Lee Chang Young, Strano Michael S
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Langmuir. 2005 May 24;21(11):5192-6. doi: 10.1021/la046867i.
Adsorption dynamics and their influence on signal transduction for carbon nanotube-based chemical sensors are explored using continuum site balance equations and a mass action model. These sensors are shown to possess both reversible and irreversible binding sites that can be modeled independently. For the case of irreversible adsorption, it is shown that the characteristic response time scales inversely with analyte concentration. It is inappropriate to report a detection limit for this type of sensor since any nonzero analyte concentration can be detected in theory but at a cost of increasing transduction time with decreasing concentration. The response curve should examine the initial rate of signal change as a function of analyte concentration. Conversely, a reversible sensor has a predefined detection limit, independent of the detector geometry with a characteristic time scaling that becomes constant in the zero analyte concentration limit. A simple analytical test is presented to distinguish between these two mechanisms from the transient response of a nanotube sensor array. Two systems appearing in the literature are shown to have an irreversible component, and regressed surface rate constants for this component are similar across different sensor geometries and analytes.
利用连续位点平衡方程和质量作用模型,探索了基于碳纳米管的化学传感器的吸附动力学及其对信号转导的影响。这些传感器具有可逆和不可逆结合位点,可独立建模。对于不可逆吸附的情况,结果表明特征响应时间与分析物浓度成反比。对于这类传感器,报告检测限是不合适的,因为理论上任何非零分析物浓度都可以检测到,但代价是随着浓度降低,转导时间会增加。响应曲线应检查信号变化的初始速率与分析物浓度的函数关系。相反,可逆传感器具有预定义的检测限,与检测器几何形状无关,在零分析物浓度极限下,特征时间尺度会变得恒定。提出了一种简单的分析测试方法,用于从纳米管传感器阵列的瞬态响应中区分这两种机制。文献中出现的两个系统显示具有不可逆成分,并且该成分的回归表面速率常数在不同的传感器几何形状和分析物之间相似。