By taking into account the surface diffuseness correction for unstable nuclei, the accuracy of the macroscopic-microscopic mass formula is further improved. The rms deviation with respect to essentially all the available mass data falls to 298 keV, crossing the 0.3 MeV accuracy threshold for the first time within the mean-field framework. Considering the surface effect of the symmetry potential which plays an important role in the evolution of the "neutron skin" toward the "neutron halo" of nuclei approaching the neutron drip line, we obtain an optimal value of the symmetry energy coefficient J=30.16 MeV. With an accuracy of 258 keV for all the available neutron separation energies and of 237 keV for the alpha-decay Q-values of super-heavy nuclei, the proposed mass formula is particularly important not only for the reliable description of the r-process of nucleosynthesis but also for the study of the synthesis of super-heavy nuclei.Comment: 2 figures, 2 tables, to appear in Phys. Lett.

The Skyrme energy density functional has been applied to the study of heavy-ion fusion reactions.The barriers for fusion reactions are calculated by the Skyrme energy density functional with proton and neutron density distributions determined by using restricted density variational (RDV) method within the same energy density functional together with semi-classical approach known as the extended semi-classical Thomas-Fermi method. Based on the fusion barrier obtained, we propose a parametrization of the empirical barrier distribution to take into account the multi-dimensional character of real barrier and then apply it to calculate the fusion excitation functions in terms of barrier penetration concept. A large number of measured fusion excitation functions spanning the fusion barriers can be reproduced well. The competition between suppression and enhancement effects on sub-barrier fusion caused by neutron-shell-closure and excess neutron effects is studied. * Electronic address: Ning.Wang@theo.

In this work, we have synthesized a thermoresponsive copolymer, alginate-g-poly(N-isopropylacrylamide) (alginate-g-PNIPAAm) by conjugating PNIPAAm to alginate, where PNIPAAm with different molecular weights and narrow molecular weight distribution was synthesized by atomic transfer radical polymerization. The copolymer dissolved in water or phosphate-buffered saline buffer solution at room temperature and formed self-assembled micelles with low critical micellization concentrations when the temperature increased to above their critical micellization temperatures. At higher concentration, that is, 7.4 wt % in water, the copolymer formed solutions at 25 °C and turned into thermosensitive hydrogels when temperature increased to the body temperature (37 °C). Herein, we hypothesized that the thermoresponsive hydrogels could produce self-assembled micelles with the dissolution of the alginate-g-PNIPAAm hydrogels in a biological fluid or drug release medium. If the drug was hydrophobic, the hydrogel eventually could release and produce drug-encapsulated micelles. In our experiments, we loaded the anticancer drug doxorubicin (DOX) into the alginate-g-PNIPAAm hydrogels and demonstrated that the hydrogels released DOX-encapsulated micelles in a sustained manner. The slowly released DOX-loaded micelles enhanced the cellular uptake of DOX in multidrug resistant AT3B-1 cells, showing the effect of overcoming the drug resistance and achieving better efficiency for killing the cancer cells. Therefore, the injectable thermoresponsive hydrogels formed by alginate-g-PNIPAAm and loaded with DOX turned into a smart drug delivery system, releasing DOX-encapsulated micelles in a sustained manner, showing great potential for overcoming the drug resistance in cancer therapy.

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We propose a semiempirical nuclear mass formula based on the macroscopic-microscopic method in which the isospin and mass dependence of model parameters are investigated with the Skyrme energy density functional. The number of model parameters is considerably reduced compared with the finite range droplet model. The rms deviation with respect to 2149 measured nuclear masses is reduced by 21%, falling to 0.516 MeV. The new magic number N = 16 in light neutron-rich nuclei and the shape coexistence phenomena for some nuclei have been examined with the model. The shell corrections of superheavy nuclei are also predicted.

The symmetry energy obtained with the effective Skyrme energy density functional is related to the values of isoscalar effective mass and isovector effective mass, which is also indirectly related to the incompressibility of symmetric nuclear matter. In this work, we analyze the values of symmetry energy and its related nuclear matter parameters in five-dimensional parameter space by describing the heavy ion collision data, such as isospin diffusion data at 35 MeV/u and 50 MeV/u, neutron skin of 208 Pb, and tidal deformability and maximum mass of neutron star. We obtain the parameter sets which can describe the isospin diffusion, neutron skin, tidal deformability and maximum mass of neutron star, and give the incompressibility K0=250.23±20.16 MeV, symmetry energy coefficient S0=31.35±2.08 MeV, the slope of symmetry energy L=59.57±10.06 MeV, isoscalar effective mass m * s /m=0.75±0.05 and quantity related to effective mass splitting fI =0.005±0.170. At two times normal density, the symmetry energy we obtained is in 35-55 MeV. To reduce the large uncertainties of fI , more critical works in heavy ion collisions at different beam energies are needed.

Heavy metal ions, such as Hg(2+) and Ag(+), pose severe risks in human health and the environment. For sensitive detection and selective removal of Hg(2+) and Ag(+) ions, here, we demonstrate a surface-enhanced Raman scattering (SERS)-active platform by employing the oligonucleotide-functionalized magnetic silica sphere (MSS)@Au nanoparticles (NPs). This system exploits mismatched T-Hg-T and C-Ag-C bridges to capture Hg(2+) and Ag(+) ions, exhibiting excellent responses for Hg(2+) ions in the range of 0.1-1000 nM and for Ag(+) in the range of 10-1000 nM. The assay is highly selective for the target ions and does not respond to other metal ions. Additionally, the Hg(2+) and Ag(+) ions in this system can be effectively removed from surrounding solutions by an external magnetic field or through spontaneous precipitation. Moreover, more than 80% of the MSS@Au NPs can be easily recycled with the help of cysteine. We anticipate that the designed strategy could be extended to other analytes that can bind to DNA molecules with a high affinity, and can be used in many potential applications such as environmental renovation, toxin detection, and groundwater analysis.

Cartilage tissue engineering highly relies on the ability to store and transport chondrocytes in order to be clinically successful. Cryopreservation is a most reliable technology for chondrocyte storage, but it suffers from the intrinsic toxicity of current state-of-the-art cryoprotectant, dimethyl sulfoxide (DMSO). In this work, we used the first fully zwitterionic compound-based approach for effective chondrocyte cryopreservation. A zwitterionic molecule combined with zwitterionic polymers could balance intra/ extracellular osmotic stress and prevent ice formation, which were the keys of successful cryopreservation. Moreover, this zwitterionic combination showed noncytotoxicity due to its high biocompatibility, superior to cytotoxic DMSO. On the basis of these performances, chondrocytes could be well cryopreserved (∼90% post-thaw survival efficiency) for a long time without any addition of DMSO, and the recovered cells could maintain their normal functionalities. In view of the association between polymer molecular weight and cryopreservation efficacy, further mechanism of cryoprotection provided by zwitterionic molecule/polymer was proposed. This work opens a new window of opportunity for DMSO-free cryopreservation using biocompatible zwitterionic materials.