The Wigner Solution and QCD Phase Transitions in a Modified PNJL Model

By employing some modification to the widely used two-flavor Polyakov-loop extended Nambu-Jona-Lasinio (PNJL) model, we discuss the Wigner solution of the quark gap equation at finite temperature and zero quark chemical potential beyond the chiral limit, and then try to explore its influences on the chiral and deconfinement phase transitions of QCD at finite temperature and zero chemical potential. The discovery of the coexistence of the Nambu and the Wigner solutions of the quark gap equation with nonzero current quark mass at zero temperature and zero chemical potential, as well as their evolutions with temperature is very interesting for the studies of the phase transitions of QCD. According to our results, the chiral phase transition might be of first order (while the deconfinement phase transition is still a crossover, as in the normal PNJL model), and the corresponding phase transition temperature is lower than that of the deconfinement phase transition, instead of coinciding with each other, which are not the same as the conclusions obtained from the normal PNJL model. In addition, we also discuss the sensibility of our final results on the choice of model parameters

\u3csup\u3e99m\u3c/sup\u3eTc-Labeled C2A Domain of Synaptotagmin I as a Target-Specific Molecular Probe for Noninvasive Imaging of Acute Myocardial Infarction

Abstract: The exposure of phosphatidylserine (PtdS) is a common molecular marker for both apoptosis and necrosis and enables the simultaneous detection of these distinct modes of cell death. Our aim was to develop a radiotracer based on the PtdS-binding activity of the C2A domain of synaptotagmin I and assess 99mTc-C2A-GST (GST is glutathione S-transferase) using a reperfused acute myocardial infarction (AMI) rat model. Methods: The binding of C2A-GST toward apoptosis and necrosis was validated in vitro. After labeling with 99mTc via 2-iminothiolane thiolation, radiochemical purity and radiostability were tested. Pharmacokinetics and biodistribution were studied in healthy rats. The uptake of 99mTc-C2A-GST within the area at risk was quantified by direct γ-counting, whereas nonspecific accumulation was estimated using inactivated 99mTc-C2A-GST. In vivo planar imaging of AMI in rats was performed on a γ-camera using a parallel-hole collimator. Radioactivity uptake was investigated by region-of-interest analysis, and postmortem tetrazolium staining versus autoradiography. Results: Fluorescently labeled and radiolabeled C2A-GST bound both apoptotic and necrotic cells. 99mTc-C2A-GST had a radiochemical purity of \u3e98% and remained stable. After intravenous injection, the uptake in the liver and kidneys was significant. For 99mTc-C2A-GST, radioactivity uptake in the area at risk reached between 2.40 and 2.63 %ID/g (%ID/g is percentage injected dose per gram) within 30 min and remained plateaued for at least 3 h. In comparison, with the inactivated tracer the radioactivity reached 1.06 ± 0.49 %ID/g at 30 min, followed by washout to 0.52 ± 0.23 %ID/g. In 7 of 7 rats, the infarct was clearly identifiable as focal uptake in planar images. At 3 h after injection, the infarct-to-lung ratios were 2.48 ± 0.27, 1.29 ± 0.09, and 1.46 ± 0.04 for acute-infarct rats with 99mTc-C2A-GST, sham-operated rats with 99mTc-C2A-GST, and acute-infarct rats with 99mTc-C2A-GST-NHS (NHS is N-hydroxy succinimide), respectively. The distribution of radioactivity was confirmed by autoradiography and histology. Conclusion: The C2A domain of synaptotagmin I labeled with fluorochromes or a radioisotope binds to both apoptotic and necrotic cells. Ex vivo and in vivo data indicate that, because of elevated vascular permeability, both specific binding and passive leakage contribute to the accumulation of the radiotracer in the area at risk. However, the latter component alone is insufficient to achieve detectable target-to-background ratios with in vivo planar imaging

Research progress on intelligent optimization techniques for energy-efficient design of ship hull forms

The design optimization of ship hull form based on hydrodynamics theory and simulation-based design (SBD) technologies generally considers ship performance and energy efficiency performance as the design objective, which plays an important role in smart design and manufacturing of green ship. An optimal design of sustainable energy system requires multidisciplinary tools to build ships with the least resistance and energy consumption. Through a systematic approach, this paper presents the research progress of energy-efficient design of ship hull forms based on intelligent optimization techniques. We discuss different methods involved in the optimization procedure, especially the latest developments of intelligent optimization algorithms and surrogate models. Moreover, current development trends and technical challenges of multidisciplinary design optimization and surrogate-assisted evolutionary algorithms for ship design are further analyzed. We explore the gaps and potential future directions, so as to paving the way towards the design of the next generation of more energy-efficient ship hull form.Comment: 30 pages, 8 figure