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The ester bond as a universal linker has recently been applied in gene delivery systems owing to its efficient gene release by electrostatic repulsion after its cleavage. However, the ester bond is nonlabile and is difficult to cleave in cells. This work reports a method in which a secondary amine was introduced to the β-position of the ester bond to generate a hydrogen-bond cyclization (HBC) structure that can make the ester bond hydrolysis ultrafast. A series of molecules comprising ultrasensitive esters that can be activated by H2O2 were synthesized, and it was found that those able to form an HBC structure showed complete ester hydrolysis within 5 h in both water and phosphate-buffered saline solution, which was several times faster than other methods reported. Then, a series of amphiphilic poly(amidoamine) dendrimers were constructed, comprising the ultrasensitive ester groups for gene delivery; it was found that they could effectively release genes under quite a low concentration of H2O2 (<200 μm ) and transport them into the nucleus within 2 h in Hela cells with high safety. Their gene transfection efficiencies were higher than that of PEI25k. The results demonstrated that the hydrogen-bond-induced ultrasensitive esters could be powerfully applied to construct gene delivery systems.  相似文献   
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Han  Jing  Sun  Youhong  Guo  Wei  Deng  Sunhua  Hou  Chuanbin  Qu  Lili  Li  Qiang 《Journal of Thermal Analysis and Calorimetry》2019,135(4):2287-2296
Journal of Thermal Analysis and Calorimetry - In this study, the non-isothermal pyrolysis method was used to investigate the pyrolysis characteristics of oil shale from four areas: namely Nongan,...  相似文献   
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Conductive hydrogels with ionic compounds possess great potential for the development of soft smart devices. A dielectric scarfskin is typically required for these devices to prevent short circuiting, leading to devices with lower stretchability than the hydrogel. Henceforth, commonly used dielectric materials, such as PDMS and Ecoflex, cannot be largely stretched. Hydrogel devices with ultrastretchability are required to accommodate hostile application environments. Herein, we propose a hydrogel fiber coated with a dielectric layer that can be stretched to over 2000% of its initial length. The fiber remains conductive when stretched to ~1300%. In addition, the core/sheath hydrogel fiber can be endowed with a variety of functional properties, such as electroluminescence (EL), photoluminescence (PL), and magnetic‐responsiveness, demonstrating scalability of the resultant fiber. The present work can pave the way for numerous next‐generation soft devices, such as smart textiles and wearable electronics. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 272–280  相似文献   
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Tetrathiatriarylmethyl (TAM, trityl) radicals have found wide applications as spin probes/labels for EPR spectroscopy and imaging, and as polarizing agents for dynamic nuclear polarization. The high hydrophilicity of TAM radicals is essential for their biomedical applications. However, the synthesis of hydrophilic TAM radicals (e.g., OX063) is extremely challenging and has only been reported in the patent literature, to date. Herein, an efficient synthesis of a highly water-soluble TAM radical bis(8-carboxyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d′]bis([1,3]dithiol-4-yl)-mono-(8-carboxyl-2,2,6,6-tetrakis(2-hydroxyethyl)benzo[1,2-d:4,5-d′]bis([1,3]dithiol-4-yl)methyl (TFO), which contains four additional hydroxylethyl groups, relative to the Finland trityl radical CT-03, is reported. Similar to OX063, TFO exhibits excellent properties, including high water solubility in phosphate buffer, low log P, low pKa, long relaxation times, and negligible binding with bovine serum albumin. On the other hand, TFO has a sharper EPR line and higher O2 sensitivity than those of OX063. Therefore, in combination with its facile synthesis, TFO should find wide applications in magnetic resonance related fields and this synthetic approach would shed new light on the synthesis of other hydrophilic TAM radicals.  相似文献   
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王曲  王刚  韩建燊  张伟  赵鑫  张琪 《人工晶体学报》2019,48(9):1698-1702
以La2O3、Al2O3、ZrO2、Cr2O3、CaCO3为原料,通过高温固相反应法制备La1-xCaxAl0.8 Cr0.2O3/CaZrO3(0≤x≤0.2)复相陶瓷材料,分别通过XRD、SEM和EDS等仪器对试样的物相组成和显微结构进行分析,利用紫外可见近红外分光光度计测量其红外吸收曲线.结果 表明:当CaZrO3理论生成量和La1-xCaxAl0.8Cr0.2O3的摩尔比小于0.20时复相陶瓷材料在0.76~2.5 μm的发射率较La0.8 Ca0.2Al0.8Cr0.2O3得到进一步提高,当CaZrO3理论生成量和La1-xCaxAl0.8Cr0.2O3的摩尔比为0.04时发射率最佳.  相似文献   
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Propagation dynamics of the cosh-Airy vortex(CAiV) beams in a chiral medium is investigated analytically with Huygens–Fresnel diffraction integral formula. The results show that the CAiV beams are split into the left circularly polarized vortex(LCPV) beams and the right circularly polarized vortex(RCPV) beams with different propagation trajectories in the chiral medium. We mainly investigate the effect of the cosh parameter on the propagation process of the CAiV beams.The propagation characteristics, including intensity distribution, propagation trajectory, peak intensity, main lobe's intensity, Poynting vector, and angular momentum are discussed in detail. We find that the cosh parameter affects the intensity distribution of the CAiV beams but not its propagation trajectory. As the cosh parameter increases, the distribution areas of the LCPV and RCPV beams become wider, and the side lobe's intensity and peak intensity become larger. Besides, the main lobe's intensity of the LCPV and RCPV beams increase with the increase of the cosh parameter at a farther propagation distance, which is confirmed by the variation trend of the Poynting vector. It is significant that we can vary the cosh parameter to control the intensity distribution, main lobe's intensity, and peak intensity of the CAiV beams without changing the propagation trajectory. Our results may provide some support for applications of the CAiV beams in optical micromanipulation.  相似文献   
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Tetrakis(4‐(1‐bromoethyl)phenyl)silane is synthesized and utilized to initiate the atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) to generate bromo‐terminated four‐armed PMMA macroinitiators, which further initiate the ATRP of methylacryloyloxyl‐2‐hydroxypropyl perfluorooctanoate (FGOA) to create fluorinated star‐shaped block copolymers PMMA‐b‐poly(FGOA)s with fluorine content ranging from 0 to 31.7 wt %. The polymerizations are well controlled with the polydispersity indices <1.30. The polymers readily dissolve in common organic solvents and show good film‐formation. Compared with the nonfluorinated sample, the fluorinated films exhibit significantly increased water contact angles owing to the enrichment of fluorine on the surface. The enhanced hydrophobicity is advantageous for the optical stability when the devices work under a moist environment. Moreover, the films possess high thermo‐optic coefficients, tunable refractive indices, and extremely low birefringence coefficients because of the presence of bulky and rigid tetraphenylsilane core and star‐shaped topological structure, showing potential application in optical waveguide devices. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1969–1977  相似文献   
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