1,921 research outputs found
Service-Learning in Undergraduate General Chemistry: A Review
Background: Service-learning is gaining recognition as a valuable pedagogy for students to gain both academic and psychosocial benefits. This high-impact practice allows students to achieve course learning objectives while contributing to their community\u27s needs. A review from 2007 revealed a lack of research focused on the topic in the prior decade, despite the interest that was shown by the American Chemical Society in 2000. Purpose: This review of recent case studies on the topic provides future researchers and practitioners with an understanding of the current state of service-learning in undergraduate chemistry courses. Methodology/Approach: To create a representative sample of recent literature for a non-exhaustive scoping review, only peer-reviewed articles addressing service-learning in undergraduate chemistry, published in reliable journals in the last two decades were included. These studies were analyzed in terms of course design, research design, and research quality. Findings/Conclusions: While the scoping review identified papers with notable contributions to establishing service-learning in undergraduate general chemistry, the review also identified several key gaps in the literature, including small sample size, reliance on subjective and indirect measures, and qualitative measures that exclude correlation analysis. Implications: Recommendations for future work for both practitioners and researchers are provided
Cloning and Expression of the PHA Synthase Gene From a Locally Isolated Chromobacterium sp. USM2
Chromobacterium sp. USM2, a locally isolated bacterium was found to synthesize poly(3-hydroxybutyrate-co-3-hydroxyvalerate), P(3HB-co-3HV) copolymer with high 3HV monomer composition. The PHA synthase gene was cloned and expressed in Cupriavidus necator PHB¯4 to investigate the possibilities of incorporating other monomer. The recombinant successfully incorporated 3-hydroxyhexanoate (3HHx) monomer when fed with crude palm kernel oil (CPKO) as the sole carbon source. Approximately 63 ± 2 wt% of P(3HB-co-3HHx) copolymer with 4 mol% of 3HHx was synthesized from 5 g/L of oil after 48 h of cultivation. In addition, P(3HB-co-3HV-co-3HHx) terpolymer with 9 mol% 3HV and 4 mol% 3HHx could be synthesized with a mixture of CPKO and sodium valerate. The presence of 3HV and 3HHx monomers in the copolymer and terpolymer was further confirmed with +H-NMR analysis. This locally isolated PHA synthase has demonstrated its ability to synthesize P(3HB-co-3HHx) copolymer from a readily available and renewable carbon source; CPKO, without the addition of 3HHx precursors
Development of platform-independent web-based telecardiology application for pilot case study
Telecardiology is one of the branches from telemedicine that transmits cardiac data such as electrocardiogram (ECG) and medical records from the patient site to cardiologist for the purpose of diagnosis by using telecommunication and information technologies. Most of the current commercialized telecardiology applications are cost expensive, vendor-specific, and dependent on computing platform and operating system (OS). There are plenty of research have been done on web-based telecardiology application either in real-time transmission or store - And-forward. In this paper, a platform-independent and OS-independent web-based telecardiology application, named VirtualDave System, is developed. The proposed system allow users to log on and access from any computer or mobile communication devices such as smart phone as long as they have internet access and web browser. The developed application allows users in categories of patient, administrator, medical officer and cardiologist, to communicate and get medical consultation without long distance traveling. With the improvement to the system dependency and functionality enhancement such as instant messaging, this web-based telecardiology could significantly help to improve the health care services especially in rural area
Towards the âultimate earthquake-proofâ building: Development of an integrated low-damage system
The 2010â2011 Canterbury earthquake sequence has highlighted the
severe mismatch between societal expectations over the reality of seismic performance
of modern buildings. A paradigm shift in performance-based design criteria
and objectives towards damage-control or low-damage design philosophy and
technologies is urgently required. The increased awareness by the general public,
tenants, building owners, territorial authorities as well as (re)insurers, of the severe
socio-economic impacts of moderate-strong earthquakes in terms of damage/dollars/
downtime, has indeed stimulated and facilitated the wider acceptance and
implementation of cost-efficient damage-control (or low-damage) technologies.
The âbarâ has been raised significantly with the request to fast-track the development
of what the wider general public would hope, and somehow expect, to live
in, i.e. an âearthquake-proofâ building system, capable of sustaining the shaking of
a severe earthquake basically unscathed.
The paper provides an overview of recent advances through extensive research,
carried out at the University of Canterbury in the past decade towards the development
of a low-damage building system as a whole, within an integrated
performance-based framework, including the skeleton of the superstructure, the
non-structural components and the interaction with the soil/foundation system.
Examples of real on site-applications of such technology in New Zealand, using
concrete, timber (engineered wood), steel or a combination of these materials, and
featuring some of the latest innovative technical solutions developed in the laboratory
are presented as examples of successful transfer of performance-based seismic
design approach and advanced technology from theory to practice
Trust as a mediator in the relationship between childhood sexual abuse and IL-6 level in adulthood
Childhood sexual abuse (CSA) has been shown to predict the coupling of depression and inflammation in adulthood. Trust within intimate relationships, a core element in marital relations, has been shown to predict positive physical and mental health outcomes, but the mediating role of trust in partners in the association between CSA and inflammation in adulthood requires further study. The present study aimed to examine the impact of CSA on inflammatory biomarkers (IL-6 and IL-1ÎČ) in adults with depression and the mediating role of trust. A cross-sectional survey data set of adults presenting with mood and sleep disturbance was used in the analysis. CSA demonstrated a significant negative correlation with IL-6 level (r = -0.28, p<0. 01) in adults with clinically significant depression, while trust showed a significant positive correlation with IL-6 level (r = 0.36, p < .01). Sobel test and bootstrapping revealed a significant mediating role for trust between CSA and IL-6 level. CSA and trust in partners were revealed to have significant associations with IL-6 level in adulthood. Counterintuitively, the directions of association were not those expected. Trust played a mediating role between CSA and adulthood levels of IL-6. Plausible explanations for these counterintuitive findings are discussed
Surface patterning of carbon nanotubes can enhance their penetration through a phospholipid bilayer
Nanotube patterning may occur naturally upon the spontaneous self-assembly of
biomolecules onto the surface of single-walled carbon nanotubes (SWNTs). It
results in periodically alternating bands of surface properties, ranging from
relatively hydrophilic to hydrophobic, along the axis of the nanotube. Single
Chain Mean Field (SCMF) theory has been used to estimate the free energy of
systems in which a surface patterned nanotube penetrates a phospholipid
bilayer. In contrast to un-patterned nanotubes with uniform surface properties,
certain patterned nanotubes have been identified that display a relatively low
and approximately constant system free energy (10 kT) as the nanotube traverses
through the bilayer. These observations support the hypothesis that the
spontaneous self-assembly of bio-molecules on the surface of SWNTs may
facilitate nanotube transduction through cell membranes.Comment: Published in ACS Nano http://pubs.acs.org/doi/abs/10.1021/nn102763
Photoluminescent diamond nanoparticles for cell labeling: study of the uptake mechanism in mammalian cells
Diamond nanoparticles (nanodiamonds) have been recently proposed as new
labels for cellular imaging. For small nanodiamonds (size <40 nm) resonant
laser scattering and Raman scattering cross-sections are too small to allow
single nanoparticle observation. Nanodiamonds can however be rendered
photoluminescent with a perfect photostability at room temperature. Such a
remarkable property allows easier single-particle tracking over long
time-scales. In this work we use photoluminescent nanodiamonds of size <50 nm
for intracellular labeling and investigate the mechanism of their uptake by
living cells . By blocking selectively different uptake processes we show that
nanodiamonds enter cells mainly by endocytosis and converging data indicate
that it is clathrin mediated. We also examine nanodiamonds intracellular
localization in endocytic vesicles using immunofluorescence and transmission
electron microscopy. We find a high degree of colocalization between vesicles
and the biggest nanoparticles or aggregates, while the smallest particles
appear free in the cytosol. Our results pave the way for the use of
photoluminescent nanodiamonds in targeted intracellular labeling or biomolecule
deliver
What makes efficient circularly polarised luminescence in the condensed phase: aggregation-induced circular dichroism and light emission
In this contribution, we conceptually present a new avenue to construction of molecular functional materials with high performance of circularly polarised luminescence (CPL) in the condensed phase. A molecule (1) containing luminogenic silole and chiral sugar moieties was synthesized and thoroughly characterized. In a solution of 1, no circular dichroism (CD) and fluorescence emission are observed, but upon molecular aggregation, both the CD and fluorescence are simultaneously turned on, showing aggregation-induced CD (AICD) and emission (AIE) effects. The AICD effect is supported by the fact that the molecules readily assemble into right-handed helical nanoribbons and superhelical ropes when aggregated. The AIE effect boosts the fluorescence quantum efficiency (ΊF) by 136 fold (ΊF, âŒ0.6% in the solution versus âŒ81.3% in the solid state), which surmounts the serious limitations of aggregation-caused quenching effect encountered by conventional luminescent materials. Time-resolved fluorescence study and theoretical calculation from first principles conclude that restriction of the low-frequency intramolecular motions is responsible for the AIE effect. The helical assemblies of 1 prefer to emit right-handed circularly polarised light and display large CPL dissymmetry factors (gem), whose absolute values are in the range of 0.08â0.32 and are two orders of magnitude higher than those of commonly reported organic materials. We demonstrate for the first time the use of a Teflon-based microfluidic technique for fabrication of the fluorescent pattern. This shows the highest gem of â0.32 possibly due to the enhanced assembling order in the confined microchannel environment. The CPL performance was preserved after more than half year storage under ambient conditions, revealing the excellent spectral stability. Computational simulation was performed to interpret how the molecules in the aggregates interact with each other at the molecular level. Our designed molecule represents the desired molecular functional material for generating efficient CPL in the solid state, and the current study shows the best results among the reported organic conjugated molecular systems in terms of emission efficiency, dissymmetry factor, and spectral stability
PEG Branched Polymer for Functionalization of Nanomaterials with Ultralong Blood Circulation
Nanomaterials have been actively pursued for biological and medical
applications in recent years. Here, we report the synthesis of several new
poly(ethylene glycol) grafted branched-polymers for functionalization of
various nanomaterials including carbon nanotubes, gold nanoparticles (NP) and
gold nanorods (NRs), affording high aqueous solubility and stability for these
materials. We synthesize different surfactant polymers based upon
poly-(g-glutamic acid) (gPGA) and poly(maleic anhydride-alt-1-octadecene)
(PMHC18). We use the abundant free carboxylic acid groups of gPGA for attaching
lipophilic species such as pyrene or phospholipid, which bind to nanomaterials
via robust physisorption. Additionally, the remaining carboxylic acids on gPGA
or the amine-reactive anhydrides of PMHC18 are then PEGylated, providing
extended hydrophilic groups, affording polymeric amphiphiles. We show that
single-walled carbon nanotubes (SWNTs), Au NPs and NRs functionalized by the
polymers exhibit high stability in aqueous solutions at different pHs, at
elevated temperatures and in serum. Morever, the polymer-coated SWNTs exhibit
remarkably long blood circulation (t1/2 22.1 h) upon intravenous injection into
mice, far exceeding the previous record of 5.4 h. The ultra-long blood
circulation time suggests greatly delayed clearance of nanomaterials by the
reticuloendothelial system (RES) of mice, a highly desired property for in vivo
applications of nanomaterials, including imaging and drug delivery
Intermolecular CT excitons enable nanosecond excited-state lifetimes in NIR-absorbing non-fullerene acceptors for efficient organic solar cells
State-of-the-art Y6-type molecular acceptors exhibit nanosecond excited-state
lifetimes despite their low optical gaps (~1.4 eV), thus allowing organic solar
cells (OSCs) to achieve highly efficient charge generation with extended
near-infrared (NIR) absorption range (up to ~1000 nm). However, the precise
molecular-level mechanism that enables low-energy excited states in Y6-type
acceptors to achieve nanosecond lifetimes has remained elusive. Here, we
demonstrate that the distinct packing of Y6 molecules in film leads to a strong
intermolecular charge-transfer (iCT) character of the lowest excited state in
Y6 aggregates, which is absent in other low-gap acceptors such as ITIC. Due to
strong electronic couplings between the adjacent Y6 molecules, the iCT-exciton
energies are greatly reduced by up to ~0.25 eV with respect to excitons formed
in separated molecules. Importantly, despite their low energies, the iCT
excitons have reduced non-adiabatic electron-vibration couplings with the
electronic ground state, thus suppressing non-radiative recombination and
allowing Y6 to overcome the well-known energy gap law. Our results reveal the
fundamental relationship between molecular packing and nanosecond excited-state
lifetimes in NIR-absorbing Y6-type acceptors underlying the outstanding
performance of Y6-based OSCs
- âŠ