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Statistical Analysis for Selective Identifications of VOCs by Using Surface Functionalized MoS2 Based Sensor Array 基于表面功能化MoS2传感器阵列的VOCs选择性识别统计分析
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10451
U. N. Thakur, Radha Bhardwaj, A. Hazra
Disease diagnosis through breath analysis has attracted significant attention in recent years due to its noninvasive nature, rapid testing ability, and applicability for patients of all ages. More than 1000 volatile organic components (VOCs) exist in human breath, but only selected VOCs are associated with specific diseases. Selective identification of those disease marker VOCs using an array of multiple sensors are highly desirable in the current scenario. The use of efficient sensors and the use of suitable classification algorithms is essential for the selective and reliable detection of those disease markers in complex breath. In the current study, we fabricated a noble metal (Au, Pd and Pt) nanoparticle-functionalized MoS2 (Chalcogenides, Sigma Aldrich, St. Louis, MO, USA)-based sensor array for the selective identification of different VOCs. Four sensors, i.e., pure MoS2, Au/MoS2, Pd/MoS2, and Pt/MoS2 were tested under exposure to different VOCs, such as acetone, benzene, ethanol, xylene, 2-propenol, methanol and toluene, at 50 °C. Initially, principal component analysis (PCA) and linear discriminant analysis (LDA) were used to discriminate those seven VOCs. As compared to the PCA, LDA was able to discriminate well between the seven VOCs. Four different machine learning algorithms such as k-nearest neighbors (kNN), decision tree, random forest, and multinomial logistic regression were used to further identify those VOCs. The classification accuracy of those seven VOCs using KNN, decision tree, random forest, and multinomial logistic regression was 97.14%, 92.43%, 84.1%, and 98.97%, respectively. These results authenticated that multinomial logistic regression performed best between the four machine learning algorithms to discriminate and differentiate the multiple VOCs that generally exist in human breath.
近年来,通过呼吸分析进行疾病诊断因其无创性、快速检测能力和适用于所有年龄的患者而备受关注。人体呼吸中存在1000多种挥发性有机成分(VOCs),但只有特定的VOCs与特定的疾病有关。在目前的情况下,使用多个传感器阵列选择性地识别这些疾病标志物VOCs是非常可取的。使用高效的传感器和使用合适的分类算法对于选择性和可靠地检测复杂呼吸中的这些疾病标志物至关重要。在本研究中,我们制作了一种贵金属(Au, Pd和Pt)纳米粒子功能化的MoS2 (Chalcogenides, Sigma Aldrich, St. Louis, MO, USA)传感器阵列,用于选择性识别不同的VOCs。在50℃的条件下,测试了纯MoS2、Au/MoS2、Pd/MoS2和Pt/MoS2四种传感器暴露于丙酮、苯、乙醇、二甲苯、2-丙烯醇、甲醇和甲苯等不同挥发性有机化合物下的性能。首先,采用主成分分析(PCA)和线性判别分析(LDA)对这7种VOCs进行了判别。与PCA相比,LDA能够很好地区分七种挥发性有机化合物。采用k近邻(kNN)、决策树、随机森林和多项逻辑回归等四种不同的机器学习算法进一步识别这些挥发性有机化合物。采用KNN、决策树、随机森林和多项逻辑回归对这7种VOCs的分类准确率分别为97.14%、92.43%、84.1%和98.97%。这些结果验证了多项逻辑回归在四种机器学习算法中表现最好,以区分和区分人类呼吸中普遍存在的多种挥发性有机化合物。
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引用次数: 2
Influence of the Type and Amount of Plasticizer on the Sensory Properties of Microspheres Sensitive to Lipophilic Ions 增塑剂种类和用量对亲脂离子敏感微球感觉性能的影响
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10487
A. Kalinowska, P. Matusiak, Sandra Skorupska, I. Grabowska-Jadach, P. Ciosek-Skibińska
Working parameters of chemical sensors, such as selectivity and sensitivity, can be adjusted by optimizing components of chemosensitive layers, including type and amount of plasticizer in the case of PVC membranes in optodes. Plasticizers are also used in the process of creating micro/nanospheres that are incorporated with chemical indicators to form micro/nano-scale optodes. This study investigated the influence of the type of plasticizer (polar o-NPOE and non-polar DOS) on the optical response of microspheres that are sensitive to lipophilic ions. Moreover, the amount of plasticizer was also adjusted in order to obtain satisfactory sensitivity in the widest linear range. The chemosensory response of the developed microspheres was studied with the use of spectrophotometry and spectrofluorimetry, while size of the optodes was estimated by confocal microscopy.
化学传感器的工作参数,如选择性和灵敏度,可以通过优化化学敏感层的成分来调整,包括在光电器件中PVC膜的增塑剂的类型和数量。增塑剂也用于制造微/纳米球的过程中,这些微/纳米球与化学指示剂结合形成微/纳米级光电器件。研究了增塑剂类型(极性o-NPOE和非极性DOS)对亲脂离子敏感微球光学响应的影响。此外,为了在最宽的线性范围内获得满意的灵敏度,还调整了增塑剂的用量。利用分光光度法和荧光光谱法研究了制备的微球的化学感觉反应,并用共聚焦显微镜估计了光电二极管的尺寸。
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引用次数: 3
Development of an Integrated In-Vehicle Driver Breath Ethanol System Based on α-Fe2O3 Sensing Material 基于α-Fe2O3传感材料的车载驾驶员呼气乙醇集成系统的研制
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10476
R. Di Chio, Monica Galtieri, N. Donato, G. Neri
Alcohol abuse is the dominant cause of fatal car accidents (about 25% of all road deaths in Europe). The large-scale implementation of systems aimed at the realization of in-vehicle driver breath ethanol detection is therefore in high demand. For this reason, we devoted our attention to the design of an inexpensive and reliable breath alcohol sensor for use in an Advanced Driver Assistance System (ADAS). The main challenge in the development of this sensor is related to the complexity of breath composition and its high humidity content, coupled with the high dilution of breath reaching the sensor. In this work, a simple α-Fe2O3 film-based sensor was developed and validated in laboratory tests. Tests were also performed by placing the ethanol sensor within the casing of the upper steering column of a car to simulate real driving conditions. Using an array provided with the developed ethanol sensor and humidity, temperature and CO2 sensors, it was possible to differentiate the signal of a driver’s breath before and after alcohol consumption.
酗酒是致命车祸的主要原因(约占欧洲所有道路死亡人数的25%)。因此,大规模实施旨在实现车载驾驶员呼气乙醇检测的系统的需求很大。因此,我们致力于设计一种廉价且可靠的呼气酒精传感器,用于高级驾驶辅助系统(ADAS)。该传感器开发的主要挑战与呼吸成分的复杂性及其高湿度含量有关,再加上到达传感器的呼吸的高度稀释。在这项工作中,开发了一种简单的α-Fe2O3薄膜传感器,并在实验室测试中得到了验证。测试还通过将乙醇传感器放置在汽车上转向柱的外壳中来模拟真实的驾驶条件。利用配备有开发的乙醇传感器和湿度、温度和二氧化碳传感器的阵列,可以区分驾驶员饮酒前后的呼吸信号。
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引用次数: 2
Electrochemical Immunosensor for Simultaneous Determination of Emerging Autoimmune Disease Biomarkers in Human Serum 同时测定人血清中新出现的自身免疫性疾病生物标志物的电化学免疫传感器
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10437
E. Sánchez-Tirado, S. Guerrero, A. González-Cortés, L. Agüí, P. Yáñez‐Sedeño, J. Pingarrón
Rheumatoid arthritis is an autoimmune disorder characterized by persistent erosive synovitis, systemic inflammation and the presence of autoantibodies, which play an important role in inducing inflammation and joint damage, releasing pro-inflammatory cytokines from monocytes and macrophages [1,2]. Likewise, neutrophil activating protein-2 (CXCL7) is a platelet-derived growth factor belonging to the CXC chemokine subfamily, which is expressed in serum, synovial fluid and synovial tissue of patients developing rheumatoid arthritis during the first twelve weeks, being useful to reflect local pathological changes [3]. Besides, matrix metalloproteinase-3 (MMP-3), which is induced by inflammatory cytokines such as interleukin-1 (IL-1) and tumor necrosis factor alpha (TNF-α) in rheumatoid synovium, degrades several extracellular matrix components of cartilage and plays central roles in rheumatoid joint destruction [4]. Therefore, monitoring serum CXCL7 and MMP-3 levels is useful for predicting the disease activity in rheumatoid arthritis. In this work, the construction and analytical performance of a dual electrochemical platform for the simultaneous determination of CXCL7 and MMP-3 is described. After the optimization of experimental variables involved in the preparation and implementation of the biosensor, the analytical usefulness of the developed configuration was demonstrated by its application to the determination of these biomarkers in serum samples from healthy individuals and patients with rheumatoid arthritis. To carry out the simultaneous determination of CXCL7 and MMP3 in human serum, just a fifty-fold sample dilution in PBS of pH 7.4 was required. In addition, the results obtained using the dual immunosensor were compared with those provided by the respective ELISA immunoassays, yielding no significant differences between the two methods. It is important to highlight that reagents consumption, four times smaller using the dual immunosensor than that required in the ELISA protocol, and an assay time of 2 h 50 min versus almost 5 h, counted in both cases after incubation of the capture antibody, are advantageous features of the dual immunosensor [5].
类风湿关节炎是一种自身免疫性疾病,其特征为持续性糜糜性滑膜炎、全身炎症和自身抗体的存在,自身抗体在诱导炎症和关节损伤、单核细胞和巨噬细胞释放促炎细胞因子中起重要作用[1,2]。同样,中性粒细胞激活蛋白-2 (neutrophil activating protein-2, CXCL7)是一种血小板衍生的生长因子,属于CXC趋化因子亚家族,在类风湿关节炎患者发病前12周的血清、滑膜液和滑膜组织中表达,有助于反映局部病理变化[3]。此外,由类风湿滑膜中白细胞介素-1 (IL-1)和肿瘤坏死因子α (TNF-α)等炎性细胞因子诱导的基质金属蛋白酶-3 (matrix metalloproteinase-3, MMP-3)降解软骨的几种细胞外基质成分,在类风湿关节破坏中起核心作用[4]。因此,监测血清CXCL7和MMP-3水平对预测类风湿关节炎的疾病活动性是有用的。本文介绍了同时测定CXCL7和MMP-3的双电化学平台的构建和分析性能。在对生物传感器的制备和实现过程中涉及的实验变量进行优化后,所开发的配置的分析有效性通过其在健康个体和类风湿关节炎患者血清样本中这些生物标志物的测定中得到了证明。同时测定人血清中CXCL7和MMP3,只需要在pH 7.4的PBS中稀释50倍。此外,将双免疫传感器获得的结果与各自ELISA免疫测定提供的结果进行了比较,两种方法之间没有显着差异。需要强调的是,使用双免疫传感器的试剂消耗比ELISA方案所需的试剂消耗少四倍,检测时间为2小时50分钟,而捕获抗体孵育后两种情况下的检测时间几乎为5小时,这是双免疫传感器的优势特征[5]。
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引用次数: 0
Cross-Sensitive Potentiometric Sensors Based on Anti-Crown (C6HgF4)3 基于反冠(C6HgF4)的交叉敏感电位传感器
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10424
Ekaterina Yuskina, K. Tugashov, V. Shur, I. A. Tikhonova, V. Babain, D. Kirsanov
In this work, we explore the possibility of using anti-crown ether (C6HgF4)3 as a membrane-active component for potentiometric cross-sensitive sensors. Anti-crown ligands have already been employed as ionophores in plasticized polymeric membranes; however, the results of these studies are contradictory. In order to clarify the electrochemical sensitivity patterns of anti-crown-based sensors, we have studied plasticized polymeric membranes containing cation and anion-exchanging additives and various solvent-plasticizers. We explored the electrochemical sensitivity of these membranes in a wide variety of aqueous solutions of inorganic salts. Alkaline, alkaline-earth, and d-element salts with different anions were studied. It was found that the sensors based on anti-crown (C6HgF4)3 exhibit cationic sensitivity, and no considerable anionic responses were observed.
在这项工作中,我们探索了使用抗冠醚(C6HgF4)3作为电位交叉敏感传感器的膜活性成分的可能性。反冠配体已作为离子载体应用于增塑型聚合物膜;然而,这些研究的结果是矛盾的。为了明确反冠传感器的电化学灵敏度模式,我们研究了含有阳离子和阴离子交换添加剂和各种溶剂增塑剂的增塑型聚合物膜。我们探索了这些膜在各种无机盐水溶液中的电化学敏感性。研究了含不同阴离子的碱盐、碱土盐和d元素盐。结果表明,基于抗冠(C6HgF4)3的传感器表现出阳离子敏感性,没有明显的阴离子响应。
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引用次数: 1
Simultaneous Quantification of Four Principal NSAIDs through Voltammetry and Artificial Neural Networks Using a Modified Carbon Paste Electrode in Pharmaceutical Samples 利用修饰碳膏电极通过伏安法和人工神经网络同时定量药物样品中四种主要非甾体抗炎药
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10450
G. Y. Aguilar-Lira, Prisciliano Hernandez, G. Álvarez-Romero, J. M. Gutiérrez
This work describes the development of a novel and low-cost methodology for the simultaneous quantification of four main nonsteroidal anti-inflammatory drugs (NSAIDs) in pharmaceutical samples using differential pulse voltammetry coupled with an artificial neural network model (ANN). The working electrode used as a detector was a carbon paste electrode (CPE) modified with multi-wall carbon nanotubes (MWCNT-CPE). The specific voltammetric determination of the drugs was performed by cyclic voltammetry (CV). Some characteristic anodic peaks were found at potentials of 0.446, 0.629, 0.883 V related to paracetamol, diclofenac, and aspirin. For naproxen, two anodic peaks were found at 0.888 and 1.14 V and for ibuprofen, an anodic peak was not observed at an optimum pH of 10 in 0.1 mol L−1 Britton–Robinson buffer. Since these drug’s oxidation process turned out to be irreversible and diffusion-controlled, drug quantification was carried out by differential pulse voltammetry (DPV). The Box Behnken design technique’s optimal parameters were: step potential of 5.85 mV, the amplitude of 50 mV, period of 750 ms, and a pulse width of 50 ms. A data pretreatment was carried out using the Discrete Wavelet Transform using the db4 wavelet at the fourth decomposition level applied to the voltammetric records obtained. An ANN was built to interpret the obtained approximation coefficients of voltammograms generated at different drug concentrations to calibrate the system. The ANN model’s architecture is based on a Multilayer Perceptron Network (MLP) that employed a Bayesian regularization training algorithm. The trained MLP achieves significant R values for the test data to simultaneous quantification of the four drugs in the presence of aspirin.
这项工作描述了一种新的低成本方法的发展,该方法使用差分脉冲伏安法与人工神经网络模型(ANN)相结合,用于同时定量药物样品中四种主要非甾体抗炎药(NSAIDs)。作为探测器的工作电极是用多壁碳纳米管(MWCNT-CPE)修饰的碳糊电极。采用循环伏安法(CV)进行药物的比伏安测定。在对乙酰氨基酚、双氯芬酸和阿司匹林的电位0.446、0.629、0.883 V处发现了一些特征阳极峰。在0.1 mol L−1 briton - robinson缓冲液中,naproxen在0.888 V和1.14 V时存在两个阳极峰,而ibuprofen在最佳pH为10时不存在阳极峰。由于这些药物的氧化过程不可逆且受扩散控制,因此采用微分脉冲伏安法(DPV)进行药物定量。Box Behnken设计技术的最佳参数为:阶跃电位5.85 mV,幅值50 mV,周期750 ms,脉宽50 ms。采用离散小波变换对得到的伏安记录进行预处理,db4小波在第四分解层进行处理。建立人工神经网络来解释不同药物浓度下产生的伏安图的近似系数,以校准系统。人工神经网络模型的结构基于多层感知器网络(MLP),该网络采用贝叶斯正则化训练算法。训练后的MLP对同时定量四种药物在阿司匹林存在下的测试数据达到显著的R值。
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引用次数: 1
Plants of the Family Asteraceae: Evaluation of Biological Properties and Identification of Phenolic Compounds 菊科植物:生物学特性评价及酚类化合物鉴定
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10486
M. Barral-Martinez, P. García-Oliveira, Bernabé Nuñez-Estevez, Aurora Silva, T. Finimundy, R. Calhelha, Marija Nenadić, M. Soković, F. Barroso, J. Simal-Gándara, I. Ferreira, L. Barros, M. Prieto
The present study focused on the biological analysis of five plants: Achillea millefolium, Arnica montana, Calendula officinalis, Chamaemelum nobile and Taraxacum officinale. The results indicated that A. montana extracts showed the highest content of phenolic compounds. Regarding the biological properties, A. millefolium had outstanding antioxidant activity, while C. officinalis had the highest rate of antimicrobial and antifungal activity. The anti-inflammatory and cytotoxic activities reflected that C. nobile showed the highest effect. In enzyme assays, C. nobile and C. officinalis extracts showed the highest inhibitory effects on acetylcholinesterase and butyrylcholinesterase enzymes. Overall, this study provides scientific evidence for the evaluation of the potential of medicinal plant extracts for the development of new products.
本文主要对五种植物——千叶阿喀琉叶、山金车、金盏菊、金缕草和蒲公英进行了生物学分析。结果表明,蒙大拿提取物中酚类化合物含量最高。在生物学特性方面,千叶合欢具有较强的抗氧化活性,而山茱萸具有较高的抗菌和抗真菌活性。抗炎活性和细胞毒活性均表现出较强的抗炎活性。对乙酰胆碱酯酶和丁基胆碱酯酶的抑制效果最好。本研究为药用植物提取物的开发潜力评价提供了科学依据。
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引用次数: 2
Electronic Nose for Bladder Cancer Detection 电子鼻用于膀胱癌检测
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10438
H. Tyagi, E. Daulton, A. Bannaga, R. Arasaradnam, J. Covington
This study outlines the use of an electronic nose as a method for the detection of VOCs as biomarkers of bladder cancer. Here, an AlphaMOS FOX 4000 electronic nose was used for the analysis of urine samples from 15 bladder cancer and 41 non-cancerous patients. The FOX 4000 consists of 18 MOS sensors that were used to differentiate the two groups. The results obtained were analysed using s MultiSens Analyzer and RStudio. The results showed a high separation with sensitivity and specificity of 0.93 and 0.88, respectively, using a Sparse Logistic Regression and 0.93 and 0.76 using a Random Forest classifier. We conclude that the electronic nose shows potential for discriminating bladder cancer from non-cancer subjects using urine samples.
本研究概述了使用电子鼻作为一种方法来检测挥发性有机化合物作为膀胱癌的生物标志物。本文使用AlphaMOS FOX 4000电子鼻对15例膀胱癌患者和41例非膀胱癌患者的尿液样本进行了分析。FOX 4000由18个MOS传感器组成,用于区分两组。使用MultiSens Analyzer和RStudio对所得结果进行分析。结果表明,使用稀疏逻辑回归和随机森林分类器分别具有0.93和0.88和0.93和0.76的高分离度和特异性。我们的结论是,电子鼻显示出利用尿液样本区分膀胱癌和非膀胱癌受试者的潜力。
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引用次数: 1
Review of the Recent Advances in Nano-Biosensors and Technologies for Healthcare Applications 纳米生物传感器和医疗保健应用技术的最新进展综述
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10473
M. Aqra, A. Ramanathan
The growing human population and the discovery of new diseases and emerging pandemics have increased the need for healthcare treatments and medications with innovative designs. The emergence of nanotechnology provides a platform for novel diagnostic and therapeutic in vivo non-invasive detection and treatment of ailments. It is now the era of the Internet of things (IoT), and data acquisition and interpretation from various parts of the human body in real time is possible with interconnected sensors and information transfer devices. Miniaturization, low power consumption and price with compatibility to existing network circuits are essential requirements in the IoT. Biosensors made of nanostructured materials are the ideal choice due to the unique structural, chemical and electronic properties of these materials with the advantage of a large surface-to-volume ratio, which makes them very successful for use as sensors for the detection of diseases, drug carriers, filters, fillers and reaction catalysts in healthcare applications. In this paper, we reviewed the recent progress made in the research and applications of biosensors in health and preventive medicine. The focus of the paper is biosensors made of nanostructured layered materials such as graphene and its structural analogs molybdenum disulphide (MoS2) and boron nitride (BN). We discussed and highlighted the present capabilities of the different nano-forms of these materials in the detection and analysis of diseases. Their efficiencies in terms of the detection limit, the sensitivity and the adaptability to different environments were be discussed. In addition, the challenges and future perspectives of using nano-biosensors to develop efficient diagnostic, therapeutic and cost-effective monitoring devices with smart technologies were explored.
不断增长的人口和新疾病的发现以及新出现的流行病增加了对具有创新设计的医疗保健治疗和药物的需求。纳米技术的出现为体内非侵入性疾病的检测和治疗提供了一个新的诊断和治疗平台。现在是物联网(IoT)时代,通过相互连接的传感器和信息传输设备,可以实时获取和解释人体各部位的数据。小型化、低功耗和价格与现有网络电路兼容是物联网的基本要求。由纳米结构材料制成的生物传感器是理想的选择,因为这些材料具有独特的结构,化学和电子特性,具有大的表面体积比的优势,这使得它们非常成功地用作检测疾病的传感器,药物载体,过滤器,填料和医疗保健应用中的反应催化剂。本文综述了近年来生物传感器在健康和预防医学中的研究和应用进展。该论文的重点是由纳米结构层状材料制成的生物传感器,如石墨烯及其结构类似物二硫化钼(MoS2)和氮化硼(BN)。我们讨论并强调了这些材料的不同纳米形式在检测和分析疾病方面的现有能力。讨论了它们在检出限、灵敏度和对不同环境的适应性等方面的效率。此外,还探讨了利用纳米生物传感器开发高效诊断、治疗和具有成本效益的智能技术监测设备的挑战和未来前景。
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引用次数: 3
Tropomyosin Analysis in Foods Using an Electrochemical Immunosensing Approach 电化学免疫传感法分析食品中的原肌球蛋白
Pub Date : 2021-06-30 DOI: 10.3390/csac2021-10471
Ricarda Torre, M. Freitas, E. Costa-Rama, H. Nouws, C. Delerue-Matos
A screen-printed carbon electrode was used as the transducer for the development of an electrochemical immunosensor for the determination of tropomyosin (a major shrimp allergen) in food samples. Monoclonal and polyclonal antibodies were used in a sandwich-type immunoassay. The analytical signal was electrochemically obtained using an alkaline phosphatase-labelled secondary antibody and a 3-indoxyl phosphate/silver nitrate substrate. The total assay time was 2 h 50 min and allowed the quantification of tropomyosin between 2.5 and 20 ng mL−1, with a limit of detection of 1.7 ng mL−1 The immunosensor was successfully applied to the analysis of commercial food products.
采用丝网印刷碳电极作为传感器,研制了一种测定食品样品中原肌球蛋白(一种主要的虾类过敏原)的电化学免疫传感器。单克隆抗体和多克隆抗体用于三明治型免疫分析。分析信号采用碱性磷酸酶标记的二抗和3-吲哚基磷酸/硝酸银底物电化学获得。总检测时间为2 h 50 min,原肌球蛋白的定量范围为2.5 ~ 20 ng mL−1,检测限为1.7 ng mL−1。该免疫传感器成功应用于商业食品的分析。
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引用次数: 1
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