Catarina Meliana , Michelle Tien Tien Tan , Hwei-San Loh , Weihua Meng , Cheng Heng Pang , Sze Shin Low
{"title":"用于食品安全致癌物质丙烯酰胺和甲醛监测的绿色电化学生物传感器","authors":"Catarina Meliana , Michelle Tien Tien Tan , Hwei-San Loh , Weihua Meng , Cheng Heng Pang , Sze Shin Low","doi":"10.1016/j.bioelechem.2025.109122","DOIUrl":null,"url":null,"abstract":"<div><div>Food safety monitoring demands practical strategies for detecting chemical hazards such as acrylamide (AA) and formaldehyde (FA), both classified as probable human carcinogens with dietary exposures often exceeding tolerable limits. Conventional methods including GC–MS and HPLC, while sensitive, are costly, labour-intensive, and unsuitable for rapid on-site testing. Here, we report green electrochemical biosensors for AA and FA detection that integrate environmentally friendly graphene with 1-pyrenebutyric acid N-hydroxysuccinamide ester (PyrNHS) on disposable screen-printed carbon electrodes (SPCEs). Graphene was synthesized via liquid-phase exfoliation in an ethanol–water system, producing few-layer structures with abundant functional groups for stable bioreceptor attachment. PyrNHS enabled noncovalent anchoring and oriented immobilization of hemoglobin (Hb) for AA and formaldehyde dehydrogenase (FDH) for FA, overcoming limitations of costly and unstable nanomaterials. The AA biosensor operated through a signal-off mechanism using differential pulse voltammetry, with a detection limit of 4.39 μM over 0–25 μM. The FA biosensor employed a signal-on enzymatic mechanism with chronoamperometry, achieving 0.02 mM detection limit across 0.1–0.6 mM. Both sensors showed high selectivity, reproducibility (RSD <1.3 %), and effective performance in instant coffee, consistent with roasting chemistry and validated by Nash assay. This work demonstrates a sustainable, low-cost, and portable platform for point-of-care (POC) carcinogen monitoring.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"168 ","pages":"Article 109122"},"PeriodicalIF":4.5000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Green electrochemical biosensor for food safety monitoring of carcinogenic acrylamide and formaldehyde\",\"authors\":\"Catarina Meliana , Michelle Tien Tien Tan , Hwei-San Loh , Weihua Meng , Cheng Heng Pang , Sze Shin Low\",\"doi\":\"10.1016/j.bioelechem.2025.109122\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Food safety monitoring demands practical strategies for detecting chemical hazards such as acrylamide (AA) and formaldehyde (FA), both classified as probable human carcinogens with dietary exposures often exceeding tolerable limits. Conventional methods including GC–MS and HPLC, while sensitive, are costly, labour-intensive, and unsuitable for rapid on-site testing. Here, we report green electrochemical biosensors for AA and FA detection that integrate environmentally friendly graphene with 1-pyrenebutyric acid N-hydroxysuccinamide ester (PyrNHS) on disposable screen-printed carbon electrodes (SPCEs). Graphene was synthesized via liquid-phase exfoliation in an ethanol–water system, producing few-layer structures with abundant functional groups for stable bioreceptor attachment. PyrNHS enabled noncovalent anchoring and oriented immobilization of hemoglobin (Hb) for AA and formaldehyde dehydrogenase (FDH) for FA, overcoming limitations of costly and unstable nanomaterials. The AA biosensor operated through a signal-off mechanism using differential pulse voltammetry, with a detection limit of 4.39 μM over 0–25 μM. The FA biosensor employed a signal-on enzymatic mechanism with chronoamperometry, achieving 0.02 mM detection limit across 0.1–0.6 mM. Both sensors showed high selectivity, reproducibility (RSD <1.3 %), and effective performance in instant coffee, consistent with roasting chemistry and validated by Nash assay. This work demonstrates a sustainable, low-cost, and portable platform for point-of-care (POC) carcinogen monitoring.</div></div>\",\"PeriodicalId\":252,\"journal\":{\"name\":\"Bioelectrochemistry\",\"volume\":\"168 \",\"pages\":\"Article 109122\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioelectrochemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1567539425002257\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioelectrochemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567539425002257","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Green electrochemical biosensor for food safety monitoring of carcinogenic acrylamide and formaldehyde
Food safety monitoring demands practical strategies for detecting chemical hazards such as acrylamide (AA) and formaldehyde (FA), both classified as probable human carcinogens with dietary exposures often exceeding tolerable limits. Conventional methods including GC–MS and HPLC, while sensitive, are costly, labour-intensive, and unsuitable for rapid on-site testing. Here, we report green electrochemical biosensors for AA and FA detection that integrate environmentally friendly graphene with 1-pyrenebutyric acid N-hydroxysuccinamide ester (PyrNHS) on disposable screen-printed carbon electrodes (SPCEs). Graphene was synthesized via liquid-phase exfoliation in an ethanol–water system, producing few-layer structures with abundant functional groups for stable bioreceptor attachment. PyrNHS enabled noncovalent anchoring and oriented immobilization of hemoglobin (Hb) for AA and formaldehyde dehydrogenase (FDH) for FA, overcoming limitations of costly and unstable nanomaterials. The AA biosensor operated through a signal-off mechanism using differential pulse voltammetry, with a detection limit of 4.39 μM over 0–25 μM. The FA biosensor employed a signal-on enzymatic mechanism with chronoamperometry, achieving 0.02 mM detection limit across 0.1–0.6 mM. Both sensors showed high selectivity, reproducibility (RSD <1.3 %), and effective performance in instant coffee, consistent with roasting chemistry and validated by Nash assay. This work demonstrates a sustainable, low-cost, and portable platform for point-of-care (POC) carcinogen monitoring.
期刊介绍:
An International Journal Devoted to Electrochemical Aspects of Biology and Biological Aspects of Electrochemistry
Bioelectrochemistry is an international journal devoted to electrochemical principles in biology and biological aspects of electrochemistry. It publishes experimental and theoretical papers dealing with the electrochemical aspects of:
• Electrified interfaces (electric double layers, adsorption, electron transfer, protein electrochemistry, basic principles of biosensors, biosensor interfaces and bio-nanosensor design and construction.
• Electric and magnetic field effects (field-dependent processes, field interactions with molecules, intramolecular field effects, sensory systems for electric and magnetic fields, molecular and cellular mechanisms)
• Bioenergetics and signal transduction (energy conversion, photosynthetic and visual membranes)
• Biomembranes and model membranes (thermodynamics and mechanics, membrane transport, electroporation, fusion and insertion)
• Electrochemical applications in medicine and biotechnology (drug delivery and gene transfer to cells and tissues, iontophoresis, skin electroporation, injury and repair).
• Organization and use of arrays in-vitro and in-vivo, including as part of feedback control.
• Electrochemical interrogation of biofilms as generated by microorganisms and tissue reaction associated with medical implants.