Relevant bibliographies by topics / SPR

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'SPR'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 January 2025

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Journal articles on the topic "SPR"

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Pinheiro, Marcelo. "SPR 2021." Neoplasias e doenças reumáticas, no. 2020 jan-mar;19(1) (March 31, 2020): 5. http://dx.doi.org/10.46833/reumatologiasp.2020.19.1.5.

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Hoshi, A. "SPR-901." Drugs of the Future 19, no. 1 (1994): 33. http://dx.doi.org/10.1358/dof.1994.019.01.234652.

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3

Rizal, Conrad, Vladimir Belotelov, Daria Ignatyeva, Anatoly K. Zvezdin, and Simone Pisana. "Surface Plasmon Resonance (SPR) to Magneto-Optic SPR." Condensed Matter 4, no. 2 (May 27, 2019): 50. http://dx.doi.org/10.3390/condmat4020050.

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In this editorial, a brief background of the surface plasmon resonance (SPR) principle is discussed, followed by several aspects of magneto-optic SPR (MOSPR) and sensing schemes from the viewpoint of fundamental studies and potential technological applications. New sensitivity metrics are introduced that would allow researchers to compare the performance of SPR and MOSPR-based sensors. Merits of MOSPR over SPR based sensors and challenges faced by MOSPR sensors in terms of their practical use and portability are also considered. The editorial ends with potential new configurations and future prospects. This work is considered highly significant to device engineers, graduate and undergraduate students, and researchers of all levels involved in developing new classes of bio-devices for sensing, imaging, environmental monitoring, toxic gas detection, and surveying applications to name a few.
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Hain, Adelaide U. P., and Jürgen Bosch. "Differential Fragment SPR (DF-SPR) for Antimalarial Drug Screening." Biophysical Journal 104, no. 2 (January 2013): 380a. http://dx.doi.org/10.1016/j.bpj.2012.11.2118.

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Sherwin, Paul F. "Correcting Diagnostic Test Sensitivity and Specificity for Patient Misclassifications Resulting from Use of an Imperfect Reference Standard." Diagnostics 13, no. 1 (December 28, 2022): 90. http://dx.doi.org/10.3390/diagnostics13010090.

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Investigational diagnostic tests are validated by using a reference standard (RS). If the RS is imperfect (i.e., it has sensitivity [Se] and/or specificity [Sp] < 1), incorrect values for the investigational test’s Se and Sp may result because of patient misclassification by the RS. Formulas were derived to correct a test’s Se and Sp that were determined by using an imperfect RS. The following derived formulas correct for misclassification and give the true numbers of disease-positive [nDP] and disease-negative patients [nDN] from the apparent number of disease-positive and disease-negative patients (anDP and anDN), and the Se and Sp of the RS (SeR, SpR): nDP = (anDP × SpR + anDN × SpR − anDN)/JR; nDN = (anDP × SeR + anDN × SeR − anDP)/JR, where JR is Youden’s Index for the RS (JR = SeR + SpR − 1). The following derived formulas give the correct Se and Sp of an investigational test (SeI and SpI): SeI = (anTPI × SpR − nDP × SeR × SpR + nDP × JR + nDN × SpR2 − nDN × SpR − SpR × anTNI + anTNI)/(nDP × JR); SpI = (anTPI − anTPI × SeR + nDP × SeR2 − nDP × SeR − SeR × nDN × SpR + nDN × JR + SeR × anTNI)/(nDN × JR), where anTPI is the apparent number of true-positive test results, and anTNI is the apparent number of true-negative test results. The derived formulas correct for patient misclassification by an imperfect RS and give the correct values of a diagnostic test’s Se and Sp.
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Wells, William. "SNPs by SPR." Genome Biology 2 (2001): spotlight—20010108–01. http://dx.doi.org/10.1186/gb-spotlight-20010108-01.

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Berger, Charles E. H., and Jan Greve. "Differential SPR immunosensing." Sensors and Actuators B: Chemical 63, no. 1-2 (April 2000): 103–8. http://dx.doi.org/10.1016/s0925-4005(00)00307-5.

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Feldman, William. "SPR Executive meets." Eos, Transactions American Geophysical Union 69, no. 11 (1988): 155. http://dx.doi.org/10.1029/88eo00107.

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Tsurutani, B. T., and M. J. Engebretson. "Assessing SPR education." Eos, Transactions American Geophysical Union 72, no. 8 (1991): 87. http://dx.doi.org/10.1029/90eo00066.

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Tsurutani, Bruce T. "SPR Awards Committee." Eos, Transactions American Geophysical Union 71, no. 33 (1990): 1028. http://dx.doi.org/10.1029/90eo00269.

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Dissertations / Theses on the topic "SPR"

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Gombau, Roigé Jordi. "Influencia de las semillas de la uva y de la suplementación con taninos enológicos comerciales sobre el color y la astringencia del vino tinto; aplicación de la resonancia de plasmones superficiales al estudio de las interacciones tanino-mucina." Doctoral thesis, Universitat Rovira i Virgili, 2020. http://hdl.handle.net/10803/670913.

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Els tanins del vi negre són determinants de la seva qualitat ja que exerceixen una gran influència sobre el color, l'astringència, el cos, la seva capacitat per a l'envelliment i en general la textura del vi. De forma tradicional els tanins del vi procedeixen de forma natural de les baies, alliberant-se de les llavors i les pells durant la vinificació, o bé de la criança o de la suplementació amb tanins comercials. Al capítol 1 d'aquesta tesi s'estudia la relació entre la morfologia de la baia i el color, la composició en tanins i la astringència dels vins negres de quatre varietats: Merlot, Cabernet Sauvignon, Ull de llebre i Garnatxa. La principal conclusió d'aquest treball va ser que el percentatge en pes de les llavors respecte del pes de la baia és un factor determinant de la concentració en tanins i la astringència del vi. Al capítol 2 de la present tesi s'estudia l'efecte com copigmentos dels tanins enològics i es conclou que tots els tanins enològics estudiats són eficaços com copigmentos. Així mateix es proposa un índex per mesurar l'eficàcia dels diferents tanins comercials. Al capítol 3 de la present tesi s'estudia la interacció entre 3 tipus de tanins i la mucina mitjançant ressonància de plasmons superficials (SPR). Per a això es van determinar les constants cinètiques i termodinàmica de la interacció així com l'índex d'astringència dels diferents tanins. Les constants de dissociació termodinàmica i cinètica de les interaccions tanins-mucina van presentar els coeficients de correlació més alts amb l'índex de astringència. Aquestes dades suggereixen que la percepció d'astringència no solament depèn de l'estabilitat termodinàmica del complex taní- proteïna sinó també probablement del temps que triga aquest complex en dissociar-se.
Los taninos del vino tinto son determinantes de su calidad ya que ejercen una gran influencia sobre el color, la astringencia, el cuerpo, su capacidad para el envejecimiento y en general la textura del vino. De forma tradicional los taninos del vino proceden de forma natural de las bayas, liberándose de las semillas y las pieles durante la vinificación, o bien de la crianza o de la suplementación con taninos comerciales. En el capítulo 1 de la presente tesis se estudia la relación entre la morfología de la baya y el color, la composición en taninos y la astringencia de los vinos tintos de cuatro variedades: Merlot, Cabernet Sauvignon, Tempranillo y Garnacha. La principal conclusión de este trabajo fue que el procentaje en peso de las semillas respecto del peso de la baya es un factor determinante de la concentración en taninos y la astringencia del vino. En el capítulo 2 de la presente tesis se estudia el efecto como copigmentos de los taninos enológicos y se concluye que todos los taninos enológicos estudiados son muy eficaces como copigmentos. Asimismo se propone un índice para medir la eficacia de los diferentes taninos comerciales. En el capítulo 3 de la presente tesis se estudia la interacción entre 3 tipos de taninos y la mucina mediante resonancia de plasmones superficiales (SPR). Para ello se determinaron las constantes cinéticas y termodinámica de la interacción así como el índice de astringencia de los diferentes taninos. Las constantes de disociación termodinámica y cinética de las interacciones taninos-mucina presentaron los coeficientes de correlación más altos con el índice de astringencia. Estos datos sugieren que la percepción de astringencia no solamente depende de la estabilidad termodinámica del complejo-tanino proteína sino también probablemente del tiempo que tarda este complejo en disociarse.
Tannins are determinants of the quality of red wine since they exert a great influence on the color, astringency, body, capacity for aging and in general on texture of the wine. Traditionally, tannins come naturally from the berries, being released from seeds and skins during vinification, or from the aging or supplementation with commercial tannins. Chapter 1 of this thesis studies the relationship between berry morphology and color, tannin composition and astringency of red wines of four varieties: Merlot, Cabernet Sauvignon, Tempranillo and Garnacha. The main conclusion of this work was that the seed percentage weight respecto to berry weight weight is the main is a determining factor tannin concentration and the astringency of the wine. In Chapter 2 of this thesis studies the effect as co-pigments of oenological tannins and it is concluded that all oenological tannins studied are very effective as co-pigments. An index is also proposed to measure the effectiveness as copigments of the different commercial tannins. Chapter 3 of this thesis studies the interaction between 3 types of tannins and mucin by means of surface plasmon resonance (SPR). With this aim, the kinetic and thermodynamic constants of the interaction were determined as well as the astringency index of the different tannins. The thermodynamic and kinetic dissociation constants of the tannin-mucin interactions had the highest correlation coefficients with the astringency index. These data suggest that astringency depends not only on the thermodynamic tendency to form the complex between tannins and salivary proteins but also probably on the time required to dissociate the complex.
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Shumaker-Parry, Jennifer Sue. "Quantitative aspects of SPR spectroscopy and SPR microscopy, applications in protein binding to immobilized vesicles and dsDNA arrays /." Thesis, Connect to this title online; UW restricted, 2002. http://hdl.handle.net/1773/11600.

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Maignan, Jordany Richarlson. "Development of Orally Bioavailable 4(1H)-Quinolones and 1,2,3,4-Tetrahydroacridin-9(10H)-ones with Potent Anti-malarial Activity." Scholar Commons, 2015. http://scholarcommons.usf.edu/etd/5873.

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Although Malaria rates are on the decline due to the efforts of the World Health Organization and other organizations dedicated to the eradication of this disease, a relaxed attitude towards the development of new antimalarial entities would be flawed. Due to the emergence of resistance in the parasite, the almost 50% world-wide reduction in malarial death rates that have been produced over the past 15 years are threatening to be lost New drugs are urgently needed and our approach focuses on the re-evaluation and optimization of the historic antimalarial ICI 56,780. Due to its causal prophylactic activity, along with its ability to prevent transmission and potent blood schizonticidal activities, it was revisited with the hopes of first understanding which functionalities were responsible to the compound's activity. Secondly, we wanted to optimize the substituents in the 3, 6 and 7-positions. Finally and most importantly, we wanted to address the cross-resistance problem of the ICI 56,780 scaffold. Initial, analogues showed the importance of the ester in facilitating the convergence of the RI towards 1. Although those analogues lost activity in W2, TM90-C2B, and Pb, they were our first glimpse at this important trend that was later exploited in our 3-halo-6-butyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one and 3-halo-6-butyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-ones which showed RI values of < 5 for our best analogues. Although our lead compound 3-bromo-6-butyl-2-methyl7-(2phenoxyethoxy)quinolin-4(1H) one possessed decreased activities as compared to ICI 56,780 at 2.60 nM for W2, 12.2 nM for TM90-C2B and 2.12 nM for Pb, it had 100% inhibition of parasite development on day 6 PE in our scouting assay and 61% inhibition on day 6in our Thompson model, increased from the < 2% value given by the ICI 56,780. Solubility and unfavorable in vivo stability were still major issues for this scaffold. Therefore, a series of piperazinyl 4(1H)-quinolones with greatly enhanced solubility were designed and tested in detailed structure activity relationships and structure property relationship studies. Initial results showed that 7-piperazinyl-4(1H)-quinolones possessed greatly increased solubilities when compared to ICI 56,780 analogues. Primarily, the linker length and the piperazine core was probed. This showed that compounds with a single carbon spacer were most active. Further testing of the 6-position gave methyl 6-methyl-4-oxo-7-((4-phenylpiperazin-1-yl)methyl)-1,4-dihydroquinoline-3-carboxylate with W2 and TM90-C2B values of 0.435 nM and 147 nM respectively. Substitution on the piperazinyl phenyl gave the most active compounds however the RI of >1500 was unacceptable. Because of this, 3-halo substituents were added to these quinolones with promising results. With RIs of < 3, the compounds were promising, however they were not active in vivo. However, methyl 6-methoxy-4-oxo-7-((4-(4-(trifluoromethyl)phenyl)piperazin-1-yl)methyl)-1,4-dihydroquinoline-3-carboxylate and methyl 6-methyl-4-oxo-7-((4-(4-(trifluoromethyl)phenyl)piperazin-1-yl)methyl)-1,4-dihydroquinoline-3-carboxylate both gave cures in our in vivo Thomson model. These studies highlight the potential in using detailed structural activity and structural property studies to re-evaluate and optimize historic antimalarials. These studies have introduced a new generation of soluble 4(1H)-quinolones with high potency against P. falciparum.
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Saxton, Julie Elizabeth. "SPR with nanoparticles for gas phase detection." Thesis, University of Cambridge, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.614753.

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Pereira, Roberta Andressa. "Morfoanatomia de Androtrichum trigynum (Spr.) Pfeiffer (Cyparaceae)." reponame:Repositório Institucional da UFSC, 2012. http://repositorio.ufsc.br/xmlui/handle/123456789/93125.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Biológicas, Programa de Pós-Graduação em Biologia Vegetal, Florianópolis, 2009.
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Androtrichum trigynum (Spr.) Pfeiffer é um gênero monotípico da família Cyperaceae ocorrendo em regiões litorâneas da costa sudoeste atlântica. Apresenta o sistema subterrâneo constituído por rizomas e raízes adventícias. Neste trabalho foram investigadas a ontogênese do sistema subterrâneo e análises quantitativas do rizoma, raízes e escapos florais de A. trigynum, coletados em dois ambientes da restinga do Parque Municipal das Dunas da Lagoa da Conceição em Florianópolis, caracterizados por dunas semifixas (DS) e baixadas úmidas (BU). Amostras do sistema subterrâneo e escapo foram coletados, fixados em FAA 70 e gluteraldeído 2,5% e processadas de acordo com as técnicas usuais em anatomia vegetal. O rizoma é espessado, plagiotrópico e simpodial, dele partem, escapos florais cuja base é coberta por catafilos, e as raízes. A partir do promeristema do rizoma diferencia-se a protoderme, o procâmbio e o meristema fundamental. Com o desenvolvimento, o meristema de espessamento primário (MEP) é observado entre a região cortical e o cilindro vascular. O MEP produz centrifugamente células parenquimáticas e centripetamente feixes vasculares anfivasais e células parenquimáticas. Posteriormente, a partir do MEP diferenciam-se a endoderme e o periciclo. Em secção longitudinal do ápice radicular são evidentes o caliptrogênio, que origina a coifa; o promeristema, o meristema fundamental, a protoderme e o procâmbio. Inicialmente a epiderme está constituída de células papilosas que secretam grande quantidade de substâncias entre estas e as células da coifa; a endoderme meristemática forma o córtex interno. Na maturidade parte do córtex interno desenvolve-se em aerênquima esquisolisígeno e as células corticais mais internas tornam-se espessadas. As células da endoderme são alongadas no sentido radial e apresentam paredes finas. O periciclo é plurisseriado. Muitos idioblastos contendo compostos fenólicos são encontrados no rizoma, raízes adventícias e escapos florais. Foram analisadas as seguintes características: diâmetro das raízes e rizoma; comprimento, diâmetro e área dos escapos florais; comprimento e diâmetro dos elementos de vaso das raízes, rizomas e escapos florais; grau de esclerofilia, densidade estomática, distância entre estômatos, comprimento total e parcial das células guarda e largura das células subsidiárias e espessura da cutícula e parede periclinal externa da epiderme do escapo floral, as médias foram comparadas por teste T de Student e estatística descritiva com o auxílio do programa Excel e BioEstat 5,0, porcentagens de similaridade e Análise de Similaridade foram usadas para contrastar a procedência e período de coleta e MDS foi empregado para mostrar a distribuição espacial das amostras. De maneira geral, os resultados indicam que a espécie apresentou maiores taxas de crescimento durante o verão, ou seja, no período mais úmido, mostrando-se adaptada ao ciclo hidrológico de alagamentos e drenagens das baixadas úmidas, ao resistir ao alagamento. Através do MDS, foi observada certa tendência à separação das características anatômicas em quatro grupos (BU inverno e verão e DS inverno e verão). A. trigynum apresentou características xeromorfas, embora elas ocorram em indivíduos de ambientes úmidos, provavelmente em conseqüência de pseudo xeromorfismo ou escleromorfismo oligotrófico, causado principalmente por falta de nutrientes no solo.
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Gamsjaeger, Roland. "AFM and SPR on biological systems applying atomic force microscopy (AFM) and surface plasmon resonance (SPR) to biologically important systems." Saarbrücken VDM Verlag Dr. Müller, 2007. http://d-nb.info/988909820/04.

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Bergström, Anna. "SPR Sensor Surfaces based on Self-Assembled Monolayers." Thesis, Linköping University, Department of Physics, Chemistry and Biology, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-16664.

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The study and understanding of molecular interactions is fundamentally important in today's field of life sciences and there is a demand for well designed surfaces for biosensor applications. The biosensor has to be able to detect specific molecular interactions, while non-specific binding of other substances to the sensor surface should be kept to a minimum.                                                                                                                                                                                The objective of this master´s thesis was to design sensor surfaces based on self-assembled monolayers (SAMs) and evaluate their structural characteristics as well as their performance in Biacore systems. By mixing different oligo (ethylene glycol) terminated thiol compounds in the SAMs, the density of functional groups for bimolecular attachment could be controlled.  Structural characteristics of the SAMs were studied using Ellipsometry, Contact Angle Goniometry, IRAS and XPS. Surfaces showing promising results were examined further with Surface Plasmon Resonance in Biacore instruments.

Mixed SAM surfaces with a tailored degree of functional COOH groups could be prepared. The surfaces showed promising characteristics in terms of stability, immobilization capacity of biomolecules, non-specific binding and kinetic assay performance, while further work needs to be dedicated to the improvement of their storage stability. In conclusion, the SAM based sensor surfaces studied in this thesis are interesting candidates for Biacore applications.

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Kärnhall, Johan. "New SPR based assays for plasma protein titer determination." Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-70044.

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Reliable analytical tools are important for time efficient and economical process development, production and batch release of pharmaceuticals. Therapeutics recovered from human plasma, called plasma protein products, involve a large pharmaceutical industry of plasma fractionation. In plasma fractionation of human immunoglobulin G (hIgG) and albumin (HSA) recommended analysis techniques are regulated by the European Pharmacopoeia and are including total protein concentration assays and zone electrophoresis for protein composition and purity. These techniques are robust, but more efficient techniques with higher resolution, specificity and less hands-on time are available. Surface plasmon resonance is an optical method to study biomolecular interactions label-free in real time. This technology was used in this master thesis to set up assays using Biacore systems for quantification of HSA and hIgG from all steps of chromatographic plasma fractionation as a tool for process development and in-process control. The analyses have simplified mass balance calculations to a high extent as they imply specific detection of the proteins compared with using total protein detection. The assays have a low hands-on time and are very simple to perform and the use of one master calibration curve during a full week decreases analysis time to a minimum. Quick, in-process control quantification of one sample is easily obtained within <10 minutes. For final QC of hIgG or for process development, an assay to quantify the distribution of the IgG subclasses (1-4) was set up on Biacore and showed significantly lower hands-on time compared with a commercial ELISA. All assays showed reliable quantification and identification performed in unattended runs with high precision, accuracy and sensitivity.
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Wijaya, Edy. "Design and optimization of Surface Plasmon Resonance (SPR) biosensors." Thesis, Lille 1, 2012. http://www.theses.fr/2012LIL10096/document.

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En terme de performance, le biocapteur idéal doit avoir très grande sensibilité, basse limite de détection et temps d’analyse qui est extrêmement court. Les biocapteurs sans marquage à base de résonance de plasmons de surface (biocapteurs SPR) possèdent naturellement le temps d’analyse le plus court parmi différent types de biocapteurs. Leur limite de détection n’est cependant pas la plus impressionnante. Il y a donc un besoin pour augmenter considérablement la sensibilité intrinsèque des biocapteurs SPR afin de permettre de plus basses limites de détection. Quelques approches pour exalter la sensibilité optique des biocapteurs SPR dans la configuration « traditionnel » de Krestchmann telles que film SPR bimétallique, plasmons à longues portées et détection dans l’infrarouge proche sont examinées dans ce travail. Des configurations « non traditionnelles » comme guides optiques planaires avec couplage par réseau et structures sub-longueur d’ondes ont été aussi théoriquement étudiées. Nouvelle stratégie de fonctionnalisation de surface à base de graphène qui augmente la sensibilité de reconnaissance biomoléculaire et peut être appliquée à quasiment toute structure SPR a été également démontrée
In terms of performance, the ideal biosensor should have high sensitivity, low limits of detection, and extremely short analysis time. Label-free surface plasmon resonance (SPR) biosensors naturally offer the shortest analysis time compared to other types of biosensors. On the other hand, the limits of detection of SPR biosensors are not the most impressive. The inherent sensitivity of SPR biosensors thus needs to be significantly improved to allow lower limits of detection. Several approaches for the enhancement of optical sensitivity of SPR biosensors in the “traditional” attenuated total reflection (ATR) Kretschmann configuration such as the use of bimetallic SPR film, long-range surface plasmons, and near-infrared operating wavelength have been investigated in this work. In addition, some “non traditional” configurations for SPR biosensors including grating-coupled planar optical waveguides and arrays of sub-wavelength structures have been theoretically studied. Novel graphene-based surface functionalization strategy with enhanced biorecognition sensitivity that can be applied to virtually any SPR structure has also been demonstrated
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Daniel, Camille. "Biopuce à aptamères anti-thrombine : exploration d'une technique alternative de détection." Phd thesis, Université de Grenoble, 2013. http://tel.archives-ouvertes.fr/tel-00954086.

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Du fait de leur haute stabilité et bas coût de production, les aptamères suscitent un intérêt croissant, depuis près de 20 ans, dans le design de biocapteurs en tant qu'élément de reconnaissance idéal. Le but de ce travail de thèse est de démontrer l'intérêt et la pertinence d'un outil tel qu'une biopuce à aptamères, associant les avantages des sondes aptamères à ceux d'une détection par SPRi (Surface Plasmon Resonance imaging), permettant une détection sans marquage et en temps réel d'interactions moléculaires. Dans ce but, deux aptamères anti-thrombine (APT1 = 5′- GGT-TGG-TGT-GGT-TGG -3′ et APT2 = 5′-AGT-CCG-TGG-TAG-GGG-AGG-TTG-GGG-TGA-CT-3′) ont été choisis comme objets d'étude modèles. Ce choix a permis d'orienter différents axes de recherche : utilisés indépendamment comme sondes lors de l'élaboration de notre biopuce, ils ont tout d'abord permis de réaliser une détection cinétique optimisée de la thrombine, avec des performances remarquables pour une détection de ce type, ainsi que le calcul de constantes de dissociation en solution et à la surface des biopuces. Mais au-delà d'un simple biocapteur, la biopuce a également pu être utilisée comme véritable plateforme d'étude de la thrombine et de ses interactions, au sein de structures plus complexes telles que la structure " sandwich " entre les deux aptamères, ou d'autres interactions impliquant la thrombine en tant qu'acteur de la cascade de coagulation (inhibition de la thrombine par l'antithrombine III et le cofacteur II de l'héparine, transformation de la prothrombine au sein du complexe prothrombinase).
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Books on the topic "SPR"

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Omar, Ahmad Wan. Saya, SPR & pilihan raya. Shah Alam, Selangor Darul Ehsan: Alaf 21 @ Grup buku Karangkraf, 2014.

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Heaslip, Peter C. The supermarket =: Spr market. London: Methuen, 1987.

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Junior, Moysés Lavander. SPR: The São Paulo Railway Co. [Brazil: s.n.], 2005.

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1961-, Borgmann Elmar-Laurent, ed. Spr@chen lernen mit neuen Medien. Frankfurt-Bockenheim: VAS, 1997.

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Binder, Ferdinand. Tanzl und Spr"uch: Innviertler Mundart. Ried: Artina-Verlag, 1985.

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name, No. Mig trstar!: Studier i Fredrika Bremers spr. Hedemora: Gidlunds, 2002.

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Hausmann, Jutta. Studien zum Menschenbild der älteren Weisheit (Spr 10ff.). Tübingen: J.C.B. Mohr (P. Siebeck), 1995.

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Living Learning Spr-Smr 2003. Augsburg Fortress Publishers, 2002.

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BRONFENBRENNER. ECON ANC SPR. Houghton Mifflin (Academic), 1989.

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Attend Chart-Spr. Abingdon Press, 1995.

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Book chapters on the topic "SPR"

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Narayan, Kartik, and Steven S. Carroll. "SPR Screening." In Applied Biophysics for Drug Discovery, 93–105. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119099512.ch6.

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Ho, Aaron Ho-Pui, Shu-Yuen Wu, Siu-Kai Kong, Zhuwen Zeng, and Ken-Tye Yong. "SPR Biosensors." In Handbook of Photonics for Biomedical Engineering, 1–19. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-6174-2_38-1.

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Ho, Aaron Ho-Pui, Shu-Yuen Wu, Siu-Kai Kong, Shuwen Zeng, and Ken-Tye Yong. "SPR Biosensors." In Handbook of Photonics for Biomedical Engineering, 1–19. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-007-6174-2_38-2.

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Ho, Aaron Ho-Pui, Shu-Yuen Wu, Siu-Kai Kong, Shuwen Zeng, and Ken-Tye Yong. "SPR Biosensors." In Handbook of Photonics for Biomedical Engineering, 123–45. Dordrecht: Springer Netherlands, 2017. http://dx.doi.org/10.1007/978-94-007-5052-4_38.

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Piliarik, Marek, and Jiří Homola. "SPR Sensor Instrumentation." In Springer Series on Chemical Sensors and Biosensors, 95–116. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/5346_016.

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Theden, Philipp, and Hubertus Colsman. "Statistische Prozessregelung (SPR)." In Qualitätstechniken, 116–24. München: Carl Hanser Verlag GmbH & Co. KG, 2013. http://dx.doi.org/10.3139/9783446437425.009.

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Azimova, Shakhnoza S., and Anna I. Glushenkova. "Murraya koenigii Spr." In Lipids, Lipophilic Components and Essential Oils from Plant Sources, 846. London: Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-323-7_2749.

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Theden, Philipp, and Hubertus Colsman. "Statistische Prozessregelung (SPR)." In Qualitätstechniken, 116–24. München, Germany: Carl Hanser Verlag GmbH & Co. KG, 2013. http://dx.doi.org/10.1007/978-3-446-43742-5_9.

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Nedelkov, Dobrin. "Integration of SPR Biosensors with Mass Spectrometry (SPR-MS)." In Methods in Molecular Biology, 261–68. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-670-2_18.

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Kyo, Motoki, Kimihiko Ohtsuka, Eiji Okamoto, and Kazuki Inamori. "High-Throughput SPR Biosensor." In Methods in Molecular Biology, 227–34. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60761-232-2_17.

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Conference papers on the topic "SPR"

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Jarvinen, Annika, Abhishek Sharma, and Sanna Auer. "MP-SPR, a Tool for Biosensor Development." In 2024 IEEE BioSensors Conference (BioSensors), 1. IEEE, 2024. http://dx.doi.org/10.1109/biosensors61405.2024.10712699.

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Yiming, Lu, Hidekazu Ishitobi, Zouheir Sekkat, and Yasushi Inouye. "A Fano resonance enhanced surface plasmon sensing for IgG/anti-IgG immunosensor with high sensitivity." In JSAP-Optica Joint Symposia, 16p_B4_9. Washington, D.C.: Optica Publishing Group, 2024. https://doi.org/10.1364/jsapo.2024.16p_b4_9.

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Abstract:
Surface plasmon resonance (SPR) is widely used as a label-free method for monitoring molecular interactions such as antigen-antibody interactions by measuring the shift in the SPR angle due to changes in the refractive index of the sensing surface. Recently, SPR sensors based on Fano resonance have been proposed to improve the sensitivity of SPR sensors [1]. In our previous report, SF11/Ag/SiO2/TiO2 multilayer system for Fano resonant SPR was developed and applied to the detection of glucose concentration, successfully improving the sensitivity by about one order of magnitude [2].
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Friedman, Stephen, Allan Carroll, Brian Van Essen, Benjamin Ylvisaker, Carl Ebeling, and Scott Hauck. "SPR." In Proceeding of the ACM/SIGDA international symposium. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1508128.1508158.

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Pal, Sarika, Narendra Pal, Y. K. Prajapati, and J. P. Saini. "Performance Evaluation of SPR Biosensor using Metamaterial over Conventional SPR and Graphene based SPR Biosensor." In 2018 5th International Conference on Signal Processing and Integrated Networks (SPIN). IEEE, 2018. http://dx.doi.org/10.1109/spin.2018.8474060.

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Liu, Chunlan, Yachen Gao, and Xingdong Tan. "Optically tuned SPR sensor." In International Conference on Optoelectronic and Microelectronic Technology and Application, edited by Jennifer Liu. SPIE, 2020. http://dx.doi.org/10.1117/12.2586386.

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Schaefer, Buerk, Michaela Harz, and Norbert Danz. "Parallel SPR diagnostic system." In Biomedical Optics 2004, edited by Tuan Vo-Dinh, Zygmunt Gryczynski, and Joseph R. Lakowicz. SPIE, 2004. http://dx.doi.org/10.1117/12.524420.

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Abdallah, C., P. Dorato, and S. Karni. "SPR Design using Feedback." In 1991 American Control Conference. IEEE, 1991. http://dx.doi.org/10.23919/acc.1991.4791682.

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Donazzan, Alberto, Alain Jody Corso, Paola Zuppella, and Maria Guglielmina Pelizzo. "Adaptive system able to switch between angular resolved SPR and SPR imaging." In SPIE Nanoscience + Engineering, edited by Satoshi Kawata and Din Ping Tsai. SPIE, 2016. http://dx.doi.org/10.1117/12.2238608.

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Simsek, Ergun. "Tunable graphene-based SPR sensors." In SPIE Defense, Security, and Sensing, edited by Brian M. Cullum and Eric S. McLamore. SPIE, 2013. http://dx.doi.org/10.1117/12.2018592.

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Rizal, Conrad. "Magneto-optic SPR-based Biosensors." In 2020 Photonics North (PN). IEEE, 2020. http://dx.doi.org/10.1109/pn50013.2020.9166966.

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Reports on the topic "SPR"

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Hinkebein, T. E., S. J. Bauer, B. L. Ehgartner, J. K. Linn, J. T. Neal, J. L. Todd, P. S. Kuhlman, C. T. Gniady, and H. N. Giles. Gas intrusion into SPR caverns. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/206492.

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Bauer, S. J. Subsidence at the Weeks Island SPR Facility. Office of Scientific and Technical Information (OSTI), January 1999. http://dx.doi.org/10.2172/3198.

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Bettin, Giorgia, David Lord, and David Keith Rudeen. SPR Hydrostatic Column Model Verification and Validation. Office of Scientific and Technical Information (OSTI), October 2015. http://dx.doi.org/10.2172/1235644.

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Munson, Darrell Eugene. Observations on vapor pressure in SPR caverns : sources. Office of Scientific and Technical Information (OSTI), May 2010. http://dx.doi.org/10.2172/986599.

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Moriarty, Dylan Michael. Historical Cavern Floor Rise for All SPR Sites. Office of Scientific and Technical Information (OSTI), September 2016. http://dx.doi.org/10.2172/1431478.

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Walter, C. E. SPR-9 concept definition study: FY 1986 summary. Office of Scientific and Technical Information (OSTI), October 1986. http://dx.doi.org/10.2172/6542640.

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Hogge, Joseph, Raquel Valdez, and David Lord. Identification of SPR Caverns with Multiple Oil Layers. Office of Scientific and Technical Information (OSTI), February 2021. http://dx.doi.org/10.2172/1765624.

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Newell, Richard, and Brian Prest. Informing SPR Policy Through Oil Futures and Inventory Dynamics. Cambridge, MA: National Bureau of Economic Research, October 2017. http://dx.doi.org/10.3386/w23974.

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Weber, Paula D., Karen A. Gutierrez, David L. Lord, and David Keith Rudeen. Analysis of SPR salt cavern remedial leach program 2013. Office of Scientific and Technical Information (OSTI), September 2013. http://dx.doi.org/10.2172/1096260.

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Suo-Anttila, Ahti Jorma. Dynamic reactor modeling with applications to SPR and ZEDNA. Office of Scientific and Technical Information (OSTI), December 2011. http://dx.doi.org/10.2172/1177062.

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