CoCu@NC具有ph可切换和双酶活性的纳米酶:阿霉素的高灵敏度比色检测和h2o2诱导的DNA损伤的裸眼检测

IF 4.7 Q2 MATERIALS SCIENCE, BIOMATERIALS
Azita Mohammadi, Rezgar Ahmadi*, Abdollah Salimi* and Shamseddin Ahmadi, 
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引用次数: 0

摘要

具有多酶活性的纳米材料用于高级传感和生物传感检测已引起人们的关注。本研究合成了Cu-Co双金属氮掺杂碳催化剂(CoCu@NC)。通过调节pH,所制备的纳米材料表现出类似过氧化氢酶和氧化酶的活性。在H2O2存在下,对对苯二甲酸(TA)荧光在pH 11下猝灭,研究了CoCu@NC的类似过氧化氢酶活性,而在O2存在下,以3,3 ',5,5 ' -四甲基联苯胺(TMB)作为显色底物在pH 3下氧化,证实了其氧化酶行为。此外,CoCu@NC的氧化酶样活性成功地用于检测1 ~ 900 nM浓度范围内的对苯二酚(HQ),检测限为0.22 nM;通过还原oxTMB为TMB,抗癌药物阿霉素(DOX)具有5 ~ 200 pM的宽线性响应和1.66 fM的极低检测限。DOX在原位与单链DNA (ssDNA)和双链DNA (dsDNA)相互作用,将其结构中的醌环还原为对苯二酚(HQ),并将鸟嘌呤碱基氧化为8-氧鸟嘌呤。基于这一现象,我们设计了一种无标记比色传感器,用于测量DNA损伤(范围为1 pM至1 μM),该传感器通过蓝色oxTMB溶液的消失和DNA/DOX的存在来工作。此外,该传感器对ssDNA和dsDNA中鸟嘌呤碱基的数量敏感。随着DNA序列中鸟嘌呤碱基(1-12)数量的增加,观察到更大的颜色变化。最后,在h2o2诱导DNA损伤的情况下,DOX与DNA损伤序列之间没有嵌层,肉眼可见颜色变化。因此,该可视化实验证明了一种低成本、简单、快速、敏感和有效的检测DOX药物和受损DNA的方法。此外,CoCu@NC磁性纳米结构可以很容易地通过施加磁场来回收和再利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CoCu@NC Nanozyme with pH-Switchable and Dual Enzymatic Activity: Highly Sensitive Colorimetric Sensing of Doxorubicin and Naked-Eye Detection of H2O2-Induced DNA Damage

CoCu@NC Nanozyme with pH-Switchable and Dual Enzymatic Activity: Highly Sensitive Colorimetric Sensing of Doxorubicin and Naked-Eye Detection of H2O2-Induced DNA Damage

The development of nanomaterials with multienzyme activity for advanced sensing and biosensing assays has attracted attention. In this study, a Cu–Co bimetallic nitrogen-doped carbon catalyst (CoCu@NC) was synthesized. The prepared nanomaterials exhibit catalase- and oxidase-like mimicking activities by adjusting the pH. The catalase-like activity of the CoCu@NC was investigated by quenching of terephthalic acid (TA) fluorescence at pH 11 in the presence of H2O2, while its oxidase behavior was confirmed by oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) as chromogenic substrate in the presence of O2 at pH 3. Furthermore, CoCu@NC’s oxidase-like activity was used successfully to detect hydroquinone (HQ) at a concentration range of 1–900 nM with a detection limit of 0.22 nM and the anticancer drug doxorubicin (DOX) with a wide linear response ranging from 5 fM to 200 pM and an exceptionally low detection limit of 1.66 fM by reduction of oxTMB to TMB. DOX interacts in situ with single-stranded (ssDNA) and double-stranded DNA (dsDNA), reducing the quinone ring in its structure to hydroquinone (HQ) and oxidizing guanine bases to 8-oxoguanine. Based on this phenomenon, we designed a label-free colorimetric sensor for measuring DNA damage (ranging from 1 pM to 1 μM), in which this sensor operates by the disappearance of the blue oxTMB solution and the presence of the DNA/DOX. Furthermore, this designed sensor is sensitive to the number of guanine bases in ssDNA and dsDNA. As the number of guanine bases (1–12) in DNA sequences increases, a greater color change is observed. Finally, in the presence of H2O2-induced DNA damage, no intercalation occurred between DOX and the DNA-damaged sequences, with the color change observable with the naked eye. Therefore, this visualization assay demonstrates a low-cost, simple, rapid, sensitive, and effective method for detecting DOX drug and damaged DNA. Additionally, CoCu@NC magnetic nanostructures could be easily recollected and reused by applying a magnetic field.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊介绍: ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.
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