The peroxidase-like catalytic activity of in situ prepared cobalt carbonate and its applications in colorimetric detection of hydrogen peroxide, glucose and ascorbic acid

过氧化氢 抗坏血酸 过氧化物酶 催化作用 化学 辣根过氧化物酶 基质(水族馆) 核化学 过氧化物 无机化学 组合化学 生物化学 有机化学 食品科学 地质学 海洋学
作者
Li‐Jing Peng,Chunyan Zhang,Weiyi Zhang,Hang‐Yu Zhou,Feng Yang
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:651: 129744-129744 被引量:18
标识
DOI:10.1016/j.colsurfa.2022.129744
摘要

In this study, the cobalt carbonate (CoCO3) was in situ prepared using cobalt (Ⅱ) and carbonate at room temperature, and the intrinsic peroxidase-like activity of CoCO3 was demonstrated for the first time through the oxidation of chromogenic substrate 3, 3', 5, 5' - tetramethylbenzidine (TMB) in the presence of hydrogen peroxide (H2O2). The effects of pH, reaction temperature, and incubation time on the catalytic activity of CoCO3 were studied. Under the optimal reaction conditions, the Michaelis constant (Km) of CoCO3 to H2O2 is 0.443 mM, which is lower than that of natural horseradish peroxidase and the previously reported peroxidase mimics. Furthermore, the mechanism exploration experiments confirm that the catalytic activity of CoCO3 is mainly attributed to the hydroxyl radical (•OH). Finally, based on the outstanding peroxidase-like activity of CoCO3, a colorimetric sensor for the detection of H2O2, glucose, and ascorbic acid (AA) was developed, which shows satisfactory selectivity and recovery. In addition, the total antioxidant capacity of three types of tea, dried lemon, three kinds of fresh fruit juice, and vitamin C tablet were determined. In short, this study reports a novel in situ generated CoCO3, which can be prepared rapidly at room temperature, eliminating the harsh, cumbersome, and time-consuming synthesis and purification process. The developed sensor based on the newly found excellent peroxidase-like activity of in situ prepared CoCO3 for the determination of H2O2, glucose, and AA is fast, simple, low cost, and high sensitivity.
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
同心渡完成签到,获得积分10
1秒前
jgn发布了新的文献求助10
1秒前
不吃了发布了新的文献求助10
1秒前
市井书生完成签到,获得积分10
1秒前
YU发布了新的文献求助30
3秒前
4秒前
zhouyan发布了新的文献求助10
4秒前
5秒前
自然心情完成签到 ,获得积分10
5秒前
5秒前
5秒前
丘比特应助wuwu采纳,获得10
6秒前
SciGPT应助无私的画笔采纳,获得10
6秒前
7秒前
yangjian完成签到,获得积分10
7秒前
8秒前
OKk完成签到,获得积分10
8秒前
魔幻雨梅发布了新的文献求助10
9秒前
日出发布了新的文献求助10
10秒前
笨笨雪碧发布了新的文献求助10
10秒前
Akim应助阿泓采纳,获得10
10秒前
wz完成签到,获得积分10
11秒前
动听藏今发布了新的文献求助10
11秒前
molihuakai应助mmyhn采纳,获得10
11秒前
聪明的阿呆完成签到,获得积分10
11秒前
11秒前
张一发布了新的文献求助10
11秒前
12秒前
molihuakai应助Hiiiiii采纳,获得30
13秒前
充电宝应助纯情的凡双采纳,获得10
13秒前
帅气大象发布了新的文献求助10
13秒前
Ava应助日出采纳,获得10
14秒前
CodeCraft应助linlineeeee采纳,获得10
14秒前
zhouyan完成签到,获得积分10
15秒前
pick发布了新的文献求助50
15秒前
TTT发布了新的文献求助10
16秒前
18秒前
Jasper应助儒雅龙采纳,获得10
18秒前
18秒前
Y888888应助小丸子呀采纳,获得10
18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
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Discerning Saints: Moralization of Intrinsic Motivation and Selective Prosociality at Work 500
Handbuch Trainingswissenschaft – Trainingslehre 500
Additive Manufacturing Design and Applications (ASM Handbook, Volume 24A) 500
Variations: A More Diverse Picture of Contemporary Art 400
Induction Heating and Heat Treatment (ASM Handbook, Volume 4C) 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7588695
求助须知:如何正确求助?哪些是违规求助? 9166861
关于积分的说明 19620186
捐赠科研通 7168621
什么是DOI,文献DOI怎么找? 3267087
关于科研通互助平台的介绍 2432000
邀请新用户注册赠送积分活动 2259085