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Gotowe bibliografie tematyczne / Biosensiing

Gotowa bibliografia na temat „Biosensiing”

Autor: Grafiati

Data publikacji: 1 kwietnia 2023

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Artykuły w czasopismach
Rozprawy doktorskie
Książki
Części książek
Streszczenia konferencji
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Artykuły w czasopismach na temat "Biosensiing":

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Kumar, Ravinder, Somvir ., Surender Singh i Kulwant . "A Review on application of Nanoscience for Biosensing". International Journal of Engineering Research 3, nr 4 (1.04.2014): 279–85. http://dx.doi.org/10.17950/ijer/v3s4/423.

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Zhou Xue, 周雪, 闫欣 Yan Xin, 张学楠 Zhang Xuenan, 王方 Wang Fang, 李曙光 Li Shuguang, 郎雷 Lang Lei i 程同蕾 Cheng Tonglei. "软玻璃光纤在生物传感领域应用的研究进展". Laser & Optoelectronics Progress 58, nr 15 (2021): 1516019. http://dx.doi.org/10.3788/lop202158.1516019.

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P.Sangeetha, P. Sangeetha, i Dr A. Vimala Juliet. "Biosensing by Cantilever Resonator for Disease Causing Pathogen Detection". Indian Journal of Applied Research 4, nr 3 (1.10.2011): 174–75. http://dx.doi.org/10.15373/2249555x/mar2014/51.

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Curtin, Kathrine, Bethany J. Fike, Brandi Binkley, Toktam Godary i Peng Li. "Recent Advances in Digital Biosensing Technology". Biosensors 12, nr 9 (23.08.2022): 673. http://dx.doi.org/10.3390/bios12090673.

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Digital biosensing assays demonstrate remarkable advantages over conventional biosensing systems because of their ability to achieve single-molecule detection and absolute quantification. Unlike traditional low-abundance biomarking screening, digital-based biosensing systems reduce sample volumes significantly to the fL-nL level, which vastly reduces overall reagent consumption, improves reaction time and throughput, and enables high sensitivity and single target detection. This review presents the current technology for compartmentalizing reactions and their applications in detecting proteins and nucleic acids. We also analyze existing challenges and future opportunities associated with digital biosensing and research opportunities for developing integrated digital biosensing systems.

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Wu, Jiyun, i Qiuyao Wu. "The Review of Biosensor and its Application in the Diagnosis of COVID-19". E3S Web of Conferences 290 (2021): 03028. http://dx.doi.org/10.1051/e3sconf/202129003028.

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The objective of this article is to summarize the available technologies for biosensing applications in COVID-19. The article is divided into three parts, an introduction to biosensing technologies, applications of mainstream biosensing technologies and a review of biosensing applications in COVID-19. The introduction of biosensors presents the history of inventing the biosensing technology, which refers to the ISFET. The resonant biosensor with the example of MEMS. the principle of optical biosensor, and the thermal biosensor. In the second part, the main use of biosensing techniques, it was discussed the field of the food industry, environmental monitoring, and the medical industry. In the part of biosensor application in COVID-19, it was mentioned that the technique of POCT, the use of RT-LAMP-NBS in the early detection in China, and the use in gRT-PCR for the detection of the DNA code to determine the presence of pathogen of COVLD-19 in the human body.

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Howell, Noura, John Chuang, Abigail De Kosnik, Greg Niemeyer i Kimiko Ryokai. "Emotional Biosensing". Proceedings of the ACM on Human-Computer Interaction 2, CSCW (listopad 2018): 1–25. http://dx.doi.org/10.1145/3274338.

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Mejía-Salazar, J. R., i Osvaldo N. Oliveira. "Plasmonic Biosensing". Chemical Reviews 118, nr 20 (24.09.2018): 10617–25. http://dx.doi.org/10.1021/acs.chemrev.8b00359.

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Fink, Dietmar, Gerardo Munoz Hernandez, Jiri Vacik i Lital Alfonta. "Pulsed Biosensing". IEEE Sensors Journal 11, nr 4 (kwiecień 2011): 1084–87. http://dx.doi.org/10.1109/jsen.2010.2073461.

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Bellassai, Noemi, Roberta D’Agata i Giuseppe Spoto. "Novel nucleic acid origami structures and conventional molecular beacon–based platforms: a comparison in biosensing applications". Analytical and Bioanalytical Chemistry 413, nr 24 (6.04.2021): 6063–77. http://dx.doi.org/10.1007/s00216-021-03309-4.

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AbstractNucleic acid nanotechnology designs and develops synthetic nucleic acid strands to fabricate nanosized functional systems. Structural properties and the conformational polymorphism of nucleic acid sequences are inherent characteristics that make nucleic acid nanostructures attractive systems in biosensing. This review critically discusses recent advances in biosensing derived from molecular beacon and DNA origami structures. Molecular beacons belong to a conventional class of nucleic acid structures used in biosensing, whereas DNA origami nanostructures are fabricated by fully exploiting possibilities offered by nucleic acid nanotechnology. We present nucleic acid scaffolds divided into conventional hairpin molecular beacons and DNA origami, and discuss some relevant examples by focusing on peculiar aspects exploited in biosensing applications. We also critically evaluate analytical uses of the synthetic nucleic acid structures in biosensing to point out similarities and differences between traditional hairpin nucleic acid sequences and DNA origami. Graphical abstract

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Soleymani, Leyla, Sudip Saha, Amanda Victorious, Sadman Sakib i Igor Zhitomirsky. "(Invited) Development of New Strategies for Bringing Photoelectrochemical Biosensing to the Point-of-Need". ECS Meeting Abstracts MA2022-01, nr 53 (7.07.2022): 2178. http://dx.doi.org/10.1149/ma2022-01532178mtgabs.

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Photoelectrochemistry combines light excitation with electrochemical readout for lowering the bias voltage needed for performing electrochemical reactions. As a result, when used in biosensing, photoelectrochemical signal readout reduces the background signals, lowering the limit-of-detection of such biosensors. To enable photoelectrochemical (PEC) signal readout to be applied to point-of-need biosensing, we have taken a three tiered approach focused on improving the understanding of signal transduction in PEC Biosensing, developing label-free assays, and creating handheld readout platforms. In this work, we developed a system using DNA as a nano-ruler to control the distance between plasmonic nanoparticles and PEC electrodes. This system was used to rationally-design PEC material systems for signal-on biosensing. Using this materials architecture, we developed a signal-on biosensor without target labeling for detecting DNA hybridization. This assay uses sequential DNA hybridization to generate a PEC signal. First, the DNA target is captured on probe-modified photoelectrodes. This is followed by hybridization of the unbound probes with DNA strands modified with plasmonic labels. The plasmonic label modulates the PEC signal, increasing the measured PEC current at low target concentrations. To enable biosensing at the point-of-need, we also developed a handheld PEC reader. The integration of plasmonic nanoparticles with PEC electrodes, label-free DNA assays, and handheld PEC readout paves the way toward bringing point-of-need PEC Biosensing.

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Rozprawy doktorskie na temat "Biosensiing":

1

Mickan, Samuel Peter. "T-ray biosensing /". Title page, table of contents and abstract only, 2003. http://web4.library.adelaide.edu.au/theses/09PH/09phm6253.pdf.

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D'Imperio, Luke A. "Biosensing-inspired Nanostructures:". Thesis, Boston College, 2019. http://hdl.handle.net/2345/bc-ir:108627.

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Thesis advisor: Michael J. Naughton
Nanoscale biosensing devices improve and enable detection mechanisms by taking advantage of properties inherent to nanoscale structures. This thesis primarily describes the development, characterization and application of two such nanoscale structures. Namely, these two biosensing devices discussed herein are (1) an extended-core coaxial nanogap electrode array, the ‘ECC’ and (2) a plasmonic resonance optical filter array, the ‘plasmonic halo’. For the former project, I discuss the materials and processing considerations that were involved in the making of the ECC device, including the nanoscale fabrication, experimental apparatuses, and the chemical and biological materials involved. I summarize the ECC sensitivity that was superior to those of conventional detection methods and proof-of-concept bio-functionalization of the sensing device. For the latter project, I discuss the path of designing a biosensing device based on the plasmonic properties observed in the plasmonic halo, including the plasmonic structures, materials, fabrication, experimental equipment, and the biological materials and protocols
Thesis (PhD) — Boston College, 2019
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Physics

3

Ravindran, Ramasamy. "An electronic biosensing platform". Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/44774.

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The objective of this research was to develop the initial constituents of a highly scalable and label-free electronic biosensing platform. Current immunoassays are becoming increasingly incapable of taking advantage of the latest advances in disease biomarker identification, hindering their utility in the potential early-stage diagnosis and treatment of many diseases. This is due primarily to their inability to simultaneously detect large numbers of biomarkers. The platform presented here - termed the electronic microplate - embodies a number of qualities necessary for clinical and laboratory relevance as a next-generation biosensing tool. Silicon nanowire (SiNW) sensors were fabricated using a purely top-down process based on those used for non-planar integrated circuits on silicon-on-insulator wafers and characterized in both dry and in biologically relevant ambients. Canonical pH measurements validated the sensing capabilities of the initial SiNW test devices. A low density SiNW array with fluidic wells constituting isolated sensing sites was fabricated using this process and used to differentiate between both cancerous and healthy cells and to capture superparamagnetic particles from solution. Through-silicon vias were then incorporated to create a high density sensor array, which was also characterized in both dry and phosphate buffered saline ambients. The result is the foundation for a platform incorporating versatile label-free detection, high sensor densities, and a separation of the sensing and electronics layers. The electronic microplate described in this work is envisioned as the heart of a next-generation biosensing platform compatible with conventional clinical and laboratory workflows and one capable of fostering the realization of personalized medicine.

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Lai, Ming-Liang. "Developing piezoelectric biosensing methods". Thesis, University of Glasgow, 2015. http://theses.gla.ac.uk/6109/.

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Biosensors are often used to detect biochemical species either in the body or from collected samples with high sensitivity and specificity. Those based on piezoelectric sensing methods employ mechanically induced changes to generate an electrical response. Reliable collection and processing of these signals is an important aspect in the design of these systems. To generate the electrical response, specific recognition layers are arranged on piezoelectric substrates in such a way that they interact with target species and so change the properties of the device surface (e.g. the mass or mechanical strain). These changes generate a change in the electrical signal output allowing the device to be used as a biosensor. The characteristics of piezoelectric biosensors are that they are competitively priced, inherently rugged, very sensitive, and intrinsically reliable. In this study, a compound label-free biosensor was developed. This sensor consists of two elements: a Love wave sensor and an electrochemical impedance sensor. The novelty of this device is that it can work in both dry and wet measurement conditions. Whilst the Love wave sensor aspect of the device is sensitive to the mass of adsorbed analytes under both dry and wet conditions with high sensitivity, the sensitivity coefficients in these two conditions may be different due to the different (mechanical) strengths of interaction between the adsorbed analyte and the substrate. The impedance sensor element of the device however is less sensitive to the mechanical strength of the bond between the analyte and the sensing surface and so can be used for in-situ calibration of the number of molecules bound to the sensing surface (with either a strong or weak link): conventional Love wave sensors are not sensitive to material loosely bound to the surface. Thus, a combination of results from these two sensors can provide more information about the analyte and the accuracy of the Love wave sensor measurements in a liquid environment. The device functions with label-free molecules and so special reagents are not needed when carrying out measurements. In addition, the fabrication of the device is not too complicated and it is easy to miniaturise. This may make the system suitable for point-of-care diagnostics and bio-material detection. The substrate used in these sensors is 64°Y–X lithium niobate (LiNbO3) which is a kind of piezoelectric material. On the substrate, there is a pair of interdigital transducers (IDTs) which are composed of 100 Ti/Au split-finger pairs with a periodicity (λ) of 40μm. The acoustic path length, between both IDTs, is 200λ and the aperture between the IDTs is 100λ. On top of the substrate and IDTs, there is a PMMA guiding layer with an optimised thickness ranging from 1000 nm to 1300 nm. In addition, a gold layer with thickness 100 nm is deposited on the guiding layer to act as the electrodes for the electrochemical impedance sensor. The biosensor in this study has been used to measure Protein A, IgG, and GABA molecules. Protein A is often coupled to other molecules such as a fluorescent dye, enzymes, biotin, and colloidal gold or radioactive iodine without affecting the antibody binding site. In addition, the capacity of Protein A to bind antibodies with such high affinity is the driving motivation for its industrial scale use in biologic pharmaceuticals. Therefore, measuring Protein A binding is a useful method with which to verify the function of the biosensor. IgG is the most abundant antibody isotype found in the circulation. By binding many kinds of pathogens including viruses, bacteria, and fungi, IgG protects the body from infection. Also, IgG can bind with Protein A well so the biosensor here could also measure IgG after a Protein A layer is immobilised on the sensing area. GABA is the main inhibitory neurotransmitter in the mammalian central nervous system. It plays an important role in regulating neuronal excitability throughout the nervous system. The conventional method to measure concentrations of GABA under the extracellular conditions is by using liquid chromatography. However, the disadvantages of chromatographic methods are baseline drift and additions of solvent and internal standards. Therefore, it is necessary to develop a simple, rapid and reliable method for direct measurement of GABA, and the sensor here is an attractive choice. When the Love wave sensor works in the liquid media, it can only be used to measure the mass of analytes but does not provide information about the conditions of molecules bound with the sensing surface. In contrast, electrochemical impedance sensing based on the diffusion of redox species to the underlying metal electrode can provide real-time monitoring of the surface coverage of bound macromolecular analytes regardless of the mechanical strength of the analyte-substrate bond: the electrochemical impedance measurement is sensitive to the size and extent of the diffusion pathways around the adsorbed macromolecules used by the redox species probe i.e. it is sensitive to the physical area of the surface covered by the macromolecular analyte and not to the mass of material that is sensed through a mechanical coupling effect (as in a Love wave device). Although electrochemical impedance measurements under the dry state are quite common when studying batteries and their redox/discharge properties, these are quite different sorts of systems to the device in this study. Therefore, integrating these two sensors (Love wave sensor and electrochemical impedance sensor) in a single device is a novel concept and should lead to better analytical performance than when each is used on their own. The new type of biosensor developed here therefore has the potential to measure analytes with greater accuracy, higher sensitivity and a lower limit of detection than found when using either a single Love wave sensor or electrochemical impedance sensor alone.

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Muñoz, Berbel Xavier. "Microsystems based on microbial biosensing". Doctoral thesis, Universitat Autònoma de Barcelona, 2008. http://hdl.handle.net/10803/3587.

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Sekretaryova, Alina. "Novel reagentless electrodes for biosensing". Licentiate thesis, Linköpings universitet, Kemiska och optiska sensorsystem, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-112345.

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Analytical chemical information is needed in all areas of human activity including health care, pharmacology, food control and environmental chemistry. Today one of the main challenges in analytical chemistry is the development of methods to perform accurate and sensitive rapid analysis and monitoring of analytes in ‘real’ samples. Electrochemical biosensors are ideally suited for these applications. Despite the wide application of electrochemical biosensors, they have some limitations. Thus, there is a demand on improvement of biosensor performance together with a necessity of simplification required for their mass production. In this thesis the work is focused on the development of electrochemical sensors with improved performance applicable for mass production, e.g. by screen printing. Biosensors using immobilized oxidases as the bio-recognition element are among the most widely used electrochemical devices. Electrical communication between redox enzymes and electrodes can be established by using natural or synthetic electron carriers as mediators. However, sensors based on soluble electronshuttling redox couples have low operational stability due to the leakage of water-soluble mediators to the solution. We have found a new hydrophobic mediator for oxidases – unsubstituted phenothiazine. Phenothiazine and glucose oxidase, lactate oxidase or cholesterol oxidase were successfully co-immobilized in a sol-gel membrane on a screen-printed electrode to construct glucose, lactate and cholesterol biosensors, respectively. All elaborated biosensors with phenothiazine as a mediator exhibited long-term operational stability. A kinetic study of the mediator has shown that phenothiazine is able to function as an efficient mediator in oxidase-based biosensors. To improve sensitivity of the biosensors and simplify their production we have developed a simple approach for production of graphite microelectrode arrays. Arrays of microband electrodes were produced by screen printing followed by scissor cutting, which enabled the realization of microband arrays at the cut edge. The analytical performance of the system is illustrated by the detection of ascorbic acid through direct oxidation and by detection of glucose using a phenothiazine mediated glucose biosensor. Both systems showed enhanced sensitivity due to improved mass transport. Moreover, the developed approach can be adapted to automated electrode recovery. Finally, two enzyme-based electrocatalytic systems with oxidation and reduction responses, respectively, have been combined into a fuel cell generating a current as an analytical output (a so-called self-powered biosensor). This was possible as a result of the development of the phenothiazine mediated enzyme electrodes, which enabled the construction of a cholesterol biosensor with self-powered configuration. The biosensor generates a current when analyte (cholesterol) is added to the cell. The biosensor has been applied for whole plasma analysis. All developed concepts in the thesis are compatible with a wide range of applications and some of them may even be possible to realize in a fully integrated biosensor unit based on printed electronics.

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Archibald, Michelle M. "Novel nanoarchitectures for electrochemical biosensing". Thesis, Boston College, 2016. http://hdl.handle.net/2345/bc-ir:106807.

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Thesis advisor: Thomas C. Chiles
Sensitive, real-time detection of biomarkers is of critical importance for rapid and accurate diagnosis of disease for point-of-care (POC) technologies. Current methods, while sensitive, do not adequately allow for POC applications due to several limitations, including complex instrumentation, high reagent consumption, and cost. We have investigated two novel nanoarchitectures, the nanocoax and the nanodendrite, as electrochemical biosensors towards the POC detection of infectious disease biomarkers to overcome these limitations. The nanocoax architecture is composed of vertically-oriented, nanoscale coaxial electrodes, with coax cores and shields serving as integrated working and counter electrodes, respectively. The dendritic structure consists of metallic nanocrystals extending from the working electrode, increasing sensor surface area. Nanocoaxial- and nanodendritic-based electrochemical sensors were fabricated and developed for the detection of bacterial toxins using an electrochemical enzyme-linked immunosorbent assay (ELISA) and differential pulse voltammetry (DPV). Proof-of-concept was demonstrated for the detection of cholera toxin (CT). Both nanoarchitectures exhibited levels of sensitivity that are comparable to the standard optical ELISA used widely in clinical applications. In addition to matching the detection profile of the standard ELISA, these electrochemical nanosensors provide a simple electrochemical readout and a miniaturized platform with multiplexing capabilities toward POC implementation. Further development as suggested in this thesis may lead to increases in sensitivity, enhancing the attractiveness of the architectures for future POC devices
Thesis (PhD) — Boston College, 2016
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Biology

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Llandro, Justin. "Magnetic rings for digital biosensing". Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611941.

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Wang, Wenxing. "Development of microcantilever biosensing platforms". Thesis, Heriot-Watt University, 2013. http://hdl.handle.net/10399/2722.

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Microcantilever sensor system as a promising field attracted much attention recently. This system has the potential to be applied for a biosensing technology which is parallel reference, label free, sensitive and real time. In this thesis, polyimide has been selected as a material to fabricate cantilever due to its excellent physical, electrical and mechanical properties, on top of its cost advantage. Importantly, we showed it is feasible to microfabricate large array of microcantilever sensors with high-power UV laser directly. It is low cost and rapid, the parameters for laser direct writing fabrication has been studied. The thesis also shows that it is possible to functionalise the polyimide film first and subsequently cut it to functionalised cantilever sensor array. The unique fabrication and functionalisation process can solve the problem of high-cost microfabrication using silicon and low-efficient functionalisation using capillary tubing all together. In addition, the fabrication process has been further developed to avoid the problem of the cross contamination from receptors on both sides. With this improvement, we developed an internally referenced microcantilever biosensors system for DNA hybridization detection. Different receptors can be coated on each side of the polymer film before fabricating to cantilever biosensors This newly developed capability enables us to coat receptors with similar but slightly different biological properties on each side of the cantilever sensor, a process which is extremely difficult by using conventional capillary tubing methods due to the possibility of thiol exchange on surfaces and hence cross-contamination. A polyimide microcantilever sensor with embedded microfluidic channel has been developed in this thesis. Photoresist material is used to form the precise microfluidic channel within the microcantilever device. The multilayer polymer film device is still soft enough to operate in static mode. The main advantage of the system presented here is that since the device is made entirely of polymer materials, the fabrication process is simple and low-cost. The magnetic beads have been used to amplify the signal of the biosensing processing; the application of polyimide microfluidic microcantilevers to the detection of Cryptosporidium and thrombin is reported in this thesis. Paper based autonomous micocantilever system has also been investigated in this thesis. We build a cantilever system without external pump or force with paper and magnetic field. The limitation of the system is that it takes too much time to pump magnetic beads through the cantilever with capillary. However, we found that it has the potential to develop a long time range timer based on the slowest property. Different methods have been investigated to slow down the speed, when liquid pass through the paper microfluidic. Finally, we demonstrate some timer devices whose ranges are from minutes to month. The devices have the potential to be used as time-based diagnostic assays, food label, etc.

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Triggs, Graham J. "Resonant grating surfaces for biosensing". Thesis, University of York, 2016. http://etheses.whiterose.ac.uk/13210/.

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Optical biosensors make up a valuable toolkit for label-free biosensing. This thesis presents a detailed study on resonant grating surfaces for biosensing. The focus is on silicon nitride gratings, which exhibit a guided-mode resonance that is highly sensitive to refractive index variations in the vicinity of the grating. A sensitivity of 143 nm/RIU (refractive index units) is measured, leading to a detection limit of 2.4×10−4 RIU. This performance is shown to be sufficient for the detection of biomolecular binding down to ng/mL concentrations. With out-of-plane excitation, these gratings can be used as a sensing surface, enabling a spatially-resolved measurement of variations in refractive index; resonance imaging. The minimum detection distance (sensing depth) is measured to be 183 nm away from the grat- ing, while the spatial resolution of resonance imaging is found to be asymmetric: 2 μm parallel to, or 6 μm perpendicular to the gratings. Using a novel approach of fabricating a resolution test pattern on top of the grating, the relationship between resolution and index contrast is studied - an important question in the context of biosensing - where it is found to decrease with index contrast. All experimental results are supplemented with theoretical and computational models. The resonant gratings are then extensively applied to the study of biofilm development, cellular imaging, and the imaging of cellular secretion. Finally, a miniaturised biosensor is demonstrated, based on a chirped resonant grating. By tuning the resonance wavelength spatially on the chip, the resonance information is directly translated into spatial informa- tion. Instrument read-out requires just a monochromatic light source and a simple CCD camera, resulting in a final device that is inexpensive, compact, robust and can be remotely operated. Performance is proven with successful detection of biomolecular binding.

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Książki na temat "Biosensiing":

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Schultz, Jerome, Milan Mrksich, Sangeeta N. Bhatia, David J. Brady, Antonio J. Ricco, David R. Walt i Charles L. Wilkins. Biosensing. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x.

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Bhattacharya, Enakshi. Biosensing with Silicon. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-92714-1.

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Chandra, Pranjal, i Kuldeep Mahato, red. Miniaturized Biosensing Devices. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-9897-2.

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Schöning, Michael J., i Arshak Poghossian, red. Label-Free Biosensing. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-75220-4.

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Merkoi, Arben, red. Biosensing Using Nanomaterials. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470447734.

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Merkoçi, A. Biosensing using nanomaterials. Hoboken: Wiley, 2009.

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Borse, Vivek, Pranjal Chandra i Rohit Srivastava, red. BioSensing, Theranostics, and Medical Devices. Singapore: Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-2782-8.

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Chandra, Pranjal, red. Biosensing and Micro-Nano Devices. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-8333-6.

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Renneberg, Reinhard, i Fred Lisdat, red. Biosensing for the 21st Century. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75201-1.

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Zhu, Jun-Jie, Jing-Jing Li, Hai-Ping Huang i Fang-Fang Cheng. Quantum Dots for DNA Biosensing. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-44910-9.

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Części książek na temat "Biosensiing":

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Schultz, Jerome. "Infrastructure Overview". W Biosensing, 1–29. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_1.

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Walt, David R. "Optical Biosensing". W Biosensing, 31–43. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_2.

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Mrksich, Milan. "Electro-Based Sensors and Surface Engineering". W Biosensing, 45–53. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_3.

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Bhatia, Sangeeta N. "Cell and Tissue-Based Sensors". W Biosensing, 55–65. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_4.

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Wilkins, Charles L. "Mass Spectrometry and Biosensing Research". W Biosensing, 67–78. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_5.

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Ricco, Antonio J. "Microfabricated Biosensing Devices: MEMS, Microfluidics, and Mass Sensors". W Biosensing, 79–106. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_6.

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Brady, David J. "Information Systems for Biosensing". W Biosensing, 107–19. Dordrecht: Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4058-x_7.

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Kheyraddini Mousavi, Arash, Zayd Chad Leseman, Manuel L. B. Palacio, Bharat Bhushan, Scott R. Schricker, Vishnu-Baba Sundaresan, Stephen Andrew Sarles i in. "Biosensing". W Encyclopedia of Nanotechnology, 329. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_100084.

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Wolf, Jean-Pierre. "Biosensing Instrumentation". W NATO Science for Peace and Security Series B: Physics and Biophysics, 131–52. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9133-5_4.

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Maeda, Mizuo. "Biosensing Materials". W Encyclopedia of Polymeric Nanomaterials, 1–5. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-36199-9_230-1.

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Streszczenia konferencji na temat "Biosensiing":

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Zhang, Bing, Kai Pang, Yi Sun i Xiaoping Wang. "High-peformance bimetallic SPR sensor for ciprofloxacin based on molecularly imprinted polymer". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320083.

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Escobar Acevedo, Marco Antonio, J. R. Guzman-Sepulveda, Carlos G. Martínez-Arias, Miguel Torres-Cisneros i Rafael Guzman-Cabrera. "Biosensing using long-range surface plasmon structures". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320281.

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Ragan, Regina, i William Thrift. "Quantitative single molecule SERS sensing enabled by machine learning (Conference Presentation)". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320297.

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Cojocaru, Ivan, Jing-Wei Fan, Joe Becker, Ilya V. Fedotov, Masfer H. Alkahtani, Abdulrahman Alajlan, Sean Blakley i in. "All-optical high resolution thermometry with color centers in diamond (Conference Presentation)". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320316.

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Chang, An-Yi, i Prabhu Arumugam. "Fabrication and characterization of boron-doped ultrananocrystalline diamond microelectrodes modified with multi-walled carbon nanotubes and nafion". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320417.

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Nishino, Tomoki, Hiroshi Tanigawa i Jun Sekiguchi. "Antifouling technology of metamaterial structure using biomimetic technology". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320471.

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Dubolazov, Olexander V., Mikhailo Sakhnovskiy, M. S. Garazduyk, A. V. Syvokorovskaya, G. B. Bodnar, V. A. Ushenko, O. I. Olar i O. Tsyhykalo. "Correlation structure of Stokes parametric images of polycrystalline films of human biological fluids". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320512.

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Sokolnyk, S. O., M. I. Sidor, Olexander V. Dubolazov, Leonid Pidkamin, Yuriy Ushenko, O. V. Olar, G. B. Bodnar i O. Prydiy. "Clinical applications of the Mueller-matrix reconstruction of the polycrystalline structure of multiple-scattering biological tissues". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320527.

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Ushenko, Alexander, V. G. Zhytaryuk, M. I. Sidor, A. V. Motrich, O. V. Pavliukovich, O. Ya Wulchulyak, I. V. Soltys i N. Pavliukovich. "Diffuse tomography of optical anisotropy of tumors of the uterus wall". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320529.

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Syvokorovskaya, A. V., M. P. Gorsky, R. Besaga, Yuriy Ushenko, Yuriy Tomka, S. O. Sokolnuik, O. Bakun, L. Yu Kushnerik i S. Golub. "System of 3D Mueller-matrix reconstruction of fibrillar networks of biological tissues of various morphological structure and physiological state". W Biosensing and Nanomedicine XI, redaktorzy Hooman Mohseni, Massoud H. Agahi i Manijeh Razeghi. SPIE, 2018. http://dx.doi.org/10.1117/12.2320535.

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Raporty organizacyjne na temat "Biosensiing":

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Anderson, G., M. Mauro, H. Mattoussi i R. Banahalli. Luminescent Nanoparticles for High Sensitivity Biosensing. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2000. http://dx.doi.org/10.21236/ada399563.

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Yan, Hao. Self-Assembled Combinatorial Nanoarrays for Multiplex Biosensing. Fort Belvoir, VA: Defense Technical Information Center, luty 2010. http://dx.doi.org/10.21236/ada518368.

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Martinez, Jennifer. Genetically encoded functional materials: regenerative medicine, optoelectronics, biosensing. Office of Scientific and Technical Information (OSTI), luty 2015. http://dx.doi.org/10.2172/1169673.

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Broach, James, Alexandre Morozov i Ron Weiss. Highly Extensible Programmed Biosensing Circuits with Fast Memory. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2011. http://dx.doi.org/10.21236/ada559064.

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Slipher, Geoffrey, Randy Mrozek, W. D. Hairston, Joseph Conroy, Wosen Wolde i William Nothwang. Stretchable Conductive Elastomers for Soldier Biosensing Applications: Final Report. Fort Belvoir, VA: Defense Technical Information Center, marzec 2016. http://dx.doi.org/10.21236/ad1005120.

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Shtenberg, Giorgi, i Shelley Minteer. Dual mode detection of heavy metal pollutants: A real-time biosensing method. United States Department of Agriculture, styczeń 2018. http://dx.doi.org/10.32747/2018.7604937.bard.

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Del Vecchio, Domitilla. Quantitative Analysis, Design, and Fabrication of Biosensing and Bioprocessing Devices in Living Cells. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2012. http://dx.doi.org/10.21236/ada582056.

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Del Vecchio, Domitilla. Quantitative Analysis, Design, and Fabrication of Biosensing and Bioprocessing Devices in Living Cells. Fort Belvoir, VA: Defense Technical Information Center, marzec 2015. http://dx.doi.org/10.21236/ada616874.

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Stukes, James, Frank Weaver, Bettye Stokes, Nancy O'Connor i Charlie Barans. Marine Science Initiative at South Carolina State College: An Investigation of the Biosensing Parameters Regulating Bacterial and Larval Attachment on Substrata. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1993. http://dx.doi.org/10.21236/ada268910.

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