Kim Do Hyoung, Oh Yoonbae, Shin Hojin, Park Cheonho, Blaha Charles D, Bennet Kevin E, Kim In Young, Lee Kendall H, Jang Dong Pyo
Department of Biomedical Engineering, Hanyang University, Seoul, Korea.
Department of Neurologic Surgery, Mayo Clinic, Rochester, MN 55905, United States.
Anal Methods. 2018 Jun 28;10(24):2834-2843. doi: 10.1039/C8AY00352A. Epub 2018 May 23.
Fast-scan cyclic voltammetry (FSCV) is an effective method for investigating electro-active neurochemical species. In recent years, FSCV has been used to measure electro-active neurotransmitters in a variety of neuroscience studies. We previously reported on the use of paired-pulse voltammetry (PPV) that enables FSCV to differentiate various analytes and minimize confounding factors by taking advantage of the adsorption characteristics of the analyte on carbon fiber microelectrodes. In spite of a number of studies regarding adsorption/desorption characteristics of neurotransmitters, the difference in adsorption/desorption properties among neurotransmitters has yet to be fully explored. To calculate adsorption/desorption constants for neurotransmitters, we propose the use of multi-waveform FSCV (M-FSCV), which consists of decade triangular waveforms in a single scan. Within the multiple waveforms, the voltammetric response of dopamine decayed exponentially because of the decreased adsorption time period. The decay pattern was mathematically described using adsorption/desorption characteristics and two additional initial points: an exponential decay constant (K) and an initial quantity (A), which were extracted from the decay equation. Using this method, we were able to quantify the decay constant (K-map) and an initial quantity (A-map) color plot in addition to a conventional pseudo color plot. M-FSCV was evaluated with two biogenic amine groups (catecholamines and indolamines) to characterize their inherent adsorption/desorption constants. As a result, the A-map showed a high correlation with concentration and the K-map for each group to be significantly differentiated. These results demonstrate that M-FSCV has the potential to be a useful technique for acquiring additional adsorption/desorption information regarding neurotransmitters.
快速扫描循环伏安法(FSCV)是研究电活性神经化学物质的有效方法。近年来,FSCV已被用于各种神经科学研究中测量电活性神经递质。我们之前报道了使用双脉冲伏安法(PPV),该方法通过利用分析物在碳纤维微电极上的吸附特性,使FSCV能够区分各种分析物并将混杂因素降至最低。尽管有许多关于神经递质吸附/解吸特性的研究,但神经递质之间吸附/解吸特性的差异尚未得到充分探索。为了计算神经递质的吸附/解吸常数,我们提出使用多波形FSCV(M-FSCV),它在单次扫描中由十进位三角波形组成。在多个波形中,多巴胺的伏安响应由于吸附时间段的减少而呈指数衰减。利用吸附/解吸特性和另外两个初始点,即从衰减方程中提取的指数衰减常数(K)和初始量(A),对衰减模式进行了数学描述。使用这种方法,除了传统的伪彩色图外,我们还能够量化衰减常数(K图)和初始量(A图)彩色图。用两个生物胺基团(儿茶酚胺和吲哚胺)对M-FSCV进行评估,以表征它们固有的吸附/解吸常数。结果,A图与浓度高度相关,并且每组的K图有明显差异。这些结果表明,M-FSCV有潜力成为获取有关神经递质额外吸附/解吸信息的有用技术。