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根据多天线(MIMO)信道空间相关特性,提出一种虚拟子信道的分析方法,从子信道角度探讨信道容量在发射端已知信道响应时预期的性能改善;在此基础上,提出一种逼近信道容量上限的波束形成方法,发掘MIMO信道矩阵最大奇异值与波束形成矢量潜在的联系,并从理论角度详细分析了单用户与多用户最大奇异值联合分布特性,实现阵列增益、空间分集和多用户分集充分融合;仿真与分析表明,利用用户间潜在的随机分布特性能有效提高用户的空间分集增益,提高系统资源利用率,对系统性能改善显著. 相似文献
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传统的反汇编是静态进行的,它难以处理逻辑陷阱、花指令、代码中的数据、动态控制流等问题,这就导致其最终的反汇编结果可能不完整,存在错误.一段特意设计的代码,可以用动态控制流替代静态控制流;一段特意设计的花指令,可以让静态控制流关系任意复杂,这都将使静态反汇编分析难以进行.让代码运行起来,动态地进行反汇编,可以解决上述静态反汇编遇到的问题.结合计算机的中断处理机制,使得代码的实际执行路径是可知的.针对实际执行到的计算机指令进行反汇编,确保了反汇编结果的准确性;反复执行代码,在时间上进行积累,可以确保反汇编结果的完整性不断增加并趋于完整. 相似文献
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基于VPN技术,提出了一种为大公司分布在不同区域的分支机构提供一种非常廉价、安全、灵活自如的网络信息传输解决方案,并通过组建试验网络的测试,证明了方案的可行性. 相似文献
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A Novel Model System for Design of Biomaterials Based on Recombinant Analogs of Spider Silk Proteins
Vladimir G. Bogush Olga S. Sokolova Lyubov I. Davydova Dmitri V. Klinov Konstantin V. Sidoruk Natalya G. Esipova Tatyana V. Neretina Igor A. Orchanskyi Vsevolod Yu Makeev Vladimir G. Tumanyan Konstantin V. Shaitan Vladimir G. Debabov Mikhail P. Kirpichnikov 《Journal of neuroimmune pharmacology》2009,4(1):17-27
Spider dragline silk possesses impressive mechanical and biochemical properties. It is synthesized by a couple of major ampullate
glands in spiders and comprises of two major structural proteins—spidroins 1 and 2. The relationship between structure and
mechanical properties of spider silk is not well understood. Here, we modeled the complete process of the spider silk assembly
using two new recombinant analogs of spidroins 1 and 2. The artificial genes sequence of the hydrophobic core regions of spidroin
1 and 2 have been designed using computer analysis of existing databases and mathematical modeling. Both proteins were expressed
in Pichia pastoris and purified using a cation exchange chromatography. Despite the absence of hydrophilic N- and C-termini, both purified proteins
spontaneously formed the nanofibrils and round micelles of about 1 μm in aqueous solutions. The electron microscopy study
has revealed the helical structure of a nanofibril with a repeating motif of 40 nm. Using the electrospinning, the thin films
with an antiparallel β-sheet structure were produced. In summary, we were able to obtain artificial structures with characteristics
that are perspective for further biomedical applications, such as producing three-dimensional matrices for tissue engineering
and drug delivery.
Vladimir G Bogush and Olga S Sokolova contributed equally to the paper.
Name(s) of guarantors of the work: Mikhail P Kirpichnikov, Vladimir G Debabov.
Meeting presentation: Russian–American Nanomedicine Workshop, Moscow, 10–12 Dec 2007. 相似文献
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A Novel System Based on a Poloxamer/ PLGA Blend as a Tetanus Toxoid Delivery Vehicle 总被引:3,自引:0,他引:3
Tobío María Nolley Jessica Guo Yuyi McIver James José Alonso María 《Pharmaceutical research》1999,16(5):682-688
Purpose. Previous work on the encapsulation of proteins and antigens in poly(lactic-co-glycolic acid) (PLGA) microspheres has led to the conclusion that microencapsulated antigens are frequently inactivated due to their interaction with the polymer. To improve the compatibility of the antigen with the polymer, we have devised a novel microencapsulated system consisting of a blend of PLGA 50:50 and poloxamer 188 (Pluronic® F68) and applied it to the delivery of tetanus antigen.
Methods. Tetanus toxoid was encapsulated in microspheres containing different amounts of poloxamer using an anhydrous procedure based on an oil-in-oil solvent extraction process. The compatibility of the polymers was studied by Fourier transform infrared (FT-IR) spectroscopy. Microspheres were assayed in vitro and in vivo for their ability to deliver active antigen for extended periods of time.
Results. Analysis by FT-IR spectroscopy evidenced the miscibility of both polymers by a hydrogen bonding mechanism. In vitro release studies revealed that microspheres containing poloxamer released anti-genically active TT, in a pulsatile manner, for up to 50 days. In addition, it was observed that the intensity and duration of the pulses were dependent on both poloxamer content and TT loading in the microspheres. The in vivo evaluation of this new system showed that the neutralizing antibodies elicited by the TT encapsulated in poloxamer-PLGA microspheres were considerably higher and more prolonged than those obtained after administration of the aluminum phosphate-adsorbed toxoid.
Conclusions. These results indicate the importance of devising new microencapsulation approaches specially adapted for preserving the activity of protein antigens incorporated within PLGA microspheres. 相似文献