A structure-switching electrochemical aptamer sensor for mercury ions based on an ordered assembled gold nanorods-modified electrode

适体 纳米棒 循环伏安法 电化学气体传感器 微分脉冲伏安法 介电谱 电化学 二茂铁 电极 化学 检出限 分析化学(期刊) 选择性 氧化还原 无机化学 材料科学 纳米技术 物理化学 色谱法 有机化学 催化作用 遗传学 生物
作者
Liying Jiang,Ninghao Liu,Dongyang Li,Peijun Yin,Xinru Xu,Chuang Shang,Fenghua Chen,Xiaoyun Qin,Zhen Zhang
出处
期刊:Solid State Sciences [Elsevier BV]
卷期号:154: 107582-107582 被引量:8
标识
DOI:10.1016/j.solidstatesciences.2024.107582
摘要

In this paper, an electrochemical aptamer sensor with high sensitivity and selectivity was proposed for the detection of mercury ion (Hg2+). The orderly assembled gold nanorods-modified screen-printed electrode (AuNRs/SPE) was used to improve the sensor with higher sensitivity and data reproducibility. The sensor was designed based on the specific recognition of Hg2+ with aptamer to form T-Hg2+-T binding structure. Two aptamer chains were applied in the designed sensor, aptamer S1 with terminal thiolate group was self-assembled on the AuNRs/SPE via Au-S bond, and complementary S2 labeled with ferrocene (Fc) would generate a strong redox electrical signal. The addition of Hg2+ would mediate the folding of the T-base of S1 to form a hairpin structure, resulting in the dissociation of the Fc-labelled S2 from the sensing system and a significant reduction in the redox current. The electrochemical properties of the sensor were further investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). The effects of aptamer reaction time, concentration, and target incubation time on the sensor response were also investigated. The results showed that the sensor had a sensitive response to Hg2+ at concentrations ranging from 1 pM to 1 μM, with a detection limit of 0.3 pM. Furthermore, the proposed sensor was applied in the determination of Hg2+ in real samples, demonstrating its potential practical value.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Hello应助搞怪以莲采纳,获得10
1秒前
老豆完成签到 ,获得积分10
3秒前
3秒前
Heuoo发布了新的文献求助10
4秒前
4秒前
dedeyy发布了新的文献求助30
4秒前
wangziyuan完成签到,获得积分10
6秒前
小蘑菇应助三岁放火烧山采纳,获得10
6秒前
dappy完成签到 ,获得积分10
6秒前
7秒前
愤怒的玉兰完成签到,获得积分10
7秒前
Jasper应助憨憨采纳,获得10
8秒前
9秒前
三三发布了新的文献求助10
9秒前
可爱的函函应助王ccccc采纳,获得10
10秒前
Wr发布了新的文献求助10
11秒前
hqq完成签到,获得积分10
11秒前
陈宇静发布了新的文献求助20
12秒前
12秒前
15秒前
horizon完成签到,获得积分10
15秒前
didihe发布了新的文献求助10
16秒前
端庄大米发布了新的文献求助10
18秒前
19秒前
隐形曼青应助冯冯采纳,获得10
20秒前
20秒前
21秒前
豆包完成签到 ,获得积分10
23秒前
dddyrrrrr完成签到 ,获得积分10
23秒前
宋佳完成签到,获得积分10
25秒前
26秒前
科目三应助liuye0202采纳,获得10
27秒前
HQK发布了新的文献求助10
28秒前
28秒前
NexusExplorer应助空古悠浪采纳,获得10
29秒前
小鱼儿完成签到,获得积分10
29秒前
29秒前
30秒前
宫傲蕾完成签到 ,获得积分10
30秒前
给大佬带病历应助xwwx采纳,获得10
31秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Rosenblum, Global Change Biology 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Physiologic specialization in Peronospora manshurica 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7777335
求助须知:如何正确求助?哪些是违规求助? 9318430
关于积分的说明 20364044
捐赠科研通 7364442
什么是DOI,文献DOI怎么找? 3318940
关于科研通互助平台的介绍 2466605
邀请新用户注册赠送积分活动 2334142