首页 > 最新文献

Sensing and Bio-Sensing Research最新文献

英文 中文
Machine learning-driven terahertz graphene-MXene-gold metasurface biosensor for dual COVID-19 and cervical cancer biomarker detection 机器学习驱动的太赫兹石墨烯- mxene -金超表面生物传感器,用于双重COVID-19和宫颈癌生物标志物检测
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-11-14 DOI: 10.1016/j.sbsr.2025.100920
Jacob Wekalao , Hussein A. Elsayed , Haifa A. Alqhtani , Mostafa R. Abukhadra , Ahmed Mehaney , Amuthakkannan Rajakannu
This study introduces a terahertz (THz) biosensor designed for rapid and precise detection of COVID-19 viral proteins and cervical cancer biomarkers. The device uses a metasurface structure composed of U-shaped MXene-coated resonators and L-shaped gold-coated elements on a graphene-functionalized circular platform built on a silicon dioxide substrate. It operates across 0.308–0.312 THz for COVID-19 detection and 0.799–0.809 THz for cervical cancer screening, achieving sensitivities of 200 GHz/RIU and 300 GHz/RIU. The corresponding figures of merit range from 2.222 to 2.667 RIU−1 for COVID-19 and 4.848–5.455 RIU−1 for cervical cancer, with quality factors above 14 for the latter. A one-dimensional convolutional neural network model optimized the sensor's response, reaching up to 95 % prediction accuracy and showing a strong linear correlation between resonance frequency and refractive index (R2 > 0.99). The architecture can be produced using standard lithography and thin-film deposition methods compatible with existing microelectronic processes. The design allows biofunctionalization with target proteins such as SARS-CoV-2 spike antigens and HPV-related biomarkers. Simulation results align with recent experimental findings in THz biosensing, supporting the feasibility of laboratory testing and clinical application.
本研究介绍了一种用于快速精确检测COVID-19病毒蛋白和宫颈癌生物标志物的太赫兹(THz)生物传感器。该装置采用了一种超表面结构,由u形mxene涂层谐振器和l形金涂层元件组成,该结构位于二氧化硅衬底上的石墨烯功能化圆形平台上。其检测范围为0.308-0.312太赫兹,宫颈癌筛查范围为0.799-0.809太赫兹,灵敏度分别为200 GHz/RIU和300 GHz/RIU。相应的优值在COVID-19的2.222 ~ 2.667 RIU−1和宫颈癌的4.848 ~ 5.455 RIU−1之间,后者的质量因子在14以上。一维卷积神经网络模型优化了传感器的响应,预测精度高达95%,共振频率与折射率之间存在很强的线性相关性(R2 > 0.99)。该结构可以使用与现有微电子工艺兼容的标准光刻和薄膜沉积方法来生产。该设计允许与靶蛋白(如SARS-CoV-2刺突抗原和hpv相关生物标志物)进行生物功能化。仿真结果与太赫兹生物传感的最新实验结果一致,支持实验室测试和临床应用的可行性。
{"title":"Machine learning-driven terahertz graphene-MXene-gold metasurface biosensor for dual COVID-19 and cervical cancer biomarker detection","authors":"Jacob Wekalao ,&nbsp;Hussein A. Elsayed ,&nbsp;Haifa A. Alqhtani ,&nbsp;Mostafa R. Abukhadra ,&nbsp;Ahmed Mehaney ,&nbsp;Amuthakkannan Rajakannu","doi":"10.1016/j.sbsr.2025.100920","DOIUrl":"10.1016/j.sbsr.2025.100920","url":null,"abstract":"<div><div>This study introduces a terahertz (THz) biosensor designed for rapid and precise detection of COVID-19 viral proteins and cervical cancer biomarkers. The device uses a metasurface structure composed of U-shaped MXene-coated resonators and L-shaped gold-coated elements on a graphene-functionalized circular platform built on a silicon dioxide substrate. It operates across 0.308–0.312 THz for COVID-19 detection and 0.799–0.809 THz for cervical cancer screening, achieving sensitivities of 200 GHz/RIU and 300 GHz/RIU. The corresponding figures of merit range from 2.222 to 2.667 RIU<sup>−1</sup> for COVID-19 and 4.848–5.455 RIU<sup>−1</sup> for cervical cancer, with quality factors above 14 for the latter. A one-dimensional convolutional neural network model optimized the sensor's response, reaching up to 95 % prediction accuracy and showing a strong linear correlation between resonance frequency and refractive index (R<sup>2</sup> &gt; 0.99). The architecture can be produced using standard lithography and thin-film deposition methods compatible with existing microelectronic processes. The design allows biofunctionalization with target proteins such as SARS-CoV-2 spike antigens and HPV-related biomarkers. Simulation results align with recent experimental findings in THz biosensing, supporting the feasibility of laboratory testing and clinical application.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100920"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145620293","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A nanobiosensor integrating FRET and MEF processes for fluorescence-based detection of Chlorpyrifos pesticide through AuNPs@ZIF-8 nanocomposite platform 通过AuNPs@ZIF-8纳米复合平台集成FRET和MEF过程的荧光检测毒死蜱农药的纳米生物传感器
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-11-14 DOI: 10.1016/j.sbsr.2025.100916
Zahra Jomeh Ghasem Abadi , Salehe Ganjali , Mehdi Dadmehr , Ziba Souri Nezami
Pesticide residues in agricultural products are considered as one of the most important health and economic challenges. Chlorpyrifos (CPF), as a widely used organophosphate pesticide in many developing countries, requires precise monitoring due to its adverse effects on human health and the environment. In this study, a novel nanobiosensor was designed and developed for the rapid and sensitive detection of CPF. The system was based on an AuNPs@ZIF-8 nanocomposite as a detection platform which coupled with fluorescence resonance energy transfer (FRET) and metal enhanced fluorescence mechanisms (MEF) processes, in which a CPF-specific aptamer was employed as the recognition element. FRET was occurred after oligonucleotides hybridization and following MEF process was observed after conjugation with nanocomposite. Subsequently, by addition of CPF target the fluorescence intensity of both applied released fluorophores was enhanced. The results demonstrated that the proposed sensor exhibited linear range between of 0.75–5.22 pM with very low detection limit (0.0817 pM). Moreover, performance evaluation in real pistachio samples showed satisfactory recovery (83–95 %) and good reproducibility (RSD: 5.3–6.4 %). Overall, this nanobiosensor can serve as an efficient and reliable tool for the rapid monitoring of chlorpyrifos in agricultural products and for improving quality control in the food industry.
农产品中的农药残留被认为是最重要的健康和经济挑战之一。毒死蜱是许多发展中国家广泛使用的有机磷农药,由于其对人类健康和环境的不利影响,需要对其进行精确监测。本研究设计并研制了一种新型的纳米生物传感器,用于快速、灵敏地检测CPF。该系统以AuNPs@ZIF-8纳米复合材料为检测平台,结合荧光共振能量转移(FRET)和金属增强荧光机制(MEF)过程,采用cpf特异性适配体作为识别元件。寡核苷酸杂交后产生FRET,与纳米复合材料偶联后观察到MEF过程。随后,通过添加CPF靶,两种应用释放的荧光团的荧光强度都得到增强。结果表明,该传感器的线性范围为0.75 ~ 5.22 pM,检出限极低(0.0817 pM)。对实际开心果样品进行性能评价,回收率为83 ~ 95%,重现性好(RSD: 5.3 ~ 6.4%)。总的来说,这种纳米生物传感器可以作为一种高效可靠的工具,用于快速监测农产品中的毒死蜱,并改善食品工业的质量控制。
{"title":"A nanobiosensor integrating FRET and MEF processes for fluorescence-based detection of Chlorpyrifos pesticide through AuNPs@ZIF-8 nanocomposite platform","authors":"Zahra Jomeh Ghasem Abadi ,&nbsp;Salehe Ganjali ,&nbsp;Mehdi Dadmehr ,&nbsp;Ziba Souri Nezami","doi":"10.1016/j.sbsr.2025.100916","DOIUrl":"10.1016/j.sbsr.2025.100916","url":null,"abstract":"<div><div>Pesticide residues in agricultural products are considered as one of the most important health and economic challenges. Chlorpyrifos (CPF), as a widely used organophosphate pesticide in many developing countries, requires precise monitoring due to its adverse effects on human health and the environment. In this study, a novel nanobiosensor was designed and developed for the rapid and sensitive detection of CPF. The system was based on an AuNPs@ZIF-8 nanocomposite as a detection platform which coupled with fluorescence resonance energy transfer (FRET) and metal enhanced fluorescence mechanisms (MEF) processes, in which a CPF-specific aptamer was employed as the recognition element. FRET was occurred after oligonucleotides hybridization and following MEF process was observed after conjugation with nanocomposite. Subsequently, by addition of CPF target the fluorescence intensity of both applied released fluorophores was enhanced. The results demonstrated that the proposed sensor exhibited linear range between of 0.75–5.22 pM with very low detection limit (0.0817 pM). Moreover, performance evaluation in real pistachio samples showed satisfactory recovery (83–95 %) and good reproducibility (RSD: 5.3–6.4 %). Overall, this nanobiosensor can serve as an efficient and reliable tool for the rapid monitoring of chlorpyrifos in agricultural products and for improving quality control in the food industry.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100916"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145575980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corrigendum to “A robust and highly sensitive electrochemical probe for detection of trace levels of NH3/NH4+ in water based on Berthelot's reaction” [Sensing and Bio-Sensing Research 47 (2025) 100760]. “基于Berthelot反应的用于检测水中痕量NH3/NH4+的坚固和高灵敏度电化学探针”[传感和生物传感研究47(2025)100760]的勘误表。
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-10-25 DOI: 10.1016/j.sbsr.2025.100905
H. Alwael , A.S. Alharthi , A. Alsolami , M. Oubaha , B. Duffy , R.M. Elshafey , M.S. El-Shahawi
{"title":"Corrigendum to “A robust and highly sensitive electrochemical probe for detection of trace levels of NH3/NH4+ in water based on Berthelot's reaction” [Sensing and Bio-Sensing Research 47 (2025) 100760].","authors":"H. Alwael ,&nbsp;A.S. Alharthi ,&nbsp;A. Alsolami ,&nbsp;M. Oubaha ,&nbsp;B. Duffy ,&nbsp;R.M. Elshafey ,&nbsp;M.S. El-Shahawi","doi":"10.1016/j.sbsr.2025.100905","DOIUrl":"10.1016/j.sbsr.2025.100905","url":null,"abstract":"","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100905"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145680794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis, characterization, and application of poly [Cu(Chr)2Cl]Cl/PGE based electrochemical sensor for the determination of Norfloxacin in pharmaceuticals and Milk samples 基于聚[Cu(Chr)2Cl]Cl/PGE电化学传感器的合成、表征及在药品和牛奶样品中诺氟沙星检测中的应用
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-10-24 DOI: 10.1016/j.sbsr.2025.100904
Abebaw Shitahun Ayicheh , Minaleshewa Atlabachew , Belete Asefa Aragaw , Amare Benor , Adane Kassa , Atakilt Abebe
Norfloxacin (Nor) is a drug belonging to the fluoroquinolones class, commonly used to treat bacterial infections of humans and animals. However, improper use, unmetabolized excretion, and overuse of Nor can lead to bacterial resistance. To mitigate this risk, sensitive, selective, and alternative analytical techniques are required. In this work, a Cu(II)-chrysine complex was synthesized, characterized and applied to modify pencil graphite electrode for electrochemical determination of Nor in pharmaceuticals and milk samples. The tip of the PGE electrode has been modified using the potentiodynamic electropolymerization method and a monomer modifier of [Cu(Chr)2Cl]Cl using the optimized potential window and film thickness. The modified electrode was characterized using EIS, UV–Vis, CV, digital optical microscopy, and contact angle. Both the developed electrochemical method and UV–Vis spectroscopic method were calibrated and used for the determination of concentration of Nor in two brands of pharmaceuticals, in milk samples, and in the presence of different potential interferences. The percent recoveries of Nor in Nofxin and Gyrablock were in the range of 93.7–99.3 % and 96.6–109.9 %, respectively, and in milk samples, recoveries ranged from 81.80 % to 91.13 %. The developed method exhibited a slope of −0.511 μA/μM, a detection limit (LoD) of 0.096 μM, and a linear dynamic range of 1–100 μM. The developed method was selective towards Nor in the presence of caffeine and paracetamol, making it a promising alternative for the determination of Nor in different matrices.
诺氟沙星(Nor)是一种氟喹诺酮类药物,通常用于治疗人类和动物的细菌感染。然而,不适当的使用,未经代谢的排泄和过度使用Nor可导致细菌耐药性。为了减轻这种风险,需要敏感的、选择性的和可替代的分析技术。本文合成了一种Cu(II)-chrysine配合物,对其进行了表征,并将其应用于修饰铅笔石墨电极,用于电化学测定药品和牛奶样品中的Nor。采用动电位电聚合法和单体改性剂[Cu(Chr)2Cl]Cl对PGE电极的尖端进行了优化的电位窗和膜厚修饰。利用EIS、UV-Vis、CV、数字光学显微镜和接触角对修饰电极进行了表征。对电化学法和紫外可见光谱法进行了标定,并用于两种品牌药品、牛奶样品和存在不同潜在干扰的情况下的Nor浓度测定。乳样品中Nor的加样回收率为81.80% ~ 91.13%,而Nofxin和Gyrablock的加样回收率分别为93.7% ~ 99.3%和996.6% ~ 109.9%。该方法的斜率为−0.511 μA/μM,检出限为0.096 μM,线性动态范围为1 ~ 100 μM。在咖啡因和扑热息痛存在的情况下,该方法对硝酸钠有选择性,可用于不同基质中硝酸钠的测定。
{"title":"Synthesis, characterization, and application of poly [Cu(Chr)2Cl]Cl/PGE based electrochemical sensor for the determination of Norfloxacin in pharmaceuticals and Milk samples","authors":"Abebaw Shitahun Ayicheh ,&nbsp;Minaleshewa Atlabachew ,&nbsp;Belete Asefa Aragaw ,&nbsp;Amare Benor ,&nbsp;Adane Kassa ,&nbsp;Atakilt Abebe","doi":"10.1016/j.sbsr.2025.100904","DOIUrl":"10.1016/j.sbsr.2025.100904","url":null,"abstract":"<div><div>Norfloxacin (Nor) is a drug belonging to the fluoroquinolones class, commonly used to treat bacterial infections of humans and animals. However, improper use, unmetabolized excretion, and overuse of Nor can lead to bacterial resistance. To mitigate this risk, sensitive, selective, and alternative analytical techniques are required. In this work, a Cu(II)-chrysine complex was synthesized, characterized and applied to modify pencil graphite electrode for electrochemical determination of Nor in pharmaceuticals and milk samples. The tip of the PGE electrode has been modified using the potentiodynamic electropolymerization method and a monomer modifier of [Cu(Chr)<sub>2</sub>Cl]Cl using the optimized potential window and film thickness. The modified electrode was characterized using EIS, UV–Vis, CV, digital optical microscopy, and contact angle. Both the developed electrochemical method and UV–Vis spectroscopic method were calibrated and used for the determination of concentration of Nor in two brands of pharmaceuticals, in milk samples, and in the presence of different potential interferences. The percent recoveries of Nor in Nofxin and Gyrablock were in the range of 93.7–99.3 % and 96.6–109.9 %, respectively, and in milk samples, recoveries ranged from 81.80 % to 91.13 %. The developed method exhibited a slope of −0.511 μA/μM, a detection limit (LoD) of 0.096 μM, and a linear dynamic range of 1–100 μM. The developed method was selective towards Nor in the presence of caffeine and paracetamol, making it a promising alternative for the determination of Nor in different matrices.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100904"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145412640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A high-performance yet cost-effective Cu/Ag bimetallic SPR biosensor augmented by halide perovskite integration: Unlocking ultra sensitivity and affordable urine-glucose sensing 卤化物钙钛矿集成增强的高性能且具有成本效益的Cu/Ag双金属SPR生物传感器:解锁超灵敏度和负担得起的尿糖传感
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-09-30 DOI: 10.1016/j.sbsr.2025.100884
M. Mishra , A. Yadav , S. Senapati , S.K. Tripathy
Metal Halide Perovskite (MHP) is introduced into Surface Plasmon Resonance (SPR) biosensor with a bimetallic CuAg configuration and urine as the biosample. The Cu/Ag pairing, prior to the application of perovskite, achieves zero reflectivity at 67.8° with a sensitivity of 147°/RIU, exhibiting improvements of 130.8 % over Ag/Cu, 267.5 % over Cu alone, and 390 %, over Ag alone. The study decisively investigates four different halide perovskites—Cesium tin iodide (CsSnI₃), Formamidinium tin iodide (FASnI₃), Potassium tin iodide (KSnI₃), and Cesium lead iodide (CsPbI₃)—integrated into the Cu/Ag structure and optimizes their thicknesses as 8 nm, 10 nm, 12 nm, and 16 nm, respectively. These materials, known for their excellent optical properties and tunability, enhance light-matter interactions, leading to significant gains in SPR sensitivity and detection accuracy. The measured sensitivity values for these perovskites are 460, 406, 352, and 399°/RIU, respectively, with corresponding detection accuracies of 0.238, 0.294, 0.312, and 0.303 RIU−1 with respective quality factors of 109.48, 119, 109.89, and 120. Evidently, CsSnI₃ is found to exhibit the highest sensitivity, supported by fair amount of detection accuracy and quality factor along with an estimated penetration depth of 150 nm, making it the most promising candidate for SPR performance enhancement in this study. Further, a layer of glucose oxidase enzyme is introduced over the halide layers which ensures the high selectivity of the proposed sensor.
将金属卤化物钙钛矿(MHP)以双金属CuAg结构引入表面等离子体共振(SPR)生物传感器中,以尿液为生物样品。在应用钙钛矿之前,Cu/Ag对在67.8°处达到零反射率,灵敏度为147°/RIU,比Ag/Cu提高130.8%,比Cu单独提高267.5%,比Ag单独提高390%。该研究决定性地研究了四种不同的卤化物钙钛矿——碘化锡铯(CsSnI₃)、碘化锡甲酰胺(FASnI₃)、碘化锡钾(KSnI₃)和碘化铅铯(CsPbI₃)——整合到Cu/Ag结构中,并优化了它们的厚度分别为8 nm、10 nm、12 nm和16 nm。这些材料以其优异的光学性能和可调性而闻名,增强了光与物质的相互作用,从而显著提高了SPR灵敏度和检测精度。这些钙钛矿的灵敏度分别为460、406、352和399°/RIU,检测精度分别为0.238、0.294、0.312和0.303 RIU−1,质量因子分别为109.48、119、109.89和120。显然,CsSnI₃被发现具有最高的灵敏度,得到相当数量的检测精度和质量因子的支持,并且估计穿透深度为150 nm,使其成为本研究中最有希望增强SPR性能的候选者。此外,在卤化物层上引入一层葡萄糖氧化酶,以确保所提出的传感器的高选择性。
{"title":"A high-performance yet cost-effective Cu/Ag bimetallic SPR biosensor augmented by halide perovskite integration: Unlocking ultra sensitivity and affordable urine-glucose sensing","authors":"M. Mishra ,&nbsp;A. Yadav ,&nbsp;S. Senapati ,&nbsp;S.K. Tripathy","doi":"10.1016/j.sbsr.2025.100884","DOIUrl":"10.1016/j.sbsr.2025.100884","url":null,"abstract":"<div><div>Metal Halide Perovskite (MHP) is introduced into Surface Plasmon Resonance (SPR) biosensor with a bimetallic Cu<img>Ag configuration and urine as the biosample. The Cu/Ag pairing, prior to the application of perovskite, achieves zero reflectivity at 67.8° with a sensitivity of 147°/RIU, exhibiting improvements of 130.8 % over Ag/Cu, 267.5 % over Cu alone, and 390 %, over Ag alone. The study decisively investigates four different halide perovskites—Cesium tin iodide (CsSnI₃), Formamidinium tin iodide (FASnI₃), Potassium tin iodide (KSnI₃), and Cesium lead iodide (CsPbI₃)—integrated into the Cu/Ag structure and optimizes their thicknesses as 8 nm, 10 nm, 12 nm, and 16 nm, respectively. These materials, known for their excellent optical properties and tunability, enhance light-matter interactions, leading to significant gains in SPR sensitivity and detection accuracy. The measured sensitivity values for these perovskites are 460, 406, 352, and 399°/RIU, respectively, with corresponding detection accuracies of 0.238, 0.294, 0.312, and 0.303 RIU<sup>−1</sup> with respective quality factors of 109.48, 119, 109.89, and 120. Evidently, CsSnI₃ is found to exhibit the highest sensitivity, supported by fair amount of detection accuracy and quality factor along with an estimated penetration depth of 150 nm, making it the most promising candidate for SPR performance enhancement in this study. Further, a layer of glucose oxidase enzyme is introduced over the halide layers which ensures the high selectivity of the proposed sensor.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100884"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145320547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nickel monoligand-MOF modified electrochemical sensor for the detection of neuroblastoma biomarker homovanillic acid 单寡镍- mof修饰的电化学传感器检测神经母细胞瘤生物标志物同质香草酸
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-11-06 DOI: 10.1016/j.sbsr.2025.100909
Shymaa S. Soliman , Amr M. Mahmoud , Dina A. El Mously

Background

Early cancer detection is vital for successful clinical outcomes and for advancing public health. It is crucial to detect cancer early for prevention and better treatment. Electrochemical sensors have been developed for disease detection, especially cancer-based on biomarkers, due to their sensitivity, selectivity, affordability, and rapid response. Neuroblastoma is a pediatric cancer originating from neural crest stem cells and is the most prevalent extracranial tumour in infants.

Method

The current study discusses the development of an electrochemical sensor for the detection of homovanillic acid (HVA), a tumour biomarker for neuroblastoma and other dopamine-related disorders. The electrochemical oxidation of HVA was investigated utilizing a carbon paste electrode modified with a nickel-based monoligand complex (ML/Ni–MOFs/CPE).

Results

This modification significantly improved the electrode's sensitivity and electrocatalytic efficiency. Under optimized conditions, the sensor displayed a linear DPV response within the concentration range of 0.1 μM to 70.0 μM and achieved a low detection limit of 0.08 μM. Morphological and elemental analyses were carried out using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray Diffraction (XRD), and infrared spectroscopy (FT-IR). These characterizations confirmed the uniform dispersion of nickel anchored onto the MOF sheets. Electrochemical performance was further evaluated using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The ML/Ni–MOFs/CPE electrode exhibited a markedly enhanced HVA oxidation peak current compared with the bare CPE, indicating improved electron transfer kinetics. The electrode demonstrated high reproducibility (RSD < 2 %) and stability, along with good selectivity against common interferents such as creatinine, ascorbic acid, uric acid, and glucose. Application to spiked human urine samples yielded recovery values between 93.25 % and 97.60 %, confirming its analytical accuracy and reliability in biological matrices. The modified electrode retained over 90 % of its initial response after 60 days of storage under ambient conditions, demonstrating outstanding stability and durability.

Significance

These findings highlight the potential of the proposed ML/Ni–MOFs/CPE sensor as a rapid, cost-effective, and reliable platform for HVA detection. Its robustness and successful application to urine samples highlight its potential for clinical diagnostics and early neuroblastoma diagnosis, supporting future integration into portable and point-of-care testing systems.
背景:恶性肿瘤的检测对于成功的临床结果和促进公众健康至关重要。早期发现癌症对于预防和更好的治疗至关重要。电化学传感器由于其灵敏度、选择性、可负担性和快速反应性,已被开发用于疾病检测,特别是基于生物标志物的癌症检测。神经母细胞瘤是一种起源于神经嵴干细胞的儿科癌症,是婴儿中最常见的颅外肿瘤。方法研制一种电化学传感器,用于检测同种香草酸(HVA)。同种香草酸是神经母细胞瘤和其他多巴胺相关疾病的肿瘤生物标志物。采用镍基单分子配合物(ML/ Ni-MOFs /CPE)修饰碳糊电极,研究了HVA的电化学氧化。结果该修饰显著提高了电极的灵敏度和电催化效率。在优化条件下,传感器在0.1 μM ~ 70.0 μM的浓度范围内具有良好的线性DPV响应,检测限低至0.08 μM。采用扫描电镜(SEM)、能量色散x射线能谱(EDX)、x射线衍射(XRD)和红外光谱(FT-IR)进行了形态和元素分析。这些表征证实了镍在MOF片上的均匀分散。利用电化学阻抗谱(EIS)和循环伏安法(CV)进一步评价了材料的电化学性能。与裸CPE相比,ML/ Ni-MOFs /CPE电极的HVA氧化峰电流明显增强,表明电子传递动力学得到改善。该电极具有高重复性(RSD < 2%)和稳定性,对常见的干扰物如肌酐、抗坏血酸、尿酸和葡萄糖具有良好的选择性。应用于加标人尿样品,回收率在93.25% ~ 97.60%之间,证实了其在生物基质中的分析准确性和可靠性。在环境条件下储存60天后,修饰电极保留了90%以上的初始响应,表现出出色的稳定性和耐用性。这些发现突出了ML/ ni - mof /CPE传感器作为HVA检测快速、经济、可靠平台的潜力。它的稳健性和对尿液样本的成功应用突出了它在临床诊断和早期神经母细胞瘤诊断方面的潜力,支持未来集成到便携式和护理点检测系统中。
{"title":"Nickel monoligand-MOF modified electrochemical sensor for the detection of neuroblastoma biomarker homovanillic acid","authors":"Shymaa S. Soliman ,&nbsp;Amr M. Mahmoud ,&nbsp;Dina A. El Mously","doi":"10.1016/j.sbsr.2025.100909","DOIUrl":"10.1016/j.sbsr.2025.100909","url":null,"abstract":"<div><h3>Background</h3><div>Early cancer detection is vital for successful clinical outcomes and for advancing public health. It is crucial to detect cancer early for prevention and better treatment. Electrochemical sensors have been developed for disease detection, especially cancer-based on biomarkers, due to their sensitivity, selectivity, affordability, and rapid response. Neuroblastoma is a pediatric cancer originating from neural crest stem cells and is the most prevalent extracranial tumour in infants.</div></div><div><h3>Method</h3><div>The current study discusses the development of an electrochemical sensor for the detection of homovanillic acid (HVA), a tumour biomarker for neuroblastoma and other dopamine-related disorders. The electrochemical oxidation of HVA was investigated utilizing a carbon paste electrode modified with a nickel-based monoligand complex (ML/Ni–MOFs/CPE).</div></div><div><h3>Results</h3><div>This modification significantly improved the electrode's sensitivity and electrocatalytic efficiency. Under optimized conditions, the sensor displayed a linear DPV response within the concentration range of 0.1 μM to 70.0 μM and achieved a low detection limit of 0.08 μM. Morphological and elemental analyses were carried out using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray Diffraction (XRD), and infrared spectroscopy (FT-IR). These characterizations confirmed the uniform dispersion of nickel anchored onto the MOF sheets. Electrochemical performance was further evaluated using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The ML/Ni–MOFs/CPE electrode exhibited a markedly enhanced HVA oxidation peak current compared with the bare CPE, indicating improved electron transfer kinetics. The electrode demonstrated high reproducibility (RSD &lt; 2 %) and stability, along with good selectivity against common interferents such as creatinine, ascorbic acid, uric acid, and glucose. Application to spiked human urine samples yielded recovery values between 93.25 % and 97.60 %, confirming its analytical accuracy and reliability in biological matrices. The modified electrode retained over 90 % of its initial response after 60 days of storage under ambient conditions, demonstrating outstanding stability and durability.</div></div><div><h3>Significance</h3><div>These findings highlight the potential of the proposed ML/Ni–MOFs/CPE sensor as a rapid, cost-effective, and reliable platform for HVA detection. Its robustness and successful application to urine samples highlight its potential for clinical diagnostics and early neuroblastoma diagnosis, supporting future integration into portable and point-of-care testing systems.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100909"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145516656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bimetallic core-shell nano-architecture of Au@Pt as an effective electrochemical mediator for ultrasensitive detection of Listeria monocytogenes in cerebrospinal fluid 双金属核壳纳米结构Au@Pt作为脑脊液中单核增生李斯特菌超灵敏检测的有效电化学介质
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-09-02 DOI: 10.1016/j.sbsr.2025.100873
Leila Mehrannia , Morteza Milani , Balal Khalilzadeh , Abolfazl Barzegari , Solmaz Sadi , Mohammad Reza Rashidi
Bacterial infections related to Listeria monocytogenes can lead to serious pathological conditions such as meningitis and meningoencephalitis in humans. Therefore, the detection of Listeria particles and byproducts is a very important issue in clinical settings. Nanostructures have been broadly utilized in different areas because of their unique physicochemical properties. Specifically, bimetallic nanostructures have been employed in the development of smart biosensor types. In the study, a simple and efficient platform utilizing bimetallic nanostructures was developed to create a diagnostic system for Listeria monocytogenes. The Au@Pt core-shell structure was synthesized and electrodeposited the glassy carbon electrode (GCE). A 24-mer thiolated single-strand probe, targeting the hly gene, was immobilized on the Au@Pt modified GCE to hybridize with the target sequence. Then, the electrochemical measurement with square wave voltammetry (SWV) technique was done to ensure the hybridization reaction. The biosensor's efficiency was validated using standard addition in real cerebrospinal fluid (CSF) samples, to assess biosensor specificity in the detection of bacterial genomics in biofluids. The obtained results indicate that the designed biosensor was able to detect the target genomic sequences. This platform was capable of detecting targets in 5 to 60 attomolar and was proved as a practical detection limit. It is suggested that the designed platform with high sensitivity and specificity for the detection of target gene sequences in biofluids.
与单核细胞增生李斯特菌有关的细菌感染可导致严重的病理状况,如人类脑膜炎和脑膜脑炎。因此,检测李斯特菌颗粒和副产物是一个非常重要的问题,在临床设置。纳米结构以其独特的物理化学性质在不同领域得到了广泛的应用。具体来说,双金属纳米结构已被用于智能生物传感器的开发。在本研究中,利用双金属纳米结构建立了一个简单高效的平台来创建单核细胞增生李斯特菌的诊断系统。合成了Au@Pt核壳结构,并电沉积了玻碳电极(GCE)。将靶向hly基因的24-mer硫代单链探针固定在Au@Pt修饰的GCE上,与目标序列杂交。然后用方波伏安法(SWV)进行电化学测量,以保证杂交反应的进行。在真实脑脊液(CSF)样品中使用标准添加验证了生物传感器的效率,以评估生物传感器检测生物体液中细菌基因组学的特异性。实验结果表明,所设计的生物传感器能够检测目标基因组序列。该平台能够检测到5 ~ 60亚摩尔的目标,并被证明是一个实用的检测极限。结果表明,该平台具有较高的灵敏度和特异性,可用于生物体液中靶基因序列的检测。
{"title":"Bimetallic core-shell nano-architecture of Au@Pt as an effective electrochemical mediator for ultrasensitive detection of Listeria monocytogenes in cerebrospinal fluid","authors":"Leila Mehrannia ,&nbsp;Morteza Milani ,&nbsp;Balal Khalilzadeh ,&nbsp;Abolfazl Barzegari ,&nbsp;Solmaz Sadi ,&nbsp;Mohammad Reza Rashidi","doi":"10.1016/j.sbsr.2025.100873","DOIUrl":"10.1016/j.sbsr.2025.100873","url":null,"abstract":"<div><div>Bacterial infections related to <em>Listeria monocytogenes</em> can lead to serious pathological conditions such as meningitis and meningoencephalitis in humans. Therefore, the detection of <em>Listeria</em> particles and byproducts is a very important issue in clinical settings. Nanostructures have been broadly utilized in different areas because of their unique physicochemical properties. Specifically, bimetallic nanostructures have been employed in the development of smart biosensor types. In the study, a simple and efficient platform utilizing bimetallic nanostructures was developed to create a diagnostic system for <em>Listeria monocytogenes</em>. The Au@Pt core-shell structure was synthesized and electrodeposited the glassy carbon electrode (GCE). A 24-mer thiolated single-strand probe, targeting the hly gene, was immobilized on the Au@Pt modified GCE to hybridize with the target sequence. Then, the electrochemical measurement with square wave voltammetry (SWV) technique was done to ensure the hybridization reaction. The biosensor's efficiency was validated using standard addition in real cerebrospinal fluid (CSF) samples, to assess biosensor specificity in the detection of bacterial genomics in biofluids. The obtained results indicate that the designed biosensor was able to detect the target genomic sequences. This platform was capable of detecting targets in 5 to 60 attomolar and was proved as a practical detection limit. It is suggested that the designed platform with high sensitivity and specificity for the detection of target gene sequences in biofluids.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100873"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144989834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Manganese-doped g-C3N4 nanozyme-based smartphone platform for rapid L-DOPA detection in clinical samples 基于锰掺杂g-C3N4纳米酶的智能手机平台快速检测临床样品中的左旋多巴
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-10-12 DOI: 10.1016/j.sbsr.2025.100895
Jianjun Kang , Xue Lin , Chen Lin , Wuyuan Pan , Jian Wang , Fang Ke
Levodopa (L-DOPA) is a crucial neurotransmitter utilized in the treatment of neurological disorders, particularly in Parkinson's disease, where its concentration in biological fluids serves as a key diagnostic marker. Despite its significance, current methods for L-DOPA detection often suffer from limitations such as prolonged detection times, low sensitivity and weak anti-interference. This study addresses these challenges by introducing a highly efficient and colorimetric sensor for the rapid detection of L-DOPA, utilizing manganese-doped graphitic carbon nitride (Mn-g-C3N4) as a peroxidase-mimetic catalyst. The sensor employs 3,3′,5,5′-tetramethylbenzidine as a substrate and achieves detection within 20 s, with a linear response over the concentration ranges of 1–10 μM and 20–90 μM, and the detection limits were 0.049 μM and 0.51 μM, respectively. The method has good specificity for L-DOPA and has been successfully applied to human serum even in the presence of interference from dopamine and other amino acids. In addition, the sensor exhibits satisfactory performance in smartphone-based L-DOPA detection. The novel sensor platform offers a simple, cost-effective, and scalable solution for real-time L-DOPA monitoring, with significant potential for applications in both clinical and environmental contexts.
左旋多巴(L-DOPA)是一种重要的神经递质,用于治疗神经系统疾病,特别是帕金森病,其在生物体液中的浓度可作为关键的诊断标志物。尽管具有重要意义,但目前的左旋多巴检测方法存在检测时间长、灵敏度低、抗干扰能力弱等局限性。本研究利用锰掺杂石墨氮化碳(Mn-g-C3N4)作为过氧化物酶模拟催化剂,引入了一种高效的L-DOPA快速检测比色传感器,解决了这些挑战。该传感器以3,3 ',5,5 ' -四甲基联苯胺为底物,在20 s内实现检测,在1 ~ 10 μM和20 ~ 90 μM的浓度范围内具有良好的线性响应,检出限分别为0.049 μM和0.51 μM。该方法对左旋多巴具有良好的特异性,即使在多巴胺和其他氨基酸干扰的情况下也能成功地应用于人血清中。此外,该传感器在基于智能手机的L-DOPA检测中表现出令人满意的性能。这种新型传感器平台为实时L-DOPA监测提供了一种简单、经济、可扩展的解决方案,在临床和环境环境中都有很大的应用潜力。
{"title":"Manganese-doped g-C3N4 nanozyme-based smartphone platform for rapid L-DOPA detection in clinical samples","authors":"Jianjun Kang ,&nbsp;Xue Lin ,&nbsp;Chen Lin ,&nbsp;Wuyuan Pan ,&nbsp;Jian Wang ,&nbsp;Fang Ke","doi":"10.1016/j.sbsr.2025.100895","DOIUrl":"10.1016/j.sbsr.2025.100895","url":null,"abstract":"<div><div>Levodopa (L-DOPA) is a crucial neurotransmitter utilized in the treatment of neurological disorders, particularly in Parkinson's disease, where its concentration in biological fluids serves as a key diagnostic marker. Despite its significance, current methods for L-DOPA detection often suffer from limitations such as prolonged detection times, low sensitivity and weak anti-interference. This study addresses these challenges by introducing a highly efficient and colorimetric sensor for the rapid detection of L-DOPA, utilizing manganese-doped graphitic carbon nitride (Mn-g-C<sub>3</sub>N<sub>4</sub>) as a peroxidase-mimetic catalyst. The sensor employs 3,3′,5,5′-tetramethylbenzidine as a substrate and achieves detection within 20 s, with a linear response over the concentration ranges of 1–10 μM and 20–90 μM, and the detection limits were 0.049 μM and 0.51 μM, respectively. The method has good specificity for L-DOPA and has been successfully applied to human serum even in the presence of interference from dopamine and other amino acids. In addition, the sensor exhibits satisfactory performance in smartphone-based L-DOPA detection. The novel sensor platform offers a simple, cost-effective, and scalable solution for real-time L-DOPA monitoring, with significant potential for applications in both clinical and environmental contexts.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100895"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145320549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Innovative aptasensor design for chlorpyrifos detection: Combining carbon nanofibers, doped carbon dots, and gold nanoparticles 毒死蜱检测的创新适体传感器设计:结合碳纳米纤维、掺杂碳点和金纳米颗粒
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-11-21 DOI: 10.1016/j.sbsr.2025.100922
Haniyeh Shantiaei, Mahmoud Roushani, Farzaneh Mohammadi
Chlorpyrifos (CPF) is an organophosphate pesticide that is essential for controlling agricultural pests. Nevertheless, residues of this compound, even at low concentrations, raise substantial concerns regarding the environment and human health, including neurotoxic, genotoxic, and reproductive effects. This study aimed to design and fabricate a highly sensitive aptamer-based electrochemical biosensor utilizing P@N, S-CDs/CNFs with gold nanoparticles (AuNPs) for the detection of CPF in fruit and vegetable samples. Initially, nitrogen- and sulfur-co-doped carbon dots (N, S-CDs) were incorporated into polyacrylonitrile (PAN) polymer, resulting in the formation of N, S-CDs/CNFs via electrospinning. Subsequently, P@N, S-CDs/CNFs were produced during the heat treatment process. The hybrid material (P@N, S-CDs/CNFs) was used to modify the surface of the glassy carbon electrode (GCE), followed by the placement of AuNPs on the GCE modified with P@N, S-CDs/CNFs using the drop casting method. The successful synthesis of the nanomaterials was confirmed through XRD, FTIR, and SEM analyses. Under optimal conditions, the aptasensor demonstrated an extensive linear range from 0.1 fg mL−1 to 800 pg mL−1, with a calculated limit of detection as low as 0.033 fg mL−1. The capability of the aptasensor to detect CPF in real samples was assessed by testing extracts of cucumber, tomato, and lettuce.
毒死蜱(Chlorpyrifos, CPF)是一种有机磷农药,是防治农业害虫的重要手段。然而,这种化合物的残留,即使浓度很低,也会引起对环境和人类健康的严重关切,包括神经毒性、遗传毒性和生殖影响。本研究旨在利用P@N, S-CDs/CNFs与金纳米颗粒(AuNPs)设计和制造一种高灵敏度的适体电化学生物传感器,用于检测水果和蔬菜样品中的CPF。首先,将氮和硫共掺杂的碳点(N, S-CDs)掺入聚丙烯腈(PAN)聚合物中,通过静电纺丝形成N, S-CDs/CNFs。随后,P@N, S-CDs/CNFs在热处理过程中产生。采用杂化材料(P@N, S-CDs/CNFs)对玻璃碳电极(GCE)表面进行修饰,然后采用滴铸法将AuNPs放置在P@N, S-CDs/CNFs修饰的GCE上。通过XRD、FTIR和SEM分析证实了纳米材料的成功合成。在最佳条件下,该传感器显示出从0.1 fg mL−1到800 pg mL−1的广泛线性范围,计算检测限低至0.033 fg mL−1。通过对黄瓜、番茄和生菜提取物的检测,评估了该传感器在实际样品中检测CPF的能力。
{"title":"Innovative aptasensor design for chlorpyrifos detection: Combining carbon nanofibers, doped carbon dots, and gold nanoparticles","authors":"Haniyeh Shantiaei,&nbsp;Mahmoud Roushani,&nbsp;Farzaneh Mohammadi","doi":"10.1016/j.sbsr.2025.100922","DOIUrl":"10.1016/j.sbsr.2025.100922","url":null,"abstract":"<div><div>Chlorpyrifos (CPF) is an organophosphate pesticide that is essential for controlling agricultural pests. Nevertheless, residues of this compound, even at low concentrations, raise substantial concerns regarding the environment and human health, including neurotoxic, genotoxic, and reproductive effects. This study aimed to design and fabricate a highly sensitive aptamer-based electrochemical biosensor utilizing P@N, S-CDs/CNFs with gold nanoparticles (AuNPs) for the detection of CPF in fruit and vegetable samples. Initially, nitrogen- and sulfur-co-doped carbon dots (N, S-CDs) were incorporated into polyacrylonitrile (PAN) polymer, resulting in the formation of N, S-CDs/CNFs via electrospinning. Subsequently, P@N, S-CDs/CNFs were produced during the heat treatment process. The hybrid material (P@N, S-CDs/CNFs) was used to modify the surface of the glassy carbon electrode (GCE), followed by the placement of AuNPs on the GCE modified with P@N, S-CDs/CNFs using the drop casting method. The successful synthesis of the nanomaterials was confirmed through XRD, FTIR, and SEM analyses. Under optimal conditions, the aptasensor demonstrated an extensive linear range from 0.1 fg mL<sup>−1</sup> to 800 pg mL<sup>−1</sup>, with a calculated limit of detection as low as 0.033 fg mL<sup>−1</sup>. The capability of the aptasensor to detect CPF in real samples was assessed by testing extracts of cucumber, tomato, and lettuce.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100922"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145575985","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dual emissive carbon dots as Ratiometric fluorescence sensors: A comprehensive review 作为比例荧光传感器的双发射碳点:综述
IF 4.9 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-01 Epub Date: 2025-11-27 DOI: 10.1016/j.sbsr.2025.100930
Samar H. Elagamy , Reem Hasan Obaydo , Aya Barseem , Hayam Lotfy
Ratiometric fluorescence sensing offers significant advantages over traditional fluorescence techniques due to its inherent self-referencing nature, enabling robust and accurate measurements. This review focuses on the utilization of Carbon Dots (CDs) as promising platforms for developing ratiometric fluorescence sensors RFS. It outlines the fundamental principles of ratiometric sensing, highlighting its advantages over traditional fluorescence methods. The sensing mechanisms employed in ratiometric sensors are discussed, including intramolecular charge transfer (ICT), fluorescence resonance energy transfer (FRET), chelation-enhanced fluorescence (CHEF), photoinduced electron transfer (PET), excited-state intramolecular proton transfer (ESIPT), aggregation-induced emission (AIE), static quenching effect (SQE), dynamic quenching (DQE) and internal filtration effect (IFE). Furthermore, various methods for constructing CD-based RFS are investigated in this review, including surface functionalization, doping, mixing strategy, hybridization/compositing, and synthesis of intrinsic dual-emissive CDs. In addition, the diverse applications of CD-based RFS in key areas are discussed, such as environmental monitoring, food safety analysis, pharmaceutical analysis, bioanalysis, and bioimaging. Finally, this review highlights the challenges associated with CD-based RFS and outlines potential directions for future research.
比率荧光传感由于其固有的自参考特性,比传统的荧光技术具有显著的优势,能够实现鲁棒和准确的测量。本文综述了利用碳点(cd)作为有前途的平台来开发比率荧光传感器。它概述了比率传感的基本原理,突出了其优于传统荧光方法的优点。讨论了用于比例传感器的传感机制,包括分子内电荷转移(ICT)、荧光共振能量转移(FRET)、螯合增强荧光(CHEF)、光诱导电子转移(PET)、激化态分子内质子转移(ESIPT)、聚集诱导发射(AIE)、静态猝灭效应(SQE)、动态猝灭效应(DQE)和内部过滤效应(IFE)。此外,本文还研究了构建基于cd的RFS的各种方法,包括表面功能化、掺杂、混合策略、杂化/复合以及合成本征双发射cd。此外,还讨论了基于cd的RFS在环境监测、食品安全分析、药物分析、生物分析和生物成像等关键领域的应用。最后,本综述强调了基于cd的RFS所面临的挑战,并概述了未来研究的潜在方向。
{"title":"Dual emissive carbon dots as Ratiometric fluorescence sensors: A comprehensive review","authors":"Samar H. Elagamy ,&nbsp;Reem Hasan Obaydo ,&nbsp;Aya Barseem ,&nbsp;Hayam Lotfy","doi":"10.1016/j.sbsr.2025.100930","DOIUrl":"10.1016/j.sbsr.2025.100930","url":null,"abstract":"<div><div>Ratiometric fluorescence sensing offers significant advantages over traditional fluorescence techniques due to its inherent self-referencing nature, enabling robust and accurate measurements. This review focuses on the utilization of Carbon Dots (CDs) as promising platforms for developing ratiometric fluorescence sensors RFS. It outlines the fundamental principles of ratiometric sensing, highlighting its advantages over traditional fluorescence methods. The sensing mechanisms employed in ratiometric sensors are discussed, including intramolecular charge transfer (ICT), fluorescence resonance energy transfer (FRET), chelation-enhanced fluorescence (CHEF), photoinduced electron transfer (PET), excited-state intramolecular proton transfer (ESIPT), aggregation-induced emission (AIE), static quenching effect (SQE), dynamic quenching (DQE) and internal filtration effect (IFE). Furthermore, various methods for constructing CD-based RFS are investigated in this review, including surface functionalization, doping, mixing strategy, hybridization/compositing, and synthesis of intrinsic dual-emissive CDs. In addition, the diverse applications of CD-based RFS in key areas are discussed, such as environmental monitoring, food safety analysis, pharmaceutical analysis, bioanalysis, and bioimaging. Finally, this review highlights the challenges associated with CD-based RFS and outlines potential directions for future research.</div></div>","PeriodicalId":424,"journal":{"name":"Sensing and Bio-Sensing Research","volume":"50 ","pages":"Article 100930"},"PeriodicalIF":4.9,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145620289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Sensing and Bio-Sensing Research
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1