Global ETD Search

31	Approche métabolomique pour une caractérisation plus fine d'extraits de plantes d'intérêts pour la santé humaine / A complementary metabolomics approach to screen metabolic fingerprints of plant extracts used in human health Delecolle, Julien 03 March 2017 (has links) Ces travaux ont pour but d’identifier des métabolites dans des teintures-mères (TMs) utilisées en homéopathie et en phytothérapie pour mieux contrôler la qualité des TMs et de mieux comprendre leur mode d’action sur la santé humaine. Nous avons étudié, par une approche de métabolomique globale, 19 TMs et un produit leader : le L52, fabriqués par les Laboratoires Lehning. Premièrement, nous avons utilisé des approches non-ciblées en construisant des banques de données GC-MS et UPLC-MS/MS, afin d’identifier un maximum de molécules dans chaque extrait. Puis, nous avons fractionné certaines TMs et purifié des métabolites inconnus pour une identification fine en HRMS. Nous avons identifié de nombreuses molécules dans chaque TM, montrant que ces dernières sont très riches en molécules pouvant être utilisées pour le contrôle-qualité des TMs et valorisées pour la santé humaine. / Tinctures defined as hydro-alcoholic extracts have been used from centuries in homeopathy and phytotherapy, but their chemical compositions remain still unknown. During my PhD, metabolomics analyses of nineteen tinctures and one leader product, L52, made by Laboratoires Lehning, were conducted using untargeted metabolomic approach. We build GC-MS and UPLC-MS/MS databases to identify a large amount of metabolites. Then, we used semi-preparative HPLC with both UV and mass detection to isolate some compounds from tinctures. We used UPLC-HRMS to obtain chemical formula, a prerequisite for metabolites identification. Finally, we identified a broad range of different metabolites in each tincture, highlighting the metabolic complexity of the TMs. These molecules can now be used for quality-control and valued for a better understanding of these products on human health. Teintures-mères GC-MS UPLC-MS/MS UPLC-HRMS HPLC-UV-MS semi-préparative Homéopathie Phytothérapie Tinctures GC-MS UPLC-MS/MS UPLC-HRMS Semi-preparative HPLC-UV-MS Homeopathy Phytotherapy 572.5 615.19
32	Cromatografia continua em leito movel simulado para a purificação dos enantiomeros do N-Boc-baclofeno-lactama / Continous chromatographic in simulated moving bed to purification of enantiomers N-Boc-baclofen-lactan Veredas, Vinícius de 18 April 2005 (has links) Orientador: Cesar Costapinto Santana / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Quimica / Made available in DSpace on 2018-08-30T12:54:54Z (GMT). No. of bitstreams: 1 Veredas, Vinicius de_D.pdf: 13205142 bytes, checksum: 97c5009c255088bef6fcdc1fd92294c3 (MD5) Previous issue date: 2005 / Doutorado / Desenvolvimento de Processos Biotecnologicos / Mestre em Engenharia Química Cromatografia contracorrente Quiralidade Enantiômeros Cromatografia líquida Adsorção Quiralidade - Aplicações industriais Countercurrent chromatography Chirality Enantiomers Liquid chromatography Adsorption Chirality - Industrial applications Simulated moving bed Chiral resolution Preparative chromatography N-Boc-baclofen-lactan
33	Analýza hlavních sacharidů vína / Analysis of main wine saccharides Horáková, Hana January 2009 (has links) This diploma thesis deals with determination of carbohydrates in wine. Theoretical part attends to production of wine from grape to treatment and training of wine. It refers saccharides in wine, especially glucose and fructose. The study provides an overview of the available sources concerning the possibilities of determination of carbohydrates in wine by chromatographic methods and Skalar automated chemistry analyser. The study shortly refers simple analytical methods for determination of wine saccharides. The experimental part based on this search deals with analysis of saccharides by high performance liquid chromatography with refractive index detector and UV detector on aminoalkyl column and determination of reducting sugars by Skalar automated chemistry analyser. Finally, the results of these methods were compared.
34	In vitro polyketide biocatalysis : triketide building-blocks and enzymology Harper, Andrew David 08 October 2013 (has links) Polyketide products are useful compounds to research and industry but can be difficult to access due to their richness in stereogenic centers. Type I polyketide synthases offer unique engineering opportunities to access natural stereocontrol and resultant complex compounds. The development of a controlled in vitro platform based around type I polyketide synthases is described. It has been used to produce a small library of polyketide fragments on an unprecedented and synthetically-relevant scale and explore polyketide synthase enzymology. / text In vitro Cell-free Preparative Polyketide Polyketide synthase Ketoreductase Malonyl-CoA ligase MatB Enzymology Chiral building blocks Chiral synthons Diketide Triketide Lactone Ketolactone Natural products Secondary metabolism Secondary metabolite Modular Type I polyketide synthase Biosynthesis Streptomyces coelicolor Saccharopolyspora erythraea Bacillus subtilis Streptomyces nodosus Saccharomyces cerevisiae Streptomyces antibioticus Streptomyces venezuelae Saccharopolyspora spinosa Streptomyces fradiae
35	Synthesis of Thiophene-Vinyl-Benzothiazole Based Ligand Analogues for Detection of Aβ and Tau Pathology in Alzheimer's Disease Johansson, Joel January 2024 (has links) As of today, Alzheimer’s disease is the leading cause of dementia among neurodegenerative disorders, affecting many millions of people worldwide. As the average life span of populations increase, more and more people succumb to the illness each year. Like other neurodegenerative disorders, Alzheimer’s disease can be attributed to the accumulation of protein aggregates in the brain. These amyloid-β peptides and tau proteins can presumably be detected in the brain many years before the onset of clinical symptoms. Development of fluorescent ligands, capable of binding to these neuropathological hallmarks and highlighting them, could serve as molecular diagnostic tools and facilitate an early diagnosis of the disease. The method could also be useful in studying disease progression and evaluating the effects of novel treatments. One such ligand is HS-259. The aim of this project was to synthetize different analogues of HS-259, and test their selectivity towards the aforementioned aggregates in brain tissue from an individual with Alzheimer’s disease. Staining of tissue samples with analogue solution enables visualization of aggregate sites through fluorescence imaging. In the end, five analogues were synthetized, albeit in relatively low overall yields. Synthetic methods included Suzuki-Miyara cross-couplings, Ullmann-type arylations and condensations. Liquid Chromatography-Mass Spectrometry (LC-MS) and Nuclear Magnetic Resonance (NMR) were used for analysis of the compounds. Two of the five analogues could be tested for staining of aggregates and assessed for photophysical characteristics, i.e. absorption- and emission spectra. One analogue stained both amyloid-β aggregates and some tau aggregates, whereas the other stained neither. Since only two analogues were tested and rendered inconsistent results, further studies are needed to assess the binding properties of HS-259 analogues in general. Alzheimer's disease neurodegenerative disorders protein aggregates molecular ligands amyloid-β Aβ amyloid-beta tau diagnosis HS-259 staining brain tissue Suzuki coupling Ullmann arylation condensation NMR nuclear magnetic resonance LC-MS liquid chromatography neuropathological hallmarks absorption spectra emission spectra synthesis plaques symptoms neuropathology thiophene-vinyl-benzothiazole TVBT ligand analogues N-arylation Knoevenagel preparative LC PBS phosphate buffered saline treatments AD mechanisms thiophene benzothiazolium fluorescence imaging bTVBT bi-thiophene-vinyl-benzothiazole detection Suzuki-Miyara Organic Chemistry Organisk kemi

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