Azita Mohammadi, Rezgar Ahmadi*, Abdollah Salimi* and Shamseddin Ahmadi,
{"title":"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","authors":"Azita Mohammadi, Rezgar Ahmadi*, Abdollah Salimi* and Shamseddin Ahmadi, ","doi":"10.1021/acsabm.5c0022610.1021/acsabm.5c00226","DOIUrl":null,"url":null,"abstract":"<p >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 H<sub>2</sub>O<sub>2</sub>, while its oxidase behavior was confirmed by oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) as chromogenic substrate in the presence of O<sub>2</sub> 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 H<sub>2</sub>O<sub>2</sub>-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.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":"8 4","pages":"3483–3497 3483–3497"},"PeriodicalIF":4.7000,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Azita Mohammadi, Rezgar Ahmadi*, Abdollah Salimi* and Shamseddin Ahmadi, \",\"doi\":\"10.1021/acsabm.5c0022610.1021/acsabm.5c00226\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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 H<sub>2</sub>O<sub>2</sub>, while its oxidase behavior was confirmed by oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) as chromogenic substrate in the presence of O<sub>2</sub> 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 H<sub>2</sub>O<sub>2</sub>-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. 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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.
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.