1 ) on the removal efficiency of PFASs in the GAC and bark filters, ii) investigate the influence of particle size of bark on the removal efficiency of PFASs and iii) establish what circumstances that potentially promotes removal of PFASs in GAC and bark filters. The results showed that GAC was the most effective method compared to bark, with a reduction of 73-93%, with increasing efficiency under low flow (10-30 L d-1 ) conditions. The removal efficiency of bark was 45% with a particle size of 2-5 mm and under low flow conditions (10-30 L d-1 ), while under high flow conditions (60 L d-1 ) with the same particle size the removal of PFASs was not efficient, instead the total PFAS concentration increased with 40%. In contrast, bark with a particle size of 5-7 mm proved to be not efficient in removing PFASs (removal efficiency = 0%). In general, the removal efficiency increased with smaller particle size of the adsorbent and lower flow rate. The results indicate that bark may be a low-cost alternative in reducing PFASs from wastewater, under certain conditions. / Per- och polyfluroalkyla ämnen (PFAS) är en familj av artificiella fluorerade organiska föreningar som har använts sedan 1950-talet i en rad olika applikationer, såsom impregnering i kläder. Studier har visat att PFAS är potentiellt toxiska och att de förekommer globalt på grund av deras persistenta och mobila egenskaper. Spillvatten från avloppsreningsverk etablerats som en betydande källa för PFAS. Bark, vilket är en biprodukt från pappers- och träindustrin, är ett poröst material vilket möjligen kan användas som adsorbent av PFAS. Denna studie har jämfört effektiviteten hos granulerat aktivt kol (GAC) och bark för att minska PFAS i avloppsvatten. Experimentet var utformat som ett småskaligt kolonn-experiment vid Kungsängsängsverket, Uppsala, och pågick under en fem veckors period. Frågeställningen var att i) studera vilka effekter flödes-hastigheten (10, 30, 40 och 60 L d-1 ) har på reduktionen av PFAS hos GAC och barkfiltren, ii) studera vilka effekter partikelstorleken hos bark har på reduktion av PFAS och iii) redogöra vilka förhållanden som potentiellt gynnar reduktionen av PFAS i GAC och bark filtren. Resultaten visade att GAC var det mest effektiva av de två materialen, med en total reduktion på 73- 93% av PFAS, med ökande effektivitet under låga flödesförhållanden (10-30 L d-1 ). Bark minskade den totala mängden av PFAS med 45% då partikelstorleken var 2-5 mm och under låga flödesförhållanden (10-30 L d-1 ) medan bark med samma partikelstorlek under ökade flödesförhållanden (60 L d-1 ) visade en ökning på 40% av PFAS i det utgående vattnet. Bark med en partikelstorlek på 5-7 mm visade ingen reduktion av PFAS. Generellt visade resultaten att reduktionen av PFAS ökar under låga flödesförhållanden och minskad partikelstorlek. Resultaten visade att bark kan vara ett alternativt material för att minska PFAS i avloppsvatten förutsatt att gynnsamma förhållanden upprätthålls.

Depuis leurs découvertes dans les années 60 par Dewar, les composés BN-hétérocycliques ont subi un développement croissant, s’accentuant pendant la dernière décennie. Ce travail de thèse mené en collaboration avec le Pr S-Y LIU de Boston Collège (États-Unis) et le Pr L. WEBER de l’Université de Bielefeld (Allemagne), a permis la synthèse, ainsi que la caractérisation par spectroscopie photoélectronique à rayonnement UV de nouveaux systèmes. Dans une première partie représentée par les chapitres II, III et IV, nous abordons l’étude de la structure électronique des composés suivants : 1,2-dihydro-1,2-azaborine (1), N-Me-1,2-BN-toluene (2), N-Me-1,3-BN-toluene (3), 1,2-dihydro-1-aza-2-boranaphtalene (4), 1,2-dihydro-1-aza-2-boranthracene (5), 1,2-dihydro-1-aza-2-boranthracene (6), 1,2-dihydro-1-aza-2-boraphenanthrene (7), 1,3,2-benzodiazaborole (8), 1,9,8-benzodiazaborole (9), N-tert-butyl[1,3,2]diazaborolo[1,5-a]-pyridine (10), 1,3,2-trihydro[1,3,2]diazaborolo[1,5-a]-pyridine (11). Afin de compléter les propriétés physico-chimiques de ces nouveaux systèmes et d’aider à l’interprétation des spectres photoélectroniques, l’utilisation de calculs quantiques tels que la théorie de la fonctionnelle de la densité (DFT), la théorie fonctionnelle de la densité en fonction du temps (TD-DFT), la fonction de Green (OVGF), la méthode du troisième ordre partiel (P3), ou encore l’interaction de configuration (SAC-CI) ont été utilisées. Dans le Chapitre V, nous présentons une étude comparative entre les énergies ionisations théoriques et expérimentales. / Since the Dewar’s discovering in 60 years, the BN-heterocycles has experienced an important development during the last decade. This thesis presents our work on the synthesis and on the electronic structure characterization by Ultra-Violet photoelectron spectroscopy (UV-PES), followed in collaboration with the Pr SY LIU from the Boston College (USA) and the Pr L. WEBER from the University of Bielefeld (Germany). The first part corresponding to the chapter II, III and IV, describe the electronic structure analysis of: 1,2-dihydro-1,2-azaborine (1), N-Me-1,2-BN-toluene (2), N-Me-1,3-BN-toluene (3), 1,2-dihydro-1-aza-2-boranaphtalene (4), 1,2-dihydro-1-aza-2-boranthracene (5), 1,2-dihydro-1-aza-2-boranthracene (6), 1,2-dihydro-1-aza-2-boraphenanthrene (7), 1,3,2-benzodiazaborole (8), 1,9,8-benzodiazaborole (9), N-tert-butyl[1,3,2]diazaborolo[1,5-a]-pyridine (10), 1,3,2-trihydro[1,3,2]diazaborolo[1,5-a]-pyridine (11). In order to provide more information on the physical chemistry properties and to interpret the photoelectron spectra, the quantum chemical calculations of ionization energies have been followed using the Density Functional Theory (DFT), the Time-Dependent Density Functional Theory (TD-DFT), the Outer Valence Green’s Function (OVGF), the Partial third order (P3), the Symmetry Adapted Cluster-Configuration Interaction (SAC-CI). Moreover, the comparative analysis of theoretical and the experimental ionization energies are presented.

Submitted by Irvana Coutinho (irvana@ufpa.br) on 2017-05-17T13:21:24Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_AcontecimentoCombateHomofobia.pdf: 2848655 bytes, checksum: 29b3ca4d6a4cfdca65c225867737d09e (MD5) / Approved for entry into archive by Irvana Coutinho (irvana@ufpa.br) on 2017-05-17T13:21:42Z (GMT) No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_AcontecimentoCombateHomofobia.pdf: 2848655 bytes, checksum: 29b3ca4d6a4cfdca65c225867737d09e (MD5) / Made available in DSpace on 2017-05-17T13:21:42Z (GMT). No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_AcontecimentoCombateHomofobia.pdf: 2848655 bytes, checksum: 29b3ca4d6a4cfdca65c225867737d09e (MD5) Previous issue date: 2016-06-24 / ‘Diferentes, porém, iguais’ – o acontecimento do combate à homofobia no Projeto Saúde e Prevenção na escola (SPE)” é o título desta tese que toma como objeto de análise as práticas discursivas e subjetividades forjadas no combate à homofobia no projeto Saúde e Prevenção na Escola. Elegemos como questão nodal de análise ‘que práticas discursivas e subjetividades são forjadas na produção do combate à homofobia no projeto SPE?’. Como desdobramentos desta questão principal definimos as seguintes problematizações: que posição ocupam os direitos humanos no combate à homofobia? De que modo a valorização da diferença e o respeito à diversidade são utilizados como estratégias para a superação da homofobia no currículo do projeto SPE? Como está feita a articulação entre a promoção da saúde e o combate à homofobia no currículo do referido projeto?. Para guiar o movimento de pensamento analítico a ser empreendido nessas problematizações adotamos as ferramentas teórico-conceituais de Michel Foucault, sobretudo, as relacionadas à genealogia, as técnicas de governo dos sujeitos, tais como a disciplina e biopolítica, e os modos de subjetivação. Como principal material empírico de análise tomamos a coleção de fascículos produzida pelo projeto SPE, e alguns documentos secundários da política de combate à homofobia, tais como as Diretrizes Curriculares Nacionais e o Programa Brasil Sem Homofobia. A análise dos documentos permitiu entender que os direitos humanos foram se formando como um dos principais alicerces do combate à homofobia na política brasileira e que as práticas discursivas no campo dos direitos humanos são produzidas para lhes atribuir um caráter de solução para todas as condições que afetam o homem em sua concepção de cidadão universal e de homem civilizado. Além disso, o SPE ao acionar o respeito à diversidade e a valorização da diferença como uma das estratégias para o combate à homofobia vinculou a diversidade sexual à uma essência da natureza humana e desenhou a diferença como uma marca que identifica aqueles que vivem a sexualidade fora dos padrões heteronormativos – isto é, aqueles que tem um ‘comportamento sexual diferenciado’. Foi possível perceber, então, a forja de dois tipos de subjetividades, aquela onde o sujeito que não é LGBT precisa reconhecer e respeitar a diferença que está em quem é LGBT, não a tomando como base para expressar qualquer tipo de preconceito; e aquela onde quem é LGBT deve se ver como portador de uma diferença que o coloca em situação especial em relação à violação de seus direitos e ao contágio de doenças, sobretudo as DST e aids. / “‘Different but equal’ – the happening of the combat to homophobia in the Project Health and Prevention at School (SPE)” is the title of this thesis which takes as object of analysis the discursive practices and subjectivities shaped in the combat to homophobia in the Project Health and Prevention at School. We have elected as nodal question of analysis: which discursive practices and subjectivities are shaped in the production of the combat to homophobia to the SPE Project? As developments of this question we defined the following questioning: which position do the human rights occupy in the combat to homophobia? In which way are the valorization of the difference and the respect to diversity used as strategies to the overcome of homophobia in the SPE curriculum? How is the articulation between the promotion of health and combat to homophobia done in the curriculum of the project mentioned? In order to guide the analytical movement of the thought to be followed in these questionings, we have adopted the Michel Foucault’s theory-conceptual tools, mainly those related to genealogy, subject-government techniques, such as discipline and bio-politics, and the ways of subjectivation. As principal empirical material of analysis we have taken the booklets collection produced by the SPE project, ‘Adolescents and youngsters to the among peers education’, and some secondary documents of the policy of combat to homophobia, such as the National Curricular Guidelines and the Program Brazil Without Homophobia. The analysis of the documents allowed us to understand that the human rights became one of the main basis of the combat to homophobia in the Brazilian politics and that discursive practices in the field of the human rights are produced so as to give a character of solution to all the conditions which affect man in his conception of universal citizen and civilized man. Besides, the SPE, by using the respect to diversity and the valorization of the difference as one of the strategies to the combat to homophobia, linked the sexual diversity to one essence of the human nature designed the difference as a mark which identifies those who live the sexuality out of the hetero-normative standards – that is, those who have a ‘differentiated sexual behavior’. It was possible to realize, thus, the shaping of the true types of subjectivity, the one where the subject who is not LGBT needs to recognize and respect the difference that exists in those who are not LGBT, not taking it as the basis to express any kind of prejudice; and that one where those who are LGBT should see themselves as holders of a difference that puts them in a special situation towards the violation of their rights and vulnerability to the contagion of diseases, mainly the STDs and AIDS.

Le principal objectif de cette thèse était de mieux comprendre l'importance des Substances Polymériques Extracellulaires (SPE) dans la structuration et la formation des biofilms benthiques ; tout en s'inscrivant dans une étude plus globale des mécanismes écologiques impliqués dans le fonctionnement des vasières intertidales. La mise au point des dosages biochimiques a été effectuée sur le mucilage de l'algue Chaetomorpha aerea et a permis en parallèle de purifier un polysaccharide sulfaté riche en galactose, présentant une activité bactéricide sélective contre la souche Staphylococcus aureus (ATCC 25923). Les études biochimiques et écologiques menées sur les SPE extraits de la vasière charentaise ont ensuite permis de quantifier leur dynamique de production et leur composition, en fonction des conditions environnementales. La présence de désoxy-sucres et d'acides uroniques au sein des SPE capsulaires a laissé supposer que ces fractions jouaient un rôle important dans la formation et le devenir du biofilm microphytobenthique. La dernière partie des travaux a permis de caractériser les propriétés acide/base de Lewis et hydrophile/hydrophobe de la surface de la micro-algue Navicula jeffreyi, impliquée dans la formation de biofilms benthiques, par des méthodes classiques d'analyse. L'utilisation d'une nouvelle méthode, la Chromatographie Gazeuse Inverse (CGI), a permis d'obtenir des résultats intéressants et relativement similaires, confirmant le caractère prometteur de la CGI pour l'étude des propriétés de surface des micro-organismes.

<p>This thesis deals with the development of analytical methods for the determination of new antimalarial drugs in biological fluids. The goal was to develop methods that facilitate clinical studies performed in the field, such as capillary blood sampling onto sampling paper.</p><p>Methods for the determination of atovaquone (ATQ) in plasma, whole blood and capillary blood applied onto sampling paper were developed and validated. </p><p>Automated solid-phase extraction (SPE) and liquid chromatography (LC) with UV absorbance detection was used to quantify ATQ. Venous blood contained higher levels of ATQ than capillary blood after a single dose of Malarone (ATQ + proguanil).</p><p>Ion-pairing LC was used to separate amodiaquine (AQ), chloroquine (CQ) and their metabolites on a CN-column. A method for quantification of AQ, CQ and their metabolites in capillary blood applied onto sampling paper was developed and validated. Perchloric acid and acetonitrile were used to facilitate the extraction of the analytes from the sampling paper. The liquid extract was further cleaned by SPE.</p><p>Methods for the determination of piperaquine (PQ) in plasma and whole blood using SPE and LC were developed and validated. Addition of trichloroacetic acid (TCA) to the samples prior to injection into the LC-system significantly enhanced the efficiency for the PQ peak. Serum and whole blood contained higher levels (about 300 nM) of PQ than plasma (about 200 nM) after a single oral dose of 340 mg PQ. This indicates that PQ may be taken up in the leucocytes and thrombocytes.</p>