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1.
Refractory wounds have always been an important issue to healthcare systems, whose healing process is always delayed by multiple factors, including bacterial infections, chronic inflammation, and excessive exudates, etc. Employing multifunctional wound dressings is recognized as an effective strategy to deal with refractory wounds, which has yielded promising outcomes in recent years. Among these advanced wound dressings, fibrous dressings have gained growing attention due to their unique merits. Such wound dressings have demonstrated great potential in delivering theranostic agents, such as antibacterial agents, anti-inflammatory drugs, growth factors, and diagnostic probes, etc., for the purposes of accelerating wound healing. This paper reviews the development of multifunctional fibrous dressings and their applications in treating refractory wounds. The construction approaches of novel fibrous dressing with capabilities of antibacterial, anti-inflammation, exudate management and diagnosis were also introduced. Furthermore, the existing problems and challenges are also discussed briefly.  相似文献   
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Tian  Xiu-Zhi  Yang  Rui  Ma  Jia-Jia  Ni  Yong-Hao  Deng  Hai-Bo  Dai  Lei  Tan  Jiao-Jun  Zhang  Mei-Yun  Jiang  Xue 《高分子科学》2022,40(7):789-798
Chinese Journal of Polymer Science - Antistatic and strength properties are of vital importance for polyurethane rubber used in moving parts of many industrial instruments. Herein, polyurethane was...  相似文献   
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为解决深度学习在图像水印算法中计算量大且模型冗余的问题,提高图像水印算法在抵抗噪声、旋转和剪裁等攻击时的鲁棒性,提出基于快速神经网络架构搜索(neural architecture search,NAS)的鲁棒图像水印网络算法。通过多项式分布学习快速神经网络架构搜索算法,在预设的搜索空间中搜索最优网络结构,进行图像水印的高效嵌入与鲁棒提取。首先,将子网络中线性连接的全卷积层设置为独立的神经单元结构,并参数化表示结构单元内节点的连接,预先设定结构单元内每个神经元操作的搜索空间;其次,在完成一个批次的数据集训练后,依据神经元操作中的被采样次数和平均损失函数值动态更新概率;最后,重新训练搜索完成的网络。水印网络模型的参数量较原始网络模型缩减了92%以上,大大缩短了模型训练时间。由于搜索得到的网络结构更为紧凑,本文算法具有较高的时间性能和较好的实验效果,在隐藏图像时,对空域信息的依赖比原始网络更少。对改进前后的2个网络进行了大量鲁棒性实验,对比发现,本文算法在CIFAR-10数据集上对抵抗椒盐噪声和旋转、移除像素行(列)等攻击优势显著;在ImageNet数据集上对抵抗椒盐高斯噪声、旋转、中值滤波、高斯滤波、JPEG压缩、裁剪等攻击优势显著,特别是对随机移除行(列)和椒盐噪声有较强的鲁棒性。  相似文献   
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International Journal of Theoretical Physics - Quantum coherence, coming from quantum superposition, occupies a significant position in the field of physics. We put forward a lower bound of the...  相似文献   
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By linking the carbazole unit to the nitrogen atom of acridone through phenyl or pyridyl, two compounds, named 10-(4-(9H-carbazol-9-yl)phenyl)acridin-9(10H)-one (AC-Ph-Cz) and 10-(5-(9H-carbazol-9-yl)pyridin-2-yl)acridin-9(10H)-one (AC-Py-Cz) were designed and synthesized. These two materials, characterized with highly twisted and rigid structure, good thermal stability, and balanced carrier-transporting properties, were employed as host materials for green phosphorescent and thermally activated delayed fluorescent organic light-emitting diodes (OLEDs). The carbazole group, despite its small contribution to the highest occupied molecular orbitals (HOMOs) of these two materials, plays an essential role as an intramolecular host in energy delivering and improving the hole transporting ability of these two hosts. The incorporation of the electron-deficient pyridyl group as a linking group slightly improves the electron transporting capability of AC-Py-Cz. The green phosphorescent OLED (PhOLED) based on AC-Py-Cz exhibited excellent device performance with a turn-on voltage of 2.5 V, a maximum power efficiency and an external quantum efficiency (ηext) of 89.8 lm W−1 and 25.2 %, respectively, benefitting from the better charge-balancing ability of AC-Py-Cz host due to the presence of the pyridyl bridge. More importantly, all the devices based on these two hosts showed low efficiency roll-off at high brightness due to the suppressed non-radiative transition in the emitting layer. In particular, the AC-Py-Cz-hosted green PhOLED exhibited an efficiency roll-off of 1.6 % from the maximum next at a high brightness of 1000 cd m−2 and a roll-off of 15.9 % at an extremely high brightness of 10000 cd m−2. This study manifests that acridone-based host materials have great potential in fabricating OLEDs with low efficiency roll-off.  相似文献   
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We studied the ring opening of propylene oxide (PO) by salen-M coordinated OH group [M = Al(III), Sc(III), Cr(III), Mn(III), Fe(III), Co(II), Co(III), Ni(II), Cu(II), Zn(II), Ru(III) and Rh(III)]. The results show that the ring-opening energy barriers for M(II) complexes are much lower than those with M(III) complexes in the gas phase, and the barriers correlate linearly with the negative charges on the OH group and the Fukui function condensed on the OH group. The nucleophilicity ordering in the gas phase can be rationalized by the ratio of formal positive charges/radius of M cations. Solvent effect greatly increases the barriers of M(II) complexes but slightly changes the results of M(III) ones, making the barriers similar. Analysis indicates that the reaction heats are linearly proportional to the reverse reaction barriers. The relationships established here can be used to estimate the ring-opening barriers and to screen epoxide ring-opening catalysts.  相似文献   
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Annals of the Institute of Statistical Mathematics - To obtain M-estimators of a response variable when the data are missing at random, we can construct three bias-corrected nonparametric...  相似文献   
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