Relevant bibliographies by topics / Chemiluminescent

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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 'Chemiluminescent'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Chemiluminescent"

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Ibragimova, D. A., O. M. Kamil, T. V. Yankova, N. A. Yashtulov, and N. K. Zaitsev. "THE EFFECT OF SURFACTANTS ON THE CHEMILUMINESCENT REACTION OF LUMINOL WITH HYDROGEN PEROXIDE." Fine Chemical Technologies 12, no. 6 (December 28, 2017): 71–76. http://dx.doi.org/10.32362/2410-6593-2017-12-6-71-76.

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The luminol-hydrogen peroxide chemiluminescent system is widely used for the creation of diagnostic systems, for chemical analysis, for studying the kinetics and mechanisms of chemical reactions, for the creation of special and emergency light sources, and for monitoring living systems. However, the use of the luminol-hydrogen peroxide chemiluminescent system is limited by the fact that there are almost no ways of managing the reaction. The introduction of organized molecular systems into the luminol-hydrogen peroxide chemiluminescent system can create an additional channel for controlling chemiluminescent reactions. The luminol-hydrogen peroxide system was not previously studied in various classes of hydrocarbon and perfluorinated micellar solutions. This work was the first to study the effect of cationic, anionic and nonionic hydrocarbon surface-active substances (cetyltrimethylammonium bromide, sodium decyl sulfate, sodium dodecyl sulfate, triton X 100) and perfluorinated surface-active substances (FT-135 and FT-248) on the chemiluminescent systems luminol-hydrogen peroxide-potassium hexacyanoferrate(III) and luminol-hydrogen peroxide-copper(II) sulphate. The systems retain the ability to chemiluminescence in the presence of a surfactant. Cationic surfactants lower the intensity of chemiluminescence, and anionic surfactants increase the intensity of chemiluminescence. The introduction of a surfactant into the system allows increasing the range of dependence of the chemiluminescence intensity on the catalyst concentration. Kinetic curves of the growth and decay of chemiluminescence were measured in the systems. The rate constants of the chemiluminescence decay were measured in the framework of the first-order kinetics model.
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Fini, Fabiana, Giorgio Gallinella, Stefano Girotti, Marialuisa Zerbini, and Monica Musiani. "Development of a Chemiluminescence Competitive PCR for the Detection and Quantification of Parvovirus B19 DNA Using a Microplate Luminometer." Clinical Chemistry 45, no. 9 (September 1, 1999): 1391–96. http://dx.doi.org/10.1093/clinchem/45.9.1391.

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Abstract Background: Quantitative PCR of viral nucleic acids can be useful clinically in diagnosis, risk assessment, and monitoring of antiviral therapy. We wished to develop a chemiluminescence competitive PCR (cPCR) for parvovirus B19. Methods: Parvovirus DNA target sequences and competitor sequences were coamplified and directly labeled. Amplified products were then separately hybridized by specific biotin-labeled probes, captured onto streptavidin-coated ELISA microplates, and detected immunoenzymatically using chemiluminescent substrates of peroxidase. Chemiluminescent signals were quantitatively analyzed by a microplate luminometer and were correlated to the amounts of amplified products. Results: Luminol-based systems displayed constant emission but had a higher detection limit (100–1000 genome copies) than the acridan-based system (20 genome copies). The detection limit of chemiluminescent substrates was lower (20 genome copies) than colorimetric substrates (50 genome copies). In chemiluminescence cPCR, the titration curves showed linear correlation above 100 target genome copies. Chemiluminescence cPCR was positive in six serum samples from patients with parvovirus infections and negative in six control sera. Conclusions: The chemiluminescence cPCR appears to be a sensitive and specific method for the quantitative detection of viral DNAs.
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Fereja, Tadesse Haile, Ariaya Hymete, and Thirumurugan Gunasekaran. "A Recent Review on Chemiluminescence Reaction, Principle and Application on Pharmaceutical Analysis." ISRN Spectroscopy 2013 (November 26, 2013): 1–12. http://dx.doi.org/10.1155/2013/230858.

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This paper provides a general review on principle of chemiluminescent reactions and their recent applications in drug analysis. The structural requirements for chemiluminescent reactions and the different factors that affect the efficiency of analysis are included in the review. Chemiluminescence application in immunoassay is the new version for this review. Practical considerations are not included in the review since the main interest is to state, through the aforementioned applications, that chemiluminescence has been, is, and will be a versatile tool for pharmaceutical analysis in future years.
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Pieńkos, Milena, and Beata Zadykowicz. "Computational Insights on the Mechanism of the Chemiluminescence Reaction of New Group of Chemiluminogens—10-Methyl-9-thiophenoxycarbonylacridinium Cations." International Journal of Molecular Sciences 21, no. 12 (June 21, 2020): 4417. http://dx.doi.org/10.3390/ijms21124417.

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Immunodiagnostics, in which one of the promising procedures is the chemiluminescent labelling, is essential to facilitate the detection of infections in a human organism. One of the standards commonly used in luminometric assays is luminol, which characterized by low quantum yield in aqueous environments. Acridinium esters have better characteristics in this topic. Therefore, the search for new derivatives, especially those characterized by the higher quantum yield of chemiluminescence, is one of the aims of the research undertaken. Using the proposed mechanism of chemiluminescence, we examined the effect of replacing a single atom within a center of reaction on the efficient transformation of substrates into electronically excited products. The density functional theory (DFT) and time dependent (TD) DFT calculated thermodynamic and kinetic data concerning the chemiluminescence and competitive dark pathways suggests that some of the scrutinized derivatives have better characteristics than the chemiluminogens used so far. Synthesis of these candidates for efficient chemiluminogens, followed by studies of their chemiluminescent properties, and ultimately in chemiluminescent labelling, are further steps to confirm their potential applicability in immunodiagnostics.
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Kudryashova, A. M., N. A. Mikhailova, and O. V. Borisova. "COMPARISON OF COLORIMETRIC AND CHEMILUMINESCENT ELISA TESTS FOR DETECTION OF IgG ANTIBODIES TO HUMAN EPO IN THE SERA OF EXPERIMENTAL ANIMALS." Medical Immunology (Russia) 20, no. 6 (December 15, 2018): 935–42. http://dx.doi.org/10.15789/1563-0625-2018-6-935-942.

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Production of antibodies to erythropoietin-stimulating drugs is an important problem of therapy with recombinant human erythropoietin (EPO). It leads to changes in the pharmacokinetic profile and decreased therapeutic efficiency. Upon long-term treatment with EPO preparations, neutralizing antibodies can result in rare cases, thus leading to complete pure red cell aplasia. Hence, detection of antibodies to EPO is an important stage in the assessment of the drug immunogenicity in preclinical and clinical studies, as well as during the treatment with EPO. We have compared colorimetric and chemiluminescent ELISA tests for detection of IgG antibodies to human EPO with 3,3’,5,5’-tetramethylbenzidine – hydrogen peroxide and luminol -hydrogen peroxide detection systems, respectively. Аntibodies to human EPO were determined in blood serum samples of experimental animals, i.e., rabbits and guinea pigs following their immunization withdifferent doses of pegylated human recombinant EPO-beta subcutaneously or intravenously. The affinitypurified rabbit polyclonal antibodies to human EPO were used as a reference material. The effects of hydrogen peroxide and luminol concentrations upon sensitivity of a chemiluminescent method were also studied. We have shown a 1.5-2-fold increase in sensitivity when using 4-iodophenol for amplification of chemiluminescence. A comparison of the chemiluminescence intensity with time has demonstrated a better stability for the substrate mixture prepared on borate buffer. A decrease in chemiluminescence signal with time was proportional to the decrease in background signal, thus rendering stability of the signal/background ratio for 3 to 30 minutes. Due to optimizing the substrate mixture composition and conditions of chemiluminescence recording, the reached detection limits for colorimetric and chemiluminescent ELISA’s were, respectively, 0.6 ng/ml and 0.08 ng/ml. The measurement range was extended by more than 20 times for chemiluminescent ELISA. The chemiluminescent ELISA for anti-erythropoietin antibody detection showed a 1.9 to 2.6-fold increase in sensitivity for rabbit serum, and 1.8 to 8.9-fold for guinea pigs serum. Good correlation of results was found for quantitative detection of antibodies in rabbit sera using the two methods (R = 0.981). Thus, chemiluminescent ELISA allowed develop a more sensitive detection technique of IgG antibodies to human erythropoietin.
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Gnaim, Samer, Anna Scomparin, Anat Eldar-Boock, Christoph R. Bauer, Ronit Satchi-Fainaro, and Doron Shabat. "Light emission enhancement by supramolecular complexation of chemiluminescence probes designed for bioimaging." Chemical Science 10, no. 10 (2019): 2945–55. http://dx.doi.org/10.1039/c8sc05174g.

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Maity, Santanu, Xiaojian Wang, Subhamoy Das, Maomao He, Lee W. Riley, and Niren Murthy. "A cephalosporin–chemiluminescent conjugate increases beta-lactamase detection sensitivity by four orders of magnitude." Chemical Communications 56, no. 24 (2020): 3516–19. http://dx.doi.org/10.1039/c9cc09498a.

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A beta-lactamase chemiluminescent probe, termed CCP, which can for the first time detect beta-lactamase activity via chemiluminescence and 4-orders of magnitude higher than commercial fluorescent probe.
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Lin, Ke Li, Tong Yang, Fang Fang Zhang, Gang Lei, Hong Yan Zou, Yuan Fang Li, and Cheng Zhi Huang. "Luminol and gold nanoparticle-co-precipitated reduced graphene oxide hybrids with long-persistent chemiluminescence for cholesterol detection." Journal of Materials Chemistry B 5, no. 35 (2017): 7335–41. http://dx.doi.org/10.1039/c7tb01607g.

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Luminol and AuNP dual-functionalized rGO hybrids (rGO/AuNP/luminol) have been synthesized to generate long-persistent chemiluminescence, which can be used as a chemiluminescent biosensing platform for the detection of cholesterol.
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Peck, Evan M., Allen G. Oliver, and Bradley D. Smith. "Enhanced Squaraine Rotaxane Endoperoxide Chemiluminescence in Acidic Alcohols." Australian Journal of Chemistry 68, no. 9 (2015): 1359. http://dx.doi.org/10.1071/ch15196.

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Squaraine rotaxane endoperoxides (SREPs) are storable chemiluminescent compounds that undergo a clean cycloreversion reaction that releases singlet oxygen and emits near-infrared light when warmed to body temperature. This study examined the effect of solvent on SREP chemiluminescence intensity and found that acidic alcohols, such as 2,2,2-trifluoroethanol, α-(trifluoromethyl)benzyl alcohol, and 1,1,1,3,3,3-hexafluoroisopropanol, greatly increased chemiluminescence. In contrast, aprotic solvents, such as trifluoroethylmethyl ether, had no effect. The interlocked rotaxane structure was necessary as no chemiluminescence was observed when the experiments were conducted with samples containing a mixture of the two non-interlocked components (squaraine thread and macrocycle endoperoxide). Spectroscopic analyses of the enhanced SREP chemiluminescent reactions showed a mixture of products. In addition to the expected squaraine rotaxane product caused by cycloreversion of the endoperoxide, a diol derivative was isolated. The results are consistent with an endoperoxide O–O bond cleavage process that is promoted by the hydrogen bonding solvent and produces light emission from a squaraine excited state.
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Agatsuma, Shinichi, Toshiyuki Nagoshi, Masaki Kobayashi, Masashi Usa, Haruo Watanabe, Hiroshi Sekino, and Humio Inaba. "Hydroxyl Radical-Induced Characteristic Chemiluminescent Spectra from Plasma of Hemodialysis Patients." Clinical Chemistry 38, no. 1 (January 1, 1992): 48–55. http://dx.doi.org/10.1093/clinchem/38.1.48.

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Abstract Plasma from hemodialysis patients evoked weak photon emissions (chemiluminescence) in a characteristic emission spectrum with a peak at 430 nm, attributed to attack by hydroxyl radicals generated from the iron-catalyzed breakdown of hydrogen peroxide (Fenton reaction), whereas plasma from normal healthy subjects showed a rather weak red chemiluminescence peak at around 680 nm, similar to that resulting from attack by hydroxyl radicals. However, the addition of hydrogen peroxide in the absence of divalent irons induced almost the same red chemiluminescent emission spectrum in both plasmas. The HPLC-gel-filtration chromatography carried out with both plasmas revealed that a primary emitter evoking a peak emission at 430 nm was located in the fraction of lower-molecular-mass substances in fractionated plasma from hemodialysis patients. In contrast, the elution peaks evoking red chemiluminescence with the addition of hydrogen peroxide were mainly observed for the higher-molecular-mass fraction, as determined by gel chromatography of both plasmas. Therefore, the observation of a chemiluminescence peak at 430 nm, induced by the generation of hydroxyl radicals, correlated well with chemiluminescent emissions in plasma samples from patients with chronic renal failure. Spectral analyses of clinical samples that show weak chemiluminescence by forced oxidation by such an active oxygen may provide a new and more sensitive method for diagnosing metabolic disorders.
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Dissertations / Theses on the topic "Chemiluminescent"

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Li, Z. "Synthesis and chemiluminescent properties of novel chemiluminescent compounds." Thesis, Swansea University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637905.

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Radioactive isotopes have been very important labelling materials in biochemistry and medicine since the 1940s. Their high detection sensitivity renders them extremely useful. However, their hazardous, limited shelf life and the difficulty of production are disadvantages. As potential substitutes for radioactive isotopes, acridinium compounds can be detected sensitively by measuring the light emitted from their reaction with hydrogen peroxide. Acridinium esters are apparently safe and can be synthesised in any laboratory in gram quantities. In addition, the unique chemiluminescent properties (multifarious wavelengths and lifetimes) of acridinium esters enable them to be used in some new analytical techniques like multiple-analyte assays. Structural factors are important to the chemiluminescent properties of acridinium esters. Therefore, the research presented in this thesis involves a) synthesis of new acridinium esters by structural modification of both the acridine ring and the phenoxy ring, and b) investigation of the effects of these modifications on the chemiluminescent properties of the acridinium esters. The first chapter gives the background of the project. The remaining chapters (chapter 2-8) detail the syntheses of twelve chemiluminescent compounds for example 2-methoxy-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinum-9-carboxylate trifluoromethanesulfonate 1, 2,6-dimethoxy-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium 9-carboxylate trifluoromethanesulfonate 2, 3-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate 3, 4-(2-succinimidyloxycarbonylethyl)phenyl 2,7-diisopropyl-10-methylacridinium-9 carboxylate trifluoromethanesulfonate 4, 4-(benzyloxycarbonylethyl)phenyl 2,7-dimethoxy-10-methylacridinium-9-carboxylate trifluoromethanesulfonate.
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Sumun, Faizal. "Chemiluminescent gene probes." Thesis, University of Sussex, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.352945.

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Chen, L. "Synthesis of new chemiluminescent compounds." Thesis, Swansea University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.636242.

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This thesis consists of five parts. In chapter 1, the background to chemiluminescence, chemiluminescent compounds and their applications is given. The synthesis and chemiluminescent behaviour of substituted phenyl acridinium esters (compounds 1 and 2), heterocyclyl acridinium esters and their analogues (compounds 3-7) and phenyl 2-halo-6-methoxy acridinium esters (compounds 8-11) are detailed in chapters 2, 3 and 4 respectively. The chemiluminescence studies include chemiluminescent kinetics, chemiluminescent efficiencies, chemiluminescent wavelengths and hydrolytic stabilities of the acridinium esters. Modifications on leaving groups show obvious effects on chemiluminescent kinetics and stabilities, but no wavelength changes were observed with such modifications. However, modifications on the acridine ring do not significantly affect chemiluminescent kinetics and stabilities. Chemiluminescent efficiency was decreased by the introduction of halogen atoms into the acridine ring. Surprisingly, chemiluminescent wavelength was found to be influenced by the introduction of halo and methoxy groups to positions 2 and 6, respectively of the acridine ring. Among the newly prepared acridinium esters, compounds 2 and 3 possess better stability and good quantum efficiency, and could be developed as better chemiluminescent labels in chemiluminescent immunoassays over the model compound. Apart from the acridinium esters, three cysteine derivatives (compounds 12-14) were also prepared for chemiluminescent immunoassay. The enantiomeric purity of the product was identified by NMR. The details are presented in chapter 5.
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Yang, J.-J. "Chemiluminescent probes for biological molecules." Thesis, Swansea University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.636704.

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This work describes the synthesis of new chemiluminescent ester compounds and their applications in immunoassay. The new compounds are 2,6-dibromo-4-(2-succinimidyl-oxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate (II), 2,6-dimethyl-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate (III), 2-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate (IV), 4,6-dibromo-2-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethane-sulfonate (V), 4,6-dimethyl-2-(2-succinimidyloxycarbonylethyl)phenyl 10-methyl-acridinium-9-carboxylate trifluoromethanesulfonate (VI) and 4-bromo-6-methyl-2-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethane-sulfonate (VII). All these compounds contain an acridinium ester unit, which provides the chemiluminescent moiety, a phenolate unit as a leaving group and a succinimidyl ester unit as a means of linking to biological molecules. The thesis is divided into two parts. The introduction gives a broad background and understanding of chemiluminescent biological probes. Initially the process of light emission is explained in brief. This is important because it is light emission from a chemical reaction that is chemiluminescence. This is followed by a description of the major chemiluminescence reagents, especially acridinium ester species as examples, and of how these can be used as labels in chemiluminescence immunoassay. The second part describes the synthesis of compounds (II), (III),(IV), (V), (VI), and (VII), together with som basic studies of theirchemiluminescent properties and attachment to Biblogical materials.
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Smith, P. A. "Dynamics of chemiluminescent atomic reactions." Thesis, University of Nottingham, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372672.

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Mu, Xiaojing. "Synthesis of novel chemiluminescent compounds." Thesis, Swansea University, 2005. https://cronfa.swan.ac.uk/Record/cronfa42926.

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Holland, Andrew Mark. "Synthesis of novel chemiluminescent compounds." Thesis, Swansea University, 2002. https://cronfa.swan.ac.uk/Record/cronfa42996.

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Barrett, Z. S. "The electrogenerated chemiluminescent imaging of metals." Thesis, Swansea University, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.636045.

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This thesis details the characterisation and development of the luminol Electrogenerated Chemiluminescence (ECL) reaction to enable it to spatially resolve dissimilar metal compositions at a single conductive metal surface. The large difference in ECL emission from iron and tin has been exploited to detect penetrative defects in the surface of commercial tinplate and is presented in chapter 4. Reaction conditions are selected based on the data shown in the chapter 3 such that the exposed iron substrate emits ECL at a greater intensity than the surrounding intact tin coating. In this way the defects are rapidly exposed and can be photographed using an image intensified CCD camera. Chapter 5 continues on the theme of defect detection but describes the use of ECL in exposing failures in five types of commercial galvanised coatings. In a similar manner to tinplate the reaction is optimised such that the exposed substrate emits a much greater light intensity when compared to the zinc coating. Given the success of the technique at studying macro features, efforts were made to develop the process further to allow observation of micro features and in particular the copper rich phases present in AA2024-T3. Chapter 6 details the investigations made to optimise ECL for micro use. In chapter 7, the newly optimised technique is used to follow the dealloying and redistribution of copper at the surface of AA2024-T3 - an important aerospace alloy. Again the dissimilar emission phenomenon is exploited, this time from copper and aluminium. It is shown that the origin of surface copper when the alloy is dealloyed in NaCl is predominantly from the copper rich S-phase particles rather than the matrix.
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Paulls, David Andrew. "Enhancement of the chemiluminescent oxidation of sulphite." Thesis, University of Hull, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337058.

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Nelstrop, Lorna. "An investigation of chemiluminescent miniaturised analytical systems." Thesis, University of Hull, 2000. http://hydra.hull.ac.uk/resources/hull:8060.

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This thesis examines the feasibility of using chemiluminescence (CL) for detection in miniaturised analytical systems. The aim of this project was to design a miniaturised device that could potentially be used for the remote sensing of metal ions. The development of miniaturised analytical devices for use with two well known chemiluminescent reactions; namely the tris(2,2'-bipyridyl)ruthenium (II) reaction and the luminol reaction, for the detection and quantification of codeine and cobalt (II) respectively are discussed. Chapter 1 introduces the concept, the manufacture, operating principles and applications of miniaturised analytical systems, while the use of chemiluminescence, its requirements and applications as a sensitive, selective yet simple method of detection are reviewed in chapter 2. Chapter 3 describes the manufacture and development of the robust and practical miniaturised analytical devices used for the analyses described in chapters 4 and 5. Several novel developments are described in this chapter. These included the use of thicker top plates that enable the reservoirs to be contained within the single unit structure. This design was intended to prolong the lifetime of the chip system and increase the available reagent volumes. A microwave furnace for thermal bonding of the two glass plates was also used and the detection of the chemiluminesence produced in the chip system was carried out from underneath the chip base. Chapter 4 details the application of the tris(2,2'-bipyridyl)ruthenium (II) (TBR) for analysis in a miniaturised analytical system. This reaction was selected as a model chemiluminescence reaction for the optimisation of the detection system in order to measure the very low levels of light produced. The incorporation of non-ionic surfactants into the analysis and their effect on the enhancement of the chemiluminescence emission intensity and the modification of electroosmotic flow is discussed. A quantitative analysis of codeine was then successfully performed using this set-up. The points for the codeine concentrations of 5x10⁻⁷ to 1x10⁻⁴ mol 1⁻¹ were plotted to give a linear calibration plot. The equation of the line was y = 6.0136x + 0.0949, R2 = 0.9999, where x was the codeine concentration in mol 1⁻¹ and y was the mean CL emission intensity in mV. A limit of detection for codeine was determined at the 95% confidence limits to be 8.3x10-7 mol 1⁻¹ codeine, with an RSD of 8% (n=5) at the 5x10⁻⁵ mol 1⁻¹ level. The sample throughput time including removal of products and water wash was found to be an average of 2 minutes. The work described in chapter 5 builds on the findings of chapter 4 and examines the use of the luminol reaction in a miniaturised analysis system for the quantification of cobalt (II) ions. A multivariate experimental design programme was carried out as part of the work described in this chapter to simultaneously optimise most of the reagent variables. The application of cationic surfactants to this reaction in the miniaturised analysis system is also discussed, with particular emphasis on the observed enhancement of chemiluminescence emission intensity and lifetime, and the modification of the electroosmotic flow characteristics. A quantitative determination of cobalt nitrate was successfully carried out with a calibration over six orders of magnitude. The equation of the linear portion of the graph (10-10- 10-8 mol 1⁻¹) was found to be y = 64.625x + 735.71 with R2 = 0.999, where x (n=3) was the concentration in mol 1⁻¹ and y was the mean CL emission in mV. The limit of detection for cobalt nitrate at the 95% confidence limits was determined as -4x10⁻¹¹ mol 1⁻¹ which equates to 0.01 ng ml⁻¹ cobalt nitrate. An RSD of 6.9% (n=3) was obtained for the 1x10-8 mol 1⁻¹ standard. The sample run time was approximately 12 minutes, which resulted in an average overall throughput time of 15 minutes. The conclusions and ideas for future work are detailed in chapter 6.
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Books on the topic "Chemiluminescent"

1

Garner, Ian. Enhanced chemiluminescent assays in the diagnosis of periodontal disease. Birmingham: University of Birmingham, 1998.

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Maxwell, Simon Robert Jenkinson. An enhanced chemiluminescent assay for antioxidant activity in biological fluids. Birmingham: University of Birmingham, 1995.

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Gary Harold Gregory Henry Thorpe. Enhanced chemiluminescent assays for horseradish peroxidase and their application in immunoassays. Birmingham: University of Birmingham, 1986.

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Commission, United States International Trade. Certain chemiluminescent compositions and components thereof and methods of using, and products incorporating, the same: Investigation no. 337-TA-285 : (Commission decision of October 11, 1989). Washington, D.C: U.S. International Trade Commission, 1991.

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Grayeski, Mary Lynn. Chemiluminescence. Washington, DC, USA: American Chemical Society, 2022. http://dx.doi.org/10.1021/acsinfocus.7e5018.

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Weeks, Ian. Chemiluminescence immunoassay. Amsterdam: Elsevier, 1992.

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Parveen, Saima, Muhammad Sohail Aslam, Lianzhe Hu, and Guobao Xu. Electrogenerated Chemiluminescence. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39555-0.

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Sojic, Neso, ed. Analytical Electrogenerated Chemiluminescence. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015776.

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Roda, Aldo, ed. Chemiluminescence and Bioluminescence. Cambridge: Royal Society of Chemistry, 2010. http://dx.doi.org/10.1039/9781849732024.

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Gundermann, Karl-Dietrich. Chemiluminescence in organic chemistry. Berlin: Springer-Verlag, 1987.

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Book chapters on the topic "Chemiluminescent"

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Gundermann, Karl-Dietrich, and Frank McCapra. "Chemiluminescent Demonstrations [1]." In Reactivity and Structure: Concepts in Organic Chemistry, 195–202. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71645-4_15.

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Mccapra, Frank. "Chemiluminescent Reactions of Acridines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 615–30. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186596.ch10.

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Weeks, Ian, and J. Stuart Woodhead. "Monoclonal Antibodies in Chemiluminescent Immunoassays." In Clinical Applications of Monoclonal Antibodies, 69–79. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1573-5_7.

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Nelstrop, Lorna J., Gillian M. Greenway, and Simon N. Port. "Investigation of Chemiluminescent Microanalytical Systems." In Micro Total Analysis Systems ’98, 355–58. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5286-0_84.

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Gundermann, Karl-Dietrich, and Frank McCapra. "Chemiluminescent Peroxide Decompositions, I (except Dioxetans)." In Reactivity and Structure: Concepts in Organic Chemistry, 33–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71645-4_4.

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Bassaneze, Vinicius, Ayumi Aurea Miyakawa, and José Eduardo Krieger. "Chemiluminescent Detection of Senescence-Associated β Galactosidase." In Methods in Molecular Biology, 157–63. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-239-1_9.

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Davidson, D. F., A. Tulgestke, C. Strand, M. F. Campbell, V. A. Troutman, V. A. Miller, and R. K. Hanson. "Rapid Chemiluminescent Imaging Behind Reflected Shock Waves." In 30th International Symposium on Shock Waves 1, 313–16. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-46213-4_52.

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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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Guy, Graeme R. "Detection of Proteins on Blots Using Chemiluminescent Systems." In Springer Protocols Handbooks, 329–35. Totowa, NJ: Humana Press, 1996. http://dx.doi.org/10.1007/978-1-60327-259-9_50.

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Costantini, F., R. M. Tiggelaar, R. Salvio, M. Nardecchia, S. Schlautmann, C. Manetti, H. J. G. E. Gardeniers, D. Caputo, A. Nascetti, and G. de Cesare. "Portable Optoelectronic System for Monitoring Enzymatic Chemiluminescent Reaction." In Lecture Notes in Electrical Engineering, 189–94. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-04324-7_25.

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Conference papers on the topic "Chemiluminescent"

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KIMURA, M., H. IGA, H. ARAKI, and M. MATSUMOTO. "RELATIONSHIP BETWEEN HEAT OF REACTION AND CHEMILUMINESCENCE EFFICIENCY OF CHEMILUMINESCENT REACTIONS." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0036.

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Atwater, James E., James R. Akse, Jeffrey DeHart, Richard R. Wheeler, and Charles E. Verostko. "Chemiluminescent Ethanol Biosensor Development." In International Conference on Environmental Systems. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1995. http://dx.doi.org/10.4271/951686.

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Haber, Ludwig C., Uri Vandsburger, William R. Saunders, and Vivek K. Khanna. "An Examination of the Relationship Between Chemiluminescent Light Emissions and Heat Release Rate Under Non-Adiabatic Conditions." In ASME Turbo Expo 2000: Power for Land, Sea, and Air. American Society of Mechanical Engineers, 2000. http://dx.doi.org/10.1115/2000-gt-0121.

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Abstract:
As combustion instability research has matured over the last decade the need for more detailed diagnostics has increased. One main gap in the diagnostics is the ability to obtain a reliable quantitative measure of unsteady heat release. In an effort to move in this direction using chemiluminescence as the measured quantity, this paper examines the formation of chemiluminescent light in the simple yet non-idealized environment of a Bunsen burner flame with co-flow of air. The results of the study show that OH* and CH* chemiluminescence can be modeled accurately using the simplified modeling approach outlined within the paper. The understanding of chemiluminescent light formation gained by the ability to model OH* and CH* light emissions accurately allows the correct interpretation of chemiluminescence in terms of heat release.
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Park, Yoon, Dean P. Neikirk, and Eric V. Anslyn. "Micromachined chemiluminescent system for explosives detection." In Optics/Photonics in Security and Defence, edited by John C. Carrano and Arturas Zukauskas. SPIE, 2006. http://dx.doi.org/10.1117/12.690200.

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AKHAVAN-TAFTI, H., R. DE SILVA, K. THAKUR, R. A. EICKHOLT, C. CHROVIAN, K. LAUWERS, R. S. HANDLEY, S. SIRIPURAPU, C. ENDRESZL, and A. P. SCHAAP. "RECENT ADVANCES IN CHEMILUMINESCENT ENZYME SUBSTRATES." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0053.

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TERANISHI, K., and T. NISHIGUCHI. "STUDY ON CHEMILUMINESCENT PROBES FOR SUPEROXIDE ANIONS: CONTROL OF CHEMILUMINESCENCE RESONANCE ENERGY TRANSFER BY CYCLOMALTOOLIGOSACCHARIDE (CYCLODEXTRIN)." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0082.

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Park, Yoon, Dean P. Neikirk, and Eric V. Anslyn. "Micromachined microfluidic chemiluminescent system for explosives detection." In Defense and Security Symposium, edited by Augustus W. Fountain III. SPIE, 2007. http://dx.doi.org/10.1117/12.719830.

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ADAMCZYK, MACIEJ, PHILLIP G. MATTINGLY, YON-YIH CHEN, and JAMES R. FINO. "MICROWAVE-ASSISTED SYNTHESIS OF CHEMILUMINESCENT ACRIDINIUM SALTS." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0051.

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ADAMCZYK, MACIEJ, JONATHAN GROTE, PHILLIP G. MATTINGLY, JEFFREY A. MOORE, and YOU PAN. "CARBONYL-REACTIVE CHEMILUMINESCENT LABELS: ACRIDINIUM HYDROXYLAMINES (AHA)." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0081.

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YANG, XIAOLIN. "AN ENHANCED CHEMILUMINESCENT IMMUNOASSAY TO DETECT INSULIN." In Bioluminescence and Chemiluminescence - Progress and Current Applications - 12th International Symposium on Bioluminescence (BL) and Chemiluminescence (CL). WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776624_0097.

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Reports on the topic "Chemiluminescent"

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Bechev, Blagovest, Moni Magrisso, Stilian Stoeff, and Pavlina Glogovska. Possible Application in Pulmonology of Neutrophil Population Functional State Evaluated by Chemiluminescent Method. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, March 2019. http://dx.doi.org/10.7546/crabs.2019.03.15.

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Nelson, Marian R., Clark L. Gross, William J. Smith, and Susan A. Kelly. Determination of ATP Levels in Sulfur Mustard-Exposed Human Peripheral Blood Lymphocytes by a Chemiluminescent Assay. Fort Belvoir, VA: Defense Technical Information Center, January 2000. http://dx.doi.org/10.21236/ada390626.

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Zare, Richard N. Surface-Catalyzed Chemiluminescence. Fort Belvoir, VA: Defense Technical Information Center, December 1990. http://dx.doi.org/10.21236/ada230176.

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DeGregoria, Anthony. Chemiluminescence and the Nomadics Spectrometer Card. Fort Belvoir, VA: Defense Technical Information Center, June 1999. http://dx.doi.org/10.21236/ada397737.

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Hastings, J. W. A Symposium on Bioluminescence and Chemiluminescence. Fort Belvoir, VA: Defense Technical Information Center, January 1998. http://dx.doi.org/10.21236/ada361122.

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Fontijn, Arthur. AASERT 98 Student Research in Chemiluminescence. Fort Belvoir, VA: Defense Technical Information Center, January 2001. http://dx.doi.org/10.21236/ada388327.

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Adler-Golden, S. Predicted NO2 IR Chemiluminescence in the Natural Atmosphere. Fort Belvoir, VA: Defense Technical Information Center, May 1986. http://dx.doi.org/10.21236/ada173812.

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Langry, K., and J. Horn. Chemiluminescence assay for the detection of biological warfare agents. Office of Scientific and Technical Information (OSTI), November 1999. http://dx.doi.org/10.2172/15013394.

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Vaghjiani, Ghanshyam L. Kinetic Studies of UV/Vis-Chemiluminescence in the CH + O2 Gas Phase Reaction. Fort Belvoir, VA: Defense Technical Information Center, February 2003. http://dx.doi.org/10.21236/ada412562.

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Vaghjiani, Ghanshyam L. Investigations of the CO-Chemiluminescence in the Reaction of Ketene With Excess Oxygen Atoms. Fort Belvoir, VA: Defense Technical Information Center, January 2000. http://dx.doi.org/10.21236/ada381370.

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