Relevant bibliographies by topics / Analyte

Academic literature on the topic 'Analyte'

Author: Grafiati
Published: 30 May 2022
Last updated: 31 May 2022

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Journal articles on the topic "Analyte"

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Jain, Bharti, J. Kumarasamy, C. Gholve, Savita Kulkarni, and M. G. R. Rajan. "A multi-analyte immunoassay for thyroid related analytes." Journal of Immunoassay and Immunochemistry 38, no. 3 (November 2016): 271–84. http://dx.doi.org/10.1080/15321819.2016.1250771.

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Kelley, Shana. "Analyte Acumen." ACS Sensors 3, no. 10 (October 26, 2018): 1892. http://dx.doi.org/10.1021/acssensors.8b01180.

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Ekins, Roger P. "Multi-analyte immunoassay." Journal of Pharmaceutical and Biomedical Analysis 7, no. 2 (January 1989): 155–68. http://dx.doi.org/10.1016/0731-7085(89)80079-2.

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Kaczmarski, K., W. Prus, C. Dobosz, P. Bojda, and T. Kowalska. "THE ROLE OF LATERAL ANALYTE–ANALYTE INTERACTIONS IN THE PROCESS OF TLC BAND FORMATION. II. DICARBOXYLIC ACIDS AS THE TEST ANALYTES." Journal of Liquid Chromatography & Related Technologies 25, no. 10-11 (July 31, 2002): 1469–82. http://dx.doi.org/10.1081/jlc-120005698.

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Metz, Michael P. "Ammonia, a troublesome analyte." Clinical Biochemistry 47, no. 9 (June 2014): 753. http://dx.doi.org/10.1016/j.clinbiochem.2014.05.044.

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Yon Hin, B. F. Y., R. S. Sethi, and C. R. Lowe. "Multi-analyte microelectronic biosensors." Sensors and Actuators B: Chemical 1, no. 1-6 (January 1990): 550–54. http://dx.doi.org/10.1016/0925-4005(90)80271-z.

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Müller, Karl-Heinz, Nereus Patel, Lee J. Hubble, James S. Cooper, and Edith Chow. "Strong enhancement of gold nanoparticle chemiresistor response to low-partitioning organic analytes induced by pre-exposure to high partitioning organics." Physical Chemistry Chemical Physics 22, no. 16 (2020): 9117–23. http://dx.doi.org/10.1039/c9cp06849j.

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A method to enhance the gold nanoparticle sensor response to weak analytes is demonstrated by pre-exposing the sensor to an analyte which elicits a strong response. This weak analyte effectively reduces the strong analyte interaction with the sensor.
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Scholz, C., T. Kraemer, and M. R. Baumgartner. "A multi-analyte approach for the quantification of 116 analytes in hair." Toxicologie Analytique et Clinique 31, no. 2 (May 2019): S22—S23. http://dx.doi.org/10.1016/j.toxac.2019.03.021.

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Bogert, James R. "Advances And Enhancements in Light Element EDXRF." Advances in X-ray Analysis 31 (1987): 449–54. http://dx.doi.org/10.1154/s0376030800022291.

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One of the strongest analytical qualities of energy-dispersive x-ray fluorescence (EDXRF) is the wide range of analyte elements that can be detected and analyzed. Historically, the technique has covered all the elements from sodium (Z=11) and above. A useful measure of specific spectrometer performance is analyte sensitivity. X-ray spectrometric sensitivity is usually expressed in terms of minimum detectable amount of analyte or rate of change of analyte line intensity with change in amount of analyte. Many factors affect analyte sensitivity in EDXRF. These include excitation conditions, specimen conditions, system geometry, atmosphere, detector and readout conditions, and of course the specific analyte line. Typically, EDXRF sensitivity is very good, and low ppm concentrations of analytes are routinely analyzed–until one encounters the light elements.
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GARCIA-SCHWARZ, G., M. BERCOVICI, L. A. MARSHALL, and J. G. SANTIAGO. "Sample dispersion in isotachophoresis." Journal of Fluid Mechanics 679 (May 12, 2011): 455–75. http://dx.doi.org/10.1017/jfm.2011.139.

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We present an analytical, numerical and experimental study of advective dispersion in isotachophoresis (ITP). We analyse the dynamics of the concentration field of a focused analyte in peak mode ITP. The analyte distribution is subject to electromigration, diffusion and advective dispersion. Advective dispersion results from strong internal pressure gradients caused by non-uniform electro-osmotic flow (EOF). Analyte dispersion strongly affects the sensitivity and resolution of ITP-based assays. We perform axisymmetric time-dependent numerical simulations of fluid flow, diffusion and electromigration. We find that analyte properties contribute greatly to dispersion in ITP. Analytes with mobility values near those of the trailing (TE) or leading electrolyte (LE) show greater penetration into the TE or LE, respectively. Local pressure gradients in the TE and LE then locally disperse these zones of analyte penetration. Based on these observations, we develop a one-dimensional analytical model of the focused sample zone. We treat the LE, TE and LE–TE interface regions separately and, in each, assume a local Taylor–Aris-type effective dispersion coefficient. We also performed well-controlled experiments in circular capillaries, which we use to validate our simulations and analytical model. Our model allows for fast and accurate prediction of the area-averaged sample distribution based on known parameters including species mobilities, EO mobility, applied current density and channel dimensions. This model elucidates the fundamental mechanisms underlying analyte advective dispersion in ITP and can be used to optimize detector placement in detection-based assays.
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Dissertations / Theses on the topic "Analyte"

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Mulrooney, Ray. "Analyte sensing with luminescent quantum dots." Thesis, Robert Gordon University, 2009. http://hdl.handle.net/10059/452.

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Semiconducting nanocrystals otherwise known as Quantum Dots (QDs) have attracted considerable attention over the last number of years due to their unique optical properties and potential applications. Their narrow size-tunable emission spectra, broad absorption spectra, resistance to photobleaching and long fluorescent lifetimes make them ideal for sensing ions and small molecules. This thesis explores the potential of QDs to function as the emissive unit in fluorescent probes. Primarily, the focus of the work is to develop QD-based sensors that operate through an electron transfer mechanism. Chapter 3 discusses the synthesis and characterisation of CdSe and CdSe/ZnS QDs. Three different sized QDs were prepared each with distinct emission wavelengths. The sizes of these nanoparticles were determined by three methods, transmission electron microscopy (TEM), dynamic light scattering (DLS) and by a UV-vis method. Surface functionalisation of these synthesised QDs (chapter 4) with mercaptosuccinic acid rendered them water soluble and were shown to display selectivity for Cu2+ over a number of biologically relevant metal ions. The negatively charged surface of the QDs and the position of copper in the Irving-William series were believed to be responsible for this interaction. Positively charged CdSe/ZnS QDs were also prepared and were shown to detect ATP and to a much lesser extent GTP over the other nucleotides screened. The greater net negative charge of the ATP and GTP when compared to their mono and diphosphate analogues was the likely cause of this discrimination. In chapter 5 the relatively unexplored field of anion sensing with QDs was examined using charge neutral urea and thiourea receptors. Based on a design by Gunnlaugsson et al, a CdSe/ZnS QD with a thiourea receptor anchored to its surface displayed similar PET-mediated fluorescence quenching as an organic dye sensor containing the same receptor. A ferrocenyl urea receptor was also anchored to a QD surface and shown to “switch off” the QD’s fluorescence emission. On addition of fluoride ions the emission was restored, most likely due to a modulation of the ferrocene’s redox activity. In chapter 6 the assembly of Schiff base receptors on the surface of preformed CdSe/ZnS QDs were shown to arrange in such a way to enable the simultaneous detection of Cu2+ and Fe3+. The intriguing aspect of this study was that the receptors themselves displayed no selectivity for any metal ion until they were assembled on the QDs. Recognition was also confirmed by a distinct colour change visible to the naked eye.
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Taylor, Carolyn. "Multi-analyte immunoassays for drugs of abuse." Thesis, University of Sunderland, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251355.

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Currently, many methods are available for the analysis of drugs of abuse in urine but they all have their drawbacks. Thus, the purpose of this research was to overcome some of these drawbacks by developing multi-analyte detection systems based on sequential or spatial techniques and immunoassays. The first system was based on a spatial technique and involved a simple indirect competitive ELISA format. This produced relatively rapid multi-analyte dip-strip ELISAs for benzoylecgonine (BE), methadone (MET) and morphine (MOR). Various enzyme-labelled antibodies, substrates and filters were investigated. A multi-analyte dip-strip assay was developed based on cellulose nitrate filters, alkaline phosphatase labelled anti-mouse second antibody and nitro blue tetrazolium / 5-bromo-4-chloro-3- indoyl phosphate (NBT /BCIP) substrate. The resulting assays gave a simple 'yes/no' result when drug was present or absent from a sample at concentrations of 1.45 f,lg ml-I , 1.55 f,lg ml-I and 1.43 f,lg ml-I for BE, MET and MOR respectively. Limitations however were encountered that caused the concentrations to be above the accepted cutoff levels for these three drugs of abuse. The second system was based on a sequential technique and involved a flow-injection nnmunoassay (FIlA). Various monoclonal antibodies, fluorotracers and immobilisation methods were investigated. For morphine, a novel simple FIlA was developed which is based on competition between a mixture of a fluorescein derivative of the drug and morphine in flow over low affinity monoclonal morphine antibodies immobilised on a N-hydroxysuccinimidyl chloroformate activated agarose immunoreactor. With this system, a split peak profile (unbound and retarded fractions) was observed under isocratic conditions with the retarded peak disappearing and the unbound peak increasing in peak height/area as the concentration of morphine increased. Using a flow-rate of 0.5 ml min-I and a fluorescein derivative dilution of 1: 100, this assay had a sample throughput of 4 samples h-I and a detection limit of 14.1 f,lg ml- I . For a flow-rate of 1.6 ml min-I and a fluorescein derivative dilution of 1: 1 00,the assay had a sample throughput of 6 samples h-I and a detection limit of 10.9 J.!g mri. The origin of the phenomenon was investigated and revealed to be due to the low association rate of the drug tracer with the morphine antibody used and the near equivalence of the monoclonal antibody affinity for its respective tracer and drug. It was found that when these values are exceeded, the "split peak" phenomenon was not observed but the reagents could be used in conventional displacement flow injection fluoroimmunoassays as was demonstrated for benzoylecgonine and methadone.
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Yamazaki, Miki. "Novel technologies for high sensitivity analyte detection." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9999.

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Microfluidic devices are attracting interest for point-of-care diagnostics due to their low unit cost, low reagent and sample usage, fast analysis times and portability. Fluorescence is the most widely used detection method in microfluidics due to its high sensitivity, excellent dynamic range, ease of implementation and non-invasive nature. Fluorescence detection has accordingly been widely used for the interrogation of microfluidic devices, with the majority of reports to date having used non-integrated laser excitation sources coupled with off-chip optics and photodetectors. For point-of-care applications, there is a growing need for self-contained systems which incorporate the microfluidic chip and all associated optical components into a compact, low-cost package. Highly compact systems of this kind would eliminate the need for expensive dedicated bench-top instrumentation. As such they would find multiple uses in the home, ambulance and GP’s surgery, where their ability to provide immediate and/or frequent testing would enable faster, more responsive and ultimately more successful treatment. Work undertaken in this thesis focuses on developing highly sensitive analyte detection systems that would enable the use of cheap optical and electronic components. To accomplish this, two separate methods, based on optical filters and time-gated detection of phosphorescent polymer beads, were investigated. We describe a simple technique for fabricating non-emissive colour filters based on the sensitisation of a highly porous nanostructured metal-oxide film with a monolayer of dye molecules. The resultant filters exhibit much less autofluorescence than conventional colour filters, and are a viable low cost alternative to interference filters. In separate work Ru(dpp)3-doped polystyrene/bisphenol A diglycidyl ether polymer phosphorescent beads developed by Dr. Edwards (Imperial College London) were used to demonstrate the feasibility of highly sensitive of low-cost time-gated detection. This method was applied to a simple biotin assay to show their bio-assay applicability.
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Tran, Ngoc L. "A fundamental study on analyte adsorption onto metallophthalocyanines." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2008. http://wwwlib.umi.com/cr/ucsd/fullcit?p3336474.

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Thesis (Ph. D.)--University of California, San Diego, 2008.
Title from first page of PDF file (viewed Dec. 16, 2008). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references (p. 91-101).
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Zhu, Tong. "Preparation of enzyme-analyte conjugates containing linker arms /." Online version of thesis, 1995. http://hdl.handle.net/1850/12161.

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Guo, Jiu-Chun. "The development of simultaneous multi-analyte fluorescence immunoassays." Thesis, Loughborough University, 1998. https://dspace.lboro.ac.uk/2134/32926.

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Fluorescence immunoassays have been established for a number of years as valuable methods of analysis in clinical chemistry and other fields, being sensitive, safe, easy to use and available in a variety formats. Those in common use are normally single analyte assays. But in many cases (e.g. forensic drug screening, therapeutic drug monitoring, screening for cancer markers, monitoring of thyroid function, or the analysis of environmental pollutants) dual- or multi-analyte assays would be much more valuable, with the advantages of increased information content, savings in time and costs, and the elimination of some sources of sampling variance. Amongst all the labels used in immunoassays, only fluorescent groups offer realistic prospects of practicable multi-analyte assays. This project has investigated single-, dual- and multi-analyte fluorescence immunoassays using several spectroscopic and software methods to resolve multicomponent fluorescence emission or synchronous spectra. The assays have been based on flow injection analysis methodology, with solid phase reactors to effect the separation of antibody-bound and unbound labelled analytes. The use of solid phase reactors incorporating thiophiIic gels to bind antibodies has also been investigated: these stationary phases have the advantage that bound antibodies can be eluted by changes of ionic strength, rather than changes of pH. This allows the use of a much wider range of fluorescence labels, clearly important in multi-analyte assays, and it has thus proved possible to develop successful dual and triple analyte assays, with results that compare well with other independent methods.
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Ranganathan, Lavakumar. "Sensor-array chip hybrid for simultaneous multiple analyte detection /." Full text open access at:, 2007. http://content.ohsu.edu/u?/etd,260.

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Easter, Renee N. "The application of elemental tags for biological analyte identification." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307043953.

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Pihlblad, Alma. "Development and comparison of bioanalytical methods to measure free analyte." Thesis, Uppsala universitet, Institutionen för biologisk grundutbildning, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413669.

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Free analyte is measured to be able to understand the pharmacological effects of a drug in the body, the binding to its ligand, and the effective drug level among other things. Thereby, it is important with correct measurements of free analyte, although it is not that easy to achieve since overestimations can occur. In this project, several immunoassays were developed for the bioanalytical methods Gyrolab and ELISA to measure free analyte, where the biotherapeutics Avastin® and Lucentis®, and the ligand VEGF were used as analytes. One difference between the methods is the short contact time of just a few seconds for Gyrolab compared to the sample incubation time of a couple of hours for ELISA. One difference between the antibodies is that Lucentis is an affinity-matured Fab region, and therefore, has a stronger affinity to VEGF compared to Avastin. When free Avastin was measured, the difference was significant, with ELISA estimating higher concentrations compared to Gyrolab. However, this was not the case for all assays. In some cases, this was probably due to differences between the methods that could not be seen. Otherwise, the results with no difference between the methods, when measuring free analyte with Lucentis as the drug, were expected due to the stronger affinity and longer halftime of dissociation. However, the difference with the longer sample incubation time for ELISA compared to the short contact time for Gyrolab seems to influence the measurement of free analyte, depending on the affinity of the components being measured.
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Andria, Sara. "Spectroelectrochemical Sensing: Novel Thin Film Characterization and Multiple Analyte Detection." University of Cincinnati / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1253548394.

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Books on the topic "Analyte"

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Royal Society of Chemistry (Great Britain), ed. Engineering the bioelectronic interface: Applications to analyte biosensing and protein detection. Cambridge, UK: RSC Pub., 2009.

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Nam, Sae-Im. On-site analysis of explosives in soil: Evaluation of thin-layer chromatography for confirmation of analyte identity. Hanover, NH: US Army Corps of Engineers, Cold Regions Research & Engineering Laboratory, 1997.

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Nam, Sae-Im. On-site analysis of explosives in soil: Evaluation of thin-layer chromatography for confirmation of analyte identity. Hanover, NH: US Army Corps of Engineers, Cold Regions Research & Engineering Laboratory, 1997.

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John, Mendham, ed. Vogel's textbook of quantitative chemical analysis. 6th ed. Harlow: Prentice Hall an imprint of Pearson Education, 2000.

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Vogel, Arthur Israel. Vogel's textbook of quantitative chemical analysis. 5th ed. Harlow: Longman, 1989.

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Vogel, Arthur Israel. Vogel's textbook of quantitative chemical analysis. 5th ed. Harlow, Essex, England: Longman Scientific & Technical, 1989.

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Tscheulin, Dieter K. Optimale Produktgestaltung: Erfolgsprognose mit analytic hierarchy process und Conjoint-Analyse. Wiesbaden: Gabler, 1992.

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Perrin, Nicolas. Italiens de Belgique: Analyses socio-démographiques et analyse des appartenances. Louvain-la-Neuve: Academia-Bruylant, 2002.

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Perrin, Nicolas. Italiens de Belgique: Analyses socio-démographiques et analyse des appartenances. Louvain-la-Neuve: Academia-Bruylant, 2005.

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Essentials of quantitative analysis. New York: McGraw-Hill Book Co., 1987.

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Book chapters on the topic "Analyte"

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Stobbe, H. "Analyte des Kleinen Blutbildes." In INSTAND-Schriftenreihe, 44–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-74928-5_2.

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Kauvar, Lawrence M., and Peter Y. K. Cheung. "Type Reactivity for Analyte Profiling." In ACS Symposium Series, 98–108. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0586.ch007.

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Riegel, Helge, Hermann Lommel, Michael Pietsch, and Wolfgang Albath. "Laboratoriumsdiagnostik (Alphabetisches Stichwortverzeichnis der Analyte)." In Vademecum der Laboratoriumsmedizin, 5–142. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-10737-9_2.

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Riegel, Helge, Hermann Lommel, Michael Pietsch, and Wolfgang Albath. "Register der Analyte und Funktionsteste." In Vademecum der Laboratoriumsmedizin, 215–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-10737-9_5.

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Rossmanith, P., J. Hedman, P. Rådström, J. Hoorfar, and M. Wagner. "Preanalytical Sample Preparation and Analyte Extraction." In Rapid Detection, Characterization, and Enumeration of Foodborne Pathogens, 121–36. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555817121.ch8.

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Juneja, Subhavna, Anujit Ghosal, and Jaydeep Bhattacharya. "Raman “Green” Spectroscopy for Ultrasensitive Analyte Detection." In Integrating Green Chemistry and Sustainable Engineering, 165–90. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2019. http://dx.doi.org/10.1002/9781119509868.ch6.

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Zia, Asif Iqbal, and Subhas Chandra Mukhopadhyay. "Inducing Analyte Selectivity in the Sensing System." In Electrochemical Sensing: Carcinogens in Beverages, 113–32. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-32655-9_6.

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Todd, P. J., and C. P. Leibman. "Organic Secondary Ion Intensity and Analyte Concentration." In Springer Series in Chemical Physics, 500–502. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_132.

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Kubalczyk, Paweł, and Edward Bald. "Methods of Analyte Concentration in a Capillary." In Springer Series in Chemical Physics, 215–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35043-6_12.

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Feifel, Sven C., Andreas Kapp, and Fred Lisdat. "Protein Multilayer Architectures on Electrodes for Analyte Detection." In Advances in Biochemical Engineering/Biotechnology, 253–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/10_2013_236.

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Conference papers on the topic "Analyte"

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Carmo, M. P., S. Po, M. Zhao, A. Lauri, P. A. Huidobro, and A. Rakovich. "Plasmonic Control of Analyte Motion." In 2020 International Conference Laser Optics (ICLO). IEEE, 2020. http://dx.doi.org/10.1109/iclo48556.2020.9285768.

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Varma, Manoj M., David D. Nolte, Halina D. Inerowicz, and Fred E. Regnier. "Multi-analyte array microdiffraction interferometry." In International Symposium on Biomedical Optics, edited by Darryl J. Bornhop, David A. Dunn, Raymond P. Mariella, Jr., Catherine J. Murphy, Dan V. Nicolau, Shuming Nie, Michelle Palmer, and Ramesh Raghavachari. SPIE, 2002. http://dx.doi.org/10.1117/12.472064.

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Parsa, H., C. D. Chin, P. Mongkolwisetwara, B. W. Lee, J. J. Wang, and S. K. Sia. "Analyte capture in microfluidic heterogeneous immunoassays." In 2010 36th Annual Northeast Bioengineering Conference. IEEE, 2010. http://dx.doi.org/10.1109/nebc.2010.5458108.

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Lavigne, John J., Axel Metzger, Kenichi Niikura, Larry A. Cabell, Steven M. Savoy, J. S. Yoo, John T. McDevitt, Dean P. Neikirk, Jason B. Shear, and Eric V. Anslyn. "Single-analyte to multianalyte fluorescence sensors." In BiOS '99 International Biomedical Optics Symposium, edited by Joseph R. Lakowicz, Steven A. Soper, and Richard B. Thompson. SPIE, 1999. http://dx.doi.org/10.1117/12.347545.

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Schlager, Kenneth J., and Timothy L. Ruchti. "Transcutaneous analyte measuring method (TAMM): a reflective, noninvasive, near-infrared blood chemistry analyzer." In Photonics West '95, edited by Gerald E. Cohn, Jeremy M. Lerner, Kevin J. Liddane, Alexander Scheeline, and Steven A. Soper. SPIE, 1995. http://dx.doi.org/10.1117/12.206017.

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Akbari, M., M. Bahrami, and D. Sinton. "Optothermal Analyte Manipulation With Temperature Gradient Focusing." In ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-38908.

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An optothermal analyte preconcentration method is introduced in this work based on temperature gradient focusing. The present approach offers a flexible, noncontact technique for focusing and transporting of analytes. Here, we use a commercial video projector and an optical system to generate heat and control the heat source position, size and power. This heater is used to focus a sample model analyte, fluorescent dye, at an arbitrary location along the microchannel. Optothermal manipulation of the focused band was demonstrated by projecting a series of images with a moving light band.
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Ashok, P. C., G. P. Singh, K. M. Tan, K. Dholakia, P. M. Champion, and L. D. Ziegler. "Microfluidic Raman Spectroscopy for Bio-Analyte Detection." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482808.

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Lin, Yu-jen, Martin Tibudan, Yiming Huang, Marcelo Nakaema, Vimal Swarup, Sandra Bishnoi, Timothy A. Keiderling, P. M. Champion, and L. D. Ziegler. "Novel Analyte Capture Method for SERS Biodetection." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482929.

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Kempen, Lothar U., Manal Beshay, and Jesus A. Delgado. "Miniature multi-analyte fiber-optic sensor probe." In SPIE Defense, Security, and Sensing, edited by Alex A. Kazemi, Nicolas Javahiraly, Allen S. Panahi, Simon Thibault, and Bernard C. Kress. SPIE, 2012. http://dx.doi.org/10.1117/12.921483.

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Rounds, Rebecca M., Seungjoon Lee, Sarah Jeffords, Bennett L. Ibey, Michael V. Pishko, and Gerard L. Coté. "Hydrogel micro-arrays for multi-analyte detection." In Biomedical Optics (BiOS) 2007, edited by Gerard L. Coté and Alexander V. Priezzhev. SPIE, 2007. http://dx.doi.org/10.1117/12.701216.

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Reports on the topic "Analyte"

1

Schlager, Kenneth J. Transcutaneous Analyte Measuring Methods (TAMM Phase 2). Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada252554.

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2

Schlager, Kenneth J. Transcutaneous Analyte Measuring Methods (TAMM). Phase 2. Fort Belvoir, VA: Defense Technical Information Center, November 1991. http://dx.doi.org/10.21236/ada243684.

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3

Ovink, R. 100-F Target Analyte List Development for Soil. Office of Scientific and Technical Information (OSTI), September 2012. http://dx.doi.org/10.2172/1084003.

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4

Ovink, R. 100-K Target Analyte List Development for Soil. Office of Scientific and Technical Information (OSTI), September 2012. http://dx.doi.org/10.2172/1084005.

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5

Wegman, Edward J. Optimization Methods for Analyte Recognition from Optical Sensor Arrays. Fort Belvoir, VA: Defense Technical Information Center, December 2002. http://dx.doi.org/10.21236/ada416421.

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6

R.W. Ovink. 100-B/C Target Analyte List Development for Soil. Office of Scientific and Technical Information (OSTI), March 2010. http://dx.doi.org/10.2172/1017507.

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7

ADAMS, M. R., and S. R. WILMARTH. Statistical Optimization Study Estimating Analyte Concentrations in Unsampled Waste Tanks. Office of Scientific and Technical Information (OSTI), July 2002. http://dx.doi.org/10.2172/807997.

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8

Brown, S. D. Studies of the analyte-carrier interface in flow injection analysis. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6794845.

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9

Velsko, S. Null Hypothesis Significance Testing for Trace Chemical Weapon Analyte Detection. Office of Scientific and Technical Information (OSTI), December 2012. http://dx.doi.org/10.2172/1059082.

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10

Brown, S. Studies of the analyte-carrier interface in flow injection analysis. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/7141292.

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