Introducing Nanoscale Electrochemistry in Small-Molecule Detection for Tackling Existing Limitations of Affinity-Based Label-Free Biosensing Applications

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Don Hui Lee, Won-Yong Lee* and Jayoung Kim*, 
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Abstract

Electrochemical sensing techniques for small molecules have progressed in many applications, including disease diagnosis and prevention as well as monitoring of health conditions. However, affinity-based detection for low-abundance small molecules is still challenging due to the imbalance in target-to-receptor size ratio as well as the lack of a highly sensitive signal transducing method. Herein, we introduced nanoscale electrochemistry in affinity-based small molecule detection by measuring the change of quantum electrochemical properties with a nanoscale artificial receptor upon binding. We prepared a nanoscale molecularly imprinted composite polymer (MICP) for cortisol by electrochemically copolymerizing β-cyclodextrin and redox-active methylene blue to offer a high target-to-receptor size ratio, thus realizing “bind-and-read” detection of cortisol as a representative target small molecule, along with extremely high sensitivity. Using the quantum conductance measurement, the present MICP-based sensor can detect cortisol from 1.00 × 10–12 to 1.00 × 10–6 M with a detection limit of 3.93 × 10–13 M (S/N = 3), which is much lower than those obtained with other electrochemical methods. Moreover, the present MICP-based cortisol sensor exhibited reversible cortisol sensing capability through a simple electrochemical regeneration process without cumbersome steps of washing and solution change, which enables “continuous detection”. In situ detection of cortisol in human saliva following circadian rhythm was carried out with the present MICP-based cortisol sensor, and the results were validated with the LC–MS/MS method. Consequently, this present cortisol sensor based on nanoscale MICP and quantum electrochemistry overcomes the limitations of affinity-based biosensors, opening up new possibilities for sensor applications in point-of-care and wearable healthcare devices.

Abstract Image

在小分子检测中引入纳米电化学,以解决基于亲和的无标签生物传感应用的现有限制
小分子电化学传感技术在疾病诊断和预防以及健康状况监测等方面的应用取得了进展。然而,由于靶标与受体大小比的不平衡以及缺乏高灵敏度的信号转导方法,基于亲和的低丰度小分子检测仍然具有挑战性。本文通过测量纳米级人工受体结合后量子电化学性质的变化,将纳米电化学引入到亲和小分子检测中。我们通过电化学共聚β-环糊精和氧化还原活性亚甲基蓝制备了一种纳米级的皮质醇分子印迹复合聚合物(MICP),提供了高的靶受体尺寸比,从而实现了以皮质醇为代表的靶小分子的“结合-读取”检测,并且具有极高的灵敏度。采用量子电导测量,该传感器可检测1.00 × 10-12 ~ 1.00 × 10-6 M范围内的皮质醇,检出限为3.93 × 10-13 M (S/N = 3),远低于其他电化学方法。此外,目前基于micp的皮质醇传感器通过简单的电化学再生过程表现出可逆的皮质醇传感能力,无需繁琐的洗涤和溶液变化步骤,从而实现“连续检测”。采用基于micp的皮质醇传感器对人唾液中的皮质醇进行了昼夜节律原位检测,并用LC-MS /MS方法对结果进行了验证。因此,目前这种基于纳米级MICP和量子电化学的皮质醇传感器克服了基于亲和的生物传感器的局限性,为传感器在护理点和可穿戴医疗设备中的应用开辟了新的可能性。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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