Le stockage optique de l’information et l’imagerie à super-résolution sont des champs d’application dont les besoins en matériaux et en molécules photocommutables sont grandissants. Une des approches consiste à associer au sein d’une même structure moléculaire des photochromes et des fluorophores au sein de laquelle des transferts d’énergie résonants sont possibles. La combinaison des propriétés photophysiques des deux types d’entités conduit à la photocommutation de fluorescence recherchée. Pour concevoir de tels systèmes, nous avons basé notre approche sur le concept de click chemistry qui permet d’avoir une grande flexibilité du point de vue synthétique. Ainsi, en utilisant des plateformes moléculaires comme les dérivés de sucres et la β-cyclodextrine, nous avons synthétisé de nombreuses architectures multichromophoriques. En variant le ratio entre le nombre de photochromes (DAE) et de fluorophores (DCM) au sein d’une même molécule, nous avons pu progresser dans la compréhension des relations entre les structures et les propriétés photophysiques de ces systèmes, impliquant des transferts d’énergie multiples entre les différentes entités. Cette démarche nous a permis, d’une part, d’appréhender les effets d’extinction non-linéaire de fluorescence, et d’autre part, de découvrir l’effet d’hystérèse photocontrôlable résultant de la compétition entre les transferts d’énergie et les réactions photochromes. / The fields of optical data storage and super-resolution imaging are in expansion and attract an increasing demand on photoswitchable materials and molecules. One approach consists in associating photochromic and fluorophores units in the same molecular structure, allowing resonant energy transfer processes. The combination of the photophysical properties of the two units leads to the expected fluorescence photoswitching. To design such systems, we based our approach on the click chemistry concept which offers a great flexibility in terms of synthesis pathways. Thus, using molecular platforms such as sugar derivatives and β-cyclodextrin, we have synthesized many multichromophoric architectures. By varying the ratio between photochromic (DAE) and fluorophore (DCM) units in the same molecule, we improved our comprehension of the structure-properties relationships, involving multiple energy transfers between the different entities. This allowed us, first, to understand the effects of non-linear fluorescence quenching, and secondly, to discover the light-controlled hysteresis effect resulting from the competition between energy transfers and photochromic reactions.

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This study examined the feasibility of using (BETA)-cyclodextrins ((BETA)CDs), which are derived from starch, as agents to stabilize volatile and leachable biocides for the protection of wood and wood composites. The encapsulation of volatile natural antimicrobial compounds, such as allyl isothiocyanate (AITC) and essential oils (EOs), in βCDs was qualitatively confirmed by Attenuated total reflection Fourier-transform infrared spectroscopy (ATR-FTIR) method and the maximum inclusion yield was quantitatively estimated by ultraviolet-visible spectrophotometry (UV/VIS) while the partial fixation of leachable borates with βCD was confirmed by ATR-FTIR and nuclear magnetic resonance (NMR) techniques. The efficacy of the βCD complexes as wood preservatives of southern yellow pine and randomly Oriented Strand Board (OSB) was examined in soil block tests (AWPA E10-16 and E22-16 standard). The results indicate that (A) (BETA)CDs suppress the premature leaching of otherwise volatile natural compounds and suggest a novel approach to the application of volatile or water-immiscible natural preservatives for wood and wood composites protection; (B) (BETA)CD can be used as an agent for partial fixation of boric acid to form boric acid esters. However, the borate esters are susceptible to leach out after AWPA E11 test and not suitable for protection against Gloeophyllum trabeum and Postia placenta in outdoor conditions.

Foods contaminated with pathogens are common sources of illness. Currently the most common and sensitive rapid detection methods involve the PCR. However, food matrices are complex and limit the sensitivity and thus detection limits. The use of coated activated carbon can effectively facilitate the removal of PCR inhibitors while not binding targeted bacterial cells from food samples. With activated carbon coated with the optimal amount of milk proteins a cell recovery at pH 7.0 of 95.7 ± 2.0% was obtained, compared to control uncoated activated carbon, which yielded a cell recovery of only 1.1 ± 0.8%. In addition, the milk protein coated activated carbon (MP-CAC) was able to absorb similar amounts of soluble compounds as uncoated activated carbon with the exception of bovine hemoglobin. This is evidence that the use of milk proteins to coat activated carbon should therefore serve as a suitable replacement for bentonite in the coating of activated carbon, which has previously been used for the removal of PCR inhibitors from food. The high amount of PCR inhibitors present in ground beef is a major factor that affects molecular based techniques such as the PCR for the detection of Salmonella enterica. In this study, a novel detection system was developed for eliminating PCR inhibitors and increasing the recovery of S. enterica in ground beef samples with the use of β-cyclodextrin and MP-CAC without enrichment of samples. invA, present in all Salmonella, was used as target the gene in the conventional PCR protocol. With ground beef containing 7.0, 15, and 27 % fat, treatment of stomached samples with 5.0, 10, and 15 % β-cyclodextrin respectively followed by treatment with MP-CAC, resulted in detection of 3 CFU/g which is equivalent to 75 CFU in 25 g samples. The total assay time was 4.5 hr. The methodology described in this study for the detection of S. enterica in ground beef without enrichment is rapid, sensitive, and has the potential to be applied to a number of food matrices to detect low numbers of food-borne bacterial pathogens before product is shipped to prevent costly recalls.

Among non-viral vectors, cationic polymers, such as poly(propylene imine) (PPI), play a prominent role in nucleic acid delivery. However, limitations of polycationic polymer-based DNA delivery systems are (i) insufficient target specificity, (ii) unsatisfactory transgene expression, and (iii) undesired transfer of therapeutic DNA into non-target cells. We developed single-chain antibody fragment (scFv)-directed hybrid polyplexes for targeted gene therapy of prostate stem cell antigen (PSCA)-positive tumors. Besides mono-biotinylated PSCA-specific single-chain antibodies (scFv(AM1-P-BAP)) conjugated to neutravidin, the hybrid polyplexes comprise -cyclodextrinmodified PPI as well as biotin/maltose-modified PPI as carriers for minicircle DNAs encoding for Sleeping Beauty transposase and a transposon encoding the gene of interest. The PSCA-specific hybrid polyplexes efficiently delivered a GFP gene in PSCA-positive tumor cells, whereas control hybrid polyplexes showed low gene transfer efficiency. In an experimental gene therapy approach, targeted transposition of a codon-optimized p53 into p53-deficient HCT116p53 /PSCA cells demonstrated decreased clonogenic survival when compared to mock controls. Noteworthily, p53 transposition in PTEN-deficient H4PSCA glioma cells caused nearly complete loss of clonogenic survival. These results demonstrate the feasibility of combining tumor-targeting hybrid polyplexes and Sleeping Beauty gene transposition, which, due to the modular design, can be extended to other target genes and tumor entities.

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<p>  </p> <p>The development of a novel technique employing the use of a linear quadrupole ion trap mass spectrometer coupled to a Nd:YAG laser and a home-built fast reagent-mixing apparatus is detailed and used to detect the short-lived tetrahedral reaction intermediate of the reaction of acetyl chloride with ethanol in microdroplets. Additionally, tandem and high-resolution mass spectrometry is used to characterize potential precursors for solution-processed metal selenide semiconductors in order to determine a synthetic route to sulfur-free thin films. Lastly, Raman MCR (multivariate curve resolution) spectroscopy is used to study the binding-induced conformational change of 1-bromopropane upon binding to α-cyclodextrin as a model system to examine guest conformational changes upon binding to a host molecule.</p>