{"title":"Hemozoin anchored MWCNTs for mediated reduction of hydrogen peroxide and real-time intracellular oxidative stress monitoring in colon cancer cells.","authors":"Sakthivel Srinivas, Mouliganesh Sekar, Kavitha Thirumurugan, Annamalai Senthil Kumar","doi":"10.1039/d4tb01902d","DOIUrl":null,"url":null,"abstract":"<p><p>Hemozoin (HZ, a malarial pigment) is an insoluble crystalline byproduct formed during the intraerythrocytic breakdown of hemoglobin by some blood-feeding parasites, such as <i>Plasmodium falciparum</i>. It consists of polymerized iron-porphyrin molecular units linked by carboxylic bonds. Due to the rigid molecular structure, studying the electron transfer activity of HZ is challenging. In this work, we report the development of a redox-active HZ-functionalized multi-walled carbon nanotube (MWCNT) modified glassy carbon electrode (GCE/MWCNT@HZ-redox). Here, HZ-redox refers to the redox-active form of hemozoin. This electrode is designed to study the electron transfer activity and mimic the peroxidase enzyme's ability to mediate hydrogen peroxide reduction in a neutral pH solution. The modified electrode exhibited a stable and well-defined redox peak at -0.385 V <i>vs.</i> Ag/AgCl in N<sub>2</sub>-purged PBS (pH 7.0) with a surface excess value of 1.64 × 10<sup>-9</sup> mol cm<sup>-2</sup>. The MWCNT@HZ-redox was characterized using Raman spectroscopy, FT-IR, and FESEM techniques. This biomimicking electrode showed excellent electrocatalytic reduction of H<sub>2</sub>O<sub>2</sub> using cyclic voltammetry. Batch-injection analysis coupled with a screen-printed electrode demonstrated the electroanalytical performance for H<sub>2</sub>O<sub>2</sub> sensing. The electrode exhibited a linear concentration range of 50-300 μM, with a sensitivity of 21 μA μM<sup>-1</sup> and a detection limit of 220 nM. As a bioanalytical application, we successfully demonstrated the <i>in situ</i> monitoring of H<sub>2</sub>O<sub>2</sub> within the reactive oxygen species of HCT-116 colon cancer cells under stimulated conditions.</p>","PeriodicalId":94089,"journal":{"name":"Journal of materials chemistry. B","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of materials chemistry. B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/d4tb01902d","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hemozoin (HZ, a malarial pigment) is an insoluble crystalline byproduct formed during the intraerythrocytic breakdown of hemoglobin by some blood-feeding parasites, such as Plasmodium falciparum. It consists of polymerized iron-porphyrin molecular units linked by carboxylic bonds. Due to the rigid molecular structure, studying the electron transfer activity of HZ is challenging. In this work, we report the development of a redox-active HZ-functionalized multi-walled carbon nanotube (MWCNT) modified glassy carbon electrode (GCE/MWCNT@HZ-redox). Here, HZ-redox refers to the redox-active form of hemozoin. This electrode is designed to study the electron transfer activity and mimic the peroxidase enzyme's ability to mediate hydrogen peroxide reduction in a neutral pH solution. The modified electrode exhibited a stable and well-defined redox peak at -0.385 V vs. Ag/AgCl in N2-purged PBS (pH 7.0) with a surface excess value of 1.64 × 10-9 mol cm-2. The MWCNT@HZ-redox was characterized using Raman spectroscopy, FT-IR, and FESEM techniques. This biomimicking electrode showed excellent electrocatalytic reduction of H2O2 using cyclic voltammetry. Batch-injection analysis coupled with a screen-printed electrode demonstrated the electroanalytical performance for H2O2 sensing. The electrode exhibited a linear concentration range of 50-300 μM, with a sensitivity of 21 μA μM-1 and a detection limit of 220 nM. As a bioanalytical application, we successfully demonstrated the in situ monitoring of H2O2 within the reactive oxygen species of HCT-116 colon cancer cells under stimulated conditions.