138 research outputs found
Near-infrared sensitivity enhancement of photorefractive polymer composites by pre-illumination
Among the various applications for reversible holographic storage media, a particularly interesting one is time-gated holographic imaging (TGHI). This technique could provide a noninvasive medical diagnosis tool, related to optical coherence tomography. In this technique, biological samples are illuminated within their transparency windowwith near-infrared light, and information about subsurface features is obtained by a detection method that distinguishes between reflected photons originating from a certain depth and those scattered from various depths. Such an application requires reversible holographic storage media with very high sensitivity in the near-infrared. Photorefractive materials, in particular certain amorphous organic systems, are in principle promising candidate media, but their sensitivity has so far been too low, mainly owing to their long response times in the near-infrared. Here we introduce an organic photorefractive materialâa composite based on the poly(arylene vinylene) copolymer TPD-PPVâthat exhibits favourable near-infrared characteristics. We show that pre-illumination of this material at a shorter wavelength before holographic recording improves the response time by a factor of 40. This process was found to be reversible. We demonstrate multiple holographic recording with this technique at video rate under practical conditions
Methodology of calculation of construction and hydrodynamic parameters of a foam layer apparatus for mass-transfer processes
ĐŃĐŸĐŒĐžŃĐ»ĐŸĐČĐ° ŃДалŃĐ·Đ°ŃŃŃ ĐŒĐ”ŃĐŸĐŽŃ ŃŃабŃĐ»ŃĐ·Đ°ŃŃŃ ĐłĐ°Đ·ĐŸŃŃĐŽĐžĐœĐœĐŸĐłĐŸ ŃĐ°ŃŃ ĐŽĐŸĐ·ĐČĐŸĐ»ŃŃ Đ·ĐœĐ°ŃĐœĐŸ ŃĐŸĐ·ŃĐžŃĐžŃĐž галŃĐ·Ń Đ·Đ°ŃŃĐŸŃŃĐČĐ°ĐœĐœŃ ĐżŃĐœĐœĐžŃ
апаŃĐ°ŃŃĐČ Ń ĐČŃĐŽĐșŃĐžĐČĐ°Ń ĐœĐŸĐČŃ ĐŒĐŸĐ¶Đ»ĐžĐČĐŸŃŃŃ ŃĐœŃĐ”ĐœŃĐžŃŃĐșĐ°ŃŃŃ ŃĐ”Ń
ĐœĐŸĐ»ĐŸĐłŃŃĐœĐžŃ
ĐżŃĐŸŃĐ”ŃŃĐČ Đ· ĐŸĐŽĐœĐŸŃĐ°ŃĐœĐžĐŒ ŃŃĐČĐŸŃĐ”ĐœĐœŃĐŒ ĐŒĐ°Đ»ĐŸĐČŃĐŽŃ
ĐŸĐŽĐœĐžŃ
ŃĐ”Ń
ĐœĐŸĐ»ĐŸĐłŃĐč. ĐŁ ŃŃĐ°ŃŃŃ ĐČŃŃĐ°ĐœĐŸĐČĐ»Đ”ĐœŃ ĐŸŃĐœĐŸĐČĐœŃ ĐżĐ°ŃĐ°ĐŒĐ”ŃŃĐž, ŃĐŸ ĐČплОĐČĐ°ŃŃŃ ĐœĐ° ĐłŃĐŽŃĐŸĐŽĐžĐœĐ°ĐŒŃĐșŃ ĐżŃĐœĐœĐžŃ
апаŃĐ°ŃŃĐČ, ŃĐŸĐ·ĐłĐ»ŃĐœŃŃŃ ĐŸŃĐœĐŸĐČĐœŃ ĐșĐŸĐœŃŃŃŃĐșŃŃŃ ŃĐ° ŃĐ”Đ¶ĐžĐŒĐž ŃĐŸĐ±ĐŸŃĐž ĐżŃĐœĐœĐžŃ
апаŃĐ°ŃŃĐČ. ĐĐžŃĐČĐ»Đ”ĐœĐŸ Đ·ĐČ'ŃĐ·ĐŸĐș ĐłŃĐŽŃĐŸĐŽĐžĐœĐ°ĐŒŃŃĐœĐžŃ
паŃĐ°ĐŒĐ”ŃŃŃĐČ. Đ ĐŸĐ·ĐłĐ»ŃĐœŃŃĐŸ ĐłŃĐŽŃĐŸĐŽĐžĐœĐ°ĐŒŃŃĐœŃ Đ·Đ°ĐșĐŸĐœĐŸĐŒŃŃĐœĐŸŃŃŃ ĐżŃĐœĐœĐŸĐłĐŸ ŃĐ°ŃŃ. ĐĐșĐ°Đ·Đ°ĐœŃ ŃĐ°ĐșŃĐŸŃĐž, ŃĐŸ ĐČплОĐČĐ°ŃŃŃ ĐœĐ° ĐżŃĐŸŃĐ”Ń ĐŒĐ°ŃĐŸĐŸĐ±ĐŒŃĐœŃ, ŃĐș ĐČ ĐłĐ°Đ·ĐŸĐČŃĐč, ŃĐ°Đș Ń ĐČ ŃŃĐŽĐșŃĐč ŃĐ°Đ·Đ°Ń
. ĐŃĐŸĐČĐ”ĐŽĐ”ĐœĐžĐč Đ°ĐœĐ°Đ»ŃĐ· ŃŃĐŽŃ ĐŽĐŸŃĐ»ŃĐŽĐ¶Đ”ĐœŃ ĐżĐŸĐșĐ°Đ·Đ°ĐČ, ŃĐŸ пДŃŃпДĐșŃĐžĐČĐœĐžĐŒ ĐœĐ°ĐżŃŃĐŒĐșĐŸĐŒ ŃĐœŃĐ”ĐœŃĐžŃŃĐșĐ°ŃŃŃ ĐżŃĐŸŃĐ”ŃŃ ĐŒĐ°ŃĐŸĐŸĐ±ĐŒŃĐœŃ Ń ŃĐŸĐ·ŃĐŸĐ±ĐșĐ° апаŃĐ°ŃŃĐČ Đ· ŃŃĐžŃĐ°Đ·ĐœĐžĐŒ ĐżŃĐ”ĐČĐŽĐŸĐ·ŃŃĐŽĐ¶Đ”ĐœĐžĐŒ ŃĐ°ŃĐŸĐŒ Đ·ŃĐŸŃŃĐČĐ°ĐœĐŸŃ ĐœĐ°ŃĐ°ĐŽĐșĐž ŃĐșĐ»Đ°ĐŽĐœĐžŃ
ŃĐŸŃĐŒ ŃĐ· ŃŃŃŃĐ°ŃŃĐžŃ
ĐŒĐ°ŃĐ”ŃŃĐ°Đ»ŃĐČ. ĐŃжД, ĐœĐ”ĐŸĐ±Ń
ŃĐŽĐœĐ” ĐżŃĐŸĐČĐ”ĐŽĐ”ĐœĐœŃ ŃпДŃŃĐ°Đ»ŃĐœĐžŃ
ĐŽĐŸŃĐ»ŃĐŽĐ¶Đ”ĐœŃ ĐłŃĐŽŃĐŸĐŽĐžĐœĐ°ĐŒŃŃĐœĐžŃ
ŃĐ”Đ¶ĐžĐŒŃĐČ ŃĐŸĐ±ĐŸŃĐž апаŃĐ°ŃŃ Đ· ŃŃŃŃĐ°ŃŃĐŸŃ ĐœĐ°ŃĐ°ĐŽĐșĐŸŃ Ń ĐČĐžĐ·ĐœĐ°ŃĐ”ĐœĐœŃĐŒ паŃĐ°ĐŒĐ”ŃŃŃĐČ, ŃĐŸ ĐČплОĐČĐ°ŃŃŃ ĐœĐ° ŃĐČОЎĐșŃŃŃŃ ĐżĐ”ŃĐ”Ń
ĐŸĐŽŃ ĐœĐ°ŃĐ°ĐŽĐșĐž Đ· ĐŸĐŽĐœĐŸĐłĐŸ ŃĐ”Đ¶ĐžĐŒŃ ĐČ ŃĐœŃĐžĐč.Industrial implementation of the stabilization method of the gas-liquid layer can significantly expand the field of use of foaming apparatus and opens up new opportunities for intensifying technological processes with the simultaneous creation of low-waste technologies. The article establishes the basic parameters influencing the hydrodynamics of foam apparatus, considers the basic constructions and operating modes of foam apparatus. The connection of hydrodynamic parameters is revealed. The hydrodynamic laws of the foam layer are considered. The indicated factors affecting the process of mass transfer, both in the gas and in the liquid phases. The conducted analysis of a number of studies showed that the perspective direction of intensification of the mass transfer process is the development of apparatuses with a three-phase fluidized bed of an irrigated nozzle of complex forms with mesh materials
The Epigenetic Landscape of Latent Kaposi Sarcoma-Associated Herpesvirus Genomes
Herpesvirus latency is generally thought to be governed by epigenetic modifications, but the dynamics of viral chromatin at early timepoints of latent infection are poorly understood. Here, we report a comprehensive spatial and temporal analysis of DNA methylation and histone modifications during latent infection with Kaposi Sarcoma-associated herpesvirus (KSHV), the etiologic agent of Kaposi Sarcoma and primary effusion lymphoma (PEL). By use of high resolution tiling microarrays in conjunction with immunoprecipitation of methylated DNA (MeDIP) or modified histones (chromatin IP, ChIP), our study revealed highly distinct landscapes of epigenetic modifications associated with latent KSHV infection in several tumor-derived cell lines as well as de novo infected endothelial cells. We find that KSHV genomes are subject to profound methylation at CpG dinucleotides, leading to the establishment of characteristic global DNA methylation patterns. However, such patterns evolve slowly and thus are unlikely to control early latency. In contrast, we observed that latency-specific histone modification patterns were rapidly established upon a de novo infection. Our analysis furthermore demonstrates that such patterns are not characterized by the absence of activating histone modifications, as H3K9/K14-ac and H3K4-me3 marks were prominently detected at several loci, including the promoter of the lytic cycle transactivator Rta. While these regions were furthermore largely devoid of the constitutive heterochromatin marker H3K9-me3, we observed rapid and widespread deposition of H3K27-me3 across latent KSHV genomes, a bivalent modification which is able to repress transcription in spite of the simultaneous presence of activating marks. Our findings suggest that the modification patterns identified here induce a poised state of repression during viral latency, which can be rapidly reversed once the lytic cycle is induced
Exposure assessment of process-related contaminants in food by biomarker monitoring
Exposure assessment is a fundamental part of the risk assessment paradigm, but can often present a number of challenges and uncertainties. This is especially the case for process contaminants formed during the processing, e.g. heating of food, since they are in part highly reactive and/or volatile, thus making exposure assessment by analysing contents in food unreliable. New approaches are therefore required to accurately assess consumer exposure and thus better inform the risk assessment. Such novel approaches may include the use of biomarkers, physiologically based kinetic (PBK) modelling-facilitated reverse dosimetry, and/or duplicate diet studies. This review focuses on the state of the art with respect to the use of biomarkers of exposure for the process contaminants acrylamide, 3-MCPD esters, glycidyl esters, furan and acrolein. From the overview presented, it becomes clear that the field of assessing human exposure to process-related contaminants in food by biomarker monitoring is promising and strongly developing. The current state of the art as well as the existing data gaps and challenges for the future were defined. They include (1) using PBK modelling and duplicate diet studies to establish, preferably in humans, correlations between external exposure and biomarkers; (2) elucidation of the possible endogenous formation of the process-related contaminants and the resulting biomarker levels; (3) the influence of inter-individual variations and how to include that in the biomarker-based exposure predictions; (4) the correction for confounding factors; (5) the value of the different biomarkers in relation to exposure scenarioâs and risk assessment, and (6) the possibilities of novel methodologies. In spite of these challenges it can be concluded that biomarker-based exposure assessment provides a unique opportunity to more accurately assess consumer exposure to process-related contaminants in food and thus to better inform risk assessment
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Functional imaging using fluorine ((19)F) MR methods: basic concepts
Kidney-associated pathologies would greatly benefit from noninvasive and robust methods that can objectively quantify changes in renal function. In the past years there has been a growing incentive to develop new applications for fluorine ((19)F) MRI in biomedical research to study functional changes during disease states. (19)F MRI represents an instrumental tool for the quantification of exogenous (19)F substances in vivo. One of the major benefits of (19)F MRI is that fluorine in its organic form is absent in eukaryotic cells. Therefore, the introduction of exogenous (19)F signals in vivo will yield background-free images, thus providing highly selective detection with absolute specificity in vivo. Here we introduce the concept of (19)F MRI, describe existing challenges, especially those pertaining to signal sensitivity, and give an overview of preclinical applications to illustrate the utility and applicability of this technique for measuring renal function in animal models. This chapter is based upon work from the COST Action PARENCHIMA, a community-driven network funded by the European Cooperation in Science and Technology (COST) program of the European Union, which aims to improve the reproducibility and standardization of renal MRI biomarkers. This introduction chapter is complemented by two separate chapters describing the experimental procedure and data analysis
- âŠ