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Sensor for Continuous and Real-Time Monitoring of Biomolecule Permeation Through Ultrathin Silicon Nanoporous Membranes

机译:通过超薄硅纳米多孔膜连续实时监测生物分子渗透的传感器

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摘要

The increase in demand for continuous and real-time monitoring of permeation of biomolecules is addressed by using highly selective ultrathin silicon nanoporous membranes (SNMs) combined with detection using ultraviolet absorption. The membranes, with an average pore size of 8.8 nm, are fabricated using semiconductor batch processes including chemical vapor deposition and rapid thermal annealing. Bovine serum albumin (BSA) of a concentration of 250 mu g/ml is used as the test molecule. The concentration of BSA diffused through the membrane is measured using optical transduction based in-house developed sensor. The photocurrent obtained from the sensor is measured every 15 min and compared with the standard Bradford assay at the same time-stamp. The concentration estimated by the sensor is found to agree with the Bradford assay with a standard deviation of 1.4%. The throughput of the membrane is increased by fabricating an array of SNMs, which showed an increase in diffusion rate by 3.8 times with respect to the single SNM. The clogging of pores by the biomolecules is analyzed using ionic conductivity experiments. The structural integrity of BSA diffused through the SNM is also analyzed.
机译:通过使用高度选择性的超薄硅纳米多孔膜(SNM)结合使用紫外线吸收的检测,可以解决对生物分子渗透的连续和实时监控的需求增加的问题。使用半导体间歇工艺(包括化学气相沉积和快速热退火)制造平均孔径为8.8 nm的膜。浓度为250μg / ml的牛血清白蛋白(BSA)用作测试分子。使用基于光学转导的内部开发的传感器测量通过膜扩散的BSA的浓度。每15分钟测量一次从传感器获得的光电流,并在同一时间戳下与标准Bradford分析进行比较。发现传感器估计的浓度与Bradford分析相符,标准偏差为1.4%。通过制造SNM阵列可以提高膜的通量,相对于单个SNM而言,SNM的扩散速率提高了3.8倍。使用离子电导率实验分析了生物分子对孔的堵塞。还分析了通过SNM扩散的BSA的结构完整性。

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