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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Bioraffinering av bark: En jämförelse mellan två extraktionsmetoder / Bark Biorefining: A Comparison between two extraction methods

Al-Bety, Salwa January 2021 (has links)
Intresset för användningen av material från förnybara råvaror ökar. Produktionen av vedmassa och material i skogsindustrin genererar dagligen stora mängder biprodukter, särskilt bark. Barken innehåller många värdefulla komponenter som kan förädlas och öka värdet för barken, men först måste de separeras. Målet med denna undersökning var att separera dessa genom att jämföra två olika typer av extraktionsmetoder. Den första metoden använde programmerbar utrustning som namnges accelerated solvent extraction (ASE) och den andra använde manuell teknik som namnges Soxhlet extraktion. Syftet med undersökningen var att avgöra vilken extraktionsmetod som kan användas till att utvinna bark komponenter mest effektivt. Metoden ASE omfattar acetonextraktion och varmvattenextraktion där trycket var 100 bar, temperaturen 100oC och tiden drygt en timme. Soxhletextraktion omfattade enbart acetonextraktion under atmosfäriskt tryck, kontinuerlig värme och tiden 90 minuter. ASE-metoden gav fyra extrakt; acetonextrakt vid 100oC samt varmvattenextrakt vid 100oC, 140oC och 160oC.  Barken som studerades var uppdelad i två fraktioner, fuktig bark och torr bark. En beräkning av utbyte % utfördes efter varje extraktion. Extrakten från fuktig bark hade mörkare färg än extrakten från torr bark. Det uppmätes pH-värden för alla vattenextrakt och den som gav lägst pH var vattenextrakt som erhölls vid 160oC. Slutligen visade utbyteresultaten inga stora skillnader mellan de utförda ASE vattenextraktionerna exklusive extraktfärgen som kan vara en indikation till skillnad i extraherade molekyler. Användningen av sand under varmvattenextraktionerna gav inga förbättringar i extraktionsmetoden. / Interest in the use of materials from renewable sources is increasing. The production of wood pulp and materials in the forest industry generates large amounts of by- products daily, especially tree bark. Bark contains many valuable components which if separated can be used in various types of applications. The aim of this study was to compare two extraction methods. The first method used programmable equipment and is named accelerated solvent extraction (ASE) and the second used manual technology and is named Soxhlet extraction.  The purpose of the study was to determine which extraction method can be used to extract bark components more efficiently. The ASE method included acetone extraction and hot water extraction where the pressure was 100 bar, the temperature 100oC and the time just over an hour. Soxhlet extraction involved only acetone extraction under atmospheric pressure, continuous heating, and a time of 90 minutes. The ASE method yielded four extracts: acetone extract at 100oC and hot water extract at 100oC, 140oC and 160oC.  The bark studied was divided into two parts, undried bark and dry bark. Total calculation of yield% was performed after each extraction. The extracts from undried bark had a darker color than the extracts from dry bark. The pH values were measured for all water extracts and the one that gave the lowest pH was obtained at 160oC. Finally, the extraction results did not show any major differences between the ASE water extractions performed excluding the extract color which may be an indication of difference in extracted molecules. The use of sand during the hot water extractions did not improve the extraction method.
2

Avaliação da exposição fetal à nicotina através da análise toxicológica em mecônio / Evaluation of fetal exposure to nicotine through the toxicological analysis in meconium

Sant\'Anna, Simone Gomes 05 October 2010 (has links)
O tabaco é uma das principais drogas consumidas mundialmente e seu uso por mulheres em idade reprodutiva, em particular, têm representado uma grande preocupação por parte de especialistas e da sociedade em geral. Apesar dos efeitos adversos associados ao ato de fumar durante a gestação serem bastante documentados e conhecidos, sabe-se que uma parcela de mulheres grávidas tem dificuldades em abandonar o hábito. A exposição fetal aos constituintes do tabaco tem sido associada com aumento do risco de aborto espontâneo e nascimentos prematuros, incidência de recém-nascidos com baixo peso, síndrome de morte súbita infantil e desordens cognitivas e neurocomportamentais. Entretanto, devido ao sentimento de culpa e medo de ações punitivas, mulheres raramente admitem terem utilizado tabaco durante a gestação. Como resultado, uma série de marcadores biológicos tem sido estudada para se diagnosticar a exposição fetal aos constituintes do tabaco. Dentre os marcadores utilizados estão a nicotina e o seu principal produto de biotransformação, a cotinina, que podem ser detectados em amostras de mecônio de recém-nascidos. No presente estudo, um método analítico foi desenvolvido visando à detecção desses marcadores em amostras de mecônio. Foi considerada neste projeto a técnica de extração acelerada por solvente (ASE) por ser uma técnica promissora para o preparo de amostras sólidas e/ou semi-sólidas. Os analitos foram identificados por cromatografia em fase-gasosa com detector de nitrogênio e fósforo (GC/NPD). Os limites de detecção foram de 3 ng/g e 30 ng/g e os de quantificação foram de 5 ng/g e 40 ng/g, para cotinina e nicotina respectivamente, e apresentaram boa linearidade na faixa de concentração estudada (5-500 ng/g), com coeficiente de correlação (r2) maior que 0,98. A precisão intra-ensaio, determinada pelo coeficiente de variação do método (CV%) foi menor que 15% e a precisão interensaio foram menor ou igual a 20% para nicotina e cotinina. A recuperação média foi de 77%. O método desenvolvido demonstrou ser rápido, preciso, prático e sensível e com uso de menores volumes de solventes orgânicos do que outros métodos descritos na literatura. O método desenvolvido e validado foi aplicado em amostras de mecônio de neonatos com suspeita ou não de exposição fetal aos constituintes do tabaco. / Tobacco is one of the main drugs consumed worldwide and its use by women of reproductive age in particular has played a major concern among experts and society in general. Despite the adverse effects associated with smoking during pregnancy are well documented, it is known that a significant proportion of pregnant women have difficulties to quit the habit. Fetal exposure to tobacco constituents has been associated with increased risk of spontaneous abortion (miscarriage) and premature births, incidence of newborns with low birth weight, sudden infant death syndrome and neurobehavioral and cognitive disorders. However, due to guilt and fear of punitive actions, women rarely admit to have used tobacco during pregnancy. As a result, a series of biological markers have been studied to diagnose fetal exposure to tobacco constituents. Nicotine and cotinine are some of these biomarkers which can be detected in meconium samples from newborns. In this study, an analytical method was developed to detect these biomarkers in meconium samples. Accelerated solvent extraction (ASE), a promising technique for solid or semi-solid sample preparation, was considered in this work the that is considered a. The analytes were identified by gas-chromatography with nitrogen phosphorus detector (GC / NPD). The limits of detection (LOD) were 3 ng/g and 30 ng/g and the limits of quantification (LOQ) were 5 ng/g and 40 ng/g for cotinine and nicotine, respectively. The method showed good linearity in the concentration range studied (5-500 ng/g), with a coefficient of correlation (r2) greater than 0.98. The intraday precision, determined by the coefficient of variation (CV %) was less than 15% and the interday precision was less or equal than 20% for nicotine and cotinine. The average recovery was 77%. The method proved to be fast, accurate, practical and sensitive and smaller volumes of organic solvents are necessary, compared to other methods published in the scientific literature. The developed and validated method was applied to meconium samples of suspected and nonsuspected neonates of having been exposed to tobacco constituents during gestation.
3

Avaliação da exposição fetal à nicotina através da análise toxicológica em mecônio / Evaluation of fetal exposure to nicotine through the toxicological analysis in meconium

Simone Gomes Sant\'Anna 05 October 2010 (has links)
O tabaco é uma das principais drogas consumidas mundialmente e seu uso por mulheres em idade reprodutiva, em particular, têm representado uma grande preocupação por parte de especialistas e da sociedade em geral. Apesar dos efeitos adversos associados ao ato de fumar durante a gestação serem bastante documentados e conhecidos, sabe-se que uma parcela de mulheres grávidas tem dificuldades em abandonar o hábito. A exposição fetal aos constituintes do tabaco tem sido associada com aumento do risco de aborto espontâneo e nascimentos prematuros, incidência de recém-nascidos com baixo peso, síndrome de morte súbita infantil e desordens cognitivas e neurocomportamentais. Entretanto, devido ao sentimento de culpa e medo de ações punitivas, mulheres raramente admitem terem utilizado tabaco durante a gestação. Como resultado, uma série de marcadores biológicos tem sido estudada para se diagnosticar a exposição fetal aos constituintes do tabaco. Dentre os marcadores utilizados estão a nicotina e o seu principal produto de biotransformação, a cotinina, que podem ser detectados em amostras de mecônio de recém-nascidos. No presente estudo, um método analítico foi desenvolvido visando à detecção desses marcadores em amostras de mecônio. Foi considerada neste projeto a técnica de extração acelerada por solvente (ASE) por ser uma técnica promissora para o preparo de amostras sólidas e/ou semi-sólidas. Os analitos foram identificados por cromatografia em fase-gasosa com detector de nitrogênio e fósforo (GC/NPD). Os limites de detecção foram de 3 ng/g e 30 ng/g e os de quantificação foram de 5 ng/g e 40 ng/g, para cotinina e nicotina respectivamente, e apresentaram boa linearidade na faixa de concentração estudada (5-500 ng/g), com coeficiente de correlação (r2) maior que 0,98. A precisão intra-ensaio, determinada pelo coeficiente de variação do método (CV%) foi menor que 15% e a precisão interensaio foram menor ou igual a 20% para nicotina e cotinina. A recuperação média foi de 77%. O método desenvolvido demonstrou ser rápido, preciso, prático e sensível e com uso de menores volumes de solventes orgânicos do que outros métodos descritos na literatura. O método desenvolvido e validado foi aplicado em amostras de mecônio de neonatos com suspeita ou não de exposição fetal aos constituintes do tabaco. / Tobacco is one of the main drugs consumed worldwide and its use by women of reproductive age in particular has played a major concern among experts and society in general. Despite the adverse effects associated with smoking during pregnancy are well documented, it is known that a significant proportion of pregnant women have difficulties to quit the habit. Fetal exposure to tobacco constituents has been associated with increased risk of spontaneous abortion (miscarriage) and premature births, incidence of newborns with low birth weight, sudden infant death syndrome and neurobehavioral and cognitive disorders. However, due to guilt and fear of punitive actions, women rarely admit to have used tobacco during pregnancy. As a result, a series of biological markers have been studied to diagnose fetal exposure to tobacco constituents. Nicotine and cotinine are some of these biomarkers which can be detected in meconium samples from newborns. In this study, an analytical method was developed to detect these biomarkers in meconium samples. Accelerated solvent extraction (ASE), a promising technique for solid or semi-solid sample preparation, was considered in this work the that is considered a. The analytes were identified by gas-chromatography with nitrogen phosphorus detector (GC / NPD). The limits of detection (LOD) were 3 ng/g and 30 ng/g and the limits of quantification (LOQ) were 5 ng/g and 40 ng/g for cotinine and nicotine, respectively. The method showed good linearity in the concentration range studied (5-500 ng/g), with a coefficient of correlation (r2) greater than 0.98. The intraday precision, determined by the coefficient of variation (CV %) was less than 15% and the interday precision was less or equal than 20% for nicotine and cotinine. The average recovery was 77%. The method proved to be fast, accurate, practical and sensitive and smaller volumes of organic solvents are necessary, compared to other methods published in the scientific literature. The developed and validated method was applied to meconium samples of suspected and nonsuspected neonates of having been exposed to tobacco constituents during gestation.
4

Optimisation de l’extraction des caroténoïdes à partir du persimmon (Diospyros kaki L.), de l’abricot (Prunus armeniaca L.) et de la pêche (Prunus persica L.) : étude photophysique en vue d’une application en thérapie photodynamique (PDT) / Optimization of carotenoids extraction from persimmon (Diospyros kaki L.), apricot (Prunus armeniaca L.) and peach (Prunus persica L.) : Photophysical study for photodynamic therapy (PDT) application

Zaghdoudi, Khalil 17 December 2015 (has links)
La thérapie photodynamique (PDT) est une technique utilisée cliniquement pour traiter certaines maladies de la peau, la dégénérescence maculaire liée à l’âge et certains types de cancer. Elle fait intervenir trois composants : une molécule photosensible ou photosensibilisateur (PS), la lumière et l’oxygène. Après administration du PS, celui-ci va se localiser plus ou moins sélectivement dans les zones tumorales où il est alors activé par irradiation lumineuse à une longueur d’onde et une puissance données. Ceci engendre la formation d’espèces réactives de l’oxygène (ROS) très réactives, dont l'oxygène singulet1 O2, qui entraînent la destruction des tissus tumoraux par nécrose ou apoptose. Afin d’améliorer la sélectivité du traitement, différentes pistes sont actuellement exploitées dont l’élaboration de « photodynamic molecular beacons » (PMB). Dans un PMB, le photosensibilisateur (PS) est associé via un peptide à un inhibiteur 1O2, appelé quencher. Ce quencher inhibe la formation d’1O2 tant que le composé n’a pas atteint sa cible. Une fois la zone cancéreuse atteinte, des enzymes spécifiques clivent le peptide, libérant ainsi le PS qui retrouve alors sa capacité à former de l’1O2. Trouver un couple PS/quencher adéquat reste un challenge en PDT. Les propriétés photophysiques particulières des caroténoïdes et leur aptitude à inhiber la production d’1O2 font de ces derniers des quenchers potentiellement utilisables pour l’élaboration de PMBs. Chez les plantes, les caroténoïdes (carotènes et xanthophylles) sont des pigments associés à la photosynthèse, qui ont deux rôles principaux : un rôle de collecteur de lumière et un rôle photoprotecteur en protégeant le(s) système(s) photosynthétique(s) contre les dommages photooxydatifs liés à une exposition trop intense à la lumière. Ceci s’opère, entre autre, via le cycle des xanthophylles. Cette aptitude à capter de l’énergie présente un intérêt potentiel à ne pas négliger dans la perspective de la conception de PMB utilisables en thérapie photodynamique. Dans le cadre de cette thèse en co-tutelle avec la Faculté des Sciences de Bizerte nous avons ciblé les caroténoïdes présents dans trois fruits produits en Tunisie à savoir les kakis (Diospyros kaki L.), les abricots (Prunus armeniaca L.) et les pêches (Prunus persica L.) connus pour leur richesse globale en ces pigments. Divers procédés d’extractions ont été étudiés : (i) L’extraction de type Soxhlet par solvants organiques à pression atmosphérique, utilisée comme référence, (ii) l'extraction accélérée par solvant organique (ASE : Accelerated solvent Extraction) effectuée sous pression, enfin (iii) l'extraction par CO2 supercritique avec l’éthanol comme cosolvant. Pour ces deux derniers procédés, une approche par plan d’expériences (surfaces de réponses) a été utilisée pour identifier les facteurs clé et les conditions optimales d’extractions de divers caroténoïdes (pression, température, débit, % de cosolvant, temps, nombre de cycles). L'analyse par chromatographie liquide à haute performance couplée à la détection UV-Visible et à la spectrométrie de masse a ensuite permis l'identification et la quantification des caroténoïdes présents dans les extraits obtenus, permettant ainsi de comparer les profils caroténoïdiques propres à chaque fruit et les performances de chaque procédé d’extraction. Cette étude ayant révélé un profil caroténoïdique particulièrement intéressant chez le kaki par rapport aux autres fruits, une extraction et une purification des caroténoïdes de ce fruit par chromatographie liquide haute pression préparative a ensuite été effectuée afin de disposer d’une quantité suffisante de chaque caroténoïde, et parfois de leurs isomères conformationnels, en vue de l’étude de leurs propriétés photophysiques (absorption, émission de fluorescence, inhibition d’1O2) et de l’évaluation de leur intérêt potentiel en tant que quencher d’1O2 dans un édifice de type PMB / Photodynamic therapy (PDT) is a clinically used technique for treating skin diseases, age-relatedmacular degeneration but mainly some types of cancer. PDT involves three components: a photosensitive molecule named photosensitizer (PS), light and oxygen. After administration of the PS, this one will be located more or less selectively in tumoral regions where it is activated by light irradiation at appropriate wavelength and power. This leads to the formation of highly reactive and cytotoxic reactive oxygen species (ROS), especially singlet oxygen, resulting in the destruction of the tumor by necrosis or apoptosis. To improve the treatment selectivity, different strategies are being exploited, one of which is the development of "photodynamic molecular beacons" (PMB). In PMB the photosensitizer is linked via a peptide to an inhibitor of 1O2 (quencher). This quencher inhibits the formation of 1O2 as long as the compound has not reached its target, namely cancer cells. In order to inhibit the toxicity of the PS in non-target cells and restore toxicity only close to the biological target, it is necessary to find an adequate PS/quencher couple. This remains a challenge for PDT. Carotenoids are interesting candidates due to their specific photophysical properties and ability to inhibit 1O2, which makes them potential quenchers for building PMBs. In plants, carotenoids (carotenes and xanthophylls) are pigments involved in the photosynthesis, in which they play two main roles: a light collecting role and a protecting role by preserving the photosynthetic systems against photoxydative damages induced by a too intense light exposure. This protection can for instance occur via the well-known xanthophylls cycle. This capacity to catch energy presents a potential interest that should not be neglected in the framework of the design of PMBs usable in photodynamic therapy. Within the framework as part of this PhD thesis in Cotutelle with the Faculty of Sciences of Bizerte, we focused on carotenoids from three fruits produced in Tunisia: persimmon (Diospyros kaki L.), apricot (Prunus armeniaca L.) and peache (Prunus persica L.), known for their global richness in these natural pigments. Three extraction processes were investigated: (i) the Soxhlet extraction based on the use of organic solvent at atmospheric pressure and used as reference, (ii) the accelerated solvent extraction (ASE) using organic solvent under high pressure, and (iii) the supercritical fluid extraction (SFE) using supercritical CO2 and ethanol as cosolvent. For these two last processes, a design of experiments (Surface Response Design) was used to identify the key factors and optimal extraction conditions of various carotenoids (pressure, temperature, flow, % cosolvent, time, number of cycles). Then, HPLC-PDA coupled with mass spectrometry (MS) enabled the identification and quantification of carotenoids from the extracts. Thus it was possible to compare the profiles in carotenoids content from each fruit as well as the performances of each extraction process. This study showed that the carotenoidic profile in the persimmon was the most interesting as compared to the profiles in the two other fruits. Extraction and purification of the carotenoids from persimmon by preparative high pressure liquid chromatography were then performed in order to have a sufficient amount of each carotenoid and sometimes of their conformational isomers. We finally performed a study of their photophysical properties (absorption, fluorescence emission, 1O2 inhibition) in order to evaluate their potential as 1O2 quencher in molecular construction such as a PMB

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