detection system

  • 文章类型: Journal Article
    这项研究涉及通过电极沉积制备具有铜和聚(3,4-亚乙基二氧噻吩)和聚苯乙烯磺酸盐(PEDOT/PSS)转化层的全固态离子选择电极(ASS-ISE)。对PEDOT/PSS薄膜的形貌进行了表征,优化了铜离子选择膜的性能。此外,设计并制备了基于铜的ASS-ISE微流控芯片。使用自构建的电位检测装置开发了具有ASS-ISE的集成微流控芯片测试系统。通过与原子吸收分光光度法(AAS)的比较测试,验证了系统的准确性。实验结果表明,集成ASS-ISE与铜微流体芯片测试系统的相对标准偏差(RSD)为4.54%,与行业标准方法相比。该值符合DL/T955-2016中RSD≤5%的规定要求。
    This study involved the preparation of an all-solid-state ion-selective electrode (ASS-ISE) with copper and a poly(3,4-ethylenedioxythiophene) and polystyrene sulfonate (PEDOT/PSS) conversion layer through electrode deposition. The morphology of the PEDOT/PSS film was characterized, and the performance of the copper ion-selective film was optimized. Additionally, a microfluidic chip for the ASS-ISE with copper was designed and prepared. An integrated microfluidic chip test system with an ASS-ISE was developed using a self-constructed potential detection device. The accuracy of the system was validated through comparison testing with atomic absorption spectrophotometry (AAS). The experimental findings indicate that the relative standard deviation (RSD) of the integrated ASS-ISE with the copper microfluidic chip test system is 4.54%, as compared to the industry standard method. This value complies with the stipulated requirement of an RSD ≤ 5% in DL/T 955-2016.
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  • 文章类型: Journal Article
    本文分析了汽车制造商EOL检测线的电气测试项目。在此基础上,针对测试速度慢的问题,提出并设计了一种集成化的自动化测试策略,对体力劳动的依赖程度高,效率低。本文主要分析了电池EOL测试中的两个主要测试:电池管理系统(BMS)测试和电气测试的各种测试。我们提出了基于各种测试项目的创新集成解决方案,包括招待会,传输,以及不同UDS协议消息的自我分析,独特的自动化电气性能测量方案,以及基于Python的集成软件端的需求和逻辑设计。实际测试的实验结果表明,集成策略的实施大大降低了测试步骤的复杂度,提高了测试效率,减少人为操作造成的错误。
    This paper analyzes the electrical test items of the EOL testing line in automotive manufacturers. On this basis, this paper proposes and designs an integrated and automated testing strategy to deal with the problems of slow testing speed, high dependence on manual labor and low efficiency. This article mainly analyzes the various tests of the two main tests in battery EOL testing: Battery Management System (BMS) testing and electrical testing. We propose an innovative integrated solution based on various testing items, including the reception, transmission, and self-analysis of different UDS protocol messages, a unique automated electrical performance measurement scheme, and a requirement and logic design of an integrated software end based on Python. The experimental results of actual testing show that the implementation of the integrated strategy greatly reduces the complexity of the testing steps, improves the testing efficiency, and reduces errors caused by human operation.
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  • 文章类型: Journal Article
    Umami是五种基本口味之一,通过研究鲜味多肽与hT1R1鲜味受体之间的相互作用来阐明其机制具有重要意义。然而,缺乏针对人类T1R1受体的鲜味肽的研究,分子机制仍然难以捉摸。这里,我们成功地建立了一个通过荧光光谱法检测人类T1R1受体的鲜味肽的系统,表面等离子体共振(SPR)和计算模拟。感官评价,计算Kd值,和四种选定的鲜味肽(GRVSNCAA,KGDEESLA,KGGGGP,和TGDPEK)和谷氨酸使用该系统进行了测试,一切都匹配得很好。GRVSNCAA的最大Ka值为479.55M-1,TGDPEK的最小亲和力为2.67M-1。计算模拟显示,hT1R1结合口袋中由于构象变化而占据的不同肽结合位点是不同味觉阈值的重要因素,肽的疏水性在调节亲和力中起着重要作用。因此,我们的研究能够快速筛选高强度鲜味肽,并开发基于T1R1受体的鲜味检测传感器。
    Umami is one of five basic tastes, the elucidation of its mechanism by the study of the interaction between umami polypeptides and hT1R1 umami receptors is of great significance. However, research on umami peptides targeting human T1R1 receptors is lacking, and the molecular mechanism remains elusive. Here, we successfully established a system to detect umami peptides targeting human T1R1 receptors by fluorescence spectroscopy, Surface Plasmon Resonance (SPR) and computational simulation. The sensory evaluation, calculated Kd value, and experimental affinity results between the four selected umami peptides (GRVSNCAA, KGDEESLA, KGGGGP, and TGDPEK) and glutamate were tested using this system, and all matched well. The maximum Ka value of GRVSNCAA was 479.55 M-1, and the minimum affinity of TGDPEK was 2.67 M-1. Computational simulations showed that the different peptide binding sites in the hT1R1 binding pocket occupied due to conformational changes are important factors for different taste thresholds, and that peptide hydrophobicity plays an important role in regulating affinity. Thus, our study enables rapid screening of high-intensity umami peptides and the development of T1R1 receptor-based umami detection sensors.
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  • 文章类型: Journal Article
    UNASSIGNED: Parkinson\'s disease (PD) is a neurodegenerative disease characterized by the impairment of facial expression, known as hypomimia. Hypomimia has serious impacts on patients\' ability to communicate, and it is difficult to detect at early stages of the disease. Furthermore, due to bradykinesia or other reasons, it is inconvenient for PD patients to visit the hospital. Therefore, it is appealing to develop an auxiliary diagnostic method that remotely detects hypomimia.
    UNASSIGNED: We proposed an automatic detection system for Parkinson\'s hypomimia based on facial expressions (DSPH-FE). DSPH-FE provides a convenient remote service for those who potentially suffer from hypomimia and only requires patients to input their facial videos. Specifically, patients can detect hypomimia through two aspects: geometric features and texture features. Geometric features focus on visually representing structures of facial muscles. Facial expression factors (FEFs) are used as the first metric to quantify the current activation state of the facial muscles. Facial expression change factors (FECFs) are subsequently used as the second metric to calculate the moving trajectories of the activation states in the videos. Geometric features primarily concentrate on spatial information, with little involvement of temporal information. Thus, the extended histogram of oriented gradients (HOG) algorithm is introduced. This algorithm can extract texture features within multiple continuous frames and incorporate the temporal information into the features. Finally, these features are applied to four machine learning algorithms to model the relationship between these features and hypomimia.
    UNASSIGNED: The DSPH-FE detection system achieved the best performance when concatenating geometric features and texture features, resulting in a F1 score of 0.9997. The best F1 scores achieved with geometric features and texture features were 0.8286 and 0.9446, respectively. This indicated that both geometric features and texture features have an ability to predict hypomimia, and demonstrated that temporal information can boost the model performance. Thus, DSPH-FE is an effective supportive tool in the medical management of PD patients.
    UNASSIGNED: Comprehensive experiments demonstrated that proposed features fit well with real-world videos and are beneficial in the clinical diagnosis of hypomimia. In particular, hypomimia had a greater impact on eyes and mouths when patients are smiling.
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  • 文章类型: Journal Article
    快速、灵敏地检测大肠杆菌的药物敏感性对人类和动物的健康非常重要。基于电化学检测和免疫检测技术构建了大肠杆菌免疫传感器,通过预处理丝网印刷电极,用交流阻抗法分析抗原抗体结合的最佳反应浓度。基于免疫传感器和电化学工作站相结合的检测系统,进行了测试,以测量大肠杆菌浓度和药物敏感性的准确性,根据电化学工作站的数据对检测系统的误差进行了校准。大肠杆菌O157:H7可在103cfu/ml~1012cfu/ml范围内检测,检测误差控制在5%以内。电化学工作站的结果和检测装置的结果一致,并且两者都显示出抗生素对大肠杆菌的抑制作用比对枯草芽孢杆菌更大。电化学检测系统高效、准确,可广泛应用于临床大肠杆菌药敏试验。
    Sensitive and rapid tests of Escherichia coli drug sensitivity is very important for health of human and animals. An E. coli immunosensor was built based on electrochemical detection and immune detection technologies, through pretreating screen-printed electrodes, and analyzing the optimal reaction concentration of antigen antibody binding with the AC impedance method. Based on the detection system combining the immunosensor and electrochemical workstation, tests were carried out to measure the accuracy of E. coli concentration and drug sensitivity, and error of the detection system was calibrated in accordance with data from the electrochemical workstation. E. coli O157:H7 can be detected in the range of 103 cfu/ml ~ 1012 cfu/ml, and the detection error controlled within 5%. Results from the electrochemical workstation and those from the detection device were consistent, and both demonstrated a greater inhibitory effect of antibiotics on E. coli than on Bacillus subtilis. The electrochemical detection system is highly efficient and accurate, and could be widely applied to E. coli drug sensitivity tests in clinical medicine.
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  • 文章类型: Journal Article
    At present, the proposed microwave power detection systems cannot provide a high dynamic detection range and measurement sensitivity at the same time. Additionally, the frequency band of these detection systems cannot cover the 5G-communication frequency band. In this work, a novel microwave power detection system is proposed to measure the power of the 5G-communication frequency band. The detection system is composed of a signal receiving module, a power detection module and a data processing module. Experiments show that the detection frequency band of this system ranges from 1.4 GHz to 5.3 GHz, the dynamic measurement range is 70 dB, the minimum detection power is -68 dBm, and the sensitivity is 22.3 mV/dBm. Compared with other detection systems, the performance of this detection system in the 5G-communication frequency band is significantly improved. Therefore, this microwave power detection system has certain reference significance and application value in the microwave signal detection of 5G communication systems.
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    文章类型: Journal Article
    针对目前蛋白质基因库异常数据检测系统存在的不足,例如低检测率和高错误检测率,设计了基于数据挖掘技术的蛋白质基因库异常数据检测系统。蛋白质基因进入系统的防火墙模块,并在不符合防火墙规则时进入免疫模块;免疫模块中的内存检测器呈现蛋白质基因,如果记忆检测器与蛋白质基因不匹配,成熟的探测器呈现蛋白质基因,如果成熟的检测器与蛋白质基因不匹配,它被确定为正常的蛋白质基因数据包,如果匹配的话,认为协同刺激模块对蛋白质基因异常数据进行了处理,C8051F060芯片控制控制模块检测蛋白质基因库的异常数据。免疫模块通过未成熟的检测器产生新的蛋白质基因序列,通过成熟的检测模块模拟蛋白质基因的免疫机制,并通过记忆检测器模拟蛋白质基因库异常数据检测系统中的二次响应。该系统将数据挖掘技术引入到检测中,采用两级动态优化算法计算蛋白质基因二级结构排列的ASG相似度值。根据这个值,通过随机生成蛋白质基因来实现蛋白质基因库的异常数据检测,否定选择,克隆选择和复制记忆细胞通过基因表达。实验结果表明,该系统能够快速检测蛋白质基因库的异常数据,确保检测效率,检测精度达到97.1%。该系统可以降低正常蛋白质基因作为异常蛋白质基因检测的错误率。
    In view of the shortcomings of the current abnormal data detection system of the protein gene library, such as low detection rate and high error detection rate, the abnormal data detection system of the protein gene library based on data mining technology is designed. The protein gene enters the firewall module of the system, and enters the immune module when it does not match the firewall rules; the memory detector in the immune module presents the protein gene, if the memory detector does not match the protein gene, the mature detector presents the protein gene, if the mature detector does not match the protein gene, it is determined as the normal protein gene data package, if it matches, it is considered that The abnormal data of protein gene was processed by the collaborative stimulation module, and the control module controlled by C8051F060 chip to detect the abnormal data of protein gene library. The immune module generates new protein gene sequences through an immature detector, simulates the immune mechanism of protein gene through a mature detector module, and simulates the secondary response in the abnormal data detection system of protein gene library through memory detector. The system introduces data mining technology into the detection and uses a two-level dynamic optimization algorithm to calculate the ASG similarity value of protein gene secondary structure arrangement. According to this value, the abnormal data detection of the protein gene library is realized by randomly generating protein genes, negative selection, clone selection and copying memory cells through gene expression. The experimental results show that the system can quickly detect abnormal data of the protein gene library, ensure the detection efficiency, and the detection accuracy reaches 97.1%. The system can reduce the error rate of normal protein gene detection as an abnormal protein gene.
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  • 文章类型: Journal Article
    Partial discharge (PD) usually reflects failures and potential hazards of equipment, so PD detection is important to protect the power system. The most reliable method now is the pulse current method (PCM), but the device of PCM is large and hard to carry. Ultraviolet (UV) pulse detection is another method to detect PD, which has a high precision, strong anti-interference ability, and a long effective distance. However, the existing detection system does not work well when the PD is weak and can hardly reflect the hidden trouble of equipment. This paper introduces an improved PD detection system, based on the UV Pulse Method, which is of high precision and can reflect early discharge. In this study, a corresponding detection device was also built. This device is handheld, non-contact, easy to use, and of high precision.
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  • 文章类型: Evaluation Study
    在本文中,提出了一种用于检测经典猪瘟病毒(CSFV)的磁弹性(ME)传感系统。检测系统包括试纸和测量电路。试纸主要由用于检测CSFV的ME生物传感器组成。基于阻抗分析技术,测量电路用于测量ME生物传感器的谐振频率。将抗CSFVIgG固定在ME传感器表面上以通过物理吸收方法形成ME生物传感器。实验结果表明,ME生物传感器的共振频率随CSFV浓度的增加而增加。通过扫描电子显微镜(SEM)图像证实了抗CSFVIgG和CSFV之间的组合的有效性,基于夹心的酶联免疫吸附测定(ELISA)分析,干扰研究和参考生物传感器测试方法。谐振频率偏移与0至2.5μg/ml范围内的浓度成线性比例,并在较高浓度下变为亚线性。用于CSFV检测的ME生物传感器的灵敏度约为95Hz/μg·ml(-1),检出限为0.6μg/ml。
    In this paper, a magnetoelastic (ME) sensing system for the detection of classical swine fever virus (CSFV) is presented. The detection system comprises a test paper and a measurement circuit. The test paper consists mainly of an ME biosensor to detect the CSFV. Based on the impedance analysis technique, the measurement circuit is designed to measure the resonance frequency of the ME biosensor. The anti-CSFV IgG is immobilized onto the ME sensor surface to form the ME biosensor through a physical absorption approach. The experimental results show that the shift in the resonance frequency of the ME biosensor increases with the augmentation of the CSFV concentration. The effectiveness of the combination between the anti-CSFV IgG and CSFV is confirmed by the scanning electron microscopy (SEM) images, the sandwich-based enzyme-linked immunosorbent assay (ELISA) analysis, the interference study and the reference biosensor test method. The resonance frequency shift is linearly proportional to the concentration in the range from 0 to 2.5μg/ml, and becomes sub-linear at higher concentrations. The ME biosensor for CSFV detection has a sensitivity of about 95Hz/μg·ml(-1), with a detection limit of 0.6μg/ml.
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