507 research outputs found
Fabrication of flexible UV nanoimprint mold with fluorinated polymer-coated PET film
UV curing nanoimprint lithography is one of the most promising techniques for the fabrication of micro- to nano-sized patterns on various substrates with high throughput and a low production cost. The UV nanoimprint process requires a transparent template with micro- to nano-sized surface protrusions, having a low surface energy and good flexibility. Therefore, the development of low-cost, transparent, and flexible templates is essential. In this study, a flexible polyethylene terephthalate (PET) film coated with a fluorinated polymer material was used as an imprinting mold. Micro- and nano-sized surface protrusion patterns were formed on the fluorinated polymer layer by the hot embossing process from a Si master template. Then, the replicated pattern of the fluorinated polymer, coated on the flexible PET film, was used as a template for the UV nanoimprint process without any anti-stiction coating process. In this way, the micro- to nano-sized patterns of the original master Si template were replicated on various substrates, including a flat Si substrate and curved acryl substrate, with high fidelity using UV nanoimprint lithography
Multi-Signal Reconstruction Using Masked Autoencoder From EEG During Polysomnography
Polysomnography (PSG) is an indispensable diagnostic tool in sleep medicine,
essential for identifying various sleep disorders. By capturing physiological
signals, including EEG, EOG, EMG, and cardiorespiratory metrics, PSG presents a
patient's sleep architecture. However, its dependency on complex equipment and
expertise confines its use to specialized clinical settings. Addressing these
limitations, our study aims to perform PSG by developing a system that requires
only a single EEG measurement. We propose a novel system capable of
reconstructing multi-signal PSG from a single-channel EEG based on a masked
autoencoder. The masked autoencoder was trained and evaluated using the
Sleep-EDF-20 dataset, with mean squared error as the metric for assessing the
similarity between original and reconstructed signals. The model demonstrated
proficiency in reconstructing multi-signal data. Our results present promise
for the development of more accessible and long-term sleep monitoring systems.
This suggests the expansion of PSG's applicability, enabling its use beyond the
confines of clinics.Comment: Proc. 12th IEEE International Winter Conference on Brain-Computer
Interfac
Relationship Between Mood, Sleepiness, and EEG Functional Connectivity by 40 Hz Monaural Beats
The monaural beat is known that it can modulate brain and personal states.
However, which changes in brain waves are related to changes in state is still
unclear. Therefore, we aimed to investigate the effects of monaural beats and
find the relationship between them. Ten participants took part in five separate
random sessions, which included a baseline session and four sessions with
monaural beats stimulation: one audible session and three inaudible sessions.
Electroencephalogram (EEG) were recorded and participants completed pre- and
post-stimulation questionnaires assessing mood and sleepiness. As a result,
audible session led to increased arousal and positive mood compared to other
conditions. From the neurophysiological analysis, statistical differences in
frontal-central, central-central, and central-parietal connectivity were
observed only in the audible session. Furthermore, a significant correlation
was identified between sleepiness and EEG power in the temporal and occipital
regions. These results suggested a more detailed correlation for stimulation to
change its personal state. These findings have implications for applications in
areas such as cognitive enhancement, mood regulation, and sleep management
Impact of Nap on Performance in Different Working Memory Tasks Using EEG
Electroencephalography (EEG) has been widely used to study the relationship
between naps and working memory, yet the effects of naps on distinct working
memory tasks remain unclear. Here, participants performed word-pair and
visuospatial working memory tasks pre- and post-nap sessions. We found marked
differences in accuracy and reaction time between tasks performed pre- and
post-nap. In order to identify the impact of naps on performance in each
working memory task, we employed clustering to classify participants as high-
or low-performers. Analysis of sleep architecture revealed significant
variations in sleep onset latency and rapid eye movement (REM) proportion. In
addition, the two groups exhibited prominent differences, especially in the
delta power of the Non-REM 3 stage linked to memory. Our results emphasize the
interplay between nap-related neural activity and working memory, underlining
specific EEG markers associated with cognitive performance.Comment: Submitted to 2024 12th IEEE International Winter Conference on
Brain-Computer Interfac
Neurophysiological Response Based on Auditory Sense for Brain Modulation Using Monaural Beat
Brain modulation is a modification process of brain activity through external
stimulations. However, which condition can induce the activation is still
unclear. Therefore, we aimed to identify brain activation conditions using 40
Hz monaural beat (MB). Under this stimulation, auditory sense status which is
determined by frequency and power range is the condition to consider. Hence, we
designed five sessions to compare; no stimulation, audible (AB), inaudible in
frequency, inaudible in power, and inaudible in frequency and power. Ten
healthy participants underwent each stimulation session for ten minutes with
electroencephalogram (EEG) recording. For analysis, we calculated the power
spectral density (PSD) of EEG for each session and compared them in frequency,
time, and five brain regions. As a result, we observed the prominent power peak
at 40 Hz in only AB. The induced EEG amplitude increase started at one minute
and increased until the end of the session. These results of AB had significant
differences in frontal, central, temporal, parietal, and occipital regions
compared to other stimulations. From the statistical analysis, the PSD of the
right temporal region was significantly higher than the left. We figure out the
role that the auditory sense is important to lead brain activation. These
findings help to understand the neurophysiological principle and effects of
auditory stimulation.Comment: Accepted to EMBC 202
Immunogenicity and safety of an AS03-adjuvanted H5N1 pandemic influenza vaccine in Korean adults: A phase IV, randomized, open-label, controlled study
AbstractBackgroundAS03-adjuvanted H5N1 pandemic influenza vaccines have been assessed in an extensive clinical development program conducted in North America, Europe, and Asia including children from 6 months of age, adults, and elderly adults. We evaluated AS03-H5N1 in Korean adults 18 through 60 years of age.MethodsThis Phase IV, randomized, study was conducted to assess the immunogenicity, reactogenicity, and safety of two doses (3.75μg of hemagglutinin antigen) of A/Indonesia/5/2005 (H5N1) adjuvanted with AS03 given 21 days apart in Korean adults. Antibody responses were assessed using hemagglutination-inhibition (HI) assays against the vaccine strain and a vaccine-heterologous strain (A/Vietnam/1194/2004) 21 days after the second dose. A control group (safety) received a licensed seasonal inactivated trivalent influenza vaccine (TIV). Reactogenicity was assessed for 7 days after each vaccination, and unsolicited adverse events were assessed for 182 days following vaccination in both study groups (NCT01730378).ResultsAS03-H5N1 was immunogenic and elicited robust HI antibody responses with seroconversion rates of 100% for the vaccine strain and 69.1% for the heterologous strain (N=81). HI antibody responses fulfilled the European licensure criteria for immunogenicity (primary endpoint). The incidence of local and systemic solicited adverse events (reactogenicity) was higher with AS03-H5N1 than TIV. There was no apparent difference in the rate of unsolicited adverse events in the AS03-H5N1 and TIV groups.ConclusionThe results indicate that AS03-H5N1 vaccine is immunogenic with reactogenicity and safety findings that are consistent with the established profile of AS03-H5N1 vaccine
Arrayed CRISPR screen with image-based assay reliably uncovers host genes required for coxsackievirus infection
Pooled CRISPR screens based on lentiviral systems have been widely applied to identify the effect of gene knockout on cellular phenotype. Although many screens were successful, they also have the limitation that genes conferring mild phenotypes or those essential for growth can be overlooked, as every genetic perturbation is incorporated in the same population. Arrayed screens, on the other hand, incorporate a single genetic perturbation in each well and could overcome these limitations. However, arrayed screens based on siRNA-mediated knockdown were recently criticized for low reproducibility caused by incomplete inhibition of gene expression. To overcome these limitations, we developed a novel arrayed CRISPR screen based on a plasmid library expressing a single guide RNA (sgRNA) and disrupted 1514 genes, encoding kinases, proteins related to endocytosis, and Golgi-localized proteins, individually using 4542 sgRNAs (three sgRNAs per gene). This screen revealed host factors required for infection by coxsackievirus B3 (CVB3) from Picornaviridae, which includes human pathogens causing diverse diseases. Many host factors that had been overlooked in a conventional pooled screen were identified for CVB3 infection, including entry-related factors, translational initiation factors, and several replication factors with different functions, demonstrating the advantage of the arrayed screen. This screen was quite reliable and reproducible, as most genes identified in the primary screen were confirmed in secondary screens. Moreover, ACBD3, whose phenotype was not affected by siRNA-mediated knockdown, was reliably identified. We propose that arrayed CRISPR screens based on sgRNA plasmid libraries are powerful tools for arrayed genetic screening and applicable to larger-scale screens.
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