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Increasing density of antibody-antigen binding on a sensor surface by controlling microfluidic environments

机译:通过控制微流体环境提高传感器表面上抗体-抗原结合的密度

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Antibody-antigen reactions are widely used in biological detection. Researchers typically use either optical or electrical measurements to examine the sensing surface for specific antigens. Poor antibody-antigen density results in poor sensitivity of biological detection. The purpose of this research is to enhance antibody-antigen density on sensing surfaces by controlling the microenvironment. Vortices of samples were produced according to the structure and conditions of the microenvironment. Finite element analysis was used to compute the velocity field, streamline, and vorticity of samples in the microenvironment. Fluorescent particles were used to show streamline of samples experimentally. Experimental results were compared to simulated ones. Finally, Turnip Yellow Mosaic Virus (TYMV) was used as the specific antigen in the experiment. Experiment results showed that the density of TYMV detected by vortex microenvironment was 16.5 times greater than the density detected by a dipping method. The duration of experiment by vortex microenvironment was 2.3×10−4 times less than the duration by dipping method. This research offers a simple and efficient design that benefits rapid and real-time detection.
机译:抗体-抗原反应被广泛用于生物检测。研究人员通常使用光学或电学测量来检查感测表面上的特定抗原。抗体-抗原密度低会导致生物学检测的敏感性差。这项研究的目的是通过控制微环境来增强传感表面上的抗体抗原密度。根据微环境的结构和条件产生样品的涡流。有限元分析用于计算微环境中样品的速度场,流线和涡度。荧光颗粒用于显示实验的流线型。实验结果与模拟结果进行了比较。最后,萝卜黄花叶病毒(TYMV)被用作实验中的特异性抗原。实验结果表明,涡旋微环境检测到的TYMV密度是浸入法检测到的16.5倍。涡流微环境下的实验时间比浸渍法的实验时间短2.3×10 −4 倍。这项研究提供了一种简单而有效的设计,可帮助快速和实时检测。

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