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Electroanalytical Immunotechnology for Minimally Invasive Assessment of Toll-Like Receptor 2, a Key Inflammatory Component in Colorectal Cancer Progression 电分析免疫技术用于微创评估toll样受体2,结直肠癌进展中的关键炎症成分
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-03-10 DOI: 10.1002/anse.202500014
Sandra Tejerina-Miranda, Maria Gamella, María Pedrero, Ana Montero-Calle, José M. Pingarrón, Rodrigo Barderas, Susana Campuzano

Toll-like receptor 2 (TLR2) is involved in infectious diseases, inflammatory processes and carcinogenesis. Soluble TLR2 (sTLR2) can be released into circulation stream acting as an endogenous negative regulator of TLR2 signaling, essential for the prevention of chronic inflammation and tissue destruction. In this context, we propose pioneering electrochemical biotechnology for the determination of sTLR2 in plasma of colorectal cancer (CRC) patients. The method involves the use of magnetic particles as micro-supports for the implementation of a sandwich immunoassay using a pair of specific antibodies and horseradish peroxidase as enzymatic tracer to carry out the amperometric transduction on screen-printed carbon electrodes in the presence of H2O2 and hydroquinone. The proposed immunoplatform shows attractive operational and analytical characteristics, reaching a low limit of detection of 241 pg mL−1 for TLR2 standards in buffered solutions, and showing an excellent reproducibility (RSD 1.4 %), and a wide dynamic range (804 to 25000 pg mL−1). It has been applied to the analysis of a cohort of 21 plasma samples from healthy individuals and CRC patients at different stages of the disease, demonstrating precise quantitative determinations, in just 45 min and requiring minimal sample amount and pre-treatments. The results demonstrate the promising utility of TRL2 plasma levels for minimally invasive monitoring of CRC progression.

toll样受体2 (TLR2)参与感染性疾病、炎症过程和癌变。可溶性TLR2 (sTLR2)可以作为TLR2信号的内源性负调节因子释放到循环流中,对预防慢性炎症和组织破坏至关重要。在这种背景下,我们提出了开创性的电化学生物技术来测定结直肠癌(CRC)患者血浆中的sTLR2。该方法包括使用磁性颗粒作为微支撑来实施夹心免疫分析,使用一对特异性抗体和辣根过氧化物酶作为酶示踪剂,在H2O2和对苯二酚存在下在丝网印刷的碳电极上进行安培转导。所提出的免疫平台具有良好的操作和分析特性,在缓冲溶液中对TLR2标准物达到241 pg mL−1的低检出限,具有良好的重现性(RSD 1.4%)和宽动态范围(804至25000 pg mL−1)。该方法已被应用于对健康个体和不同阶段CRC患者的21个血浆样本的队列分析,显示出精确的定量测定,仅需45分钟,所需样本量和预处理最少。结果表明,TRL2血浆水平在微创监测结直肠癌进展方面具有很好的应用前景。
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引用次数: 0
Front Cover: Titanium Mxene: A Promising Material for Next-Generation Optical Biosensors and Machine Learning Integration (Anal. Sens. 2/2025) 封面二茂钛:下一代光学生物传感器和机器学习集成的前景看好的材料(Anal. Sens.)
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-03-10 DOI: 10.1002/anse.202580201
Athulya Aravind, Durgalakshmi Dhinasekaran, Ajay Rakkesh Rajendran

2D MXenes offer exceptional advancements in biosensing owing to their tunable optical properties with large surface area of interaction and hydrophilicity. This revolutionizes the biosensing of analytes using advanced sensing modes such as surface enhanced Raman scattering (SERS), surface plasmon resonance (SPR), and colorimetry with high selectivity and sensitivity in biomedical application. More in the Review by Durgalakshmi Dhinasekaran and co-workers.

2D MXenes由于其可调的光学特性,具有大的相互作用表面积和亲水性,在生物传感方面取得了非凡的进步。这彻底改变了分析物的生物传感,使用先进的传感模式,如表面增强拉曼散射(SERS),表面等离子体共振(SPR),以及在生物医学应用中具有高选择性和灵敏度的比色法。Durgalakshmi Dhinasekaran及其同事的评论。
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引用次数: 0
Dicyanovinyl Appended Carbazole Based Colorimetric Sensor for Volatile Organic Amines 双氰乙烯基附加咔唑基挥发性有机胺比色传感器
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-03-07 DOI: 10.1002/anse.202400109
S. Arunkumar, Gokul Raj Mini Rajendran, Aniket Chowdhury, George Rajendra Kumar

Herein we report synthesis, photophysical properties and amine sensing applications of a carbazole-dicyanovinyl based sensor (2). Sensor molecule 2 shows solid state fluorescence (φ=~41 %), mechanochromic fluorescence and aggregation induced emission. Presence of donor and acceptor groups in 2 resulted in strong absorption bands in the visible region of electromagnetic spectrum which is exploited for colorimetric sensing of primary amines. Amine sensing mechanism of 2 is established using 1H NMR titration studies. Test kit developed using probe 2 showed prominent color change in presence of biogenic amines generated from decomposed meat product.

本文报道了一种咔唑-二氰乙烯基传感器的合成、光物理性质和胺传感应用(2)。传感器分子2表现出固态荧光(φ=~ 41%)、机械致变色荧光和聚集诱导发光。2中供体和受体基团的存在导致电磁波谱可见区有很强的吸收带,用于伯胺的比色检测。利用1H NMR滴定法建立了2的胺感机制。使用探针2开发的测试试剂盒显示,分解肉制品产生的生物胺存在显著的颜色变化。
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引用次数: 0
Immobilization of Ru(II) Complex Onto the Glassy Carbon Electrode for the Detection of Tetracycline Residue in Chicken Egg and Cow Milk Ru(II)配合物在玻璃碳电极上固定化检测鸡蛋和牛奶中四环素残留
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-03-04 DOI: 10.1002/anse.202500005
P. Jeba Sagana, T. Shankar, K. Swarnalatha

This study highlights the electrochemical drug (ECD) sensor with a glassy carbon electrode modified with ruthenium(II) complex (RBNH), which showed a stronger response to the detection of tetracycline (TC) antibiotic residue in real samples like chicken eggs and cow milk compared to other substrate materials. Glassy carbon electrodes are covalently functionalized with ruthenium(II) complex containing the redox active 2, 2 bipyridine, and a hydrazone ligand (BNH) via., drop casting method. This results in the electrocatalytic behavior of the modified electrode (GCE/RBNH) on the oxidation of TC. Further, the modified electrode′s sustainability was tested with various antibiotics, including different concentrations of tetracycline, and scan rates by different techniques like cyclic voltammetry (CV), linear sweep voltammetry (LSV). Then a GCE/RBNH was used to create a linear calibration curve for TC concentrations ranging from 10 to 100 μmol L−1 (R2=0.99), with a limit of detection and quantification 0.0675 μmol L−1 and 0.224 μmol L−1. The current approach, which possesses an effortless electrode modification step and offers the lowest detection limit and a comparatively wider linear dynamic range, performed better for determining TC in chicken eggs and milk samples than recently reported voltammetric methods.

本研究重点研究了钌(II)配合物修饰的玻璃碳电极电化学药物(ECD)传感器,与其他底物材料相比,该电极对鸡蛋和牛奶等实际样品中四环素(TC)抗生素残留的检测表现出更强的响应。玻璃碳电极通过含有氧化还原活性2,2联吡啶的钌(II)配合物和腙配体(BNH)共价功能化。、滴铸法。结果表明,改性电极(GCE/RBNH)对TC的氧化具有电催化作用。此外,通过循环伏安法(CV)、线性扫描伏安法(LSV)等不同技术测试了各种抗生素(包括不同浓度的四环素)和扫描速率下修饰电极的可持续性。采用GCE/RBNH建立了10 ~ 100 μmol L−1浓度范围内的线性校准曲线(R2=0.99),检测限和定量限分别为0.0675和0.224 μmol L−1。目前的方法具有简单的电极修饰步骤,具有最低的检测限和相对较宽的线性动态范围,比最近报道的伏安法更好地测定鸡蛋和牛奶样品中的TC。
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引用次数: 0
Modifying the Morphology, Doping, and Electroanalytical Performance of Carbon Nanofibers by Varying the Ratio of Etchant and Feedstock Gases 通过改变蚀刻剂和原料气体的比例来改变碳纳米纤维的形貌、掺杂和电分析性能
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-02-23 DOI: 10.1002/anse.202400097
Ishan Pande, Khadijeh Nekoueian, Jani Sainio, Tomi Laurila

Ammonia (NH3) is a widely used etchant gas in the plasma-enhanced chemical vapor deposition (PECVD) synthesis of carbon nanofibers (CNFs). In addition to being an effective etchant, NH3 also serves as a dopant by providing N heteroatoms. However, this secondary role has not been comprehensively investigated. Moreover, the influence of N-doping on the electroanalytical performance of CNFs has not been thoroughly assessed. In this work, we have prepared CNFs of two varieties by altering the ratio of etchant and feedstock gases (NH3 and C2H2, respectively), resulting in N-doped CNFs with different doping levels. Differences were also observed in the morphology and electrochemical characteristics of the CNFs. While inner sphere redox (ISR) characteristics were not significantly affected, a significant shift between the peak potentials of ascorbic acid (AA) and dopamine (DA) was detected in the higher doped CNFs, resulting in enhanced selectivity towards DA. Our results demonstrate a simple yet effective method for enhancing the electroanalytical properties of CNFs.

氨(NH3)是等离子体增强化学气相沉积(PECVD)法合成纳米碳纤维(CNFs)中广泛使用的蚀刻气体。NH3除了是一种有效的蚀刻剂外,还可以提供N杂原子作为掺杂剂。然而,这一次要作用尚未得到全面调查。此外,n掺杂对CNFs电分析性能的影响尚未得到全面评估。在这项工作中,我们通过改变蚀刻剂和原料气体(分别为NH3和C2H2)的比例,制备了两个品种的CNFs,从而得到了不同掺杂水平的n掺杂CNFs。在形态和电化学特性上也观察到不同的CNFs。虽然内球氧化还原(ISR)特性没有受到显著影响,但在高掺杂CNFs中检测到抗坏血酸(AA)和多巴胺(DA)峰电位之间的显著变化,导致对DA的选择性增强。我们的结果证明了一种简单而有效的方法来提高CNFs的电分析性能。
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引用次数: 0
On-Paper Enzyme-Linked and Metal-Linked Immunosorbent Assays for Low-Cost Decentralized Testing of Carcinoembryonic Antigen 纸上酶联和金属联免疫吸附法低成本分散检测癌胚抗原
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-02-11 DOI: 10.1002/anse.202400113
Electra Mermiga, Dr. Varvara Pagkali, Dionysios Soulis, Dr. Christos Kokkinos, Prof. Anastasios Economou

This work reports two simplified paper-based approaches for immunosensing of carcinoembryonic antigen (CEA) in serum. On-paper enzyme-linked immunosorbent assay (p-ELISA) (using enzymatic generation of a colored product) and metal-linked immunosorbent assay (p-MeLISA) (using gold nanoparticles (AuNPs) as labels) were implemented using low-cost diagnostic bio-conjugated paper mini disks as platforms for the fast colorimetric immunosensing of CEA in human serum. The colour intensity was captured with a commercial scanner and analyzed using an open-source software. Different parameters of the preparation of the bioconjugated disks and of the immunoassays were studied and, under the selected conditions, LODs of 0.4 ng mL−1 with p-ELISA and 0.1 ng mL−1 with p-MeLISA were achieved while recoveries of CEA in serum samples were in the range from 88 to 112 % with coefficient of variation of <12 %. The assay time was 90 s for p-ELISA and 85 s for p-MeLISA. The immunoassays exhibited satisfactory selectivity in the presence of other cancer biomarkers and good stability under storage. Thanks to simple and rapid fabrication and modification, simple analysis protocol, affordability (<0.05 € per device), equipment-free quantification, low sample and reagents requirments, stability and satisfactory analytical characteristics, these approaches are fit-for-purpose for assay of CEA in serum at the point-of care in resource-limited settings.

本工作报告了两种简化的基于纸张的血清癌胚抗原(CEA)免疫传感方法。采用低成本的诊断性生物偶联纸迷你盘作为平台,实现了纸上酶联免疫吸附测定(p-ELISA)(使用酶促生成有色产物)和金属联免疫吸附测定(p-MeLISA)(使用金纳米颗粒(AuNPs)作为标记)对人血清中CEA的快速比色免疫传感。颜色强度是用商用扫描仪捕获的,并使用开源软件进行分析。在选择的条件下,p-ELISA法和p-MeLISA法的检出限分别为0.4 ng mL - 1和0.1 ng mL - 1,血清样品中CEA的回收率为88% ~ 112%,变异系数为12%。p-ELISA法测定时间为90 s, p-MeLISA法测定时间为85 s。在其他癌症生物标志物存在的情况下,免疫测定具有令人满意的选择性和良好的储存稳定性。由于简单快速的制造和修改,简单的分析方案,价格低廉(每台设备0.05欧元),无设备定量,低样品和试剂要求,稳定性和令人满意的分析特性,这些方法适合在资源有限的环境中在护理点检测血清中CEA。
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引用次数: 0
Paper Electrochemical Sensor Utilizing Nano Ag-Decorated Cu2O Nanoparticles for Ascorbic Acid Detection in Tablets 利用纳米ag修饰Cu2O纳米颗粒的纸质电化学传感器检测片剂中的抗坏血酸
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-02-04 DOI: 10.1002/anse.202400118
A. Venkadesh, Anumol Mathew, Thayyil K. Fahmeeda, J. Sonia, B. N. Kumara, K. Sudhakara Prasad

The accurate and selective detection of vitamins are very much needed in the food, and pharmaceutical industries and health care. In this study, a new sustainable disposable electrochemical platform was fabricated with nano silver/Cu2O composite (nAg/Cu2O) for sensing ascorbic acid (vitamin C). The modified electrode exhibited reduced resistance to charge transfer and improved electro active area. The analyte displayed excellent electrochemical activity on the surface of nAg/Cu2O modified paper electrode and showed a concentration-dependent response between 0.05 to 500 μM with a detection limit (S/N=3), 0.04 μM. Furthermore, the anti-interference studies revealed that the nAg/Cu2O nanocomposites have high selectivity towards ascorbic acid. Notably, the sensor based on nAg/Cu2O showed exceptional stability and reproducibility, with a relative standard deviation for peak currents measuring approximately 7 % or less while testing for a week of time. The real-world application and analytical performance was realized by identifying ascorbic acid in commercial vitamin C tablets with satisfactory results.

在食品、医药工业和卫生保健中非常需要对维生素进行准确和选择性的检测。本研究以纳米银/Cu2O复合材料(nAg/Cu2O)为材料,制备了一种新型的可持续的一次性电化学平台,用于检测抗坏血酸(维生素C)。改性电极的电荷转移电阻降低,电活性面积增大。分析物在nAg/Cu2O修饰纸电极表面表现出优异的电化学活性,在0.05 ~ 500 μM范围内具有浓度依赖性,检出限(S/N=3)为0.04 μM。此外,抗干扰研究表明,nAg/Cu2O纳米复合材料对抗坏血酸具有较高的选择性。值得注意的是,基于nAg/Cu2O的传感器表现出出色的稳定性和可重复性,在一周的测试时间内,峰值电流的相对标准偏差测量约为7%或更低。通过对市售维生素C片中抗坏血酸的鉴别,实现了该方法的实际应用和分析性能。
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引用次数: 0
Advancing Breath Biomarker Detection with Chemiresistive Metal Oxide Nanostructures: A Pathway to Next-Generation Diagnostic Tools 利用化学阻性金属氧化物纳米结构推进呼吸生物标志物检测:通往下一代诊断工具的途径
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-02-03 DOI: 10.1002/anse.202400111
Jesse Nii Okai Amu-Darko

Breath biomarker detection represents a transformative frontier in non-invasive diagnostics, offering rapid, real-time insights into health conditions ranging from metabolic disorders to cancer. Metal oxide nanostructures (MONs) have emerged as key materials in this research because of their large surface area, adjustable electrical characteristics, and sensitivity to gaseous biomarkers at trace quantities. This paper examines current advances in chemiresistive MON-based sensors, focusing on the importance of structural optimization, hybrid material systems, and functionalization strategies in improving performance. Exploring the study of complicated datasets, the prediction of biomarker signatures, and dynamic aims in tuning the quality of the sensors. Functionalization strategies also play a vital role in enhancing the performance of MON-based sensors. By modifying the surface chemistry of chemiresistive metal oxides, researchers can tailor the sensors to preferentially adsorb certain gaseous biomarkers while minimizing interference from other compounds present in breath. Future opportunities include the development of multimodal sensors, simplified and portable devices, and durable, reusable platforms capable of long-term operation in real-world environments. With the confluence of nanotechnology and data-driven analytics, MON-based breath sensors have the potential to transform customized healthcare by providing worldwide early detection, illness monitoring, and preventative medication.

呼吸生物标志物检测代表了非侵入性诊断的变革前沿,提供从代谢紊乱到癌症等健康状况的快速、实时洞察。金属氧化物纳米结构(MONs)由于其大表面积、可调节的电特性和对微量气体生物标志物的敏感性而成为这项研究的关键材料。本文综述了化学阻性氮化镓传感器的最新进展,重点介绍了结构优化、混合材料系统和功能化策略在提高性能方面的重要性。探索复杂数据集的研究,生物标志物特征的预测,以及调整传感器质量的动态目标。功能化策略在提高基于mon的传感器性能方面也起着至关重要的作用。通过修改耐化学金属氧化物的表面化学性质,研究人员可以定制传感器,使其优先吸附某些气体生物标志物,同时最大限度地减少呼吸中其他化合物的干扰。未来的机会包括开发多模态传感器、简化和便携式设备,以及能够在现实环境中长期运行的耐用、可重复使用的平台。随着纳米技术和数据驱动分析的融合,基于mon的呼吸传感器有可能通过提供全球早期检测、疾病监测和预防性药物来改变定制医疗保健。
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引用次数: 0
A Smartphone-Integrated Coated Microneedle Sensor for In-Situ Extraction and Rapid Detection of Total Phenols in Fruits and Vegetables 智能手机集成涂层微针传感器用于果蔬中总酚的原位提取和快速检测
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-01-24 DOI: 10.1002/anse.202400114
Rui Li, Shiyu Liu, Long Chen, Chao Huang, Prof. Xin Jia

As interest in monitoring the nutritional and antioxidant levels in fruits and vegetables grows, the need for efficient, non-invasive detection methods increases. In this work, a novel coated microneedle colorimetric sensing platform is designed to rapidly and sensitively detect total phenolic compounds (TPC) in fruits and vegetables, which is the key indicator of their nutritional and antioxidant properties. The platform utilizes a swollen microneedle structure to efficiently collect juice samples, enhancing detection efficiency through colorimetric analysis and eliminating the complexity of traditional methods. The microneedles are fabricated from a composite material consisting of 10,12-pentacosadiynoic acid (PCDA) and methacrylated gelatin (GelMA), with a secondary layer containing α-cyclodextrin to selectively bind polyphenols, thereby inducing a visible color change for the specific detection of TPC. The colorimetric response is directly correlated with the concentration of TPC, facilitating on-site analysis. Using phenol as a model molecule, the detection range of the system for phenol is 10–60 mM, with an LOD of 0.5 mM. Furthermore, a mobile application enables portable detection and analysis, reducing detection time from several hours to just 30 min. This technology offers a promising approach for the rapid, reliable monitoring of phenolic content in fresh produce, with potential applications in food quality control, nutritional analysis, and agricultural monitoring.

随着人们对监测水果和蔬菜中的营养和抗氧化水平的兴趣的增长,对高效、非侵入性检测方法的需求也在增加。本文设计了一种新型的包被微针比色传感平台,用于快速、灵敏地检测水果和蔬菜中的总酚类化合物(TPC),这是衡量水果和蔬菜营养和抗氧化性能的关键指标。该平台采用膨胀微针结构,高效采集果汁样品,通过比色分析提高检测效率,消除了传统方法的复杂性。该微针由10,12-五甲酸(PCDA)和甲基丙烯酸明胶(GelMA)组成的复合材料制成,第二层含有α-环糊精选择性结合多酚,从而诱导可见的颜色变化,用于TPC的特异性检测。比色响应与TPC浓度直接相关,便于现场分析。以苯酚为模型分子,该系统对苯酚的检测范围为10 - 60mm, LOD为0.5 mM。此外,移动应用程序可以实现便携式检测和分析,将检测时间从几个小时缩短到30分钟。该技术为快速、可靠地监测新鲜农产品中酚类物质含量提供了一种有前景的方法,在食品质量控制、营养分析和农业监测方面具有潜在的应用前景。
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引用次数: 0
Front Cover: Metal-Organic Frameworks (MOFs) for Glucose Sensing: Advancing Non-Invasive Detection Strategies in Diabetes Management (Anal. Sens. 1/2025) 封面:用于葡萄糖传感的金属有机框架(MOFs):推进糖尿病管理中的非侵入性检测策略。参议员1/2025)
IF 2.9 Q2 CHEMISTRY, ANALYTICAL Pub Date : 2025-01-13 DOI: 10.1002/anse.202580101
P. N. Blessy Rebecca, D. Durgalakshmi, R. Ajay Rakkesh

Metal-organic frameworks (MOFs) offer an impeccable platform for glucose sensing, contributing in both enzymatic- and non-enzymatic-based electrochemical detection. Comprising metal ions and organic ligands, MOFs with their exceptional properties including tunable porosity, high surface area, diverse structural configuration, strong adsorptive capacity, electrocatalytic behavior, and abundant active sites pave way for improving healthcare diagnostics. More in the Review by R. Ajay Rakkesh and co-workers.

金属有机框架(mof)为葡萄糖传感提供了一个完美的平台,有助于酶和非酶的电化学检测。mof由金属离子和有机配体组成,具有孔隙度可调、比表面积高、结构构型多样、吸附能力强、电催化性能好、活性位点丰富等特点,为改善医疗诊断铺平了道路。R. Ajay Rakkesh及其同事的更多评论。
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引用次数: 0
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