2,760 research outputs found
Topological Quantum Phase Transition in Synthetic Non-Abelian Gauge Potential
The method of synthetic gauge potentials opens up a new avenue for our
understanding and discovering novel quantum states of matter. We investigate
the topological quantum phase transition of Fermi gases trapped in a honeycomb
lattice in the presence of a synthetic non- Abelian gauge potential. We develop
a systematic fermionic effective field theory to describe a topological quantum
phase transition tuned by the non-Abelian gauge potential and ex- plore its
various important experimental consequences. Numerical calculations on lattice
scales are performed to compare with the results achieved by the fermionic
effective field theory. Several possible experimental detection methods of
topological quantum phase tran- sition are proposed. In contrast to condensed
matter experiments where only gauge invariant quantities can be measured, both
gauge invariant and non-gauge invariant quantities can be measured by
experimentally generating various non-Abelian gauges corresponding to the same
set of Wilson loops
The preparation, characterization, and pharmacokinetic studies of chitosan nanoparticles loaded with paclitaxel/dimethyl-β-cyclodextrin inclusion complexes.
A novel biocompatible and biodegradable drug-delivery nanoparticle (NP) has been developed to minimize the severe side effects of the poorly water-soluble anticancer drug paclitaxel (PTX) for clinical use. PTX was loaded into the hydrophobic cavity of a hydrophilic cyclodextrin derivative, heptakis (2,6-di-O-methyl)-β-cyclodextrin (DM-β-CD), using an aqueous solution-stirring method followed by lyophilization. The resulting PTX/DM-β-CD inclusion complex dramatically enhanced the solubility of PTX in water and was directly incorporated into chitosan (CS) to form NPs (with a size of 323.9–407.8 nm in diameter) using an ionic gelation method. The formed NPs had a zeta potential of +15.9–23.3 mV and showed high colloidal stability. With the same weight ratio of PTX to CS of 0.7, the loading efficiency of the PTX/DM-β-CD inclusion complex-loaded CS NPs was 30.3-fold higher than that of the PTX-loaded CS NPs. Moreover, it is notable that PTX was released from the DM-β-CD/CS NPs in a sustained-release manner. The pharmacokinetic studies revealed that, compared with reference formulation (Taxol(®)), the PTX/DM-β-CD inclusion complex-loaded CS NPs exhibited a significant increase in AUC(0→24h) (the area under the plasma drug concentration–time curve over the period of 24 hours) and mean residence time by 2.7-fold and 1.4-fold, respectively. Therefore, the novel drug/DM-β-CD inclusion complex-loaded CS NPs have promising applications for the significantly improved delivery and controlled release of the poorly water-soluble drug PTX or its derivatives, thus possibly leading to enhanced therapeutic efficacy and less severe side effects
The prevalence of environmentral colonization of Legionella in hospital water systems in Taiwan – a 20 hospital surveillance
Comparison of the Accuracy of HSV1 and HSV2 Antibody Tests with PCR in the Diagnosis of Recurrent Genital Herpes
Jia Deng, Yu-Jian Ye, Qiu-Ping Chen, Yi-Jin Zhang, Ji-Feng Liu Department of Dermatology, Hangzhou Third People’s Hospital, Hangzhou, People’s Republic of ChinaCorrespondence: Ji-Feng Liu, Department of Dermatology, Hangzhou Third People’s Hospital, No. 38 of West Lake Road, Shangcheng District, Hangzhou, Zhejiang, 310009, People’s Republic of China, Tel/Fax +86 0571-87827514, Email [email protected]: To assess the accuracy of HSV1and HSV2 antibody testing in identifying genital herpes infection.Methods: A cohort of 299 patients previously diagnosed with recurrent genital herpes, confirmed via PCR, were tested using ELISA for HSV1 and HSV2 IgM and IgG antibodies. The study compared the accuracy of HSV1 and HSV2 antibody tests in diagnosing genital herpes.Results: Among 299 patients, 14 tested positives for HSV1 DNA. Of these, 9 had HSV1 IgG antibodies, but none had HSV2 IgG antibody. Among 278 patients with HSV2 DNA, 149 had HSV1 IgG, 9 had HSV2 IgG, and 97 had both. Seven patients had both HSV1 and HSV2 DNA; 3 had HSV1 IgG, 1 had HSV2 IgG, and 3 had both. The accuracy of HSV1 IgG for HSV1 infection was 64.2%, and for HSV1 and HSV2 co-infection, 85.7%. The accuracy of HSV2 IgG for HSV2 infection was 38.1%, and for HSV1 and HSV2 co-infection, 57.1%. The combined antibody positivity accuracy was 34.9%.Conclusion: Genital herpes is primarily caused by HSV2 (92.98%). A smaller percentage is HSV1 (4.67%) or co-infection (2.34%). Despite relatively low diagnostic accuracy (34.9– 85.7%) for antibody detection, combined antibody testing is necessary. Herpes DNA testing is recommended for accurate diagnosis. Absence of antibodies does not rule out genital herpes and clinical assessment is essential.Keywords: antibody test, DNA test, genital herpes, HSV-1, HSV-
Design of arbitrarily shaped planar microstrip antenna arrays with improved efficiency
A design technique is described for an arbitrarily shaped planar microstrip antenna array with improved radiation efficiency. In order to fully utilize the limited antenna aperture, several basic modules are proposed from which we construct the array. A consideration of the aperture shape shows that with several practical examples a proper combination of these basic modules not only allows the convenient design of arbitrarily-shaped microstrip array, but also helps to improve the aperture radiation efficiency. To confirm the feasibility of the approach, a circular array with 256 elements was constructed and fabricated. Both computed and measured aperture radiation results are compared and these demonstrate that the design technique is effective for arbitrarily-shaped planar microstrip arrays. © 2013 Sheng Ye et al
Extent of Safety Database in Pediatric Drug Development: Types of Assessment, Analytical Precision, and Pathway for Extrapolation through On-Target Effects
Pediatric patients should have access to medicines that have been
appropriately evaluated for safety and efficacy. Given this goal of revised
labelling, the adequacy of the pediatric clinical development plan and
resulting safety database must inform a favorable benefit-risk assessment for
the intended use of the medicinal product. While extrapolation from adults can
be used to support efficacy of drugs in children, there may be a reluctance to
use the same approach in safety assessments, wiping out potential gains in
trial efficiency through a reduction of sample size. To address this
reluctance, we explore safety review in pediatric trials, including factors
affecting these data, specific types of safety assessments, and precision on
the estimation of event rates for specific adverse events (AEs) that can be
achieved. In addition, we discuss the assessments which can provide a benchmark
for the use of extrapolation of safety that focuses on on-target effects.
Finally, we explore a unified approach for understanding precision using
Bayesian approaches as the most appropriate methodology to describe/ascertain
risk in probabilistic terms for the estimate of the event rate of specific AEs
Mining features of products from Chinese customer online reviews
2008-2009 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe
The impact of physiological loading on immune cell infiltration and myocardial function evaluated by cardiac MRI: a comparison between non-working heart and working heart transplant models
Computational Complexity of Atomic Chemical Reaction Networks
Informally, a chemical reaction network is "atomic" if each reaction may be
interpreted as the rearrangement of indivisible units of matter. There are
several reasonable definitions formalizing this idea. We investigate the
computational complexity of deciding whether a given network is atomic
according to each of these definitions.
Our first definition, primitive atomic, which requires each reaction to
preserve the total number of atoms, is to shown to be equivalent to mass
conservation. Since it is known that it can be decided in polynomial time
whether a given chemical reaction network is mass-conserving, the equivalence
gives an efficient algorithm to decide primitive atomicity.
Another definition, subset atomic, further requires that all atoms are
species. We show that deciding whether a given network is subset atomic is in
, and the problem "is a network subset atomic with respect to a
given atom set" is strongly -.
A third definition, reachably atomic, studied by Adleman, Gopalkrishnan et
al., further requires that each species has a sequence of reactions splitting
it into its constituent atoms. We show that there is a to decide whether a given network is reachably atomic, improving
upon the result of Adleman et al. that the problem is . We
show that the reachability problem for reachably atomic networks is
-.
Finally, we demonstrate equivalence relationships between our definitions and
some special cases of another existing definition of atomicity due to Gnacadja
Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels
PMCID: PMC3480949This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited
- …