Location privacy preservation approach towards to content sharing on mobile online social network

A privacy access control model for content sharing was presented to fine-grained control users' location infor-mation associated with sharing content in mobile social network. A k-anonymity privacy algorithm for privacy settings was given to protect against inference attack on a content sharing service provider server. To balance the privacy and quality of service, a location shifting method was presented. Finally experimental results demonstrate the validity and practicality of the proposed approach.     

Fast reused code tracing method based on simhash and inverted index

A novel method for fast and accurately tracing reused code was proposed. Based on simhash and inverted in-dex, the method can fast trace similar functions in massive code. First of all, a code database with three-level inverted in-dex structures was constructed. For the function to be traced, similar code blocks could be found quickly according to simhash value of the code block in the function code. Then the potential similar functions could be fast traced using in-verted index. Finally, really similar functions could be identified by comparing jump relationships of similar code blocks. Further, malware samples containing similar functions could be traced. The experimental results show that the method can quickly identify the functions inserted by compilers and the reused functions based on the code database under the premise of high accuracy and recall rate.     

聚甲基丙烯酸甲酯/星形聚乙二醇半互穿聚合物网络的形状记忆性能和分子机理

采用非共价复合方法,设计并合成了具有星形结构的聚甲基丙烯酸甲酯/星形聚乙二醇半互穿聚合物网络(PMMA/SPEG)和聚甲基丙烯酸甲酯/线性聚乙二醇半互穿聚合物网络(PMMA/LPEG).研究了PEG分子量对PMMA/SPEG和PMMA/LPEG的热性能、机械性能、动态机械性能和形状记忆性能的影响.结果表明,与PMMA/LPEG相比,星形结构的嵌入显著提高了PMMA/SPEG复合物的机械性能、形状回复率和回复速度.采用Edwards管道模型理论对其形状记忆效应的分子机理进行了阐释,利用材料的应力松弛特性对机理分析进行了验证.     

The Efect of Queueing Strategy on Network Trafc

In recent years,the transportation system has been faced by increasing challenge in congestion and inefciency,and research in trafc network has become a significant area of interest.In this paper,we introduce a dynamic-information-based(DIB)queueing strategy into network trafc model under the efcient routing strategy.DIB makes a packet with higher priority to be delivered if there are less packets travelling along its path from the current node to the destination.It is found that,compared with the traditional first-in-first-out(FIFO)queueing strategy,DIB can efectively balance the trafc load of the system via delaying packets to be delivered to congested nodes.Although the network capacity has no obvious changes,some other indexes which reflect transportation efciency are efciently improved in the congestion state.Besides,extensive simulation results and discussions are provided to explain the phenomena.The results may provide novel insights for research on trafc systems.     

个人便携式网络硬件防水墙设计

文中介绍了防水墙技术和数据包过滤技术,针对个人计算机网络安全的问题,设计了一种便携式的防水墙系统。本系统运用了防水墙技术和网络数据包过滤技术,采用MEGA128单片机控制DM9000网络控制器的方法,对本地计算机发出的数据进行过滤,达到了防止信息被窃取的目的。     

Synthesis of H (type 4) trisaccharide,key structural fragment of globo-H and fucosyl-GM1 cancer-associated antigens

A convenient synthesis of Fucα1-2Galβ1-3GalNAcβ-OCH₂CH₂CH₂NH₂ (trisaccharide H type 4) is described. This glycan is the terminal part of glycosphingolipids globo-H and fucosyl-GM1 known as cancer-associated carbohydrate antigens.     

The efficient in‐situ reduction and cyclization reaction of aromatic aldehyde, 1,3‐cyclopentanedione (tetronic acid), and nitro‐compound under SnCl2·2H2O‐THF medium

An efficient in‐situ reduction and cyclization reaction for the synthesis of pyrazolo[4,3‐f]quinoline, pyrazolo[3,4‐f]quinoline, and pyrazolo[3,2‐f]quinoline derivatives directly form 5‐nitroindazole, 6‐nitroindazole and 5‐nitroindole in the presence of SnCl₂·2H₂O was reported. Compared to traditional synthetic methods, this approach has the advantages of stable reagents, easy obtaining raw material, and high yields. In this research, SnCl₂·2H₂O is the efficient reducing agent for the in‐situ reduction and cyclization reaction of nitro‐compound. In addition, this process provided an alternative approach for the synthesis of target compounds.     

Single Beacon Cruise Positioning Algorithm in Wireless Sensor Networks

Node localization is important in WSNs （Wireless sensor networks） applications. We present a new cruise positioning algorithm, where a single beacon node cruises an entire network, broadcasting its position periodically with fixed signal strength. Meawhile, an unknown node obtains the location and the corresponding distance of the beacon node. Two possible position coordinate sets for the unknown node can then be calculated, and the coordinate mean of the point set with a small variance is an unbiased estimator of the unknown node＇s coordinate. The positioning algorithm＇s computation is simple, positioning accuracy is not limited by a physical distance measuring tool, and there are no restrictions on the path of motion, which makes it more realistic. An algorithm simulation is presented to compare the original and cruise location algorithm. Numerical results show that the cruise localization algorithm can achieve good positioning accuracy.     

Switchable peptide-equipped protein/cucurbit[7]uril supramolecular assembly for targeted drug delivery

ABSTRACT

Herein, we develop a switchable peptide-equipped protein/cucurbit[7]uril (CB[7]) supramolecular assembly as novel targeted drug vector. Specifically, bovine serum albumin (BSA) is used to interact with CB[7], serving as the core of drug vector. Then, a peptide shield layer is formed on the surface of BSA/CB[7], yielding peptide-equipped supramolecular assembly (Pep@BSA@CB[7]). The equipped peptide shield layer is composed of switchable peptide probes consisting of a polycationic cell-penetrating peptide (CPP) motif, a polyanionic motif and a linking motif, and therefore provides a variety of desirable properties. First, the CPP motif displays excellent cell penetration ability and can facilitate internalisation of the drug vector. Secondly, the polyanionic motif performs intramolecular electrostatic interaction with CPP motif and thereby can reduce non-targeted delivery towards normal cells. Thirdly, the linking motif can be specifically cleaved by matrix metalloproteinases 2 that is up-regulated in tumour microenvironment, thus enabling precise cancer-targeting. As a consequent, Pep@BSA@CB[7] can serve as a promising drug vector that exhibits superior targeting ability and high uptake efficiency towards cancer cells, which may be of great potential in cancer-targeted treatment.