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Paper-based electrochemiluminescence telomerase activity detection using hybridization chain reaction and CRISPR/Cas12a dual signal amplification
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-26 DOI: 10.1016/j.bioelechem.2025.108916
Yun Zhang , Liang Gao , Zhe Shi , Qiong Wu , Xiangmin Miao
Sensitive telomerase activity detection becomes particularly significance since the important value of it in early cancer diagnosis as a potential biomarker. Herein, we developed a paper-based analytical devices (PADs) for telomerase activity detection, using positively charged Au@luminol nanoparticles ((+)Au@luminol NPs) as electrochemiluminescence (ECL) signal probe coupling with hybridization chain reaction (HCR) and CRISPR/Cas12a dual signal amplification. Firstly, the initial strong ECL signal was obtained based on the electrostatic adsorption of (+)Au@luminol NPs onto the surface of HCR double-stranded hybrid aggregates. In the presence of telomerase, the primer was efficiently elongated with telomeric repeats of (TTAGGG)n to release activator DNA and trigger the CRISPR/Cas12a, which can prevent the happen of HCR and the adsorption of (+)Au@luminol NPs through cleaving the capture probe on the electrode surface, such results directly inducing the decrease of the ECL signal that was proportional to telomerase concentration, due to the efficient signal amplification of HCR and CRISPR/Cas12a, a low detection limit of 2.3 cells/mL for telomerase could be detected. Moreover, the sensor realized the effective application for telomerase extracts analysis in human serum samples, making it possess potential application value for telomerase activity assays in cancer diagnostics.
{"title":"Paper-based electrochemiluminescence telomerase activity detection using hybridization chain reaction and CRISPR/Cas12a dual signal amplification","authors":"Yun Zhang ,&nbsp;Liang Gao ,&nbsp;Zhe Shi ,&nbsp;Qiong Wu ,&nbsp;Xiangmin Miao","doi":"10.1016/j.bioelechem.2025.108916","DOIUrl":"10.1016/j.bioelechem.2025.108916","url":null,"abstract":"<div><div>Sensitive telomerase activity detection becomes particularly significance since the important value of it in early cancer diagnosis as a potential biomarker. Herein, we developed a paper-based analytical devices (PADs) for telomerase activity detection, using positively charged Au@luminol nanoparticles ((+)Au@luminol NPs) as electrochemiluminescence (ECL) signal probe coupling with hybridization chain reaction (HCR) and CRISPR/Cas12a dual signal amplification. Firstly, the initial strong ECL signal was obtained based on the electrostatic adsorption of (+)Au@luminol NPs onto the surface of HCR double-stranded hybrid aggregates. In the presence of telomerase, the primer was efficiently elongated with telomeric repeats of (TTAGGG)<sub>n</sub> to release activator DNA and trigger the CRISPR/Cas12a, which can prevent the happen of HCR and the adsorption of (+)Au@luminol NPs through cleaving the capture probe on the electrode surface, such results directly inducing the decrease of the ECL signal that was proportional to telomerase concentration, due to the efficient signal amplification of HCR and CRISPR/Cas12a, a low detection limit of 2.3 cells/mL for telomerase could be detected. Moreover, the sensor realized the effective application for telomerase extracts analysis in human serum samples, making it possess potential application value for telomerase activity assays in cancer diagnostics.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"164 ","pages":"Article 108916"},"PeriodicalIF":4.8,"publicationDate":"2025-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143155422","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An electrochemiluminescence strategy with proximity ligation triggered multiple catalytic hairpin assembly induced CRISPR/Cas 12a system for analysis of paraquat
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-25 DOI: 10.1016/j.bioelechem.2025.108915
Wen-Jie Zhong , Wei-Guo Yang , Ying Zhang , Tao Li , Ming-Li Su , Ruo Yuan , Shangcheng Xu , Wen-Bin Liang
Paraquat (PQ) as a widely used non-selective herbicides has gained attention in agricultural residue detection and food safety. Herein, a novel quantitative analysis approach for PQ was proposed based on a novel kind of aggregation-induced emission electrochemiluminescence (AIECL) emitters, tetraphenylethylene-luminol (TPE-L) with a small molecule-induced multiple catalytic hairpin assembly (CHA) amplification strategy, the competitive immune reaction and CRISPR/Cas12a system. The target molecule PQ is introduced into a signal cycle, and auxiliary sensitization cycles are constructed by virtue of the cleavage characteristics of the CRISPR/Cas12a system, which realized the multiple utilization of the target by using both cis- and trans-cleavage activities. In addition, the new multiple CHA amplification strategy was attributed to cross-catalytic hairpin assembly caused by the products of the CHA cycle as the initiator chain of the next CHA cycle, realizing the efficient utilization of cyclic products and producing high-efficiency signal amplification. Thus, the ECL biosensor for ultrasensitive analysis of PQ was successfully constructed with a limit of detection of 0.7 pg/mL. Importantly, it could be easily-extended to other small molecules simply by replacing paired antibodies, providing prospects in agricultural residue detection, food safety and related medical applications.
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引用次数: 0
Advanced cortisol detection: A cMWCNTs-enhanced MB@Zr-MOF ratiometric electrochemical aptasensor
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-23 DOI: 10.1016/j.bioelechem.2025.108914
Runran Ma , Te Li , Xueying Li , Jianwei Han , Xin Zhang , Tingting Di , Jiabo Wang , Weijun Kong
A ratiometric electrochemical aptasensor was developed for ultra-sensitive detection of cortisol using aptamer (Apt) as recognition element, methylene blue (MB) as signal probe, and zirconium metal–organic framework (Zr-MOF) as carrier loaded with abundant MB for signal amplification. The carboxylated multi-walled carbon nanotubes (cMWCNTs)-modified Au electrode showed excellent electrochemical performance to immobilize complementary DNA (cDNA) for hybridizing with MB@Zr-MOF-Apt via amide bonds. In the presence of cortisol, it would compete with cDNA for binding the Apt, resulting in the detachment of MB@Zr-MOF-Apt complex from the electrode surface, and the electrochemical signal of MB was decreased, while that of [Fe(CN)6]3−/4− was basically unchanged. The ratio of the electrochemical signals of [Fe(CN)6]3−/4− to MB was proportional to the cortisol concentration. Due to the greatly enhanced conductivity of the cMWCNTs-decorated Au electrode and the largely improved EC signals of Zr-MOF encapsulated MB probes, this ratiometric electrochemical aptasensor offered high sensitivity with an ultra-low detection limit of 0.0046 nM and a wide linearity of 0.01–1000 nM, as well as satisfactory accuracy with recoveries of 93.79–106.76 % in artificial sweat samples, providing a potential strategy for the detection of more trace hormones in different clinical samples by simply replacing the corresponding aptamers.
以适配体(Apt)为识别元件,亚甲基蓝(MB)为信号探针,锆金属有机框架(Zr-MOF)为载体,负载丰富的甲基蓝(MB)进行信号放大,开发了一种用于超灵敏检测皮质醇的比率计量电化学适配体传感器。羧化多壁碳纳米管(cMWCNTs)修饰的金电极显示出优异的电化学性能,可固定互补 DNA(cDNA),通过酰胺键与 MB@Zr-MOF-Apt 杂交。在皮质醇存在的情况下,皮质醇会与 cDNA 竞争结合 Apt,导致 MB@Zr-MOF-Apt 复合物从电极表面脱离,MB 的电化学信号降低,而[Fe(CN)6]3-/4- 的电化学信号基本不变。[Fe(CN)6]3-/4-与甲基溴电化学信号的比值与可的松浓度成正比。由于经 cMWCNTs 装饰的金电极的电导率大大提高,而封装了 Zr-MOF 的甲基溴探针的电化学信号也有很大改善,因此这种比率电化学传感器灵敏度高,检出限超低,仅为 0.0046 nM 的超低检测限和 0.01-1000 nM 的宽线性度,以及令人满意的准确度(在人工汗液样品中的回收率为 93.79-106.76 %)。
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引用次数: 0
An electrochemical aptasensor based on bimetallic carbon nanocomposites AuPt@rGO for ultrasensitive detection of adenosine on portable potentiostat
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-22 DOI: 10.1016/j.bioelechem.2025.108906
Zheng Gong , Hongli Zhao , Yi Mao , Fangfang Zhou , Zehui Shi , Minbo Lan
Adenosine plays a crucial role in the cardiovascular and nervous systems of living organisms. Excessive adenosine can lead to arrhythmias or heart failure, making the accurate detection of adenosine highly valuable. Given the widespread use of sensors for detecting small molecules, we propose a sensitive electrochemical aptasensor for adenosine detection in this study. The aptasensor utilized reduced graphene oxide (rGO) as the base material, and its performance was further enhanced by loading gold-platinum nanoparticles (AuPt@rGO) to improve the current response. The AuPt@rGO composite was synthesized using a simple process and was modified onto screen-printed electrodes (SPE) fabricated in the laboratory. This modification increased the effective area of the working electrode, providing more contact sites and enhancing sensitivity for adenosine detection. As a result, the sensor exhibited excellent performance in selectivity, sensitivity, and stability, with a linear response range for adenosine from 10 nM to 10 μM and a detection limit of 1.28 nM (n = 3). Furthermore, successful detection of adenosine levels in real samples was achieved using a portable potentiostat, demonstrating excellent recovery rates (95.99 %–103.4 %). These results indicate the aptasensor’s significant potential for future applications in field analysis and medical diagnostics.
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引用次数: 0
Cytochrome P450 electrochemical biosensors transforming in vitro metabolism testing – Opportunities and challenges
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-21 DOI: 10.1016/j.bioelechem.2025.108913
Carina S.P. Vieira, Marcela A. Segundo, Alberto N. Araújo
The ability of the living world to flourish in the face of constant exposure to dangerous chemicals depends on the management ability of a widespread group of enzymes known as heme-thiolate monooxygenases or cytochrome P450 superfamily. About three-quarters of all reactions determining the metabolism of endogenous compounds, of those carried in foods, of taken drugs, or even of synthetic chemicals discarded into the environment depend on their catalytic performance. The chromatographic and (photo)luminometric methods routinely used as predictive and analytical tools in laboratories have significant drawbacks ranging from limited shelf-life of reagents, use of synthetic substrates, laborious and tedious procedures for highly sensitive detection. In this review, alternative electrochemical biosensors using the cytochrome P450 enzymes as bio-element are emphasized in their main aspects as well regarding their implementation and usefulness. Despite the various schemes proposed for the implementation, reports on real applications are scant for several reasons, including low reaction rates, broad substrate specificity, uncoupling reactions occurrence, and the need for expensive electron transfer partners to promote electron transfer. Finally, the prospect for future developments is introduced, focusing on integrating miniaturized systems with electrochemical techniques, alongside optimizing enzyme immobilization methods and electrode modifications to improve enzymatic stability and enhance sensor reliability. This progress represents a crucial step towards the creation of portable biosensors that mimic human physiological responses, supporting the precision medicine approach.
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引用次数: 0
Real-time prediction of heparin concentration in blood extracorporeal circulation by relaxation time distribution (RTD)
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-20 DOI: 10.1016/j.bioelechem.2025.108912
Soichiro Ueno , Daisuke Kawashima , Katsuhiro Matsuura , Hiromichi Obara , Ryou Tanaka , Masahiro Takei
<div><div>Heparin concentration <span><math><mrow><mi>c</mi></mrow></math></span> in a blood extracorporeal circulation has been real-timely predicted based on the relaxation strength <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mi>m</mi></msub></mrow></math></span> at relaxation frequency <span><math><mrow><msub><mi>f</mi><mi>m</mi></msub></mrow></math></span> extracted by relaxation time distribution (RTD). The simulated extracorporeal circulation was conducted to optimize the number of <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mi>m</mi></msub></mrow></math></span> for the prediction of <em>c</em> using the porcine whole blood (WB) and low-leukocyte and −platelet blood (LLPB) under the condition of the gradual increment of <span><math><mrow><mi>c</mi></mrow></math></span> from 0 to 8 U/mL with constant flow rate and blood temperature. The experimental results show that among the three relaxation strengths <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>1</mn></msub></mrow></math></span>, <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>2</mn></msub></mrow></math></span> and <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>3</mn></msub></mrow></math></span> (in ascending order of frequency), <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>2</mn></msub></mrow></math></span> at <span><math><mrow><msub><mi>f</mi><mn>2</mn></msub></mrow></math></span> = 5.2 ∼ 6.2 MHz and <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>3</mn></msub></mrow></math></span> at <span><math><mrow><msub><mi>f</mi><mn>3</mn></msub></mrow></math></span> = 42 ∼ 50 MHz were correlated to <span><math><mrow><mi>c</mi></mrow></math></span>. The <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>3</mn></msub></mrow></math></span> was decreasing with increasing <span><math><mrow><mi>c</mi></mrow></math></span> in both cases, which was influenced by the plasma macromolecular concentrations, while the <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>2</mn></msub></mrow></math></span> was increased with increasing <em>c</em> in WB case but was hardly changed in LLPB case because the <span><math><mrow><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>2</mn></msub></mrow></math></span> is influenced by the blood cell concentrations and the shape changes of blood cell membranes. Heparin concentration <span><math><mrow><mi>c</mi></mrow></math></span> is estimated by the linear regression formula <span><math><mrow><msup><mrow><mi>c</mi></mrow><mrow><mi>P</mi><mi>R</mi><mi>E</mi></mrow></msup><mo>=</mo><msub><mi>a</mi><mn>1</mn></msub><msub><mrow><mo>(</mo><mi>Δ</mi><mi>ε</mi></mrow><mn>2</mn></msub><mo>-</mo><msubsup><mrow><mi>Δ</mi><mi>ε</mi></mrow><mrow><mn>2</mn></mrow><mrow><mi>c</mi><mo>=</mo><mn>0</mn></mrow></msubsup><mrow><mo>)</mo><mo>+</mo></mrow><msub><mi>a</mi><mn>2</mn></msub><mrow><mo>(</mo><msub><mrow><mi>Δ</mi><mi>ε</mi></mrow><mn>3</mn></msub><mo>-</mo><msubsup><mrow><
{"title":"Real-time prediction of heparin concentration in blood extracorporeal circulation by relaxation time distribution (RTD)","authors":"Soichiro Ueno ,&nbsp;Daisuke Kawashima ,&nbsp;Katsuhiro Matsuura ,&nbsp;Hiromichi Obara ,&nbsp;Ryou Tanaka ,&nbsp;Masahiro Takei","doi":"10.1016/j.bioelechem.2025.108912","DOIUrl":"10.1016/j.bioelechem.2025.108912","url":null,"abstract":"&lt;div&gt;&lt;div&gt;Heparin concentration &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; in a blood extracorporeal circulation has been real-timely predicted based on the relaxation strength &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mi&gt;m&lt;/mi&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; at relaxation frequency &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mi&gt;f&lt;/mi&gt;&lt;mi&gt;m&lt;/mi&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; extracted by relaxation time distribution (RTD). The simulated extracorporeal circulation was conducted to optimize the number of &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mi&gt;m&lt;/mi&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; for the prediction of &lt;em&gt;c&lt;/em&gt; using the porcine whole blood (WB) and low-leukocyte and −platelet blood (LLPB) under the condition of the gradual increment of &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; from 0 to 8 U/mL with constant flow rate and blood temperature. The experimental results show that among the three relaxation strengths &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;1&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt;, &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; and &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;3&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; (in ascending order of frequency), &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; at &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mi&gt;f&lt;/mi&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; = 5.2 ∼ 6.2 MHz and &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;3&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; at &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mi&gt;f&lt;/mi&gt;&lt;mn&gt;3&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; = 42 ∼ 50 MHz were correlated to &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt;. The &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;3&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; was decreasing with increasing &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; in both cases, which was influenced by the plasma macromolecular concentrations, while the &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; was increased with increasing &lt;em&gt;c&lt;/em&gt; in WB case but was hardly changed in LLPB case because the &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; is influenced by the blood cell concentrations and the shape changes of blood cell membranes. Heparin concentration &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;/mrow&gt;&lt;/math&gt;&lt;/span&gt; is estimated by the linear regression formula &lt;span&gt;&lt;math&gt;&lt;mrow&gt;&lt;msup&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mi&gt;P&lt;/mi&gt;&lt;mi&gt;R&lt;/mi&gt;&lt;mi&gt;E&lt;/mi&gt;&lt;/mrow&gt;&lt;/msup&gt;&lt;mo&gt;=&lt;/mo&gt;&lt;msub&gt;&lt;mi&gt;a&lt;/mi&gt;&lt;mn&gt;1&lt;/mn&gt;&lt;/msub&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mo&gt;(&lt;/mo&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;mo&gt;-&lt;/mo&gt;&lt;msubsup&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mi&gt;c&lt;/mi&gt;&lt;mo&gt;=&lt;/mo&gt;&lt;mn&gt;0&lt;/mn&gt;&lt;/mrow&gt;&lt;/msubsup&gt;&lt;mrow&gt;&lt;mo&gt;)&lt;/mo&gt;&lt;mo&gt;+&lt;/mo&gt;&lt;/mrow&gt;&lt;msub&gt;&lt;mi&gt;a&lt;/mi&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/msub&gt;&lt;mrow&gt;&lt;mo&gt;(&lt;/mo&gt;&lt;msub&gt;&lt;mrow&gt;&lt;mi&gt;Δ&lt;/mi&gt;&lt;mi&gt;ε&lt;/mi&gt;&lt;/mrow&gt;&lt;mn&gt;3&lt;/mn&gt;&lt;/msub&gt;&lt;mo&gt;-&lt;/mo&gt;&lt;msubsup&gt;&lt;mrow&gt;&lt;","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"163 ","pages":"Article 108912"},"PeriodicalIF":4.8,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143035352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of micro-nanostructured film with antibacterial, anticorrosive and thermal conductivity properties on copper surface
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-15 DOI: 10.1016/j.bioelechem.2025.108905
Li Lai, Muqiu Xia, Mengyu Fu, Yuanyuan Gao, Jiahao Sun, Guangzhou Liu, Shiqiang Chen
A micro-nano sharkskin like film (Cu-MNS-FA) was synthesized on copper surface through chemical etching followed by formate passivation, and its anticorrosive, antibacterial and thermal conductivity properties were investigated. Results show that after 7 d of exposure to nature, Pseudomonas aeruginosa and Desulfovibrio vulgaris seawater, the charge transfer resistance of Cu-MNS-FA is more than three times higher than that of unmodified copper. In particular, in D. vulgaris seawater, the Rct value of modified copper is 7 times higher than that of unmodified copper after the same exposure duration. The counts of sessile cells, specifically P. aeruginosa and D. vulgaris, on the surface of modified copper are reduced by > 88 % after 3 days of immersion. Furthermore, thermal conductivity remains 10 % higher than that of untreated copper after 7 d of immersion. This film improves the performance characteristics of copper in seawater heat exchange systems.
{"title":"Development of micro-nanostructured film with antibacterial, anticorrosive and thermal conductivity properties on copper surface","authors":"Li Lai,&nbsp;Muqiu Xia,&nbsp;Mengyu Fu,&nbsp;Yuanyuan Gao,&nbsp;Jiahao Sun,&nbsp;Guangzhou Liu,&nbsp;Shiqiang Chen","doi":"10.1016/j.bioelechem.2025.108905","DOIUrl":"10.1016/j.bioelechem.2025.108905","url":null,"abstract":"<div><div>A micro-nano sharkskin like film (Cu-MNS-FA) was synthesized on copper surface through chemical etching followed by formate passivation, and its anticorrosive, antibacterial and thermal conductivity properties were investigated. Results show that after 7 d of exposure to nature, <em>Pseudomonas aeruginosa</em> and <em>Desulfovibrio vulgaris</em> seawater, the charge transfer resistance of Cu-MNS-FA is more than three times higher than that of unmodified copper. In particular, in <em>D. vulgaris</em> seawater, the <em>R</em><sub>ct</sub> value of modified copper is 7 times higher than that of unmodified copper after the same exposure duration. The counts of sessile cells, specifically <em>P. aeruginosa</em> and <em>D. vulgaris</em>, on the surface of modified copper are reduced by &gt; 88 % after 3 days of immersion. Furthermore, thermal conductivity remains 10 % higher than that of untreated copper after 7 d of immersion. This film improves the performance characteristics of copper in seawater heat exchange systems.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"163 ","pages":"Article 108905"},"PeriodicalIF":4.8,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143027451","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Print-Light-Synthesis of ruthenium oxide thin film electrodes for electrochemical sensing applications
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-15 DOI: 10.1016/j.bioelechem.2025.108909
Stefano Gianvittorio , Marco Malferrari , Horst Pick , Stefania Rapino , Andreas Lesch
Print-Light-Synthesis (PLS) combines the inkjet printing of a ruthenium precursor ink with the simultaneous photo-induced generation of ruthenium oxide films. During PLS, inkjet-printing generates on conductive as well as insulating substrates micrometer-thin reaction volumes that contain with high precision defined precursor loadings. Upon direct UV light irradiation, the Ru precursor converts to RuO2 while all other ink components escape in the gas phase. No post PLS processes are required, and the as-obtained RuO2 films can be immediately used as electrochemical devices. Two-dimensional RuO2 patterns with micrometric resolution and highly-controlled ruthenium loadings (few µg/cm2) are realized. Thin RuO2 films are generated on insulating substrates, such as polyimide, as well as individual RuO2 particles on conductive substrates, such as graphene layers. The RuO2 films are characterized by electron microscopy and spectroscopic techniques. The sensoristic applicability of the PLS-RuO2 electrodes is demonstrated by potentiometric pH sensing in cell cultures and amperometric detection of L-cysteine. For pH sensing the RuO2 film electrodes show Nernstian sensitivity. L-cysteine detection of RuO2-modified graphene electrodes showed an electrocatalytical effect and resulted in the possibility of selectively detecting L-Cysteine also in presence of the interfering compound uric acid.
{"title":"Print-Light-Synthesis of ruthenium oxide thin film electrodes for electrochemical sensing applications","authors":"Stefano Gianvittorio ,&nbsp;Marco Malferrari ,&nbsp;Horst Pick ,&nbsp;Stefania Rapino ,&nbsp;Andreas Lesch","doi":"10.1016/j.bioelechem.2025.108909","DOIUrl":"10.1016/j.bioelechem.2025.108909","url":null,"abstract":"<div><div>Print-Light-Synthesis (PLS) combines the inkjet printing of a ruthenium precursor ink with the simultaneous photo-induced generation of ruthenium oxide films. During PLS, inkjet-printing generates on conductive as well as insulating substrates micrometer-thin reaction volumes that contain with high precision defined precursor loadings. Upon direct UV light irradiation, the Ru precursor converts to RuO<sub>2</sub> while all other ink components escape in the gas phase. No post PLS processes are required, and the as-obtained RuO<sub>2</sub> films can be immediately used as electrochemical devices. Two-dimensional RuO<sub>2</sub> patterns with micrometric resolution and highly-controlled ruthenium loadings (few µg/cm<sup>2</sup>) are realized. Thin RuO<sub>2</sub> films are generated on insulating substrates, such as polyimide, as well as individual RuO<sub>2</sub> particles on conductive substrates, such as graphene layers. The RuO<sub>2</sub> films are characterized by electron microscopy and spectroscopic techniques. The sensoristic applicability of the PLS-RuO<sub>2</sub> electrodes is demonstrated by potentiometric pH sensing in cell cultures and amperometric detection of L-cysteine. For pH sensing the RuO<sub>2</sub> film electrodes show Nernstian sensitivity. L-cysteine detection of RuO<sub>2</sub>-modified graphene electrodes showed an electrocatalytical effect and resulted in the possibility of selectively detecting L-Cysteine also in presence of the interfering compound uric acid.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"163 ","pages":"Article 108909"},"PeriodicalIF":4.8,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143035350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced detection of Cystatin C for predicting adverse outcomes in gestational diabetes mellitus using a point-of-care immunosensor 利用即时免疫传感器增强胱抑素C检测,预测妊娠期糖尿病的不良结局。
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-13 DOI: 10.1016/j.bioelechem.2025.108907
Ya Jin , Yongmei Chen , Xiaoqin Li , Songjun Han , Lei Mou , Nan Li
Cystatin C (Cys-C) is emerging as a critical biomarker for assess gestational diabetes mellitus (GDM), a condition that significantly impacts maternal and fetal health. In this study, we developed a novel label-free electrochemical immunosensor designed for point-of-care applications, offering lower reagent consumption and rapid detection of Cys-C in pregnant women with GDM. Compared to traditional enzyme-linked immunosorbent assays (ELISA), the sensor demonstrates enhanced sensitivity, reduced reagent usage, and faster detection. In a cohort study involving 150 pregnant women with GDM and 150 healthy controls, serum Cys-C levels were analyzed using the developed sensor. Serum samples were collected and analyzed for Cys-C levels using our immunosensor. Serum Cys-C levels were significantly elevated in GDM patients compared to controls (P < 0.05), and higher levels were observed in GDM complicated by pregnancy-induced hypertension (PIH) and fetal growth restriction (FGR). Furthermore, elevated Cys-C levels were positively correlated with adverse pregnancy outcomes, including premature birth, fetal distress, and cesarean section (P < 0.05). This study underscores the potential of Cys-C as a reliable biomarker for GDM and highlights the advantages of our novel sensor for quick, accurate, and scalable GDM diagnosis and management.
妊娠期糖尿病(GDM)是一种严重影响母体和胎儿健康的疾病,胱抑素C (Cys-C)正成为评估妊娠期糖尿病(GDM)的关键生物标志物。在这项研究中,我们开发了一种新型的无标签电化学免疫传感器,设计用于护理点应用,提供更低的试剂消耗和快速检测GDM孕妇的Cys-C。与传统的酶联免疫吸附测定法(ELISA)相比,该传感器具有更高的灵敏度、更少的试剂使用量和更快的检测速度。在一项包括150名GDM孕妇和150名健康对照者的队列研究中,使用开发的传感器分析了血清Cys-C水平。使用我们的免疫传感器收集血清样本并分析Cys-C水平。GDM患者血清Cys-C水平显著高于对照组(P < 0.05),且GDM合并妊高征(PIH)和胎儿生长受限(FGR)患者血清Cys-C水平更高。此外,Cys-C水平升高与早产、胎儿窘迫、剖宫产等不良妊娠结局呈正相关(P < 0.05)。这项研究强调了Cys-C作为一种可靠的GDM生物标志物的潜力,并强调了我们的新型传感器在快速、准确和可扩展的GDM诊断和管理方面的优势。
{"title":"Enhanced detection of Cystatin C for predicting adverse outcomes in gestational diabetes mellitus using a point-of-care immunosensor","authors":"Ya Jin ,&nbsp;Yongmei Chen ,&nbsp;Xiaoqin Li ,&nbsp;Songjun Han ,&nbsp;Lei Mou ,&nbsp;Nan Li","doi":"10.1016/j.bioelechem.2025.108907","DOIUrl":"10.1016/j.bioelechem.2025.108907","url":null,"abstract":"<div><div>Cystatin C (Cys-C) is emerging as a critical biomarker for assess gestational diabetes mellitus (GDM), a condition that significantly impacts maternal and fetal health. In this study, we developed a novel label-free electrochemical immunosensor designed for point-of-care applications, offering lower reagent consumption and rapid detection of Cys-C in pregnant women with GDM. Compared to traditional enzyme-linked immunosorbent assays (ELISA), the sensor demonstrates enhanced sensitivity, reduced reagent usage, and faster detection. In a cohort study involving 150 pregnant women with GDM and 150 healthy controls, serum Cys-C levels were analyzed using the developed sensor. Serum samples were collected and analyzed for Cys-C levels using our immunosensor. Serum Cys-C levels were significantly elevated in GDM patients compared to controls (P &lt; 0.05), and higher levels were observed in GDM complicated by pregnancy-induced hypertension (PIH) and fetal growth restriction (FGR). Furthermore, elevated Cys-C levels were positively correlated with adverse pregnancy outcomes, including premature birth, fetal distress, and cesarean section (P &lt; 0.05). This study underscores the potential of Cys-C as a reliable biomarker for GDM and highlights the advantages of our novel sensor for quick, accurate, and scalable GDM diagnosis and management.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"163 ","pages":"Article 108907"},"PeriodicalIF":4.8,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142997142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conductive and flexible gold-coated polylactic acid nanofiber-based electrochemical aptasensor for monitoring cortisol level in sweat and saliva 用于监测汗液和唾液中皮质醇水平的导电柔性金包覆聚乳酸纳米纤维电化学适体传感器。
IF 4.8 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-01-13 DOI: 10.1016/j.bioelechem.2025.108908
Mkliwa Koumbia, Takai Madoka
Conductive nanofibers can exhibit excellent mechanical properties such as flexibility, elasticity, porosity, large surface area-to-volume ratio, etc making them suitable for a wide range of applications including biosensor development. Their large surface area provides more active sites for immobilization of large amount of bioreceptors enabling more interaction sites with the target analytes, enhancing sensitivity and detection capabilities. However, engineering conductive nanofibers with such excellent properties is challenging limiting their effective deployment for intended applications. In this research, we propose a novel approach for easy fabrication of highly conductive and flexible nanofiber leveraging the electrospinning, electroless deposition and have applied it to cortisol monitoring; a common biomarker for stress which is often quantified through enzyme-linked immunoassays using blood or saliva samples. By adopting the nanofiber sheet as a transducer for aptamer immobilization and cortisol sensing our developed biosensor was able to detect cortisol in buffer, artificial saliva, and artificial sweat within five minutes, from 10 pg/mL to 10 µg/mL (27.59 pM to 27.59 µM) with a low detection limit of 1 pg/ml (2.76 pM). The Au-coated PLA nanofiber-based electrochemical biosensor’s flexibility allows for compact manufacturing, rendering it an optimal choice for integration into point-of-care testing and wearable systems.
导电纳米纤维具有优异的机械性能,如柔韧性、弹性、孔隙率、大表面积体积比等,适用于包括生物传感器开发在内的广泛应用。它们的大表面积为大量生物受体的固定化提供了更多的活性位点,使其与目标分析物有更多的相互作用位点,提高了灵敏度和检测能力。然而,具有如此优异性能的工程导电纳米纤维是一项挑战,限制了它们在预期应用中的有效部署。在这项研究中,我们提出了一种利用静电纺丝、化学沉积制备高导电性和柔性纳米纤维的新方法,并将其应用于皮质醇监测;一种常见的压力生物标志物,通常通过使用血液或唾液样本进行酶联免疫测定来量化。通过采用纳米纤维片作为适体固定和皮质醇传感的传感器,我们开发的生物传感器能够在5分钟内检测缓冲液,人工唾液和人工汗液中的皮质醇,检测范围从10 pg/mL到10µg/mL (27.59 pM到27.59µM),低检测限为1 pg/mL (2.76 pM)。基于au涂层PLA纳米纤维的电化学生物传感器的灵活性允许紧凑型制造,使其成为集成到护理点测试和可穿戴系统中的最佳选择。
{"title":"Conductive and flexible gold-coated polylactic acid nanofiber-based electrochemical aptasensor for monitoring cortisol level in sweat and saliva","authors":"Mkliwa Koumbia,&nbsp;Takai Madoka","doi":"10.1016/j.bioelechem.2025.108908","DOIUrl":"10.1016/j.bioelechem.2025.108908","url":null,"abstract":"<div><div>Conductive nanofibers can exhibit excellent mechanical properties such as flexibility, elasticity, porosity, large surface area-to-volume ratio, etc making them suitable for a wide range of applications including biosensor development. Their large surface area provides more active sites for immobilization of large amount of bioreceptors enabling more interaction sites with the target analytes, enhancing sensitivity and detection capabilities. However, engineering conductive nanofibers with such excellent properties is challenging limiting their effective deployment for intended applications. In this research, we propose a novel approach for easy fabrication of highly conductive and flexible nanofiber leveraging the electrospinning, electroless deposition and have applied it to cortisol monitoring; a common biomarker for stress which is often quantified through enzyme-linked immunoassays using blood or saliva samples. By adopting the nanofiber sheet as a transducer for aptamer immobilization and cortisol sensing our developed biosensor was able to detect cortisol in buffer, artificial saliva, and artificial sweat within five minutes, from 10 pg/mL to 10 µg/mL (27.59 pM to 27.59 µM) with a low detection limit of 1 pg/ml (2.76 pM). The Au-coated PLA nanofiber-based electrochemical biosensor’s flexibility allows for compact manufacturing, rendering it an optimal choice for integration into point-of-care testing and wearable systems.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"163 ","pages":"Article 108908"},"PeriodicalIF":4.8,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142997139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Bioelectrochemistry
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