Relevant bibliographies by topics / Luminol

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

Academic literature on the topic 'Luminol'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 April 2022

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Journal articles on the topic "Luminol"

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Neumann, Helfried, Stefan Klaus, Markus Klawonn, Dirk Strübing, Sandra Hübner, Dirk Gördes, Axel Jacobi von Wangelin, Michael Lalk, and Matthias Beller. "A New Efficient Synthesis of Substituted Luminols Using Multicomponent Reactions." Zeitschrift für Naturforschung B 59, no. 4 (April 1, 2004): 431–38. http://dx.doi.org/10.1515/znb-2004-0411.

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AbstractA new general synthesis of substituted luminols (5-amino-2,3-dihydrophthalazine-1,4-diones) is presented. Diversely substituted luminol derivatives can be synthesized in three steps. The products are of interest as new materials, which exhibit chemiluminescence.
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Young, Jay A. "Luminol (3-Aminophthalhydrazide)." Journal of Chemical Education 82, no. 10 (October 2005): 1465. http://dx.doi.org/10.1021/ed082p1465.

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Nakazono, Manabu, Makoto Asechi, and Kiyoshi Zaitsu. "Synthesis of photosensitive luminol releasing compound, luminol-O-2-nitrobenzylate." Journal of Photochemistry and Photobiology A: Chemistry 163, no. 1-2 (April 2004): 149–52. http://dx.doi.org/10.1016/j.jphotochem.2003.11.006.

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Radi, R., T. P. Cosgrove, J. S. Beckman, and B. A. Freeman. "Peroxynitrite-induced luminol chemiluminescence." Biochemical Journal 290, no. 1 (February 15, 1993): 51–57. http://dx.doi.org/10.1042/bj2900051.

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Vascular endothelial cells, smooth muscle cells, macrophages, neutrophils, Kupffer cells and other diverse cell types generate superoxide (O2.-) and nitric oxide (.NO), which can react to form the potent oxidant peroxynitrite anion (ONOO-). Peroxynitrite reacted with luminol to yield chemiluminescence which was greatly enhanced by bicarbonate. The quantum chemiluminescence yield of the ONOO- reaction with luminol in bicarbonate was approx. 10(-3). Chemiluminescence was superoxide dismutase-inhibitable, indicating that O2.- was a key intermediate for chemiexcitation. O2.- appears to be formed secondarily to the reaction of a bicarbonate-peroxynitrite complex with luminol, yielding luminol radical and O2.-. Luminol radical reacts with O2.- to form the unstable luminol endoperoxide, which follows the light-emitting pathway. Neither .NO nor O2.- alone were capable of directly inducing significant luminol chemiluminescence in our assay systems. These results suggest that ONOO- can be a critical unrecognized mediator of cell-derived luminol chemiluminescence reported in previous studies. In addition, it is shown that bicarbonate can participate in secondary oxidation reactions after reacting with ONOO-.
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Allen, Robert C. "Haloperoxidase-Catalyzed Luminol Luminescence." Antioxidants 11, no. 3 (March 8, 2022): 518. http://dx.doi.org/10.3390/antiox11030518.

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Common peroxidase action and haloperoxidase action are quantifiable as light emission from dioxygenation of luminol (5-amino-2,3-dihydrophthalazine-1,4-dione). The velocity of enzyme action is dependent on the concentration of reactants. Thus, the reaction order of each participant reactant in luminol luminescence was determined. Horseradish peroxidase (HRP)-catalyzed luminol luminescence is first order for hydrogen peroxide (H2O2), but myeloperoxidase (MPO) and eosinophil peroxidase (EPO) are second order for H2O2. For MPO, reaction is first order for chloride (Cl−) or bromide (Br−). For EPO, reaction is first order for Br−. HRP action has no halide requirement. For MPO and EPO, reaction is first order for luminol, but for HRP, reaction is greater than first order for luminol. Haloperoxidase-catalyzed luminol luminescence requires acidity, but HRP action requires alkalinity. Unlike the radical mechanism of common peroxidase, haloperoxidases (XPO) catalyze non-radical oxidation of halide to hypohalite. That reaction is second order for H2O2 is consistent with the non-enzymatic reaction of hypohalite with a second H2O2 to produce singlet molecular oxygen (1O2*) for luminol dioxygenation. Alternatively, luminol dehydrogenation by hypohalite followed by reaction with H2O2 yields dioxygenation consistent with the same reaction order. Haloperoxidase action, Cl−, and Br− are specifically quantifiable as luminol luminescence in an acidic milieu.
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O'Keefe, D. A., D. R. James, W. R. Ware, and N. O. Petersen. "Kinetics of a rapid, luminol dependent chemiluminescence signal induced in HL-60 cells by amphotericin B and other stimulants." Biochemistry and Cell Biology 69, no. 9 (September 1, 1991): 618–23. http://dx.doi.org/10.1139/o91-091.

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Addition of the polyene antibiotic amphotericin B or tissue culture medium to nondifferentiated HL-60 cells in the presence of luminol induces a chemiluminescence signal that reaches a peak value within a few seconds and decays exponentially in less than a minute. The kinetics of the signal and its modulation by superoxide dismutase, catalase, and horseradish peroxidase are consistent with a series of solution biochemical processes with a rate-determining step corresponding to the disproportionation of a luminal–superoxide complex. The effects of the enzymes demonstrate that superoxide is a precursor to the rate-determining intermediate and that both catalase and peroxide enhance a reaction that competes with the rate-limiting process.Key words: chemiluminescence, luminol, amphotericin B, superoxide, HL-60 cells.
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Schechinger, Linda, and Amy Sue Waldman. "A Convenient Luminol Demonstration." Journal of Chemical Education 72, no. 3 (March 1995): 243. http://dx.doi.org/10.1021/ed072p243.

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Yankova, T. V., P. V. Melnikov, and N. K. Zaitsev. "Chemiluminescence Reactions of Luminol and N-Octyl Luminol with Hypochlorite in Anionic Surfactants." Moscow University Chemistry Bulletin 74, no. 3 (May 2019): 116–21. http://dx.doi.org/10.3103/s002713141903012x.

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Salehnia, Foad, Morteza Hosseini, and Mohammad Reza Ganjali. "Enhanced electrochemiluminescence of luminol by an in situ silver nanoparticle-decorated graphene dot for glucose analysis." Analytical Methods 10, no. 5 (2018): 508–14. http://dx.doi.org/10.1039/c7ay02375h.

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Herein, a rapid, linker-free, single-step strategy for in situ synthesis of graphene quantum dot–luminol–Ag nanoparticle (GQD–luminol–AgNP) nanocomposites was designed by reducing AgNO3 with an electrochemiluminescent reagent, luminol, in the presence of GQDs.
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Jiao, Ti Feng, Yuan Yuan Xing, and Jing Xin Zhou. "Synthesis and Characterization of Functional Cholesteryl Substituted Luminol Derivative." Materials Science Forum 694 (July 2011): 565–69. http://dx.doi.org/10.4028/www.scientific.net/msf.694.565.

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Functional luminol derivative with cholesteryl substituted group has been designed and synthesized from the reaction of the corresponding precursor cholesteryl chloroformate with luminol. It has been found that depending on cholesteryl substituted group, the formed luminol derivative showed different properties, indicating distinct regulation of molecular skeleton. UV and IR data confirmed commonly the formation of imide group as well as cholesteryl segment in molecular structure. Thermal analysis showed that the thermal stability of luminol derivative with cholesteryl segment was different from luminol. The difference of thermal stability is mainly attributed to the formation of imide group and cholesteryl substituent group in molecular structure. The present results have demonstrated that the special properties of luminol derivative can be turned by modifying molecular structure of objective compound with proper substituted groups, which show potential application in functional material fields such as liquid crystal and ECL sensor.
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Dissertations / Theses on the topic "Luminol"

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Cedrón, Juan Carlos. "Luminol." Revista de Química, 2013. http://repositorio.pucp.edu.pe/index/handle/123456789/100502.

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La investigación forense tiene un pequeño aliado desde hace casi un siglo: el luminol. Esta simple molécula ha ayudado a resolver muchos crímenes por su peculiaridad de emitir luz en contacto con pequeños restos de sangre.
Forensic investigation has a small partner for almost a century: luminol. This simple molecule has helped to solve many murders because of its peculiarity of emitting light upon contact with tiny amounts of blood residues.
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Scowen, N. R. "Peroxidatic oxidation of luminol." Thesis, University of Newcastle upon Tyne, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384006.

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Patel, Jayprakash Lakman. "Luminol chemiluminescence and its applications." Thesis, Imperial College London, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266344.

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Martínez, Muñoz Daniel. "Theoretical studies of the chemiluminescence reactions; luminol." Thesis, Uppsala universitet, Institutionen för kemi - BMC, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-255902.

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The vast majority of chemical reactions occurs only in the ground state, however photochemical reactions like chemiluminescence take place in ground and excited states. In almost all chemiluminescence processes oxygen-oxygen bond breakage is involved. But, there is no general reason to explain why these processes occur via an oxygen-oxygen cleavage. These types of phenomena are usually highly exothermic. Computational chemistry has risen as a powerful tool to characterize and analyze chemical phenomena. Quantum mechanics are utilized to explain chemical observations. Applying these equations, one can compute the chemical properties of any system in any state. In the present study, three chemiluminescence reactions derived from luminol are modeled; nitrogen based, oxygen based and dianion nitrogen based models. The key factor of oxygen-oxygen bond rupture is discussed and rationalized. The electronic potential energy surfaces of the three compounds are computed at complete active space self-consistent field theory. Peroxide compounds compared to the dinitrogenated  compounds show a lower activation energy and they are more exothermic. This study allows us to rationalize why luminol needs to be presented in a basic medium and oxidized in order to produce chemiluminescence.
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Ferreira, Ernesto Correa. "Aplicações analiticas do estudo da reação quimiluminescente de luminol." [s.n.], 2001. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250060.

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Orientador: Adriana Vitorino Rossi
Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica
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Alshetaiwi, Hamad S. "Luminol luminescence-based theranostics for pre-clinical breast adenocarcinoma." Thesis, Kansas State University, 2014. http://hdl.handle.net/2097/17378.

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Master of Science
Department of Anatomy & Physiology
Deryl L. Troyer
Breast cancer ranks second as a cause of cancer death in women in the USA. Detection of early tumors and tumor-targeted treatments could decrease the problems associated with breast cancer management. Photodynamic therapy (PDT) is a cancer treatment that uses a photosensitizer and a specific wavelength of light and is currently in clinical trials for breast cancer. When tumor cells which have absorbed photosensitizer are exposed to the correct wavelength of light, reactive oxygen species are generated, resulting in tumor cell death. Poor tissue penetration of light is a major limitation in PDT, restricting its use to treatment of localized tumors. Light generation at the tumor area might increase the effectiveness of PDT. Polymorphonuclear neutrophils (PMNs) are known to often infiltrate breast adenocarcinoma, and their activatation in tumor stroma produces luminescence in the presence of luminol. Here, we hypothesized that luminol can be used as a theranostic agent for luminescence-based early tumor detection (diagnosis) and in situ PDT (treatment). BALB/c mice were transplanted with 4T1 mammary adenocarcinoma cells to establish a breast adenocarcinoma model. The early tumor detection objective was tested by daily intraperitoneal injection of luminol and in vivo luminescence imaging. To test the PDT treatment objective,the photosensitizer 5-aminolevulinic acid (ALA) and luminol were administered to mice through intraperitoneal and intravenous routes, respectively. This treatment regimen was repeated six times and ALA alone/luminol alone/saline treated tumor-bearing mice were used as controls. Results demonstrated that luminol allowed detection of activated PMNs only two days after 4T1 cell transplantation, even though tumors were not yet palpable. Relative differences in the increase of tumor volume and final tumor weights were analyzed to test the in situ PDT. Analysis of the data showed luminol treatments resulted in breast adenocarcinoma tumor growth attenuation. In conclusion this study provides evidence that luminol can be a theranostic agent for breast adenocarcinoma.
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Santos, Luciana Maia Escher dos. "ANÁLISE DO PERFIL MOLECULAR DE VESTÍGIOS SANGUÍNEOS PROVENIENTES DE LOCAIS DE CRIME APÓS APLICAÇÃO DE REAGENTE QUIMIOLUMINESCENTE." Pontifícia Universidade Católica de Goiás, 2013. http://localhost:8080/tede/handle/tede/2371.

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Molecular Biology shown to be an effective tool in forensic laboratories for the ability to identify an individual from minute amounts of biological samples such as blood, bones, semen, hair, teeth, nails, spittle, urine and other biological fluids recovered from the crime scene. One of the main biological evidence found at a crime scene are traces of bloodstains. This study aimed to analyze the molecular profiles of biological samples exposed to the chemiluminescent reagent luminol based on different storage times (48 hours and 30 days). With the measurement of all samples can be inferred that in the first 48 hours of storage, there was obtained DNA and varying concentrations after application of the chemiluminescent reagent. The samples were amplified by PCR using a multiplex system AmpFlSTR ® Select NGM and capillary electrophoresis. Molecular profiles were obtained complete and incomplete denoting specificity as the quality and quantity of the sample analyzed. The selection of molecular markers mini-STRs greatly contributed to the success of these profiles, allowing the study and analysis of degraded material. Our data suggest that the degradation of the DNA molecule exposed to the chemiluminescent reagent was higher in the samples compared to those containing diluted whole blood impregnation. Therefore, analyzing the bloodstains samples exposed to luminol in shorter storage provide molecular profiles compatible to clash samples.
A Biologia Molecular mostrou-se uma ferramenta efetiva nos laboratórios forenses pela capacidade de identificar um indivíduo a partir de quantidades ínfimas de amostras biológicas como sangue, ossos, sêmen, cabelo, dentes, unhas, saliva, urina, entre outros fluidos biológicos recuperados no local do crime. Uma das principais evidências biológicas encontradas em local de crime são vestígios de substâncias hematóides. Esta pesquisa visou a análise de perfis moleculares de amostras biológicas expostas ao reagente quimioluminescente a base de luminol em diferentes tempos de armazenamento (48 horas e 30 dias). Com a quantificação de todas as amostras pode-se inferir que nas primeiras 48 horas de armazenamento, obtiveram-se concentrações variáveis de DNA e após a aplicação do reagente quimioluminescente. As amostras foram amplificadas por PCR utilizando um sistema multiplex AmpFlSTR® NGM SElect e eletroforese capilar. Foram obtidos perfis moleculares completos e incompletos denotando inespecificidade conforme a qualidade e quantidade da amostra analisada. A seleção dos 17 marcadores moleculares mini-STRs em muito contribuiu para o sucesso desses perfis, permitindo estudo e análise de material degradado. Os dados indicam que a degradação da molécula de DNA exposta ao reagente quimioluminescente foi maior nas amostras diluídas em relação àquelas contendo impregnação com sangue total. A análise estatística das amostras com e sem exposição ao reagente quimioluminescente comparado ao grupo controle e em diferentes concentrações, mostrou não haver diferença estatísticamente significativa entre os valores quantificados obtidos. Ainda assim, analisar as amostras hematóides expostas ao luminol em menor tempo de armazenamento proporcionarão perfis moleculares compatíveis ao confronto de amostras.
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Oliveira, Sandro de. "Determinação da capacidade antirradicalar de produtos naturais utilizando-se a quimiluminescência do luminol e ensaios fotométricos com radicais estáveis." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-05122011-114158/.

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Os organismos vivos estão expostos à ação oxidativa de espécies reativas de oxigênio (ERO), causando uma série de doenças degenerativas como câncer, aterosclerose, diabetes, artrite e doenças do coração. Estudos têm demonstrado que o consumo de substâncias antioxidantes na dieta diária podem prevenir estes processos oxidativos que provocam o envelhecimento precoce do organismo. Nas últimas décadas tem se destacado o interesse em encontrar antioxidantes naturais para o emprego em produtos alimentícios ou farmacêuticos, com a finalidade de substituir antioxidantes sintéticos, os quais apresentam restrições devido ao seu potencial tóxico. Nesse trabalho, são comparados os resultados de medidas da capacidade antirradicalar de vários derivados fenólicos incluindo produtos naturais obtidos com os ensaios utilizando o radical estável DPPH• e o cátion radical ABTS•+, que apresentam vantagens em relação à simplicidade do método analítico e facilidade na coleta de dados, além da reprodutibilidade dos resultados. Além disso, desenvolveu-se um ensaio com DPPH• para avaliar a capacidade antirradicalar de compostos fenólicos em meio ácido, hidroalcoólico e tamponado, para possibilitar a obtenção de valores da capacidade antirradicalar de flavonoides e compostos análogos em meio aquoso em diferentes estados de ionização. Também, foi utilizado o ensaio quimiluminescente com luminol/hemina/H2O2, desenvolvido pelo nosso grupo de pesquisa, para a determinação da capacidade antirradicalar de extratos, fases e frações de Baccharis regnelli e proposto o novo parâmetro \"Porcentagem de Trolox\" para expressar adequadamente esta capacidade em misturas complexas. A sensibilidade do ensaio luminol comprovou ser maior que a de outros métodos e adequado para medir a capacidade antirradicalar de misturas complexas de produtos naturais, auxiliando no isolamento de novas substâncias com atividade antirradicalar.
Living organisms are exposed to the oxidative action of reactive oxygen species (ROS), causing a series of degenerative diseases such as cancer, atherosclerosis, diabetes, arthritis and heart disease. Studies have shown that consumption of antioxidant substances in the daily diet can prevent these oxidative processes that cause premature aging of the organism. Much attention has been paid in the last decades on the discovery of new natural antioxidants for its use in food or pharmaceutical industry, with the aim of replace synthetic antioxidants, which have restrictions due to their toxic potential. In this study, we compared the results from antiradical capacity determinations of several phenolic derivatives including natural products obtained by two different assays. One of them utilizes the stable radical DPPH• and the other the radical cation ABTS•+ as reagents and both have the advantage of a simple analytical method and ease in data collection as well as high data reproducibility. Furthermore, we have developed a method with DPPH• for the evaluation of the antirradicalar capacity of phenolic compounds in acid and buffered hydroalcoholic media, in order to facilitate the determination of the antiradical capacity of flavonoids and similar compounds in aqueous ambient and to allow differentiation between the capacity of different ionization states of these derivatives. Finally the chemiluminescent luminol/hemin/H2O2 assay, developed by our research group, has been utilized for the determination of the antiradical capacity of extracts, phases and fractions of Baccharis regnelli and the new parameter \"Trolox Percentage\" is being proposed to adequately express the antiradical capacity of complex mixtures. The sensibility of the luminol assay has been found to be higher than that of other methods and is shown to be suitable for the determination of antiradical activity parameters of complex natural product mixtures, contributing to the isolation of new substances with antiradical activity.
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Eckert, Camila Rodrigues. "Determinação da atividade anti-radicalar de flavonóides e extratos de espécies de Baccharis através da reação quimiluminescente do luminol." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-24042007-082922/.

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Nesse trabalho foi realizado um estudo da atividade anti-radicalar de flavonóides frente ao ensaio com o sistema luminol/hemina/H2O2 desenvolvido por nosso Grupo de Pesquisa. Na tentativa de esclarecer a relação estrutura-atividade de flavonóides, foi realizada também uma investigação das propriedades de derivados fenólicos como compostos-modelo utilizando-se a reação quimiluminescente do luminol. Os resultados obtidos com os compostos-modelo com o ensaio luminol foram comparados com aqueles obtidos para estes aditivos em um ensaio que utiliza o radical estável DPPH como sonda. Além disso, foi realizado um estudo fitoquímico monitorado através da atividade anti-radicalar de extratos de Baccharis. Foram identificados dois componentes ativos da fase em acetato de etila obtida das folhas de Baccharis regnellii e a sua atividade anti-radicalar determinada.
In this work a systematic study on the antiradical activity of flavonoids was performed, using the assay luminol/hemin/H2O2 developed by our research group. With the objective to establish a structure activity relationship for flavonoids, a study on the antioxidant properties of several phenolic derivatives as model compounds was also performed, using luminol chemiluminescence. The results obtained with the model compounds from the luminol assay are compared to those obtained by an assay which utilizes the stable DPPH radical as probe. Furthermore, a phytochemical study, monitored by the antiradical activity, was performed on extracts of Baccharis. This study led to the identification of two active components in the ethyl acetate phase of Baccharis regnellii leafs and the determination of its antiradical activity.
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King, David. "Sonochemical analysis of the output of ultrasonic dental descalers." Thesis, University of Bath, 2010. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538276.

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Ultrasonic descalers are used in dentistry to remove calculus and other contaminants from teeth. One mechanism which may assist in the cleaning is cavitation generated in cooling water around the descaler. The spatial distribution of cavitation around three designs of descaler tips and under three load conditions has been observed using sonochemiluminescence from a luminol solution and compared with the vibratory motion of the tips in a water bath, characterised by scanning laser vibrometry. The type of cavitation was confirmed by acoustic emission analysed by a ‘Cavimeter’ supplied by NPL. Surface profilometry and SEM of eroded hydroxyapatite pellets was performed to quantitatively study the erosion caused by a descaler tip in both contact and non-contact modes. Densitometry was used to study the erosion of black ink from a glass microscope slide, and determined that under the majority of conditions, no erosion was demonstrated via cavitation, by descalers operating in non-contact mode, although significant erosion was demonstrated with the tip in contact with the slide.
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Books on the topic "Luminol"

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Chʻoe, Sang-gyu. Luminol. Sŏul: Chʻŏngnim Chʻulpʻan, 1991.

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Joyce, Laura E. Luminol Theory. Brooklyn, NY: punctum books, 2017.

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Santacroce, Isabella. Luminal. Milano: Feltrinelli, 1998.

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Ferguson, V. S. Inanna hyper-luminal. Seattle, Wash: Thel Dar Pub., 1996.

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Luminous. London: Millennium, 1999.

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Wiethüchter, Blanca. Luminar. La Paz, Bolivia: Ediciones del Hombrecito Sentado, 2005.

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Lozano, Orietta. Luminar. Cali, Colombia: Ediciones Universidad del Valle, 1994.

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Luminous. New York: Dutton Books, 2011.

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Egan, Greg. Luminous. London: Millennium, 1998.

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Jobin, L. J. The Luminoc insect trap. Sainte-Foy, Quebec: Forestry Canada, Quebec Region, 1992.

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Book chapters on the topic "Luminol"

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Gundermann, Karl-Dietrich, and Frank McCapra. "Luminol and Related Compounds." In Reactivity and Structure: Concepts in Organic Chemistry, 77–108. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71645-4_7.

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Heindl, Dieter, and Hans-Peter Josel. "Chemiluminescent Detection with Horseradish Peroxidase and Luminol." In Nonradioactive Analysis of Biomolecules, 258–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57206-7_18.

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Peter, M., P. Wendt, A. Stemberger, R. Lange, A. G. Gatthof, and G. Blümel. "Untersuchungen zur Wertigkeit der Luminol Chemiluminescenz im Vollblut." In Kongreß der Deutschen Gesellschaft für Chirurgie München, 10.–13. April 1985, 81–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70325-6_17.

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Greenway, Gillian M., Lorna J. Nelstrop, Tom McCreedy, and Paul Greenwood. "Luminol Chemiluminescence Systems for Metal Analysis by μTAS." In Micro Total Analysis Systems 2000, 363–66. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-017-2264-3_84.

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Warren, J. T., A. H. Esa, G. R. Pettit, and W. S. May. "Bryostatin Stimulation of Human Neutrophil Luminol and DBA (Lucigenin) Chemiluminescence." In Oxygen Radicals in Biology and Medicine, 223–27. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5568-7_34.

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Schiff, H. I., G. I. Mackay, C. Castledine, G. W. Harris, and Q. Tran. "Atmospheric Measurements of Nitrogen Dioxide with a Sensitive Luminol Instrument." In Acidic Precipitation, 105–14. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-3385-9_9.

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Trujillo, Marco. "Analysis of the lmmunity-Related Oxidative Bursts by a Luminol-Based Assay." In Methods in Molecular Biology, 323–29. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3356-3_26.

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Guerrieri, Patrizia, Paolo Montemaggi, Volker Budach, Carmen Stromberger, Volker Budach, Volker Budach, Anthony E. Dragun, et al. "Luminal Subtypes." In Encyclopedia of Radiation Oncology, 460. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-85516-3_1164.

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Hildebrandt, Alfred G., Andreas Weimann, and Regine Kahl. "Use of the Chemiluminigenic Probes Luminol and Lucigenin for the Detection of Active Oxygen Species in Hepatic Microsomes and in Intact Hepatocytes." In Biological Reactive Intermediates III, 971–80. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5134-4_94.

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Gooch, Jan W. "Luminous." In Encyclopedic Dictionary of Polymers, 435. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7067.

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Conference papers on the topic "Luminol"

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NAKAZONO, M., and K. ZAITSU. "PHOTOSENSITIVE LUMINOL RELEASING COMPOUND, LUMINOL-O-4,5-DIMETHOXY -2-NITROBENZYLATE." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0042.

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Carvalho, Francisco Dheyson de Quadro, and Estevão Bombonato Pereira. "Estudo fotofísico do Luminol." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020138.

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The 5-Amino-2,3-dihydro-1,4-phthalazinedione known as Luminol is used mainly in hidden blood investigations. Therefore, the objective of this work is to develop a calculations routine using computational chemistry methods that properly describe the structure of luminol and its derivatives. Posteriorly, this routine will be used for the analysis and the proposition of new structures comparing the results with experimental data obtained in appropriate literature. Firstly, the Density Functional Theory (DFT) was used with the functional B3LYP/G, and the base function def2-TZVP in the ORCA program for modeling the structures. Thus, was verified the interference of the presence of solvent molecules close to the luminol molecule, the use of solvent as a dielectric continuum, the combination of both for a description of the solvent effect, and the use of relativistic functions to optimize results. Therefore, having obtained the preliminary results, we did the comparison with experimental data collected by other researchers.
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MARZOCCHI, E., S. GRILLI, L. DELLA CIANA, M. MIRASOLI, P. SIMONI, L. PRODI, and A. RODA. "NUCLEOPHILIC ACYLATION CATALYSTS EFFECT ON LUMINOL CHEMILUMINESCENCE." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0030.

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Guo, Wenying, Jilin Yan, and Yifeng Tu. "Sensitization of luminol electrochemiluminescence by metallic oxide nano-particles." In 2010 IEEE 3rd International Nanoelectronics Conference (INEC). IEEE, 2010. http://dx.doi.org/10.1109/inec.2010.5424922.

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Alshetaiwi, Hamad S., Tej B. Shrestha, Sivasai Balivada, Matthew T. Basel, Marla Pyle, Hongwang Wang, Stefan H. Bossmann, and Deryl L. Troyer. "Abstract 4920: Luminol-basedin situphotodynamic therapy for breast adenocarcinoma." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4920.

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MERRILL, GERALD A., and ROBERT C. ALLEN. "INHIBITION ANALYSIS OF CHICKEN HETEROPHIL LUMINOL AND LUCIGENIN LUMINESCENCE." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0104.

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Matsuo, Ruru, and Ryosuke Matsumoto. "Diffusion and Mixing in Microchannel Analyzed by the Luminol Chemiluminescence." In ASME 2013 11th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icnmm2013-73113.

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This study focused on the diffusion and mixing phenomena investigated by using luminol chemiluminescence (CL) to estimate the local chemical reaction rate in the T-junction microchannel. Generally, the degree of mixing in microchannel is calculated by the deviation of the obtained concentration profiles from the uniform concentration profile by using fluorescence technique. Thus, the degree of mixing is a macroscopic estimate for the whole microchannel, which is inappropriate for understanding the diffusion and mixing phenomena in the mixing layer. In this study, the luminol CL reaction is applied to visualize the local chemical reaction and to estimate the local diffusion and mixing phenomena at an interface between two liquids in microchannel. Luminol emits blue chemiluminescence when it reacts with the hydrogen peroxide at the mixing layer. Experiments were carried out on the T-junction microchannel with 200 microns in width and 50 microns in depth casted in the PDMS chip. The chemiluminescence intensity profiles clearly show the mixing layer at an interface between two liquids. The experimental results are compared with the results of numerical simulation that involves solving the mass transport equations including the chemical reaction term. By calibrating CL intensity to the chemical reaction rate estimated by the numerical simulation, the local chemical reaction profile can be quantitatively estimated from the CL intensity profile.
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Sakai, Harumasa, Hugo Oppelaar, Paul Baas, Nico Van Zandwijk, and Fiona A. Stewart. "Detection of singlet oxygen yield from new photosensitizers using luminol." In Fifth International Photodynamic Association Biennial Meeting, edited by Denis A. Cortese. SPIE, 1994. http://dx.doi.org/10.1117/12.203354.

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Cantrell, Chris A., Richard E. Shetter, John A. Lind, Curt A. Gilliland, and Jack G. Calvert. "Chemical amplifier for peroxy radical measurements based on luminol chemiluminescence." In Optics, Electro-Optics, and Laser Applications in Science and Engineering, edited by Harold I. Schiff. SPIE, 1991. http://dx.doi.org/10.1117/12.46180.

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ZILIOTTO, Luis Henrique Carra, and Isaac Newton Lima DA SILVA. "ANALYSIS OF FALSE-POSITIVE RESULTS AND THE REAL EFFECTIVENESS OF LUMINOL IN THE DETECTION OF BLOOD SPOTS." In SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 2021 INTERNATIONAL VIRTUAL CONFERENCE. DR. D. SCIENTIFIC CONSULTING, 2022. http://dx.doi.org/10.48141/sbjchem.21scon.28_abstract_ziliotto.pdf.

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Forensic investigators have widely used luminol for more than 90 years in the identification of blood in life crime scenes. When mixed with an alkaline solution and sprayed on a catalyst (iron present in blood hemoglobin), it reproduces a chemiluminescent reaction with a bluish color. As it is a presumptive blood test, the present study sought to demonstrate that only the photons emission is not a prerogative to attest that the result is indeed human blood. In this perspective, 24 samples of both liquid and solid substances that can easily be found in residences and potentially used by criminals to impair the interpretation of the investigator at the crime scene were prepared. Out of the total of the analyzed samples, there was a chemical reaction with sodium hypochlorite and wood varnish, proving the known understanding that some samples may cause interference in the examination with luminol.
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Reports on the topic "Luminol"

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Gaffney, J. S., N. A. Marley, and P. J. Drayton. Aircraft measurements of nitrogen dioxide and peroxyacyl nitrates using luminol chemiluminescence with fast capillary gas chromatography. Office of Scientific and Technical Information (OSTI), September 1997. http://dx.doi.org/10.2172/564167.

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Jackson, Mitchell. Luminous Days. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.7105.

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Li, Christopher, Arul Chinnaiyan, and Peggy Porter. Advancing Our Understanding of the Etiologies and Mutational Landscapes of Basal-Like, Luminal A, and Luminal B Breast Cancers. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada613073.

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Chinnaiyan, Arul, Christopher Li, and Peggy Porter. Advancing Our Understanding of the Etiologies and Mutational Landscapes of Basal-Like, Luminal A, and Luminal B Breast Cancers. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada613074.

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Li, Christopher. Advancing Our Understanding of the Etiologies and Mutational Landscapes of Basal-Like, Luminal A, and Luminal B Breast Cancers. Fort Belvoir, VA: Defense Technical Information Center, October 2013. http://dx.doi.org/10.21236/ada597854.

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Chinnaiyan, Arul. Advancing Our Understanding of the Etiologies and Mutational Landscapes of Basal-Like, Luminal A, and Luminal B Breast Cancers. Fort Belvoir, VA: Defense Technical Information Center, October 2013. http://dx.doi.org/10.21236/ada598332.

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Du, Cheng. Transdifferentiation between Luminal- and Basal-Type Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, December 2013. http://dx.doi.org/10.21236/ada601036.

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Vaught, David B. Neuregulin Driven Cell Differentiation, Transformation, and Parity of Luminal Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, December 2013. http://dx.doi.org/10.21236/ada598353.

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Leung, Y., Y. Zhang, B. Yanny, K. Herner, J. Annis, A. Palmese, A. Sampaio-Santos, et al. The Diffuse Light Envelope of Luminous Red Galaxies. Office of Scientific and Technical Information (OSTI), May 2020. http://dx.doi.org/10.2172/1637638.

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Wood, Keith V. Luciferases of Luminous Beetles: Evolution, Color Variation, and Applications. Fort Belvoir, VA: Defense Technical Information Center, March 1992. http://dx.doi.org/10.21236/ada251122.

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