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A Portable, Electromagnetically-Driven Microfluidic System for Molecular Diagnosis of SARS-CoV-2 and Influenza A/B Viruses 便携式电磁驱动微流控系统用于SARS-CoV-2和流感A/B病毒的分子诊断
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-13 DOI: 10.1016/j.snb.2025.139324
Ko-Hua Lin, Chih-Hung Wang, Ying-Jun Lin, Wen-Yen Huang, Yan-Shen Shan, Huey-Pin Tsai, Gwo-Bin Lee
The clinical symptoms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are similar to those of influenza viruses (such as type A, Inf A and type B, Inf B). However, the treatment and vaccines for COVID-19 and the Flu diseases differ, respectively. There exists a critical unmet clinical need for development of rapid, sensitive, and accurate point-of-care (POC) devices to detect these three viruses. Although traditional real-time reverse transcription polymerase chain reaction (qRT-PCR) is sensitive and specific, it requires large-scale equipment and skilled personnel in clinical setting. To address this issue, we developed a compact (25 × 25 × 17cm), electromagnetically-driven microfluidic system capable of performing virus capture, lysis, qRT-PCR, and fluorescence quantification within 100minutes with only 50μL of sample. The integrated microfluidic system was employed to conduct 50 blinded clinical assessments, which included 8 simulated co-infection samples. The system’s performance was compared with the gold standard by using accuracy, sensitivity, specificity, positive predictive value, and negative predictive value. For SARS-CoV-2 (E and RdRp genes), the metrics were 97.6%, 100.0%, 96.5%, 92.8%, and 100.0%. For Inf A, they were 95.2%, 90.0%, 96.8%, 90.0%, and 96.8%. For Inf B, all metrics reached 100.0%. This confirms that this portable, automated, easy-to-operate microfluidic system, with its optimized optical detection system, is suitable for POC testing.
严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的临床症状与流感病毒(如A型、Inf A型和B型、Inf B型)相似。然而,COVID-19和流感的治疗方法和疫苗各不相同。开发快速、灵敏和准确的即时护理(POC)设备检测这三种病毒的临床需求尚未得到满足。虽然传统的实时逆转录聚合酶链式反应(qRT-PCR)具有敏感性和特异性,但在临床上需要大量的设备和熟练的人员。为了解决这个问题,我们开发了一个紧凑的(25 × 25 × 17cm),电磁驱动的微流控系统,能够在100分钟内进行病毒捕获,裂解,qRT-PCR和荧光定量,只有50μL的样品。采用集成微流控系统进行50例盲法临床评估,包括8例模拟共感染样本。通过准确度、灵敏度、特异性、阳性预测值和阴性预测值与金标准进行比较。对于SARS-CoV-2 (E和RdRp基因),指标分别为97.6%、100.0%、96.5%、92.8%和100.0%。对干扰素,分别为95.2%、90.0%、96.8%、90.0%和96.8%。对于Inf B,所有指标都达到了100.0%。这证实了这种便携式、自动化、易于操作的微流体系统及其优化的光学检测系统适合POC测试。
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引用次数: 0
Surface Engineering of Ionized Carbon Nanotube Sensors for Enhanced Detection of SF₆ Decomposition Gases in High-Voltage Circuit Breakers 离子碳纳米管传感器对高压断路器中货号分解气体检测的表面工程
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-12 DOI: 10.1016/j.snb.2025.139319
Saif Aldeen Saad Obayes AL-KADHIM, Yong Zhang, Waqas Muhammad, Jinghui Shi
This study presents surface-engineered ionized carbon nanotube (CNT) sensors for detecting sulfur hexafluoride (SF₆) decomposition products, achieving exceptional sensitivity and selectivity in real-time gas monitoring. SF₆ is widely used as an insulating gas in high-voltage electrical equipment, but under fault conditions decomposes into by-products such as sulfur dioxide (SO₂) and thionyl fluoride (SOF₂), which are crucial indicators of equipment degradation requiring precise detection for predictive maintenance.Conventional methods including gas chromatography (GC), infrared spectroscopy (IR), and semiconductor metal-oxide (MOX) sensors face limitations in continuous on-site monitoring due to complex instrumentation, high operating temperatures (>200°C), or inadequate selectivity. To overcome these challenges, a three-electrode field-ionization CNT sensor was developed featuring a uniform gold nanoparticle coating that enhances electron emission efficiency through work function reduction. The sensor achieved experimentally determined detection limits of 1 ppm for SOF₂ and 20 ppb for SO₂, with maximum sensitivities of −1.10 nA/ppm (40°C) and −0.964 nA/ppm (50°C) for SOF₂, respectively—representing 5- to 14-fold improvements over conventional benchmarks. Optimization of electrode spacing (60 µm and 75 µm) balanced electric field strength and detection range up to 540 ppm. The sensor demonstrated rapid response kinetics (t₉₀ = 11–14 s) at 40–50°C operating temperature, excellent repeatability (CV < 5%), and acceptable reproducibility across three independently fabricated sensors (CV < 33%). Cross-sensitivity remained low (maximum 3.22%/ppm), confirming robust selectivity in SF₆ matrices. This work provides a high-performance solution for real-time monitoring, predictive maintenance, and enhanced operational safety in high-voltage circuit breakers.
本研究提出了用于检测六氟化硫(SF₆)分解产物的表面工程电离碳纳米管(CNT)传感器,在实时气体监测中实现了卓越的灵敏度和选择性。顺丰货号是一种广泛用于高压电气设备的绝缘气体,但在故障情况下会分解成二氧化硫(SO₂)和亚硫酰氟(sof2)等副产品,这些副产品是设备退化的关键指标,需要精确检测以进行预测性维护。传统的方法包括气相色谱(GC)、红外光谱(IR)和半导体金属氧化物(MOX)传感器,由于仪器复杂、工作温度高(>200°C)或选择性不足,在连续现场监测中面临限制。为了克服这些挑战,研究人员开发了一种三电极场电离碳纳米管传感器,该传感器具有均匀的金纳米颗粒涂层,通过减少功函数来提高电子发射效率。该传感器通过实验确定的sof2检测限为1 ppm, so2检测限为20 ppb, sof2的最大灵敏度分别为- 1.10 nA/ppm(40°C)和- 0.964 nA/ppm(50°C),比传统基准提高了5至14倍。优化电极间距(60µm和75µm)平衡电场强度和检测范围高达540 ppm。该传感器在40-50°C的工作温度下表现出快速的响应动力学(t₉₀= 11-14 s),出色的重复性(CV < 5%),以及三个独立制造的传感器的可重复性(CV < 33%)。交叉灵敏度仍然很低(最大3.22%/ppm),证实了SF₆矩阵的强大选择性。这项工作为高压断路器的实时监控、预测性维护和提高运行安全性提供了高性能解决方案。
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引用次数: 0
Electrochemical Multiplex Immunosensor Based on 3D Printing for Dengue NS1 Protein and Antibody Detection 基于3D打印的登革热NS1蛋白和抗体检测电化学复合免疫传感器
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-12 DOI: 10.1016/j.snb.2025.139321
Thomas A.C. Martins, Gustavo Martins, Maurício A.P. Papi, Luiz Humberto Marcolino-Junior, Márcio F. Bergamini
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引用次数: 0
Logic-gate driven ratiometric fluorescent platform for smartphone-based danofloxacin quantification using thymidine-lanthanide cooperative carbon dots with high selectivity 高选择性胸苷-镧系协同碳点在智能手机上定量danoflo沙星的逻辑门驱动比例荧光平台
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-12 DOI: 10.1016/j.snb.2025.139317
Yawen Zhao, Lei Jia, Xiangzhen Chen, Jun Xu, Tongqian Zhao
Based on the selective fluorescence enhancement effect of danofloxacin (DANO) on a novel europium (Eu) complex, this study developed a fluorescence detection method utilizing a thymidine-Eu (T-Eu) complex as the fluorescent platform and green fluorescent carbon dots (CDs) as an internal standard reference signal. This method was successfully applied to the determination of DANO content in real samples. The newly synthesized T-Eu complex utilizes the energy transfer mechanism between thymidine and rare earth elements, exhibiting weak red fluorescence upon excitation with 365 nm UV light. Notably, the fluorescence intensity was significantly enhanced in the presence of DANO through the so-called “antenna effect”. Meanwhile, green fluorescent carbon dots were synthesized using catechol as the carbon source and ethylenediamine as the nitrogen dopant. Experimental results demonstrated that the developed CDs/T-Eu fluorescent probe exhibited favorable linear responses within DANO concentration ranges of 0-10 μM and 10-25 μM, with correlation coefficients (R2) of 0.9821 and 0.9848, respectively. The limit of detection (LOD) was determined as low as 5.94 nM. Furthermore, the probe exhibited excellent selectivity and stability in practical food sample analysis, while also being simple to operate, safe, and environmentally friendly. Additionally, this study incorporated the design of logic gate circuits, thereby expanding the potential applications of fluorescent nanoprobes in intelligent device systems. In conclusion, the proposed method holds significant promise for DANO detection and offers novel strategies and technical support for the trace analysis of other environmental pollutants.
基于丹氧氟沙星(danoflo沙星,DANO)对一种新型铕(Eu)配合物的选择性荧光增强作用,本研究建立了以胸腺嘧啶-铕(T-Eu)配合物为荧光平台,绿色荧光碳点(CDs)为内标参考信号的荧光检测方法。该方法成功地应用于实际样品中DANO含量的测定。新合成的T-Eu配合物利用胸腺嘧啶与稀土元素之间的能量转移机制,在365 nm紫外光激发下表现出弱红色荧光。值得注意的是,在DANO存在下,荧光强度通过所谓的“天线效应”显著增强。同时,以儿茶酚为碳源,乙二胺为氮掺杂剂,合成了绿色荧光碳点。实验结果表明,CDs/T-Eu荧光探针在DANO浓度0 ~ 10 μM和10 ~ 25 μM范围内具有良好的线性响应,相关系数(R2)分别为0.9821和0.9848。检测限(LOD)低至5.94 nM。该探针在实际食品样品分析中具有良好的选择性和稳定性,同时操作简单、安全、环保。此外,本研究结合了逻辑门电路的设计,从而扩大了荧光纳米探针在智能设备系统中的潜在应用。总之,所提出的方法对DANO检测具有重要的前景,并为其他环境污染物的痕量分析提供了新的策略和技术支持。
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引用次数: 0
Fluorescence-enhanced biosensor based on conversion of RNA-to-DNA aptamer for detecting neomycin in food samples 基于rna - dna适配体转化的荧光增强生物传感器检测食品样品中的新霉素
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-12 DOI: 10.1016/j.snb.2025.139318
Hualin Guo, Pengfei Ma, Zhouping Wang
Neomycin (NEO) poses risks such as ototoxicity and nephrotoxicity through residual contamination. Therefore, it is urgent to develop an aptamer biosensor for highly sensitive identification of NEO. Compared to DNA aptamers, RNA aptamers are less commonly used due to their lower stability against nucleases. Herein, we carried out the transformation of a previously NEO RNA aptamer into DNA aptamer. Through systematic molecular dynamics studies, the conformational changes of RNA and DNA aptamers in the recognition of NEO were systematically explored. Additionally, a fluorescence-enhanced nanomaterial MOF@CuNCs was synthesized and integrated with the DNA aptamer to achieve the rapid, sensitive and efficient detection of NEO in milk and honey. The biosensor demonstrated excellent detection performance with a sensitive detection limit of 0.912 pg/mL. This work provides new strategies for aptamer redesign and supports biosensor development in food biosensing field.
新霉素(NEO)通过残留污染造成耳毒性和肾毒性等风险。因此,迫切需要开发一种适合NEO的高灵敏度生物传感器。与DNA适配体相比,RNA适配体较少使用,因为它们对核酸酶的稳定性较低。在此,我们将先前的NEO RNA适体转化为DNA适体。通过系统的分子动力学研究,系统探讨了RNA和DNA适体在NEO识别过程中的构象变化。此外,合成了荧光增强纳米材料MOF@CuNCs,并与DNA适体结合,实现了牛奶和蜂蜜中NEO的快速、灵敏、高效检测。该传感器具有良好的检测性能,检测限为0.912 pg/mL。该研究为适配体的重新设计提供了新的策略,并为食品生物传感领域生物传感器的发展提供了支持。
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引用次数: 0
A portable digital RT-LAMP platform for rapid detection of various viruses 便携式数字RT-LAMP平台,用于快速检测各种病毒
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-12 DOI: 10.1016/j.snb.2025.139320
Liang Yu, Xiaoyang Jin, Tao Yang, Qiang Shu, Wei Li, Xingyu Lin
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引用次数: 0
Wafer-level High Performance MIM Humidity Sensor Based on Nanofiber-Microcavity Hierarchical Structures 基于纳米纤维-微腔分层结构的晶圆级高性能MIM湿度传感器
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-12 DOI: 10.1016/j.snb.2025.139301
Wenbin Qiang, Litao Qin, Shuairong Deng, Quanfeng Zhou, Tingting Yang, Xiangyu Sun
Humidity sensors are essential for environmental monitoring, human-machine interaction, and medical diagnosis. However, most research lacks mature large-scale manufacturing technologies, limiting practical application and mass production. In this work, a wafer-level metal-insulator-metal (MIM) humidity sensor based on a polyimide (PI) hierarchical structure is proposed. By employing an innovative two-step plasma etching strategy, we constructed a nanofiber-microcavity hierarchical structure on the PI sensing layer, synergistically enhancing sensitivity and dynamic response. Firstly, the PI layer was isotropically etched via microwave plasma asher (MPA) to construct microcavities, which effectively increased the water vapor adsorption area and shortened diffusion paths. Subsequently, a high-aspect-ratio nanofiber array was precisely fabricated on the microcavity surface via reactive ion etching (RIE). The resulting enlargement of specific surface area and increase in abundant hydrophilic groups facilitate efficient moisture transport. The sensor exhibits high sensitivity (1.12 pF/%RH within 60%-90% RH), fast response and recovery times (2.75 s/3.5 s), and low hysteresis (1.2%RH). In addition, the sensor demonstrates good temperature stability, long-term stability, and anti-interference capability. This process is compatible with wafer-level CMOS manufacturing, offering a solution for the large-scale fabrication of high-performance humidity sensors. It shows application potential in the fields of non-contact control and respiratory monitoring.
湿度传感器对于环境监测、人机交互和医疗诊断是必不可少的。然而,大多数研究缺乏成熟的大规模制造技术,限制了实际应用和批量生产。本文提出了一种基于聚酰亚胺(PI)层次化结构的晶圆级金属-绝缘体-金属(MIM)湿度传感器。通过采用创新的两步等离子体刻蚀策略,我们在PI传感层上构建了纳米纤维-微腔分层结构,协同提高了灵敏度和动态响应。首先,利用微波等离子体asher (MPA)对PI层进行各向同性刻蚀,形成微腔,有效地增加了水蒸气吸附面积,缩短了扩散路径;随后,通过反应离子刻蚀(RIE)在微腔表面精确制备了高纵横比纳米纤维阵列。由此产生的比表面积的扩大和丰富的亲水基团的增加促进了有效的水分输送。该传感器具有高灵敏度(60% ~ 90% RH范围内1.12 pF/%RH)、快速响应和恢复时间(2.75 s/3.5 s)、低迟滞(1.2%RH)等特点。此外,该传感器具有良好的温度稳定性、长期稳定性和抗干扰能力。该工艺与晶圆级CMOS制造兼容,为大规模制造高性能湿度传感器提供了解决方案。它在非接触控制和呼吸监测领域具有应用潜力。
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引用次数: 0
Dynamic Coordination of ROS and PI3K/Akt Pathway in iPSC Differentiation Monitored by SERS Technology SERS技术监测iPSC分化过程中ROS和PI3K/Akt通路的动态协调
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-11 DOI: 10.1016/j.snb.2025.139309
Jianhui Wan, Weina Zhang, Weile Zhu, Jingyu Hou, Shuyi Long, Liyun Zhong
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引用次数: 0
Study on synergistic effect of titanium sources on structure and gas sensibility of the Ti/Zn-NDI-bimetallic MOF film optical waveguide 钛源对Ti/ zn - ndi双金属MOF薄膜光波导结构和气敏性的协同效应研究
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-11 DOI: 10.1016/j.snb.2025.139308
Patima Nizamidin, Huifang Chen, Zhiqiong Yang, Yanmei Li, Haijiao Xie
In this paper, we report the structural diversity and gas sensing selectivity of bimetallic titanium/zinc organic framework (Ti/Zn-NDI-bimetallic MOF) films constructed from Zn, two different Ti sources (tetrabutyl titanate, tbT; titanium tetrachloride, Ttc), and 1,4,5,8-naphthalenetetracarboxdiimide (NDI) organic ligands. The Ti/Zn-NDI-bimetallic MOF films were grown on the surface of titanium dioxide (TiO2) substrate using solvothermal method. A graphene structured (Ti/Zn-NDI- bimetallic MOF-1) and straw leaf structured (Ti/Zn-NDI-bimetallic MOF-2) films were obtained under the same fabrication condition, after selectively using the Ttc and tbT as the titanium sources, respectively. The structure diversity was assumed to be the consequence of free combination or specific site barrier effect of Ttc and tbT under strong acidic condition (pH=1.8). As the means of optical waveguide sensor (OWGS), Ti/Zn-NDI-bimetallic MOF-1 film OWGS shows a greater selective response to ethylenediamine (EDA) and H2S, when exposed to the same concentration (100 ppm) of amines and acidic gases. The Lewis acid-base interaction preferentially occurred between the film and EDA/H2S owing to the acid-base amphoteric nature of Ti/Zn-NDI-bimetallic MOF-1 frame. Within 10 ppm-100 ppt of EDA detection range, Ti/Zn-NDI-bimetallic MOF-1 film OWGS exhibits a fast (2 s) and significant response (the signal-to-noise ratios (S/N) for 100 ppt EDA was 3.52) with lower LODEDA=1.30 ppb and humidity immunitive. While, the Ti/Zn-NDI-bimetallic MOF-2 film OWGS only responds to SO2, due to the dipole-dipole host-guest interaction. Ti/Zn-NDI- bimetallic MOF-2 film OWGS has a fast response (2 s) for SO2 in the detection range of 10 ppm-100 ppt, with a S/N=4.22 (100 ppt) and LODSO2= 0.85 ppb.
在本文中,我们报道了由锌、两种不同的钛源(钛酸四丁酯,tbT;四氯化钛,Ttc)和1,4,5,8-萘四羧基二亚胺(NDI)有机配体构建的双金属钛/锌有机骨架(Ti/Zn-NDI-双金属MOF)薄膜的结构多样性和气敏选择性。采用溶剂热法在二氧化钛(TiO2)衬底表面生长了Ti/ zn - ndi双金属MOF薄膜。在相同的制备条件下,分别选择Ttc和tbT作为钛源,获得了石墨烯结构(Ti/Zn-NDI-双金属MOF-1)和秸秆叶结构(Ti/Zn-NDI-双金属MOF-2)薄膜。这种结构多样性被认为是Ttc和tbT在强酸条件下(pH=1.8)自由结合或特异位点屏障作用的结果。作为光波导传感器(OWGS)的手段,Ti/ zn - ndi -双金属MOF-1薄膜OWGS在暴露于相同浓度(100 ppm)的胺和酸性气体时,对乙二胺(EDA)和H2S具有更大的选择性响应。由于Ti/ zn - ndi - MOF-1双金属框架的酸碱两性性质,膜与EDA/H2S之间优先发生Lewis酸碱相互作用。在10 ppm-100 ppt的EDA检测范围内,Ti/ zn - ndi -双金属MOF-1薄膜OWGS表现出快速(2 s)和显著的响应(100 ppt EDA的信噪比(s /N)为3.52),低LODEDA=1.30 ppb,并且具有湿度免疫。而Ti/ zn - ndi -双金属MOF-2薄膜OWGS仅对SO2有响应,这是由于偶极子-偶极子主客体相互作用。Ti/Zn-NDI-双金属MOF-2薄膜OWGS在10 ppm-100 ppt的检测范围内对SO2具有快速响应(2 s), s /N=4.22 (100 ppt), LODSO2= 0.85 ppb。
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引用次数: 0
An Electrochemiluminescence Biosensor Based on Ti₃C₂/AuNPs/CsPbBr₃ Nanocomposite and PAM-Regulated CRISPR-Cas12a Signal Amplification for Highly Sensitive Detection of APE1 基于Ti₃C₂/AuNPs/CsPbBr₃纳米复合材料和pam调控CRISPR-Cas12a信号放大的高灵敏度检测APE1的电化学发光生物传感器
IF 8.4 1区 化学 Q1 CHEMISTRY, ANALYTICAL Pub Date : 2025-12-11 DOI: 10.1016/j.snb.2025.139316
Zhengfang Liang, Shuwei Xiao, Junhong Li, Guoli Zuo, Jihua Wei, Yuanxun Gong, Qianli Tang, Kai Zhang, Xianjiu Liao
Apurinic/apyrimidinic endonuclease 1 (APE1), a key enzyme in the base excision repair pathway, is frequently overexpressed in multiple cancers and has emerged as an important biomarker for early diagnosis and therapeutic response evaluation. In this work, a highly sensitive electrochemiluminescence (ECL) biosensor was developed for APE1 detection by integrating a PAM-regulated CRISPR-Cas12a activation mechanism with a multifunctional nanocomposite-modified electrode. A Ti₃C₂/AuNPs/CsPbBr₃ ternary nanocomposite was fabricated through ultrasonic assembly to provide enhanced conductivity, water stability, and probe-loading capacity. Meanwhile, a DNA duplex containing an AP site within the PAM region was engineered to regulate Cas12a activation through APE1-mediated cleavage and polymerase-assisted repair, thereby minimizing background interference and enabling highly specific signal generation. Ferrocene-labeled DNA tetrahedrons (TDNs) were further introduced as a spatially ordered probe scaffold to improve hybridization efficiency and facilitate Cas12a trans-cleavage–mediated signal release. This work presents three key innovations: (1) Construction of a Ti₃C₂/AuNPs/CsPbBr₃ nanocomposite that simultaneously enhances ECL stability, conductivity, and electron-transfer efficiency, addressing the inherent water-instability of perovskite emitters. (2) Coupling of a PAM-regulated APE1–KF repair mechanism with Cas12a activation to achieve highly specific AP-site recognition and selective signal generation. (3) Introduction of a TDN-based probe architecture that provides rigid spatial orientation and high-density probe loading, markedly improving hybridization efficiency and Cas12a trans-cleavage performance. Benefiting from these synergistic innovations, the biosensor achieves a detection limit of 6.28 × 10⁻⁸ U μL⁻¹ and a wide linear range (1 × 10⁻⁷ to 1 × 10⁻1 U μL⁻¹). The platform also demonstrates excellent specificity, reproducibility, and reliable performance in diluted serum, highlighting its promise for clinical and biochemical applications.
APE1是碱基切除修复途径的关键酶,在多种癌症中经常过表达,已成为早期诊断和治疗反应评估的重要生物标志物。在这项工作中,通过将pam调控的CRISPR-Cas12a激活机制与多功能纳米复合修饰电极结合,开发了一种高灵敏度的电化学发光(ECL)生物传感器,用于检测APE1。通过超声波组装制备了Ti₃C₂/AuNPs/CsPbBr₃三元纳米复合材料,以提高其导电性、水稳定性和探针负载能力。同时,在PAM区域中含有AP位点的DNA双工被设计成通过ape1介导的切割和聚合酶辅助修复来调节Cas12a的激活,从而最大限度地减少背景干扰并实现高度特异性的信号产生。二铁标记的DNA四面体(TDNs)被进一步引入作为空间有序的探针支架,以提高杂交效率并促进Cas12a反式切割介导的信号释放。这项工作提出了三个关键的创新:(1)构建Ti₃C₂/AuNPs/CsPbBr₃纳米复合材料,同时提高了ECL的稳定性、电导率和电子转移效率,解决了钙钛矿发射体固有的水不稳定性。(2) pam调控的APE1-KF修复机制与Cas12a激活耦合,实现高度特异性的ap位点识别和选择性信号生成。(3)引入基于tdn的探针结构,提供刚性空间取向和高密度探针负载,显著提高杂交效率和Cas12a反式裂解性能。得益于这些协同创新,该生物传感器的检测限为6.28 × 10⁻U μL⁻¹,线性范围宽(1 × 10⁻⁷至1 × 10 μL⁻¹)。该平台在稀释血清中也表现出出色的特异性、可重复性和可靠的性能,突出了其在临床和生化应用方面的前景。
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