98 research outputs found
Adopting Maximum Pupil Diameter to Detect Subtle Usability Issues of a Smartphone Application, Conflict Solver
With the increasing popularity and unparalleled ubiquity of smartphones, researchers in various fields are designing and developing novel applications for this platform as part of the solution to the challenging problems they face. Usability lies at the core of the user experience of such applications. However, the assessments used are often limited to summative and post-event methods, which can overlook subtle yet impactful issues. Objective and instantaneous measures of cognitive workloads provide a solution to this shortcoming. Our previous research has established the reliability of maximum pupil dilation, measured with Tobii Pro Nano, as a preeminent indicator of cognitive workload surges in mobile application users. In this study, we used this measure to locate user cognitive workload peaks while using Conflict Solver and discovered subtle user interface issues that were not reported in the post-usability interview. A total of 30 participants completed a Conflict Solver usability experiment with two phases. In phase 1, the participants performed two “Add a Term” tasks on the original Conflict Solver, followed by a semi-structured interview about their experience with the application. A few subtle usability issues with a drop-down menu were detected through identifying user cognitive workload peaks. In phase 2, the same participants completed the same tasks on Conflict Solver with a redesigned and extended drop-down menu. The results showed that the new design solved the usability issues, and the participants became more favor the drop-down menu over the input box. In conclusion, including maximum pupil dilation into the usability assessment toolkit would provide a more objective and comprehensive usability assessment of a smartphone application. It can also be used to verify the successfulness of a user interface design solution.</p
Designing Recognition Molecules and Tailoring Functional Surfaces for In Vivo Monitoring of Small Molecules in the Brain
ConspectusThe in vivo analysis of chemical signals in brain extracellular
fluid (ECF) using implanted electrochemical biosensors is a vital
way to study brain functions and brain activity mapping. This approach
offers excellent spatial (10–200 μm) and temporal (approximately
second) resolution and the major advantage of long-term stability.
By implantation of a microelectrode in a specific brain region, changes
in the concentration of a variety of ECF chemical species can be monitored
through applying a suitable electrical signal and, typically, recording
the resulting Faradaic current. However, the high performance requirements
for in vivo biosensors greatly limit our understanding of the roles
that biomolecules play in the brain. Since a large number of biological
species, including reactive oxygen species (ROS), metal ions, amino
acids, and proteins, coexist in the brain and interact with each other,
developing in vivo biosensors with high selectivity is a great challenge.
Meanwhile, it is difficult to quantitatively determine target molecules
in the brain because of the variation in the distinct environments
for monitoring biomolecules in vitro and in vivo. Thus, there are
large errors in the quantification of concentrations in the brain
using calibration curves obtained in artificial cerebrospinal fluid
(aCSF). More importantly, to gain a full understanding of the physiological
and pathological processes in the brain, the development of novel
approaches for the simultaneous determination of multiple species
in vivo is urgently needed.This Account provides insight into
the basic design principles
and criteria required to convert chemical/electrochemical reactions
into electric signals, while satisfying the increasing requirements,
including high selectivity, sensitivity, and accuracy, for the in
vivo analysis of biomolecules in the brain. Recent developments in
designing various functional surfaces, such as self-assembled monolayers,
gold nanostructures, and nanostructured semiconductors for facilitating
electron transfer from specific enzymes, including superoxide dismutase
(SOD), and further application to an O<sub>2</sub><sup>•–</sup> biosensor are summarized. This Account also aims to highlight the
design principles for the selective biosensing of Cu<sup>2+</sup> and
pH in the brain through the rational design and synthesis of specific
recognition molecules. Additionally, electrochemical ratiometric biosensors
with current signal output have been constructed to correct the effect
of distinct environments in a timely manner, thus greatly improving
the accuracy of the determination of Cu<sup>2+</sup> in the live brain.
This method of using a built-in element has been extended to biosensors
with the potential signal output for in vivo pH analysis. More importantly,
the new concept of both current and potential signal outputs provides
an avenue to simultaneously determine dual species in the brain.The extension of the design principles and developed strategy demonstrated
in this Account to other biomolecules, which may be closely correlated
to the biological processes of brain events, is promising. The final
section of this Account outlines potential future directions in tailoring
functional surfaces and designing recognition molecules based on recent
advances in molecular science, nanoscience and nanotechnology, and
biological chemistry for the design of advanced devices with multiple
target species to map the molecular imaging of the brain. There are
still opportunities to engineer surfaces that improve on this approach
by constructing implantable, multifunctional nanodevices that promise
to combine the benefits of multiple sensing and therapeutic modules
Solid-State NMR Analyses Reveal the Structure Dependence of the Molecular Dynamics for ω-Amino Acids
The molecular dynamics of metabolites is structure dependent
and
vitally important for the interactive functions in their potential
applications as natural materials. To understand the relationship
between molecular structure and dynamics, the molecular motions of
four structurally related ω-amino acids (β-alanine, γ-aminobutyric
acid, 5-aminovaleric acid, and 6-aminocaproic acid) were investigated
by measuring their proton spin–lattice relaxation times (<i>T</i><sub>1</sub>, <i>T</i><sub>1ρ</sub>) as
a function of temperature (180–440 K). <sup>13</sup>C CPMAS
NMR and DSC analyses were performed to obtain complementary information.
All of these ω-amino acids showed no phase transition in the
temperature range studied but had outstandingly long proton <i>T</i><sub>1</sub> at 300 MHz and even at 20 MHz for the deuterated
forms. The molecular dynamics of all these ω-amino acids were
dominated by the reorientation motions of amino groups and backbone
motions except in β-alanine. The activation energies for amino
group reorientations were positively correlated with the strength
of hydrogen bonds involving these groups in the crystals and the carbon-chain
lengths, whereas such energies for the backbone motions were inversely
correlated with the carbon-chain lengths. These findings provided
essential information for the molecular dynamics of ω-amino
acids and demonstrated the combined solid-state NMR methods as a useful
approach for understanding the structural dependence of molecular
dynamics
Comparison with state-of-the-art tracking algorithms.
The tracker DOSiam gets best tracking results in challenging environments of fast motion, scale variation, motion blur, in-plane and out-plane rotations.</p
Illustration of DOSiam.
It consists of the feature extraction subnetwork and cross-correlation operation. The feature extraction subnetwork contains conventional convolution layers and DO-Conv.</p
Ratiometric Electrochemical Sensor for Selective Monitoring of Cadmium Ions Using Biomolecular Recognition
A selective, accurate, and sensitive
method for monitoring of cadmium
ions (Cd<sup>2+</sup>) based on a ratiometric electrochemical sensor
was developed, by simultaneously modifying with protoporphyrin IX
and 6-(ferroceney) hexanethiol (FcHT) on Au particle-deposited glassy
carbon electrode. On the basis of high affinity of biomolecular recognition
between protoporphyrin IX and Cd<sup>2+</sup>, the functionalized
electrode showed high selectivity toward Cd<sup>2+</sup> over other
metal ions such as Cu<sup>2+</sup>, Fe<sup>3+</sup>, Ca<sup>2+</sup>, and so on. Electroactive FcHT played the role as the inner reference
element to provide a built-in correction, thus improving the accuracy
for determination of Cd<sup>2+</sup> in the complicated environments.
The sensitivity of the electrochemical sensor for Cd<sup>2+</sup> was
enhanced by ∼3-fold through the signal amplification of electrodeposited
gold nanoparticles. Accordingly, the present ratiometric method demonstrated
high sensitivity, broad linear range from 100 nM to 10 μM, and
low detection limit down to 10 nM (2.2 ppb), lower than EPA and WHO
guidelines. Finally, the ratiometric electrochemical sensor was successfully
applied in the determination of Cd<sup>2+</sup> in water samples,
and the obtained results agreed well with those obtained by the conventional
ICP-MS method
Illustration of DO-Conv.
The deep convolution and conventional convolution kernel are included in DO-Conv. ∘ means the depthwise convolution operator and * means convolution operator.</p
A comparison of the DOSiam with state-of-the-art trackers in terms of success rate and precision on VOT2016 and VOT2018 with different attributes, respectively.
A comparison of the DOSiam with state-of-the-art trackers in terms of success rate and precision on VOT2016 and VOT2018 with different attributes, respectively.</p
A comparison of the DOSiam with state-of-the-art trackers in terms of success rate and precision on OTB2015 with different attributes.
A comparison of the DOSiam with state-of-the-art trackers in terms of success rate and precision on OTB2015 with different attributes.</p
- …