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]
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
张张完成签到,获得积分10
1秒前
yuxinyue应助文件撤销了驳回
1秒前
王w发布了新的文献求助30
2秒前
2秒前
科研通AI6.2应助春深半夏采纳,获得10
3秒前
万能图书馆应助孙靖博采纳,获得10
3秒前
搜集达人应助yeahokk采纳,获得10
4秒前
4秒前
captainHc完成签到 ,获得积分10
6秒前
科研通AI6.2应助zh采纳,获得20
6秒前
丘比特应助认真的失败者采纳,获得10
6秒前
瑾色发布了新的文献求助10
7秒前
7秒前
俗人应助zz采纳,获得10
8秒前
压力是多的完成签到,获得积分10
8秒前
资明轩发布了新的文献求助10
10秒前
10秒前
yyx发布了新的文献求助10
12秒前
12秒前
12秒前
12秒前
13秒前
yjjslbyfbgfwz发布了新的文献求助10
13秒前
Akim应助狂野的皮带采纳,获得10
13秒前
我是老大应助xxz采纳,获得10
13秒前
ys1008发布了新的文献求助10
14秒前
14秒前
Zoeytam完成签到,获得积分10
14秒前
斯文败类应助一二三采纳,获得10
14秒前
14秒前
英俊的铭应助明亮从霜采纳,获得10
15秒前
思源应助曾经尔岚采纳,获得10
16秒前
今天喝咖啡吗完成签到,获得积分10
17秒前
吁慧洋发布了新的文献求助10
17秒前
karyoter发布了新的文献求助10
17秒前
汉堡包应助yjjslbyfbgfwz采纳,获得10
18秒前
汉堡包应助超帅孱采纳,获得30
19秒前
20秒前
th完成签到,获得积分10
20秒前
20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
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Les Mantodea de guyane 2500
Feldspar inclusion dating of ceramics and burnt stones 1000
What is the Future of Psychotherapy in a Digital Age? 801
The Psychological Quest for Meaning 800
Digital and Social Media Marketing 600
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5969202
求助须知:如何正确求助?哪些是违规求助? 7270802
关于积分的说明 15982574
捐赠科研通 5106528
什么是DOI,文献DOI怎么找? 2742565
邀请新用户注册赠送积分活动 1707584
关于科研通互助平台的介绍 1620960