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White Spot lesions are a common iatrogenic occurrence on patients who are treated with fixed orthodontic appliances. There is a dynamic chemical interaction between enamel and saliva at the tooth surface that allow a lesion to have phase changes involving demineralization of enamel and remineralization. This is due to calcium and phosphate dissolved in saliva that is deposited onto the tooth surface or removed depending on the surrounding pH. Caseinphosphopeptide-amorphous calcium phosphate (CPP-ACP) is gaining popularity in dentistry as a way to increase the available level of calcium and phosphate in plaque and saliva to improve the chemical gradient so that if favors remineralization. The aim of our investigation is to search the available current literature and formulate a recommendation for use of CPP-ACP in orthodontics. Publications from the following electronic databases were searched: PubMed, Web of Science, Cochrane Library and Science Direct. Searches from August 2010 to April 1st 2012 were performed under the terms "MI Paste OR Recaldent OR caseinphosphopeptide-amorphous calcium phosphate OR CPP-ACP or tooth mousse". The searches yielded 155 articles, These were reviewed for relevance based on inclusion and exclusion criteria. Articles with inappropriate study design or no outcome measures at both baseline and end point were also excluded. 13 articles were deemed of relevance with a high quality study design and were included in this study for evaluation. The current literature suggests a preventative treatment regimen in which MI Paste Plus is used. It should be delivered once daily prior to bed after oral hygiene for 3 minutes in a fluoride tray, throughout orthodontic treatment. It should be recommended for high risk patients determined by poor oral hygiene, as seen by the inability to remove plaque from teeth and appliances. This protocol may prevent or assist in the remineralization of enamel white spot lesions during and after orthodontic treatment. / Oral Biology

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The dissociative anesthetic ketamine has been subject to growing abuse worldwide, particularly in adolescents. This project compared the effects of ketamine in conditioned place preference and intravenous self-administration in adolescent (PND 28-50) and adult (>PND70) Sprague-Dawley rats. Cocaine served as a positive control. In CPP, adolescents demonstrated preferences for ketamine, while adults developed an aversion. In the self-administration procedure, adults acquired the behavior more rapidly, but there was no difference in the percentage of subjects reaching acquisition nor in responding under a progressive ratio schedule for either drug. The CPP results suggest that adolescents have a greater sensitivity to the rewarding and tolerance to the aversive effects of ketamine. The divergent results for ketamine in the adults may reflect differences in the two procedures. However, because cocaine produced only hedonic effects in both age groups, it also suggests unique characteristics of ketamine and differences in its effects based on age.

Développement et évaluation de nouvelles stratégies pour le traitement des hépatites B chroniques, dans le modèle du canard de Pékin infecté par le DHBVL’infection chronique par le HBV est la cause majeure de cirrhose hépatique et de carcinome hépatocellulaire, conduisant à plus d’un million de décès chaque année. Le faible taux de réussite des thérapies actuelles des hépatites B montre la nécessité du recours à des méthodes thérapeutiques alternatives. Ainsi, nous avons étudié une stratégie pertinente reposant sur l’utilisation de molécules antisens (PNAs) couplées à des peptides perméabilisants (CPPs). Nous avons démontré que les PNAs ciblant le signal d’encapsidation du DHBV couplés au CPP pénétraient dans les cellules et conduisait à une inhibition de la réplication virale. De plus, nous avons mis en évidence une activité antivirale du CPP (Arg)8 seul. Nous avons ensuite évaluer le mécanisme d’action antivirale du CPP in vitro et avons démontré qu’il inhibait les stades tardifs de la morphogénèse virale, conduisant à une inhibition forte de la sécrétion des particules virales. Par ailleurs, nous nous sommes intéressés à l’évaluation de stratégies immunothérapeutiques, reposant sur la vaccination génétique. Nous avons démontré les bénéfices de la co-administration de cytokines (IFNγ), avec un vaccin à ADN dirigé contre la grande protéine d’enveloppe du DHBV (preS/S), sur l’amplitude de la réponse humorale et sur le pouvoir neutralisant des anticorps induits. Enfin nous avons évalué les bénéfices d’une approche d’immunisation hétérologue « prime-boost » associant l’immunisation à ADN et un vecteur viral (AdénoCELO) recombinant, codant la protéine preS/S du DHBV et l’IFNγ. Nous avons montré que l’immunisation hétérologue induisait une réponse humorale plus forte que celle induite par l’immunisation homologue. / Development and evaluation of new strategies for treating chronic hepatitis B in the model of Peking duck infected with DHBVChronic infection with Hepatitis B virus (HBV) is the major cause of liver cirrhosis and hepatocellular carcinoma, leading to more than one million deaths each year. The low success rate of current therapies against HBV infection shows the need of alternative therapeutics. Thus, we studied a new strategy based on the use of antisense molecules (PNAs) coupled with cell penetrating peptides (CPPs). We have shown that PNAs targeting the DHBV encapsidation signal coupled to CPPs penetrated into the cells and led to an inhibition of viral replication. In addition, we have demonstrated an antiviral activity of the CCP (Arg)8 itself. We then evaluate the mechanism of antiviral action of this CPP in vitro and have shown that it inhibited the late stages of viral morphogenesis, leading to a strong inhibition of the release of viral particles. Furthermore, we were interested in evaluating immunotherapeutic strategies, based on DNA vaccination. We have demonstrated the benefits of co-administration of cytokines (IFNy), with a DNA vaccine directed against the DHBV large envelope protein (preS/S), enhancing the magnitude of humoral response and enhancing neutralizing anti-DHBV antibody response. Finally we evaluated the benefits of a heterologous immunization approach or prime-boost immunization involving DNA vaccination and a recombinant viral vector (AdenoCELO) encoding the DHBV preS/S and IFNy proteins. We have shown that heterologous immunization induced a humoral response stronger than that induced by homologous immunization. By contrast, the heterologous prime-boost strategy was less effective than homologous DNA immunization for therapy of chronic DHBV-carrier ducks.

Made available in DSpace on 2015-02-04T21:45:28Z (GMT). No. of bitstreams: 1 Adilson J da Silva.pdf: 1679669 bytes, checksum: 027c6b4ba0a531ee2c3cb3524d5d47bf (MD5) Previous issue date: 2006-12-19 / A necessidade de cortar custos e aumentar a produtividade, aliada à crescente disponibilização de padrões que visam garantir a interoperabilidade entre aplicações distintas, têm levado um crescente número de empresas a utilizar a Internet como principal meio de comunicação com os seus parceiros comerciais, estimulando o crescimento do comércio eletrônico B2B e conseqüentemente aumentando o interesse na automatização da fase de negociação, que normalmente precede a fase de interação eletrônica entre os parceiros comerciais, buscando assim a agilização de todo o processo de colaboração. O desenvolvimento de negociações eletrônicas de forma automatizada implica na definição de regras e mensagens que devem ser utilizadas pelas partes, durante o processo de negociação. O padrão ebXML (Electronic Business Extensible Markup Language) especifica os componentes CPP (Collaboration Protocol Profile) e CPA (Collaboration Protocol Agreement) para serem utilizados na fase de negociação. O CPP descreve o perfil da empresa com relação a suas capacidades técnicas para o estabelecimento de um processo de negócio com outras empresas e o CPA é o acordo resultante da intersecção dos CPP dos parceiros comerciais envolvidos em um processo de colaboração de negócios. Estes componentes podem ser utilizados na automatização do processo de negociação, mas a especificação ebXML deixa em aberto a forma de geração automática do acordo de colaboração (CPA), assim como a forma de interação entre as empresas nesta fase. O problema é como efetuar a automatização desta interação e gerar automaticamente o acordo (CPA), a partir dos perfis (CPP) de cada empresa. Neste trabalho são analisadas as especificações ebXML e elaborada uma proposta para agilizar o processo de negociação, através da automatização da troca de mensagens que ocorre durante a fase de negociação e a geração de informações para auxiliar um negociador humano a tomar uma decisão final sobre um determinado processo de negociação, com a conseqüente geração de um acordo de colaboração (CPA). A proposta abrange a definição de um protocolo de negociação baseado em XML, para a troca de mensagens durante a fase de interação e a modelagem de um sistema para o controle destas mensagens e comparação das propostas de acordo, até a finalização do processo de negociação e, em caso de sucesso, com a geração do documento de acordo de colaboração. Para a validação da proposta foi desenvolvido um protótipo utilizando a linguagem Java e plataforma J2EE, abrangendo requisitos básicos para suportar um processo de negociação. Este protótipo foi implementado em um ambiente de testes com um cenário de uso envolvendo um processo de negociação entre duas empresas, visando estabelecer um processo de negócio de compra e venda.

The focus of this dissertation is on the development of a solid freeform fabrication (SFF) process for the design and manufacture of porous biodegradable orthopaedic implants from calcium polyphosphate (CPP). Porous CPP structures are used as bone substitutes for regenerating bone defects and/or as substrates in formation of so-called “biphasic” implants for repair of damaged osteochondral tissues. The CPP implants can be utilized in the treatment of many musculoskeletal diseases, osteochondral defects, and bone tumours while replacement of the defect site is required. In this study, the fabrication of CPP structures was developed through a powder-based SFF technique known as adhesive bonding 3D-printing. SFF is an advanced alternative to the “conventional” fabrication method consisting of gravity sintering of CPP pre-forms followed by machining to final form, as SFF enables rapid manufacturing of complex-shaped bio-structures with controlled internal architecture. To address the physical and structural properties of the porous SFF-made components, they were characterized using scanning electron microscopy, micro-CT scanning and mercury intrusion porosimetry. Specific surface area and permeability of the porous structures were also determined. Additionally, the chemical properties (crystallinity) of the specimens were identified by X-ray diffraction. The mechanical properties of the crystalline CPP material were also measured by micro- and nano-indentation. Moreover, the porous structures were tested by uniaxial and diametral mechanical compression to determine the compressive and tensile strengths, respectively. Furthermore, the effect of the stacked-layer orientation on the mechanical properties of the SFF-made constructs was investigated through the production of samples with horizontal or vertical stacked-layers. The properties of the SFF-made samples were compared with those of the conventionally-made CPP constructs. The SFF-made implants showed drastically higher compressive mechanical strength compared to the conventionally-formed samples with identical porosity. It was also shown that the orientation of the stacked-layer has substantial influence on the mechanical strengths. Moreover, this thesis examined the ability of in vitro forming of cartilaginous tissue on the SFF-made substrates where the chondrocytes cellular response to the CPP implants was evaluated histologically and biochemically. In addition, an initial in vivo assessment of the CPP structures as bone substitutes was conducted using a rabbit medial femoral site model. Significant amount of new-bone was formed within the CPP porous constructs during the 6-week implantation period demonstrating appropriate biological response of SFF-made CPP structures for bone substitute applications. Another accomplishment of this thesis was the development of a mathematical model which predicts the compact density of powder layers spread by a counter-rotating roller in the SFF technique. The results may be used in the control of the apparent density of the final implant. The potential of the developed SFF method as an efficient and reproducible technique for the production of porous CPP structures for use in orthopaedics and musculoskeletal tissue regenerative applications was concluded.

The attribution of incentive salience to cues that become associated with drugs of abuse is a critical characteristic of individuals who may be vulnerable to drug addiction. Rodents with the propensity to sign track are thought to be vulnerable to drug abuse. The goal of the current work was to investigate whether sign trackers (STs) would acquire cocaine conditioned place preference (CPP) to a discrete cue using an avian species. In Experiment 1, sign and goal trackers (GTs) were first identified using a one third rank order split. Following identification, cocaine-CPP was conducted with a discrete cue in each end chamber. Contrary to previous research, results showed that GTs showed a CPP to the discrete cue but STs did not. Experiment 2 was conducted to determine whether sign and GTs had been misclassified with the rank order split. Experiment 2 compared the rank order method with a t-test method (absolute criterion). Misclassification of both sign and GTs occurred using the rank order split. The findings indicated that use of a more accurate method to identify sign and GTs may have led to different results for Experiment 1. The t-test method may be useful for models that require identification of STs.

Die Rasterionenleitfähigkeitsmikroskopie (scanning ion conductance microscopy, SICM) stellt eine kontaktfreie Methode zur Ermittlung sowohl der Topographie als auch lokalen Ionenleitfähigkeit einer Oberfläche dar. Besonders vorteilhaft ist die Vermeidung mechanischer Beeinflussung bei der Untersuchung flexibler Strukturen, z.B. Lipiddoppelschichten wie Zellen oder künstlich erzeugter Lipidmembranen. Porenüberspannende Membranen (pore-suspending membranes, PSMs) verbinden als ein Beispiel für Modellsysteme eine hohe Stabilität mit lateraler Mobilität und dem Vorhandensein wässriger Kompartimente ober- und unterhalb der Doppelschicht, wie sie auch in der Natur gefunden werden. Ein wichtiges Forschungsgebiet stellt die Untersuchung der Wechselwirkung von Peptiden, besonders zellpenetrierenden Peptiden (cell penetrating peptides, CPPs), mit Lipiden und anderen Membranbestandteilen dar. Häufig untersuchte Beispiele sind Melittin, Hauptbestandteil des Giftes der Honigbiene Apis mellifera, sowie Penetratin, dritte Helix der Antennapedia Homöodomäne von Drosophila melanogaster. Generalisierte Protokolle zur Herstellung lösungsmittelfreier PSMs werden vorgestellt. Riesige unilamellare Vesikel (giant unilamellar vesicles, GUVs) unterschiedlicher Lipidzusammensetzung wurden hierzu auf porösem Siliziumnitrid (Si3N4), welches mit Cholesterylpolyethylenoxythiol (CPEO3, hydrophob) bzw. Mercaptoethanol (ME, hydrophil) funktionalisiert worden war, gespreitet. Verwendet wurden GUVs aus reinen Phosphatidylcholin (PC)-Lipiden sowie aus Mischungen von PC-Lipiden mit Cholesterol und PC-Lipiden mit Phosphatidylserin (PS)-Lipiden. Der Erfolg des Spreitvorgangs wurde durch Abbilden mittels konfokaler Rasterlasermikroskopie (confocal laser scanning microscopy, CLSM) und SICM verifiziert. Der Hauptteil dieser Arbeit behandelte die Entwicklung und Anwendung CLSM- und SICM-basierter CPP-Titrationsassays zur Aufklärung des Einflusses der Substratfunktionalisierung und der Lipidzusammensetzung der Membranen auf die Wechselwirkung zwischen Melittin bzw. Penetratin und den Lipiddoppelschichten. CLSM-Experimente wurden mit Melittin auf allen zur Verfügung stehenden PSMs sowohl auf hydrophob als auch hydrophil funktiona-lisierten Substraten durchgeführt, während Penetratin auf den drei unterschiedlichen PSMs auf hydrophil funktionalisierten Substraten verwendet wurde. Ein Reißen der Membranen wurde im Fall hydrophil funktionalisierter Substrate für beide Peptide im Bereich von 1–3 µM beobachtet. Bei hydrophob funktionalisierten Substraten induzierte eine dreifach geringere Melittinkonzentration die Zerstörung der Membranen. Sowohl auf hydrophob als auch auf hydrophil funktionalisierten Substraten wurde bei einem Cholesterolanteil von 10% eine Erhöhung der zum Reißen notwendigen Melittinkonzentratin erhalten, während bei 20% PS-Anteil eine Verschiebung zu geringeren Konzentrationen evident wurde. SICM-Experimente wurden mit Melittin auf PC/Cholesterol-PSMs auf hydrophob und hydrophil funktionalisierten Substraten und mit reinen PC-PSMs auf hydrophil funktionalisierten Membranen durchgeführt. Es wurden keine signifikanten Konzentrationsunterschiede beobachtet; die gefundenen Konzentrationsbereiche jedoch stimmten mit denen der CLSM-Experimente überein. Darüberhinaus wurde vor dem Reißen der Membranen ein Ansteigen der Porentiefe gefunden, das mit einer erhöhten Membranpermeabilität korrespondiert.