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The design of wound dressings with excellent self-healing ability, adequate adhesion, good biocompatibility, and potential antibacterial ability is of great significance for the healing of infected wounds arising from human activities. Herein, a series of multi-functional hydrogel dressings, poly(ionized isocyanoethyl methacrylate-glutamine)/poly(hexamethylene guanidine) (iGx/PHMGy) hydrogels, were obtained through homopolymerization of fully ionized isocyanoethyl methacrylate-glutamine (iIEM-Gln) in the presence of poly(hexamethylene guanidine) (PHMG), in which strong hydrogen bonds were formed among urea groups in the P (iIEM-Gln) chain to form a stable hydrogel network. The prepared iGx/PHMGy hydrogels exhibited adequate self-healing ability and tissue adhesion, which could be firmly adhered to the wound surface and remained intact during application. In addition, the presence of PHMG imparted good antibacterial activity to the hydrogels for the effective promotion of the wound healing in S. aureus infected skin wound on mice. Overall, this multi-functional hydrogel provides a facile and effective strategy for the design of infected wound dressings, and may show great potential in clinical applications.  相似文献   
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Lai  Chun-Kit  Tang  Sui 《Acta Appl Math》2019,164(1):65-81

We characterize the completeness and frame/basis property of a union of under-sampled windowed exponentials of the form

$$ {\mathcal{F}}(g): =\bigl\{ e^{2\pi i n x}: n\ge 0\bigr\} \cup \bigl\{ g(x)e^{2\pi i nx}: n< 0\bigr\} $$

for \(L^{2}[-1/2,1/2]\) by the spectra of the Toeplitz operators with the symbol \(g\). Using this characterization, we classify all real-valued functions \(g\) such that \({\mathcal{F}}(g)\) is complete or forms a frame/basis. Conversely, we use the classical non-harmonic Fourier series theory to determine all \(\xi \) such that the Toeplitz operators with the symbol \(e^{2\pi i \xi x}\) is injective or invertible. These results demonstrate an elegant interaction between frame theory of windowed exponentials and Toeplitz operators. Finally, we use our results to answer some open questions in dynamical sampling, and derivative samplings on Paley-Wiener spaces of bandlimited functions.

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Herein, we reported the formation mechanism of hybrid crystalline (cylindrite) in isotactic polypropylene (iPP)/carbon fiber (CF) via pulling a CF within the iPP melt. The α‐row nuclei layer closely attached to the surface of CF acts as a self‐nucleation site, rather than a heterogeneous nucleation one, to grow cylindrites. As a result, the polymorphic feature of iPP/CF cylindrite is significantly influenced by the microstructure of α‐row nuclei. With decreasing crystallization temperature (Tc), the polymorphic cylindrite changes from pure α‐form to mixed α‐/β‐form and to β‐rich form. The main characteristics of this change include: (a) the outlines of α‐row nuclei layer correspond to wave‐like, saw‐like, and straight lines; (b) the orientation level of iPP molecules in the α‐row nuclei layer become higher; (c) the α‐lamellae rearrange from loose to compact; and (d) the distance between the growth sites of β‐sectors and the surface of CF is evidently longer than in the case of α‐sectors. Moreover, this study provides a guideline for developing the interfacial enhanced iPP/CF composites through manipulation of polymorphic structure in cylindrites. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 368–377  相似文献   
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张成  许海涛  朱园园  汤俊  韦穗 《光子学报》2020,49(9):168-179
针对现有光学加密方法进行彩色图像加密时加密容量低、解密图像失真度高等问题,提出一种基于压缩全息和空分复用的多彩色图像加密方法.在光学加密阶段,结合改进的Mach-Zehnder干涉仪与空分复用技术,通过不同的随机相位掩膜对多幅彩色图像进行同时加密,仅需单次曝光即可得到由多幅彩色图像加密的全息图.在解密过程中,由于记录全息图的过程可建模为压缩感知过程,使用两步迭代收缩/阈值算法即可求解.实验结果表明,提出的加密系统加密容量大,解密重建图像质量高,结合压缩感知理论,有效地消除了同轴全息中平方场项对解密重建性能的影响,解密图像平均峰值信噪比仅下降约2~5dB;密钥安全性高,随机相位掩膜与传播距离均起到密钥的作用,在随机相位掩膜错误或传播距离仅偏移0.25%时,便无法解密出原始彩色图像;且对噪声与遮挡性攻击具有良好的鲁棒性,解密重建性能随噪声增大下降趋势缓慢,加密全息图80%信息受到遮挡性攻击时,仍可取得良好的解密重建结果.  相似文献   
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Journal of Solid State Electrochemistry - Self-supporting porous Ni film with uniform honeycomb-like micropores and a thickness of up to 66&nbsp;μm is electrodeposited by dynamic hydrogen...  相似文献   
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In this paper, the problem of the uniform stability for a class of fuzzy fractional-order genetic regulatory networks with random discrete delays, distributed delays, and parameter uncertainties is studied. Although there is a portion of literature on using fixed point theorems to study the stability of fractional neural networks, most of them required the fractional order to be in 1 2 , 1 . However, the case of the fractional-order belonging to ( 0 , 1 2 ) has not been discussed. To solve it, this work proposes a novel idea of using fixed point theory to study the stability of fuzzy (0,1) order neural networks, the problem of the uniqueness of the solution of the considered genetic regulatory networks is resolved, and a novel sufficient condition to guarantee the uniform stability of above genetic regulatory networks is also derived. Eventually, an example is given to demonstrate that the obtained result is effective.  相似文献   
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The pH‐sensitive tertiary amino groups were introduced to synthesize temperature and pH dual‐sensitive degradable polyaspartamide derivatives (phe/DEAE‐g‐PHPA) containing pendant aromatic structures and ionizable tertiary amino groups. The thermo/pH‐responsive behavior of phe/DEAE‐g‐PHPA polymer can be tuned by adjusting the graft copolymer composition. Due to the pH sensitivity of the phe/DEAE‐g‐PHPA‐g‐mPEG polymer with hydrophilic long PEG chain, the micelles and the anticancer drug‐loaded micelles were prepared by a quick pH‐changing method without using toxic organic solvent. The obtained polymeric micelles, paclitaxel‐loaded micelles and doxorubicin‐loaded micelles were stable under physiological conditions. Both the drug‐loaded micelles showed much faster release at pH 5 than at pH 7.4. The doxorubicin‐loaded micelles showed obvious and better anticancer activity against both HepG2 and HeLa cells than free doxorubicin. Thus these nontoxic, dual thermo‐ and pH‐sensitive phe/DEAE‐g‐PHPA‐g‐mPEG micelles may be a promising anticancer drug delivery system. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 879–888  相似文献   
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