In der vorliegenden Arbeit wurden stickstoffhaltige Monomere ausgehend von aromatischen Aminen oder Lactamen durch Umsetzung mit Chlorsilanen synthetisiert. Die so erhaltenen Derivate wurden mit Hilfe spektroskopischer und thermischer Analysenmethoden umfassend charakterisiert. Auf Basis der stickstoffhaltigen Monomere wurden über unterschiedliche Synthesestrategien organisch-anorganische, nanostrukturierte Hybridmaterialien hergestellt. Durch die thermisch induzierte Zwillingspolymerisation der Monomere 2,2‘-Spirobi[3,4-dihydro-1H-1,3,2-benzodiazasilin] und 1,1’,4,4‘-Tetrahydro-2,2‘-spirobi[benzo[d][1,3,2]-oxazasilin] gelang es, Hybridmaterialien bestehend aus Polyanilin-Formaldehyd-Harzen und Polysilazanen bzw. Siliciumdioxid unter Variation der Reaktionstemperatur herzustellen. Die Untersuchung der entstandenen Materialien erfolgte mittels spektroskopischer Methoden. Die Lactam-Monomere wurden durch die Zugabe von Aminocarbonsäuren zu Polyamid 6/SiO2- bzw. Polysiloxan-Kompositen umgesetzt. Hier stand die Ermittlung der molekularen Struktur, wie auch die Bestimmung des thermischen Verhaltens und der Homogenität der Materialien im Vordergrund. Es konnte gezeigt werden, dass die Synthese der thermoplastischen Kompositmaterialien auch in vergrößertem Maßstab reproduzierbar ist und die Produkte zudem zu Folien extrudierbar sind. / In the present work nitrogen-containing monomers have been synthesized by reactions of silicon tetrachloride with amines or lactames and were characterized by different spectroscopic and thermal analysis methods. The twin monomers 2,2‘-spirobi[3,4-dihydro-1H-1,3,2-benzodiazasiline] and 1,1’,4,4‘-tetrahydro-2,2‘-spirobi[benzo[d][1,3,2]¬oxazasiline] can be converted to hybrid materials containing polyaniline-formaldehyde resins and polysilazane or SiO2 by thermal induced twin polymerization under variation of the reaction temperature. The obtained nano composites were investigated by spectroscopic methods and electron microscopy. The lactam containing monomers were polymerized to polyamide 6/SiO2-composites by addition of aminocarbonic acids and -caprolactam. The analysis of the molecular structure as well as the investigation of the thermal behavior and the homogeneity of materials was emphasized. It could be shown, that the synthesis can be performed reproducible. Furthermore, it is possible to extrude the thermoplastic composite materials to films.

Arthropod hemocyanin and phenoloxidase are members of a group of proteins called the Type-3 copper oxygen-binding proteins, both possessing a highly conserved oxygen-binding site containing two copper atoms each coordinated by three histidine residues (Decker and Tuczek, 2000). Despite similarities in their active site, these proteins have very different physiological functions. Phenoloxidase possesses both tyrosinase and o-diphenoloxidase activity, and is predominantly involved in reactions which protect insects from infection (Kopàcek et al., 1995). Hemocyanin is a large multi-subunit protein with a primary function as a respiratory protein, reversibly binding and transporting molecular O2 (Decker and Rimke, 1998; Decker and Tuczek, 2000). Recently, it has been demonstrated in vitro that arthropod hemocyanin possesses an inducible phenoloxidase activity when incubated with denaturants, detergents, phospholipids or proteolytic enzymes. This activity appears to be restricted to only a few subunit types, and it has been hypothesised that it may be accompanied by conformational change which opens the active site increasing access for larger phenolic substrates (Decker and Jaenicke, 2004; Decker et al., 2001; Decker and Tuczek, 2000). This possibly suggests a dual role of hemocyanin in arthropods. The presented thesis deals with two distinct aims. The first was to isolate and sequence a phenoloxidase gene from the insect Spodoptera littoralis (Egyptian Cottonleaf Worm). Despite efforts, progress was hindered by a number of experimental problems which are outlined within the relevant chapters. The second aim was to characterise the mode of SDS induced phenoloxidase activity in arthropod hemocyanin from the ancient chelicerates Limulus polyphemus (horseshoe crab) and Eurypelma californicum (tarantula) and the more modern chelicerate Pandinus imperator (scorpion), using a number of biophysical techniques. The results indicated that the SDS induced phenoloxidase activity is associated with localised tertiary and secondary conformational changes in hemocyanin, most likely in the vicinity of the dicopper centre, thus enhancing access for larger phenolic substrates. Experiments indicate that copper remains associated with the protein during these structural changes; however the nature of the association is unclear. SDS concentrations approximating the CMC appeared critical in causing the necessary structural changes required for a significant increase in the detectable phenoloxidase activity to be exhibited.

Η ανάπτυξη ευφυών υλικών, ή καλύτερα ευφυών συστημάτων, βασίζεται στην αξιοποίηση των λειτουργικών ιδιοτήτων μιας σειράς υλικών με κυριότερους εκπροσώπους τα υλικά με μνήμη σχήματος, τα ηλεκτρορεολογικά αιωρήματα και τα πιεζο/σιδηροηλεκτρικά στοιχεία. Το επιστημονικό και τεχνολογικό πεδίο των «ευφυών υλικών» επιχειρεί να αναπτύξει συστήματα υλικών των οποίων η επιτυχία δε θα βασίζεται στην εκπλήρωση πολύ υψηλών και σταθερών προδιαγραφών, αλλά στη δυνατότητα ελεγχόμενης μεταβολής της συμπεριφοράς τους. Η εργασία αυτή αναφέρεται σε κράματα με μνήμη σχήματος και στη μελέτη των συντελούμενων σε αυτά κρυσταλλογραφικών μετασχηματισμών, με τη μέθοδο της διαφορικής θερμιδομετρίας σάρωσης και τη μέθοδο της δυναμικής μηχανικής ανάλυσης. Στόχος της παρούσας εργασίας ήταν η μελέτη των μετασχηματισμών φάσεων προτανυσμένων συρμάτων SMA που είναι ενσωματωμένα στο εσωτερικό πολυμερικής μήτρας. Για λόγους αναφοράς εξετάσθηκε και η θερμική απόκριση των συνιστωσών υλικών. Το πρώτο μέρος της εργασίας προσφέρει μια βιβλιογραφική επισκόπηση του αντίστοιχου επιστημονικού πεδίου και το δεύτερο μέρος αναφέρεται στην πειραματική μελέτη του ίδιου θέματος. Στη συνέχεια δίνεται μια συνοπτική περιγραφή της διάρθρωσης της παρούσης εργασίας. Στο πρώτο κεφάλαιο γίνεται λόγος για τα ευφυή υλικά. Ως ευφυή υλικά αναφέρονται συστήματα που έχουν την ικανότητα να μεταβάλλουν τη συμπεριφορά τους ή ορισμένα χαρακτηριστικά τους (σχήμα, ιδιοσυχνότητα, συντελεστή απόσβεσης δονήσεων και άλλα) με δεδομένο και ελεγχόμενο τρόπο, εξ’ αιτίας μιας διέγερσης. Τα συστήματα αυτά ενσωματώνουν αισθητήρες και ενεργοποιητές, οι οποίοι συνδέονται μεταξύ τους με έναν κατάλληλο βρόχο ελέγχου. Στο ίδιο κεφάλαιο αναφέρονται τα υλικά που μπορούν να χρησιμοποιηθούν ως αισθητήρες και ενεργοποιητές και οι τύποι τους, τα είδη ελέγχου που έχουν επιτευχθεί, καθώς και εφαρμογές των ευφυών συστημάτων. Στο δεύτερο κεφάλαιο γίνεται αναφορά στα σύνθετα υλικά. Ως σύνθετο υλικό χαρακτηρίζεται ένα σύστημα δύο ή περισσότερων, διαφορετικών σε σύσταση και χημική δομή, υλικών τα οποία είναι φυσικά συνδεδεμένα μεταξύ τους. Τα σύνθετα υλικά αποτελούνται από μια συνεχή φάση, που λέγεται «μήτρα», ενισχυμένη με κάποιο υλικό που συνήθως αποκαλείται «ενισχυτικό ή πληρωτικό μέσο» και μια τρίτη φάση τη «διεπιφάνεια». Στο κεφάλαιο αυτό αναφέρονται οι κατηγορίες των σύνθετων υλικών, τα είδη μήτρας και εγκλεισμάτων, καθώς και τα χαρακτηριστικά της διεπιφάνειας. Στο τρίτο κεφάλαιο παρουσιάζονται τα ευφυή σύνθετα υλικά με ενσωματωμένα σύρματα με μνήμη σχήματος. Τα κράματα με μνήμη σχήματος εμφανίζουν την ικανότητα να μεταβάλλουν αντιστρεπτά ορισμένες φυσικές ιδιότητες του υλικού καθώς και το σχήμα τους. Εδώ αναλύεται ο ευθύς και αντίστροφος μαρτενσιτικός μετασχηματισμός, το φαινόμενο μνήμης σχήματος, τα κυριότερα κράματα μνήμης σχήματος που χρησιμοποιούνται και οι μηχανικές τους ιδιότητες, ενώ γίνεται αναφορά στις δυνατότητες και στους περιορισμούς των κραμάτων στις διάφορες εφαρμογές. Στο τέταρτο κεφάλαιο αναφέρονται τα υλικά που χρησιμοποιήθηκαν για την παρασκευή των ευφυών συστημάτων στην παρούσα εργασία. Αρχικά γίνεται λόγος για τη χημική δομή, τη θερμική κατεργασία και τις εφαρμογές εποξειδικών ρητινών. Στη συνέχεια αναφέρονται οι ίνες Kevlar® και αναλύεται η χημική δομή τους, τα είδη των ινών Kevlar® που υπάρχουν και οι εφαρμογές τους. Στο κεφάλαιο αυτό παρουσιάζονται και τα σύρματα με μνήμη σχήματος. Στο πέμπτο κεφάλαιο περιγράφεται ο τρόπος με τον οποίο παρασκευάστηκαν τα σύνθετα με ενσωματωμένα σύρματα με μνήμη σχήματος. Στο έκτο κεφάλαιο αναφέρονται οι πειραματικές τεχνικές που χρησιμοποιήθηκαν για τη μελέτη των δοκιμίων. Εδώ αναφέρονται σε συντομία γενικά στοιχεία για τη μέθοδο της διαφορικής θερμιδομετρίας σάρωσης (DSC) και για τη μέθοδο της δυναμικής μηχανικής ανάλυσης (DMA). Επίσης, περιγράφονται οι συσκευές της διαφορικής θερμιδομετρίας σάρωσης και της δυναμικής μηχανικής ανάλυσης που χρησιμοποιήθηκαν για τη μελέτη της θερμικής και μηχανικής απόκρισης των δοκιμίων. Στο έβδομο κεφάλαιο παρατίθενται τα πειραματικά αποτελέσματα για δοκίμια Ni-Ti, Ni-Ti-Cu με 6% σε Cu, Ni-Ti-Cu με 12% σε Cu και για σύνθετα δοκίμια NiTi με προτάνυση 3%, NiTiCu (6% Cu) με προτάνυση 2%, NiTiCu (12% Cu) με προτάνυση 3%, που μελετήθηκαν με τη διάταξη της διαφορικής θερμιδομετρίας σάρωσης (DSC). Επιπλέον, παρουσιάζονται τα πειραματικά αποτελέσματα για σύρματα Ni-Ti-Cu με 12% σε Cu και Ni-Ti, καθώς και για σύνθετα Ni-Ti-Cu (12% Cu) με 3% προτάνυση και για ρητίνη με ίνες Kevlar 29®, που μελετήθηκαν με διάταξη δυναμικής μηχανικής ανάλυσης (DMA). Στο επόμενο κεφάλαιο σχολιάζονται τα αποτελέσματα αυτά, ενώ στο τελευταίο κεφάλαιο αναφέρονται τα συμπεράσματα που προκύπτουν από τη μελέτη των αποτελεσμάτων. / Exploiting the functional properties of materials such as shape memory alloys, electrorheological suspensions and piezo/ferroelectric elements results in the development of smart materials or systems. In the scientific and technological field of smart materials the major achievement is not related to the values of specific physical properties but to the “adopted” ability to control their own behaviour. The subject of the present work concerns the crystallographic transformations of Shape Memory Alloys (SMA) under constrained conditions. The occurring transitions are studied experimentally by means of Differential Scanning Calorimetry (DSC) and Dynamic Mechanical Analysis (DMA). The first part of this work is a bibliographical review of the field, while the second one is the experimental study of the same subject. In the following lines, a short description, of the present thesis is given. The first chapter gives an introduction to smart materials. Composite systems, which under the influence of an external cause, can vary their behaviour or some characteristics (shape, natural vibration frequency, damping coefficient etc) in a specific and controllable way, are referred as smart materials. These systems incorporate sensors and actuators, which in turn are connected by a suitable control loop. Suitable materials for being employed as sensors and actuators, as well as the types of the, up to now, achieved control are also discussed. Chapter two covers briefly, fundamental aspects of composite materials. A system of two or more different, in composition and chemical structure, materials physically bonded between of them is characterised as a composite material. Composite materials are consisted from a continuous phase, often called “matrix”, and a discrete phase, called “reinforcing or filling phase”. Composite materials exhibit always a third phase, namely interface, between matrix and reinforcement. In this chapter the types of composites, matrices, fillers and the characteristics of interface are referred. Chapter three presents smart composite systems with embedded shape memory alloys (SMA). Shape memory alloys have the ability to change, reversibly, a number of characteristics, including their own shape. In this chapter direct and reverse martensitic transformation, shape memory effect, important shape memory alloys and their mechanical properties, as well as a short description of the manufacturing procedure of smart systems with embedded shape memory alloys, is presented. In the fourth chapter the employed materials for the production of the smart systems are discussed. The chemical structure, the curing procedure and the applications of epoxy resins are referred. Aramid fibres, such as Kevlar® fibres are also discussed, connecting their reinforcing role with their microstructure. Chapter five describes analytically the preparation procedure of the specimens. Next chapter describes the main characteristics of differential scanning calorimetry, dynamic mechanical analysis, as well and the devices used to study the thermal and mechanical response of the specimens. Chapters seven and eight present the experimental results of all the examined specimens and the resulting discussion respectively. Finally, concluding remarks and possible future work are included in chapter nine.

The majority of structural studies on DNA have been carried out using fibre diffraction, while studies of its dynamics and thermal behaviour have been mainly performed in solution. When the DNA double helix is heated, it exhibits local separation of the two strands that grow in size with temperature and lead to their complete separation. This work has investigated various aspects of this phenomenon. The experiments reported in this thesis were carried out on films of oriented fibres of DNA prepared with the Wet Spinning Apparatus. Thus, sample preparation and characterisation are essential parts of the research. The structures of two forms of DNA, A and B, have been explored as a function of relative humidity at fixed ionic conditions. A method to eliminate traces of ever-present B-form contamination in A-form samples was established. The high orientation of the DNA molecules within the samples allowed us to investigate dynamical fluctuations and the melting transition of DNA using neutron scattering, which can provide the spatial information crucial to understand a phase transition, probing the static correlation length along the molecule as a function of temperature. The transition has been investigated for A and B-forms in order to understand its dependence on molecular configuration.Furthermore, after the first melting, denatured DNA films show typical glass behaviour. Their thermal relaxation has been explored using calorimetry.Neutron and X-ray inelastic scattering (INS and IXS) were used in the past to measure longitudinal phonons in fibre DNA, and the results shown disagreement. Recent INS measurements supported with phonon simulations have been crucial to understand the different dispersion curves reported to date. Experiments using INS and IXS have been carried out to continue with this investigation. Attempts to observe the transverse fluctuations associated to the thermal denaturing of DNA, never experimentally investigated before, have been made.

Cette thèse décrit la synthèse, la caractérisation, les réactivités, et les propriétés physiques de complexes divalents et trivalents de Ni formés à partir de nouveaux ligands «pincer» de type POCN. Les ligands POCN de type amine sont préparés d’une façon simple et efficace via l’amination réductrice de 3-hydroxybenzaldéhyde avec NaBH4 et plusieurs amines, suivie par la phosphination de l’amino alcool résultant pour installer la fonction phosphinite (OPR2); le ligand POCN de type imine 1,3-(i-Pr)2PC6H4C(H)=N(CH2Ph) est préparé de façon similaire en faisant usage de PhCH2NH2 en l’absence de NaBH4. La réaction de ces ligands «pincer» de type POCN avec NiBr2(CH3CN)x en présence d’une base résulte en un bon rendement de la cyclométalation du lien C-H situé en ortho aux fonctions amine et phosphinite. Il fut découvert que la base est essentielle pour la propreté et le haut rendement de la formation des complexes «pincer» désirés. Nous avons préparé des complexes «pincer» plan- carrés de type POCN, (POCNRR΄)NiBr, possédant des fonctions amines secondaires et tertiaires qui démontrent des réactivités différentes selon les substituants R et R΄. Par exemple, les complexes possédant des fonctions amines tertiaires ArCH2NR2 (NR2= NMe2, NEt2, and morpholinyl) démontrent des propriétés rédox intéressantes et pourraient être convertis en leurs analogues trivalents (POCNR2)NiBr2 lorsque réagis avec Br2 ou N-bromosuccinimide (NBS). Les complexes trivalents paramagnétiques à 17 électrons adoptent une géométrie de type plan-carré déformée, les atomes de Br occupant les positions axiale et équatoriale. Les analyses «DSC» et «TGA» des ces composés ont démontré qu’ils sont thermiquement stables jusqu’à ~170 °C; tandis que la spectroscopie d’absorption en solution a démontré qu’ils se décomposent thermiquement à beaucoup plus basse température pour regénérer les complexes divalents ne possédant qu’un seul Br; l’encombrement stérique des substitutants amines accélère cette route de décomposition de façon significative. Les analogues NMe2 et N(morpholinyl) de ces espèces de NiIII sont actifs pour catalyser la réaction d’addition de Kharasch, de CX4 à des oléfines telles que le styrène, tandis qu’il fut découvert que l’analogue le moins thermiquement stable (POCNEt2)Ni est complètement inerte pour catalyser cette réaction. Les complexes (POCNRH)NiBr possédant des fonctions amines secondaires permettent l’accès à des fonctions amines substituées de façon non symétrique via leur réaction avec des halogénures d’alkyle. Un autre avantage important de ces complexes réside dans la possibilité de déprotonation pour préparer des complexes POCN de type amide. De telles tentatives pour déprotoner les fonctions NRH nous ont permis de préparer des espèces dimériques possédant des ligands amides pontants. La nature dimérique des ces complexes [P,C,N,N-(2,6-(i-Pr)2PC6H3CH2NR)Ni]2 (R= PhCH2 et Ph) fut établie par des études de diffraction des rayons-X qui ont démontré différentes géométries pour les cœurs Ni2N2 selon le substituant N : l’analogue (PhCH2)N possède une orientation syn des substitutants benzyles et un arrangement ressemblant à celui du cyclobutane du Ni et des atomes d’azote, tandis que l’analogue PhN adopte un arrangement de type diamant quasi-planaire des atomes du Ni et des atomes d’azote et une orientation anti des substituants phényles. Les espèces dimériques ne se dissocient pas en présence d’alcools, mais elles promouvoient l’alcoolyse catalytique de l’acrylonitrile. De façon intéressante, les rendements de ces réactions sont plus élevés avec les alcools possédant des fonctions O-H plus acides, avec un nombre de «turnover» catalytique pouvant atteindre 2000 dans le cas de m-cresol. Nous croyons que ces réactions d’alcoolyse procèdent par activation hétérolytique de l’alcool par l’espèce dimérique via des liaisons hydrogènes avec une ou deux des fonctions amides du dimère. Les espèces dimériques de Ni (II) s’oxydent facilement électrochimiquement et par reaction avec NBS ou Br2. De façon surprenante, l’oxydation chimique mène à l’isolation de nouveaux produits monomériques dans lesquels le centre métallique et le ligand sont oxydés. Le mécanisme d’oxydation fut aussi investigué par RMN, «UV-vis-NIR», «DFT» et spectroélectrochimie. / This thesis describes the synthesis, characterization, reactivities, and physical properties of divalent and trivalent complexes of Nickel based on new POCN-type pincer ligands. The amino-type POCN ligands were prepared in a simple and efficient manner via reductive amination of 3-hydroxybenzaldehyde with NaBH4 and various amines, followed by phosphination of the resulting amino alcohol to install the phosphinite (OPR2) functionality. The imino-type POCN ligand 1,3-(i-Pr)2PC6H4C(H)=N(CH2Ph) was prepared similarly using PhCH2NH2 in the absence of NaBH4. Reaction of these POCN-type pincer ligands with NiBr2(CH3CN)x in the presence of a base results in the high yield cyclometalation of the C-H bond which is ortho to the amine and phosphinite functionalities. The base was found to be essential for a clean and high yield formation of the desired pincer complexes. We have thus prepared square planar POCN-type pincer complexes (POCNRR΄)NiBr featuring tertiary or secondary amine moieties that exhibit different reactivities as a function of amine substituents R and R΄. For instance, complexes bearing the tertiary amine moieties ArCH2NR2 (NR2= NMe2, NEt2, and morpholinyl) displayed interesting redox properties and could be converted into their trivalent analogues (POCNR2)NiBr2 when reacted with Br2 or N-bromosuccinimide (NBS). These 17-electron, paramagnetic trivalent complexes adopt a distorted square pyramidal geometry with Br atoms at axial and equatorial positions. DSC and TGA analyses of these compounds revealed them to be thermally stable up to ~170 °C; whereas absorption spectroscopy in solution showed that they undergo thermal decomposition at much lower temperatures to regenerate the monobromo divalent complexes; increased steric bulk of the amine substituents accelerate this decomposition pathway significantly. The NMe2 and N(morpholinyl) analogues of these NiIII species are active catalysts for the Kharasch addition of CX4 to olefins such as styrene, whereas the least thermally stable analogue (POCNEt2)Ni was found to be completely inert for this reaction. The complexes (POCNRH)NiBr featuring secondary amine moieties allow access to unsymmetrically substituted amine moieties via reaction with alkyl halides. Another important advantage of these complexes lies in the possibility of deprotonation to prepare amide-type POCN complexes. Such attempts at deprotonating the NRH moieties have allowed us to prepare dimeric species featuring bridging amido ligands. The dimeric nature of these complexes [P,C,N,N-(2,6-(i-Pr)2PC6H3CH2NR)Ni]2 (R= PhCH2 and Ph) was established through X-ray diffraction studies that showed different geometries for the Ni2N2 cores as a function of N-substituent: the (PhCH2)N analogue featured a syn orientation of the benzyl substituents and a cyclobutane-like arrangement of Ni and of the nitrogen atoms, whereas the PhN analogue adopted a nearly planar diamond-like arrangement of the Ni and of the nitrogen atoms and an anti orientation of the phenyl substituents. These dimeric species do not dissociate in the presence of alcohols, but they promote the catalytic alcoholysis of acrylonitrile. Interestingly, yields of these reactions are higher with alcohols possessing more acidic O-H moieties, with a catalytic turnover number reaching up to 2000 in the case of m-cresol. These alcoholysis reactions are believed to proceed through heterolytic activation of the alcohol by dimeric species via hydrogen bonding with one or two amido moieties in the dimer. The dimeric Ni (II) species were found to undergo facile oxidation both electrochemically and in reaction with NBS or Br2. Surprisingly, chemical oxidation led to isolation of new monomeric products in which both the metallic center and the ligand were oxidized. giving a trivalent species featuring an imine-type POCN ligand. Oxidation mechanism was investigated in detail by NMR, UV-vis-NIR, DFT and spectroelectrochemistry.

In dieser Arbeit wurde die Möglichkeit untersucht, Bortrihalogenide mit Wasserstoff unter milden Bedingungen (T < 100 °C, p(H2) < 50 bar) zu hydrieren. Um eine Triebkraft für die thermodynamisch ungünstige Reaktion zu erhalten, wurden Amine als Hilfsbasen zugesetzt, welche den bei der Reaktion entstehenden Halogenwasserstoff als Ammoniumsalz binden und damit das Reaktionsgleichgewicht in Richtung der Produkte verschieben. Es wurden dafür verschiedene Amin-Boran bzw. Amin-HCl Addukte synthetisiert und mittels IR, NMR und DSC charakterisiert. Bei den anschließenden Hydrierungsversuchen wurden verschiedene Katalysatoren auf ihre Eignung getestet und weiterentwickelt. Unterstützt wurden die experimentellen Arbeiten durch Berechnungen mit Gaussian 03. IR- und NMR-Spektren vieler Addukte wurden berechnet und freie Reaktionsenthalpien der Hydrierung in Abhängigkeit des verwendeten Amins und Borhalogenids bestimmt. Mögliche Übergangszustände wurden diskutiert und ihre Aktivierungsenergien ermittelt.

Consistently, reports in the literature have identified that a sedentary lifestyle contributes to the progression of a range of chronic degenerative diseases. The measurement of energy expenditure and physical activity pattern in children is a challenge for all professionals interested in paediatric health and from a broader perspective, the public health fraternity charged with considering longer term health consequences of physical inactivity. The primary objective of this thesis was to identify a suitable indirect and objective measurement technique for the assessment of energy expenditure and physical activity pattern in children. The ideal characteristics of such a technique are that it should be reproducible and have been validated against a criterion reference method. To achieve this goal, a series of methodological studies were undertaken (Chapters II and III). This work was essential to increase accuracy during the individualised laboratory calibration process and further minimise prediction errors when analysing data from 7 days of monitoring under free-living conditions in the second part of the study (Chapters IV and V). In the first study to verify the combined effect of body position, apparatus and distraction on children's resting metabolic rate (RMR), experiments were carried out on 14 children aged 8-12 (mean age = 10.1 years ± 1.4). Each participant underwent 2 test sessions, one week apart under three different situations: a) using mouthpiece and nose-clip (MN) or facemask (FM); b) sitting (SEAT) or lying (LY) and c) TV viewing (TV) or no TV viewing. In the first session, following 20 min rest and watching TV, the following protocol was used: LY: 20 min - stabilisation; 10 min using MN and 10 min using FM. Body position was then changed to seated: 20 min stabilisation; 10 min using FM; 10 min using MN. In the second session, FM and MN order was changed and participants did not watch TV. Data were analysed according to the eight combinations among the three studied parameters. Repeated measures ANOVA indicated statistically significant differences for &VO2 (p=0.01) and RMR (p=0.02), with TVMNSEAT showing higher values than TVFMLY. Bland-Altman analysis showed a bias for &VO2, &VCO2, RQ and RMR between TVFMLY and TVMNSEAT of -17.8±14.5 ml.min-1, -8.8±14.5 ml. min-1, 0.03±0.05 and -115.2±101.9 kcal.d-1, respectively. There were no differences in RMR measurements due to body position and apparatus when each variable was isolated. Analyses of distraction in three of four combinations indicated no difference between TV and no TV. In summary, different parameter combinations can result in increased bias and variability and thereby reported differences among children's RMR measurement. The second study dealt with treadmill adaptation and determination of self-selected (SS) walking speed. Assessment of individual and group differences in metabolic energy expenditure using oxygen uptake requires that individuals are comfortable with, and can accommodate to, the equipment being utilised. In this study, a detailed proposal for an adaptation protocol based on the SS was developed. Experiments were carried out on 27 children aged 8-12 (mean age = 10.3±1.2 yr). Results from three treadmill tests following the adaptation protocol showed similar results for step length with no significant differences among tests and lower and no statistically significant variability within- and between-days. Additionally, no statistically significant differences between SS determined over-ground and on a treadmill were verified. These results suggest that SS speed determined over-ground is reproducible on a treadmill and the 10 min familiarisation protocol based on this speed provided sufficient exposure to achieve accommodation to the treadmill. The purpose of the third study was to verify within- and between-day repeatability and variability in children's oxygen uptake ( &VO2), gross economy (GE) [ &VO2 divided by speed] and heart rate (HR) during treadmill walking based on SS. 14 children (mean age = 10.2±1.4 yr) undertook 3 testing sessions over 2 days in which four walking speeds, including SS, were tested. Within- and between-day repeatability was assessed using the Bland and Altman method and coefficients of variability (CV) were determined for each child across exercise bouts and averaged to obtain a mean group CV value for &VO2, GE and HR per speed. Repeated measures ANOVA showed no statistically significant differences in within- or between-day CV for &VO2, GE or HR at any speed. Repeatability within and between-day for &VO2, GE and HR for all speeds was verified. These results suggest that submaximal &V O2 during treadmill walking is stable and reproducible at a range of speeds based on children's SS. In the fourth study, the objective was to establish the effect of walking speed on substrate oxidation during a treadmill protocol based on SS. Experiments were carried out on 12 girls aged 8-12 (mean age = 9.9±1.4 yr). Each participant underwent 2 test sessions, one week apart. Workloads on the treadmill included 2 speeds slower than SS (1.6 [V1] and 0.8 km.h-1 [V2] slower than SS), SS (V3), and a speed 0.8 km.h-1 faster than SS (V4). Indirect calorimetry from respired gas measurements enabled total fat (FO) and carbohydrate (CHO) oxidation rates to be calculated according to the non-protein respiratory quotient (Peronnet and Massicote, 1991) and percentage of CHO and FO calculations using equations from McGilvery and Goldstein (1983). Repeated measures ANOVA followed by a Tukey Post Hoc test (p< 0.05) was used to verify differences in CHO and FO rates among speeds. Paired T-test was used to verify differences in CHO and FO rates between tests per velocity. The reliability between-day was assessed using intraclass correlation coefficient (ICC). Results showed significant differences for CHO among all speeds, as well as significant differences for FO between V1 and V2 against V3 and V4 in both tests. Analyses between trials per velocity showed no significant substrate use differences as well as acceptable reliability. At the self-selected speed (V3) there was an accentuation in FO reduction as well as an increase in CHO oxidation. The purpose of the fifth study was to determine whether there were differences in substrate oxidation between girls (G) and women (W) during a treadmill protocol based on SS. Experiments were carried out on 12 G aged 8-12 (mean age = 9.9±1.4 yr) and 12 W aged 25-38 (mean age = 32.3±3.8 yr). The treadmill protocol included 6 min workloads followed by 5 min rest periods. Workloads included 2 speeds slower than SS (1.6 (V1) and 0.8 km.h-1 (V2) slower than SS), SS (V3), and a speed 0.8 km.h-1 faster than SS (V4). Total fat and carbohydrate (CHO) oxidation rates were calculated from indirect calorimetry according to the non-protein respiratory quotient. Repeated measures ANOVA followed by a Tukey Post Hoc test was used to verify intra-test differences in CHO and fat oxidation rates among speeds. Intergroup differences were analysed using paired T-test. Fat utilisation in W achieved a plateau at a relative velocity 0.8 km.h-1 slower than SS, but for G, fat utilisation increased until SS, and then stabilised upon reaching the higher velocity. CHO oxidation curves rose abruptly above V2 for W, while for G the acute increase occurred after SS (V3). Collectively, these results indicate that as walking intensity increases G are able to meet the energy demands of the work by increasing fat oxidation together with the increased CHO oxidation up to SS. In contrast for W, increasing CHO oxidation is associated with an early decrease in fat utilisation at a velocity slower than the self-selected speed. The sixth study dealt with validation of indirect techniques for the measurement of energy expenditure in free-living conditions against the DLW technique. Experiments were carried out on 19 children aged 8-12 (mean age = 10.3±1.0 yr). To indirectly predict energy expenditure 12 different procedures were used. Only one procedure, combining activity and heart rate (AHbranched), was based on a group equation, the others were based on individualised regression. Three of the individually-based techniques were able to accurately predict energy expenditure in free-living conditions. These tecniques were HRPAnetRMR using HRnet [HR exercise minus sleep HR (SHR)] against PAnet (measured PA exercise minus measured RMR) and upper and lower body equations corrected by RMR; HRPAnet4act using the same procedure but corrected by the mean resting &VO2 for 4 resting activities [(4act) = supine watching TV, sitting watching TV, sitting playing computer games and standing], and HRPALBnet4act using only lower body activities and corrected by 4act. HRPAnetRMR was only slightly more accurate than HRPAnet4act and HRPALBnet4act, but this technique is only adjusted by RMR whereas the other two are heavily dependent on more complex laboratory calibration. Bland and Altman (1986) analyses showed no significant differences between AHbranched predicted and measured TEE using the DLW technique. A SEE of 79 kcal.d-1 and a mean difference of 72 kcal.d-1, with a 95% CI ranging from -238 to 93.9 kcal.d-1 was found. In addition, no significant differences between predicted HRPAnetRMR and measured TEE using DLW were found, showing an SEE of 99 kcal.d-1 and a mean difference of -67 kcal.d-1, and a 95% CI ranging from -276.6 to 141.9 kcal.d-1. AHbranched and HRPAnetRMR were both valid and similarly suitable for the prediction of energy expenditure in children under free-living conditions. Significant associations between DLWAEE and the after-school time window indicated that this time window as an important discretionary period representative of children physical activity. However, the duration of the after-school time windows should be more carefully considered. Accelerometer data showed a better association between the largest after-school time window (3.5 hr) and measured TEE. The final study, completed with 19 children aged 8-12 (10.3±1.0 yr) highlighted, under laboratory conditions across a range of walking and running speeds, the inadequacy of the use of the standard MET in children. This traditional approach overestimates energy expenditure with an increased difference linearly related to speed increments. Minute-by-minute analyses of 7 days of free-living monitoring showed an average overestimation of 64 minutes per day for moderate-to-vigorousphysical- activity (MVPA) using the standard MET compared with the individually measured MET. For all intensities, these differences were statistically significant (p< 0.001). The second part of this study showed a variability of 20% in the average time spent at MVPA when comparing HR I 140 bpm and HR > 50%P &VO2 (P &VO2 = the highest &VO2 observed during an exercise test to exhaustion). Results of the current study compared to observations in the literature showed that HR I 140 bpm consistently estimates lower MVPA time than HR > 50%P &VO2. When these two PA indices were compared with individual and standard MET measured minute-byminute, statistically significant differences were verified among all of them at MPA, but no differences were verified at VPA, except between individual and standard METs. However, whether each one of the PA indices used are under- or overestimating time at MVPA is still debatable due to the lack of a gold standard. Finally, each index used in this study classified different numbers of participants as achieving the PA target of 60 min.d-1. The wide variability between indices when attempting to classify children who are achieving the recommended target is cause for great concern because habitually these indices are utilised as screening tools in paediatric and public health settings and used to guide behavioural interventions.

There is an increase in the prevalence of obesity among people with schizophrenia thought to be due in part to the weight enhancing side-effects of medications commonly used to treat the symptoms of schizophrenia. Despite the deleterious health effects associated with obesity and its impact on quality of life and medication compliance, little is known about body composition and energy expenditure in this clinical group. The primary purpose of this thesis was to enhance understanding of body composition and energy expenditure, particularly resting energy expenditure in men with schizophrenia who take atypical antipsychotic medications. Unique to this investigation is the evaluation of clinical tools used to predict body composition and energy expenditure against reference methodologies in men with schizophrenia. Further, given the known links between obesity and physical activity, an additional but less comprehensive component of the thesis was a consideration of total and activity energy expenditure in addition to the interaction between psychiatric symptoms, side-effects of antipsychotic medications and physical activity also occurred as part of this thesis. Collectively, the goals of this thesis were addressed through a series of studies – the first two studies were related to the measurement and characteristics of body composition in men with schizophrenia, while the third and fourth studies were related to the measurement and characteristics of resting energy expenditure in men with schizophrenia. The fifth and sixth studies the utilised doubly labelled water technique to quantify activity and total energy expenditure in a small group of men with schizophrenia and explored the use of accelerometry in this cohort. The final study briefly considered the impact of psychiatric symptoms and self-reported medication side-effects on objectively measured physical activity. In the first study, thirty-one male adults previously diagnosed with schizophrenia and sixteen healthy male controls were recruited. Estimates of body composition derived from an anthropometry-based equation and from bioelectric impedance analysis (BIA) using deuterium dilution as the reference methodology to determine total body water were compared. The study also determined the validity of equations commonly used to predict body composition from BIA in the men with schizophrenia. A further aim was to determine the superiority of either BIA or body mass index (BMI) as an indicator of obesity in this cohort. The inclusion of the control group, closely matched for age, body size and body composition demonstrated that there was no difference in the ability of body composition prediction methods to distinguish between fat and fat-free mass (FFM) in controls and men with schizophrenia when both groups had similar body composition. However this study indicated that an anthropometry-based equation previously used in people with schizophrenia was a poor predictor of body composition in this cohort, as evidenced by wide limits of agreement (25%) and systematic variation of the bias. In comparison, the best predictor of percentage body fat (%BF) in this group was gained when impedance values were used to predict percentage body fat via the equation published by Lukaski et al (1986). Although percentage body fat was underpredicted using the Lukaski et al. (1986) equation, the mean magnitude was relatively small (1.3%), with the limits of agreement approximately 13%. Linear regression analysis revealed that %BF predicted using the Lukaski et al. (1986) equation explained 25% more of the variance in percentage body fat than BMI. Further, this study also indicated that BIA was more sensitive than BMI in distinguishing between overweight and obesity in this cohort of men with schizophrenia. Because of the almost exclusive use of BMI as an indicator of obesity in people with schizophrenia, the level of excess body fat may be in excess of that previously indicated. The second study extended the examination of body composition in men with schizophrenia. In this study, the thirty-one participants with schizophrenia (age, 34.2 ± 5.7 years; BMI, 30.2 ± 5.7 kg/m2) were individually matched with sedentary controls by age, weight and BMI. Deuterium dilution was used to distinguish between FFM and fat mass. The previous study had indicated that while BIA was a suitable group measure for obesity, on an individual level the technique lacked the precision required for investigating body composition in men with schizophrenia. Waist circumference was used as an indicator of body fat distribution. The findings of this study indicated that in comparison with healthy sedentary controls of similar body size and age, men with schizophrenia had higher levels of body fat which was more centrally distributed. Percentage body fat was on average 4% higher and waist circumference, on average 5 cm greater in men with schizophrenia than the sedentary controls of the same age and BMI. Further, this study indicates that the use of BMI to predict body fat in men with schizophrenia will result in greater bias than when it is used to predict body fat in other sedentary men. Commonly used regression equations to predict energy requirements at rest are based on the relationships between weight and resting energy expenditure (REE) and in such equations, weight acts as a surrogate measure of FFM. The objectives of study three were to measure REE in a small group of men with schizophrenia who were taking the antipsychotic medication clozapine and to determine whether REE can be predicted with sufficient accuracy to substitute for the measurement of REE in the clinical and/or research settings. Body composition was determined using deuterium dilution and REE was measured using a Deltatrac Metabolic Cart via a ventilated hood. The male participants, (aged 28.0 ± 6.7 yrs, BMI 29.8 ± 6.8 kg/m2) were weight stable at the time of the study and had been taking clozapine for 20.5 ± 12.8 months, with doses of 450 ± 140 mg/day. Of the six prediction equations evaluated, the equation of Mifflin et al. (1990) with no systematic bias, the lowest bias and the lowest limits of agreement proved to be the most suitable equation to predict REE in this cohort. The overestimation of REE can be corrected for by deducting 160 kcal/day from the predicted REE value when using the Mifflin et al. (1990) equations. However, the magnitude of the error associated with the prediction of REE for an individual is 370 kcal/day. The findings of this study indicate that REE cannot be predicted with sufficient individual accuracy in men with schizophrenia, therefore it was necessary to measure rather than predict REE in subsequent studies. In the fourth study, indirect calorimetry (Deltatrac Metabolic Cart via ventilated hood) and deuterium dilution were used to accurately determine REE, respiratory quotient (RQ) and FFM in 31 men with schizophrenia and healthy sedentary controls individually matched for age and BMI. Data from this study indicated that gross REE was lower in men with schizophrenia than in healthy sedentary controls of a similar age and body size. However, there was no difference between the groups in REE when REE was adjusted for FFM using the mathematically correct method (analysis of covariance with FFM as the covariate). There was however a statistically and clinically significant difference in resting, fasted RQ between men with schizophrenia and controls, suggesting that RQ rather than REE may be an important correlate worthy of further investigation in men with schizophrenia who take antipsychotic medications. Studies five and six involved the application of the doubly labelled water (DLW) technique to accurately determine total energy expenditure (TEE) and activity energy expenditure (AEE) in a small group of men with schizophrenia who had been taking the atypical antipsychotic medication clozapine. The participants were those who took part in study three. The purpose of these studies was to assess the validity of a commercially available tri-axial accelerometer (RT3) for predicting free-living AEE and to investigate TEE and AEE in men with schizophrenia. There was poor agreement between AEE measured using DLW and AEE predicted using the RT3. However, using the RT3 to measure inactivity explained over two-thirds of the variance in AEE. This study found that the relationship between current AEE per kilogram of body weight and change from baseline weight in men taking clozapine was strong although not significant. The sedentary nature of the group of participants in this study was reflected in physical activity levels, (PAL, 1.39 ± 0.27), AEE (435 ±352 kcal/day) and TEE (2511 ± 606 kcal/day) that fell well short of values recommended by WHO (2000) for optimal health and to prevent weight gain. Given the increasing recognition of the importance of sedentary behaviour to weight gain in the general community, further examination of the unique contributing factors such as medication side effects and symptoms of mental illness to activity levels in this clinical group is warranted. The final study used accelerometry (RT3) to objectively measure activity in a group of 31 men with schizophrenia who had been taking atypical antipsychotic medications for more than four months. The purpose of this study was to explore the relationships between psychiatric symptomatology, side-effects of medication and physical activity. Accelerometry output was analysed to provide a measure of inactivity and moderate intensity activity (MIA). The well-validated and reliable standardised clinical interview, the Positive and Negative Syndrome Scale (PANSS) was used as a measure of psychiatric symptoms. Perceived side-effects of medication were assessed using the Liverpool University Neuroleptic Rating Side-Effects Scale (LUNSER). Surprisingly, there was no relationship reported between any measures of negative symptoms and physical inactivity. However, self-reported measures of medication side-effects relating to fatigue, sleepiness during the day and extrapyramidal symptoms explained 40% of the variance in inactivity. This study found significant relationships between some negative symptoms and moderate intensity activity. Despite the expectation that as symptoms of mental illness reduce, inactivity may diminish and moderate intensity activity will increase, it may not be surprising that in practice this is an overly simplistic view. It may be that measures of social functioning and possibly therefore cognition may be better predictors of physical activity than psychiatric symptomatology per se.

Η υπέρταση είναι ένας από τους σημαντικότερους παράγοντες που αυξάνει τα καρδιαγγειακά επεισόδια τα οποία ευθύνονται περίπου για το ήμισυ των θανατηφόρων επεισοδίων στους ενήλικους. To σύστημα ρενίνης-αγγειοτασίνης-αλδοστερόνης (ΣΡΑΑ) διαδραματίζει καθοριστικό ρόλο στην παθοφυσιολογία των καρδιαγγειακών νόσων. Η αναστολή του ΣΡΑΑ σε παθολογικές καταστάσεις μπορεί να πραγματοποιηθεί με αναστολή του ενζύμου της ρενίνης ή παρεμπόδιση της σύνδεσης της ΑΙΙ με τους υποδοχείς ΑΤ1. Έχει διατυπωθεί η υπόθεση ότι τα αμφοτερικά μόρια για να αλληλεπιδράσουν με τον υποδοχέα θα πρέπει πρώτα να εισδύσουν σε κατάλληλη τοπογραφική θέση στις βιολογικές μεμβράνες και μετά με διάχυση να προσεγγίσουν το ενεργό κέντρο όπου όταν προσδεθούν με μία σειρά αντιδράσεων θα εξασκήσουν τη βιολογική τους δράση. Για την κατανόηση του ρόλου των μεμβρανών στο σύστημα ΣΡΑΑ μελετήθηκαν οι αλληλεπιδράσεις της αλισκιρένης (αναστολέας ρενίνης) και ολμεσαρτάνης (ανταγωνιστής αγγειοτασίνης ΙΙ) σε μοντέλα διπλοστιβάδων διπαλμιτικής φωσφατιδυλοχολίνης με ή χωρίς χοληστερόλη. Οι μελέτες διεξήχθησαν κάνοντας χρήση Πυρηνικού Μαγνητικού Συντονισμού (υγρής και στερεής κατάστασης), Διαφορικής Θερμιδομετρίας Σάρωσης, Φασματοσκοπίας Raman και Περίθλασης Ακτίνων-Χ. Σύγκριση των πειραματικών αποτελεσμάτων με άλλες σαρτάνες που μελετήθηκαν κάνοντας χρήση τις ίδιες τεχνικές απόδειξαν ότι όλα τα φάρμακα του ΣΡΑΑ εντοπίζονται στην ενδιάμεση φάση όπου εξασκούν διαφορετικές υδρόφιλες και λιπόφιλες αλληλεπιδράσεις. Επομένως το κάθε φάρμακο αποτυπώνει τη δική του σφραγίδα μέσα στις λιπιδικές διπλοστιβάδες. Αυτή η μοναδικότητα στις αλληλεπιδράσεις κάθε φαρμάκου με τις λιπιδικές διπλοστιβάδες ίσως να σχετίζεται και με τη μοναδικότητα του στο φαρμακευτικό του προφίλ. Ένα άλλο ενδιαφέρον αποτέλεσμα που προέκυψε από τις μελέτες είναι ότι η ολμεσαρτάνη σε μεθανολικό διάλυμα τόσο σε χαμηλή θερμοκρασία όσο και σε θερμοκρασία δωματίου δεν είναι σταθερή και μετατρέπεται στο αιθερικό της παράγωγο το οποίο ταυτοποιήθηκε φασματοσκοπικά. Στις ίδιες συνθήκες δεν παρατηρήθηκε εστεροποίηση. / Hypertension is one of the major risk factors responsible for the increase of half of the cardiovascular episodes in the adults. The system of Renin-Angiotensin-Aldosterone (RAAS) plays a determinative role in the pathophysiology of cardiovascular diseases. In a pathological state the aim is to block the generation of Angiotensin II through inhibition of rennin or angiotensin converting enzymes or its action on AT1 receptor. It has been hypothesized that amphiphilic molecules in order to exert their action on the receptor site, they have first to enter into the lipidic core of the lipid bilayers and then diffuse towards the active site. Thus, if this mechanism is applied, the lipidic part of the membrane bilayers appears to play an important role in the membrane action. To comprehend on the membrane:drug interactions we have studied the effects of olmesartan and aliskiren using dipalmitoylphosphatidylcholine bilayers with or without cholesterol. Various physical chemical methodologies such as liquid and solid state NMR , x-ray diffraction, Raman spectroscopy and Differential Scanning Calorimetry have been applied. The comparative results with other SARTANs showed that all drugs of the RAAS system act on the polar group and upper part of the alkyl chain, but exert different interactions. Thus, each drug is characterized by its own fingerprint in terms of its interactions and this may explain its unique pharmacological profile. Another, intriguing result derived from this thesis dissertation is the observation that olmesartan in methanolic solution is converted to its ether analogue. This isolated product was unambiguously structurally elucidated using a combination of LC-MS and 2D NMR spectroscopy.

This dissertation has focused on studying the effect of four glycine derivatives on the solid state properties of mannitol, glycine, and sucrose when freeze dried into blended mixtures. The primary goal was to assess their value for use in the stabilisation of vaccines in the solid state, by examining key physical and chemical characteristics, which have been documented to be beneficial to the stabilisation of biopharmaceutical formulations. The novel excipients; dimethyl glycine, and trimethyl glycine, were shown to retard the crystallisation and increase the overall glass transition temperature, of mannitol, when freeze dried as evidenced by DSC and Powder X-ray diffraction. Mannitol’s glass transition temperature increased from 100C to 12.650C and 13.610C when mixed with methyl-glycine and dimethyl glycine respectively. The glycine derivatives did not show the same effect on sucrose which remained amorphous regardless of the concentration of the other excipient. The different behaviour with the sucrose system was thought to be due to relatively high glass transition temperature of sucrose. Conversely glycine remained highly crystalline due it’s relatively low glass transition temperature. The novel excipient formulations were also assessed for their effect on the aggregation of the adjuvant aluminium hydroxide when freeze dried by Dynamic Light Scattering (DLS).The formulations containing the glycine derivatives all caused a decrease in the aggregation size of the adjuvant from ~26 μm, to 185 nm in the presence of methyl glycine. The effects of lysozyme and viral antigen on the adjuvants were also examined showing that the addition of the virus did not affect the size of the aggregates formed, however lysozyme showed significant decreases in the aggregates formed. Examination of the freezing method were also made showing that faster freezing rates produced smaller aggregates of the adjuvant. When investigating the rate at which the excipients lost water during secondary drying there was evidence of the formation of hydrates of glycine, trimethyl glycine, and mannitol has shown that the glycine derivatives have attributes which would be beneficial in stabilising vaccines in the solid state when freeze dried.