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991.
Selenium nanoparticles (SeNPs) are considered to be the new selenium supplement forms with high biological activity and low toxicity; however, the molecular mechanism by which SeNPs exert the biological function is unclear. Here, we reported that biocompatibility SeNPs possessed intrinsic oxidase-like activity. Using Na2SeO3 as a precursor and glutathione as a reductant, biocompatibility SeNPs were synthesized by the wet chemical reduction method in the presence of bovine serum albumin (BSA). The results of structure characterization revealed that synthesized SeNPs were amorphous red elementary selenium with spherical morphology, and ranged in size from 25 to 70 nm size with a narrow distribution (41.4 ± 6.7 nm). The oxidase-like activity of the as-synthesized SeNPs was tested with 3,3′,5,5′-tetramethylbenzidine (TMB) as a substrate. The results indicated that SeNPs could catalyze the oxidization of TMB by dissolved oxygen. These SeNPs showed an optimum catalytic activity at pH 4 and 30 °C, and the oxidase-like activity was higher as the concentration of SeNPs increased and the size of SeNPs decreased. The Michaelis constant (K m) values and maximal reaction velocity (V max) of the SeNPs for TMB oxidation were 0.0083 mol/L and 3.042 μmol/L min, respectively.  相似文献   
992.
The lateral current-induced spin polarization in InGaN/GaN superlattices (SLs) without an applied magnetic field is reported. The fact that the sign of the nonequilibrium spin changes as the current reverses and is opposite for the two edges provides a clear signature for the spin Hall effect. In addition, it is discovered that the spin Hall effect can be strongly manipulated by the internal strains. A theoretical work has also been developed to understand the observed strain-induced spin polarization. Our result paves an alternative way for the generation of spin polarized current.  相似文献   
993.
Jiang H  Wen H  Zheng X  Liu Z  Wang K  Zhang H  Guo Y 《Optics letters》2007,32(17):2580-2582
By employing the self-modulation birefringence difference in a semiconductor optical amplifier (SOA), an improved method is proposed to generate a complete optical single-sideband (OSSB) signal. Over 30 dB sideband suppression ratios (SSRs) of lower OSSB signals are obtained over a 12 dB input power range and a 36 nm wavelength span, with a maximum of over 35 dB. Upper OSSB signals with an SSR of over 15 dB are observed using a SOA for what is believed to be the first time. This method is effective even for the carrier-suppressed signal. The theory for OSSB generation in an SOA is extended and verified by experiment.  相似文献   
994.
We consider the influence of the local squeezed vacuum fields on two initially entangled two-qubit system. By considering the upper bound of entanglement under time evolution, we find that the decay of the quantum entanglement shows different behavior for different time scales (t?max{(2βA)−1,(2βB)−1}t?max{(2βA)−1,(2βB)−1} and t?min{(2βA)−1,(2βB)−1}t?min{(2βA)−1,(2βB)−1}). The relative phase of the squeezing environment can also affect the entanglement dynamics profoundly.  相似文献   
995.
996.
Polyethylene glycol-modified canine uricase (PEG-UHC) was prepared by modifying the ε-amino group of lysine residues on the canine uricase (UHC) protein to near-saturation with 5 kDa monomethoxyl-polyethylene glycol succinimide (mPEG-SPA-5k). In order to accurately determine the PEGylation uniformity of PEG-UHC, CZE, 3–8% gradient gel SDS-PAGE, and imaging CIEF (iCIEF) analyses were compared. CZE could not effectively separate PEG-UHC proteins with different degrees of modification, 3–8% gradient gel SDS-PAGE could separate PEG-UHC into seven gel bands; however, most of the gel bands were smeared or blurred, and the separation of PEG-UHC samples by iCIEF was significantly better than that by 3–8% gradient gel SDS-PAGE. Under denatured conditions, iCIEF separated 12 pI peaks, and could also accurately quantify the relative monomer PEG-UHC content. More than 85% of the total monomeric PEG-UHC was conjugated with 7–12 PEG molecules; of this 85%, approximately 40% was conjugated with 9–10 PEG molecules. These results demonstrated that iCIEF exhibits good potential for determining the PEGylation homogeneity of PEGylated protein drugs.  相似文献   
997.
Journal of Radioanalytical and Nuclear Chemistry - The rapid measurement of radon progeny concentration is of great significance for improving the efficiency of radon exposure dose evaluation in a...  相似文献   
998.
研究高活性和稳定性的非贵金属基析氢催化剂对解决当前能源危机和环境污染问题具有重要意义.碳化钨具有与贵金属Pt类似的d带电子结构,因而成为一类新兴的非贵金属析氢催化剂,受到广泛关注.磷掺杂是提高催化剂析氢活性的有效方法之一,然而目前最常见的构筑磷掺杂方法是使用多金属氧酸盐(POMs,如H3PW12O40),其固定的W/P原子比导致W2C中的掺杂浓度难以调控,并且磷掺杂主要是进入碳载体而不是碳化物本身,从而导致无法明确杂原子对其电催化析氢活性的贡献.本文采用植酸(PA)为磷源设计合成了可控磷掺杂W2C纳米颗粒,并探讨了催化剂组分、杂原子掺杂位置与析氢性能之间的关系.深入研究了磷掺杂碳化钨(WCP)的化学结构和析氢活性.与原始的W2C催化剂相比,WCP具有更高的本征活性、更快的电子转移速率和更多的活性位数量,并且在酸性和碱性条件下均表现出较好的析氢性能.特别是过电位为-200 mV时,WCP催化剂的本征活性在酸性和碱性条件下分别为0.07和0.56 H2 s-1,高出纯W2C(0.01和0.05 H2 S-1)数倍.同时,在电流密度为-10 mA cm-2时,优化后的WCP催化剂在酸性和碱性条件下的析氢过电位分别降低了96和88 mV.XPS及EDS元素分析结果表明,随磷源添加量增加,磷掺杂从碳化钨表面逐渐向内部扩散,进一步说明磷取代位置与析氢活性之间的构效关系,高浓度的表面磷取代可以加速质子捕获过程,从而显著提高其析氢活性,而过量的内部磷取代会破坏W2C结构,降低电子转移速率,从而导致析氢性能下降.利用密度泛函理论计算深入研究了WCP具有较好析氢性能的原因,与内部磷取代相比,表面磷取代会使碳化钨表现出更合适的氢吸附自由能,并且更加有效地降低了氢释放势垒,从而优化了析氢反应动力学.综上,本文为元素掺杂工艺提供了新的思路,同时研究了表面异质原子对析氢活性的关键作用,为该类催化材料的构效关系研究提供了新思路.  相似文献   
999.
Guo  Leilei  Wang  Quanxiu  Shi  Qingqing  Guan  Ruolin  Zhao  Liping  Yang  Hanmin 《Transition Metal Chemistry》2021,46(1):37-47
Transition Metal Chemistry - In this study, the shape-controlled synthesis of ruthenium (Ru) nanostructures was examined using microwave irradiation. Dendritic Ru nanostructures, with an average...  相似文献   
1000.
The abuse of antibiotics will cause an increase of drug-resistant strains and environmental pollution,which in turn will affect human health.Therefore,it is important to develop effective detection techniques to determine the level of antibiotics contamination in various fields.Compared with traditional detection methods,electrochemical sensors have received extensive attention due to their advantages such as high sensitivity,low detection limit,and good selectivity.In this mini review,we summarized the latest developments and new trends in electrochemical sensors for antibiotics.Here,modification methods and materials of electrode are discussed.We also pay more attention to the practical applications of antibiotics electrochemical sensors in different fields.In addition,the existing problems and the future challenges ahead have been proposed.We hope that this review can provide new ideas for the development of electrochemical sensors for antibiotics in the future.  相似文献   
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