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Nanotip analysis for dielectrophoretic concentration of nanosized viral particles

机译:纳米提示分析纳米颗粒病毒的介电泳浓度

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Rapid and sensitive detection of low-abundance viral particles is strongly demanded in health care, environmental control, military defense, and homeland security. Current detection methods, however, lack either assay speed or sensitivity, mainly due to the nanosized viral particles. In this paper, we compare a dendritic, multi-terminal nanotip ('dendritic nanotip') with a single terminal nanotip ('single nanotip') for dielectrophoretic (DEP) concentration of viral particles. The numerical computation studies the concentration efficiency of viral particles ranging from 25 to 100 nm in radius for both nanotips. With DEP and Brownian motion considered, when the particle radius decreases by two times, the concentration time for both nanotips increases by 4-5 times. In the computational study, a dendritic nanotip shows about 1.5 times faster concentration than a single nanotip for the viral particles because the dendritic structure increases the DEP-effective area to overcome the Brownian motion. For the qualitative support of the numerical results, the comparison experiment of a dendritic nanotip and a single nanotip is conducted. Under 1 min of concentration time, a dendritic nanotip shows a higher sensitivity than a single nanotip. When the concentration time is 5 min, the sensitivity of a dendritic nanotip for T7 phage is 10~4 particles ml~(-1). The dendritic nanotip-based concentrator has the potential for rapid identification of viral particles.
机译:在医疗保健,环境控制,军事防御和国土安全方面,强烈需要快速,灵敏地检测低丰度病毒颗粒。然而,当前的检测方法缺乏测定速度或灵敏度,这主要是由于纳米级的病毒颗粒。在本文中,我们比较了树突状,多末端纳米尖端(“ dendritic nanotip”)和单末端纳米尖端(“ single nanotip”)的病毒颗粒介电电泳(DEP)浓度。数值计算研究了两个纳米尖端的半径为25至100 nm的病毒颗粒的浓缩效率。考虑DEP和布朗运动,当粒子半径减小两倍时,两个纳米尖端的浓缩时间都会增加4-5倍。在计算研究中,树突状纳米尖端显示的浓度比单个纳米尖端约快1.5倍,因为树突状结构增加了DEP有效面积以克服布朗运动。为了对数值结果提供定性支持,进行了树枝状纳米尖端和单个纳米尖端的比较实验。在1分钟的浓缩时间下,树状纳米尖端的灵敏度高于单个纳米尖端。当浓缩时间为5 min时,树突状纳米尖端对T7噬菌体的敏感性为10〜4个颗粒ml〜(-1)。基于树突纳米尖端的浓缩器具有快速识别病毒颗粒的潜力。

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