Bibliographies thématiques / Fluorimetry

Littérature scientifique sur le sujet « Fluorimetry »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 3 mars 2023

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Articles de revues sur le sujet "Fluorimetry":

Thakur, Shikha, Neha Bajwa et Ashish Baldi. « NEW ANALYTICAL METHODS FOR ESTIMATION OF ARTEETHER BY UV AND FLUORESCENCE SPECTROPHOTOMETRY : DEVELOPMENT AND VALIDATION ». Journal of Drug Delivery and Therapeutics 8, n^o 5 (15 septembre 2018) : 151–58. http://dx.doi.org/10.22270/jddt.v8i5.1797.

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The present research work discusses the development and validation of two different spectrophotometric methods for estimation of Î±-Î² arteether using UV spectrophotometer and spectrofluorimeter for the first time. Two simple, accurate, precise, sensitiveand economical methods has been developed and validated for the estimation of Î±-Î² arteether in bulk and pharmaceutical dosage form as per ICH guidelines Q2(R1). The solvent used for UV spectroscopy was methanol and HCl (8:2) and methanol was used for fluorimeter. For qualitative and quantitative analysis, 254 nm was used in UV spectroscopy and excitation and emission wavelengths were set at 354 nm and 697 nm respectively for fluorimetry. Coefficients of correlation were found to be 0.993 and 0.992 for UV spectroscopy and fluorimetry. Both methods show good accuracy and precision and were compared statistically by using two way ANOVA which shows no significant difference between these methods. So the proposed methods were found to have equal applicability for estimation and routine analysis of arteether in pharmaceutical formulations. Keywords: Arteether, Analytical method, Fluorimeter, Pharmaceutical formulation, UV spectrophotometer.

Smith, B. W., B. T. Jones et J. D. Winefordner. « High-Precision Fluorimetry with a Light-Emitting Diode Source ». Applied Spectroscopy 42, n^o 8 (novembre 1988) : 1469–72. http://dx.doi.org/10.1366/0003702884429535.

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A simple fluorimeter which uses a light-emitting diode as a source of excitation and a photodiode as a detector has been constructed and evaluated. The exceptional stability of both the detector and the source make it possible to make concentration measurements by fluorimetry with a precision of at least 0.002%. Furthermore, the system exhibited excellent linear dynamic range and a limit of detection of 20 ng/L for the dye Oxazine 720 in methanol.

Westerlund-Karlsson, Annette, Katriina Suonpää, Matti Ankelo, Jorma Ilonen, Mikael Knip et Ari E. Hinkkanen. « Detection of Autoantibodies to Protein Tyrosine Phosphatase-like Protein IA-2 with a Novel Time-resolved Fluorimetric Assay ». Clinical Chemistry 49, n^o 6 (1 juin 2003) : 916–23. http://dx.doi.org/10.1373/49.6.916.

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Abstract Background: Circulating autoantibodies to pancreatic glutamic acid decarboxylase (GAD65; the 65-kDa isoform of glutamic acid decarboxylase), protein tyrosine phosphatase-like protein IA-2, and insulin can be used as predictive markers of type 1 diabetes. We developed a novel assay for the detection of IA-2 autoantibodies (IA-2As) in serum based on time-resolved fluorimetry, hypothesizing that this kind of assay could provide several advantages over methods described to date, including radiobinding assays (RBAs) and ELISAs. Methods: The intracellular part of IA-2 (IA-2ic) was biotinylated and bound to streptavidin-coated 96-well plates by simultaneous incubation with serum samples and glutathione S-transferase (GST)-IA-2ic fusion protein. GST-IA-2ic captured by autoantibodies in the serum was detected with europium-labeled anti-GST antibody, and the signal was measured in a time-resolved fluorimeter. A serum sample panel from 100 patients with newly diagnosed type 1 diabetes and 100 unaffected controls was analyzed with the new assay and a conventional RBA. Results: Among the 100 serum samples from patients with type 1 diabetes, the time-resolved fluorimetric assay identified 74 IA-2A-containing sera, whereas the RBA detected 80 IA-2A-positive samples. Five of the six samples positive in the RBA but not detected by the time-resolved fluorimetric assay were only weakly positive in the RBA. The performance time of the time-resolved fluorimetric assay was 2.5 h compared with 10–12 h required by the RBA. Conclusions: The time-resolved fluorimetric assay provides a simple, nonradioactive analysis method for the detection of IA-2As with a specificity and a sensitivity comparable to the RBA method. This assay allows substantial reduction in performance time compared with the conventional RBA.

Valcárcel, M., A. Gómez-Hens et S. Rubio. « Simultaneous determination of epinephrine and norepinephrine in urine by derivative synchronous fluorescence spectroscopy. » Clinical Chemistry 31, n^o 11 (1 novembre 1985) : 1790–94. http://dx.doi.org/10.1093/clinchem/31.11.1790.

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Abstract The combination of synchronous and derivative fluorimetry, potentially useful in resolving mixtures that present strongly overlapping conventional fluorescence spectra, appears suitable for determining epinephrine and norepinephrine in urine. We describe a simple, rapid, and inexpensive method for simultaneous assay of these compounds in a single scan of urine specimens from normal adults. The catecholamines are extracted from the sample on cation-exchange columns and subsequently determined by formation of trihydroxyindoles. Analytical recovery is about 94% for epinephrine, 91% for norepinephrine, with a CV of approximately 5%. No sophisticated detection equipment is necessary, a conventional modern fluorimeter being adequate.

Neher, Erwin. « Quantitative Aspects of Calcium Fluorimetry ». Cold Spring Harbor Protocols 2013, n^o 10 (octobre 2013) : pdb.top078204. http://dx.doi.org/10.1101/pdb.top078204.

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Fidanza, Joëlle, et Jean-Jacques Aaron. « Evaluation of filter papers as substrates for solid-surface room-temperature fluorimetry and photochemical fluorimetry ». Talanta 33, n^o 3 (mars 1986) : 215–18. http://dx.doi.org/10.1016/0039-9140(86)80054-6.

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Lesher-Pérez, Sasha Cai, Ge-Ah Kim, Chuan-hsien Kuo, Brendan M. Leung, Sanda Mong, Taisuke Kojima, Christopher Moraes, M. D. Thouless, Gary D. Luker et Shuichi Takayama. « Dispersible oxygen microsensors map oxygen gradients in three-dimensional cell cultures ». Biomaterials Science 5, n^o 10 (2017) : 2106–13. http://dx.doi.org/10.1039/c7bm00119c.

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Velmurugan, K., A. Raman, Derin Don, Lijun Tang, S. Easwaramoorthi et R. Nandhakumar. « Quinoline benzimidazole-conjugate for the highly selective detection of Zn(ii) by dual colorimetric and fluorescent turn-on responses ». RSC Advances 5, n^o 55 (2015) : 44463–69. http://dx.doi.org/10.1039/c5ra04523a.

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Askin, Samuel, Thomas E. H. Bond, Alanna E. Sorenson, Morgane J. J. Moreau, Helma Antony, Rohan A. Davis et Patrick M. Schaeffer. « Selective protein unfolding : a universal mechanism of action for the development of irreversible inhibitors ». Chemical Communications 54, n^o 14 (2018) : 1738–41. http://dx.doi.org/10.1039/c8cc00090e.

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Sadeghi, Susan, et Samieh Oliaei. « Optimization of ionic liquid based dispersive liquid–liquid microextraction combined with dispersive micro-solid phase extraction for the spectrofluorimetric determination of sulfasalazine in aqueous samples by response surface methodology ». RSC Advances 6, n^o 114 (2016) : 113551–60. http://dx.doi.org/10.1039/c6ra20223c.

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Thèses sur le sujet "Fluorimetry":

Aminuddin, Mohammad. « New aromatic dialdehyde labels for analytical fluorimetry ». Thesis, Loughborough University, 1987. https://dspace.lboro.ac.uk/2134/27565.

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Fluorigenic aromatic molecules have found wide application in Fluorescence Spectroscopy. Commercially available fluorigenic reagents have been used to detect amines, amino acids, peptides and proteins. Orthophthalaldehyde (OPA) is an aromatic dialdehyde which is specific for a primary amino group. Three polyaromatic dialdehyde molecules similar to this compound have been synthesised and investigated for their analytical applications. They are: (1) naphthalene-2,3- dicarboxaldehyde (NDA), (2) 1-phenylnaphthalene-2, 3- dicarboxaldehyde (0NDA) and (3) anthracene-2,3- dicarboxaldehyde (ADA).

Tse, Oi Ling. « Development of humidity sensor based on fluorimetric optode membrane ». HKBU Institutional Repository, 1999. http://repository.hkbu.edu.hk/etd_ra/191.

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Horne, Andrew James. « Insights into Kv1.2 activation and deactivation using voltage clamp fluorimetry ». Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/27083.

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Voltage-gated potassium (Kv) channels are essential membrane proteins in modulating membrane excitability and related cellular processes. Many details associated with the voltage response are unclear, particularly the complete role of the voltage sensing domain, and not just the densely charged S4 helix. Based on its crystal structure, the Kv1.2 channel represents an ideal model in which to study these questions. This thesis investigates Kv1.2 activation and deactivation gating, using the voltage clamp fluorimetry technique. This technique utilizes an environmentally sensitive fluorophore introduced at locations of interest in order to visualize conformational changes in protein structure. Labelling of Kv1.2 channels at the extracellular end of S4 reports a fast quenching of fluorescence emission upon depolarization that correlates extremely well with gating current measurements, suggesting it is a report of voltage-dependent S4 translocation. In addition, a slow quenching component is observed with a very negative voltage-dependence (V₁/₂ = -73.9 mV ± 1.4 mV), not seen in any other Kv channels studied to date, that involves regions of the voltage sensing domain in S1 and S2. This slow quenching is selectively removed from the fluorescence report with transfer of extracellular S1-S2 or S3-S4 linkers from the homologous Shaker potassium channel, suggesting that it arises from channel-specific interactions between the Kv1.2 linker segments. However, transfer of Kv1.2 linker segments into Shaker fail to recapitulate this quenching component, suggesting that these linker interactions likely underlie further differences in voltage sensor domain gating and/or structure. This slow quenching component correlates with deactivation of ionic current, and is prolonged with co-expression of the N-type inactivation-conferring Kvβ1.2 subunit. In the presence of the beta subunit, this likely reflects unbinding of the inactivation moiety from the pore domain, allowing deactivation and S4 return, but in the α-subunit alone we suggest that this may be a report of a voltage-dependent rearrangement in the voltage sensor domain that stabilizes the S4 in an activated conformation. Such interactions have been reported in other voltage-gated proteins, and provides further evidence that we must consider more than just S4 translocation when it comes to understanding the complete potassium channel voltage response, Kv1.2 or otherwise.

Drzewianowski, Andrea F. « Temporal Changes in Phytoplankton Variable Fluroescence (FV/FM) and Absorption as a Result of Daily Exposure to High Light ». Fogler Library, University of Maine, 2008. http://www.library.umaine.edu/theses/pdf/DrzewianowskiAF2008.pdf.

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Simpson, K. M. « Studies of cosmic ray composition using a hybrid fluorescence detector / ». Title page, contents and abstract only, 2001. http://web4.library.adelaide.edu.au/theses/09PH/09phs61261.pdf.

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Afonin, Kirill A. « Design and characterization of novel bio-sensor platform for sequence specific, label-free, fluorescent detection of native RNA molecules ». Bowling Green, Ohio : Bowling Green State University, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=bgsu1206395144.

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Passmore, James B. « Calibration of a laser induced fluorescence system by raman scattering in hydrogen with application to the detection of hydroxyl radicals ». Thesis, Georgia Institute of Technology, 1992. http://hdl.handle.net/1853/27150.

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Primo, Afranio Reis Rodrigues. « Avaliação da influência do reservatório do funil na qualidade da água do rio Paraíba do Sul ». Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/46/46133/tde-20042007-100003/.

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O rio Paraíba do Sul, após formar o reservatório do Funil, abastece cidades ribeirinhas e a cidade do Rio de Janeiro. A INB, uma empresa da área nuclear, está localizada na margem norte deste reservatório. Neste trabalho, Ag, Al, As, Ba, Cd, Co, Cr, Fe, Mn, Ni e Pb foram determinados por ICP OES em água e sedimentos em pontos a montante e a jusante do Funil e neste. Urânio, usando fluorimetria, também foi determinado em amostras coletadas a montante e a jusante do ponto de descarga de efluentes da INB, no ribeirão da Água Branca. O estudo não mostrou evidências que a INB está provocando impacto ambiental nesse ribeirão. As, Ni e Pb em todos os pontos de amostragem e Al, Cr e Fe na maioria desses pontos apresentaram concentrações em água acima do máximo permitido pela CONAMA 357. A maioria dos elementos apresentou concentrações nas amostras de água a montante do reservatório do Funil superiores às verficadas a jusante, para ambas as estações chuvosa e seca. Os sedimentos estão impactados por As, Cd, Cr e Pb em quase todos os pontos estudados.
The Paraiba do Sul River after forming the Funil Reservoir serves as the major source of potable water for downstream cities and for the city of Rio de Janeiro. INB, a company of the nuclear area, is located in the north margin of this reservoir. In the present study, Ag, Al, As, Ba, Cd, Co, Cr, Fe, Mn, Ni and Pb were determined by ICP OES in water and sediments samples at points upstream and downstream from Funil and in this one. Uranium, using fluorimetry, was also determined in samples collected upstream and downstream from the INB effluent discharge point at the Água Branca Creek. The study did not show evidences that INB is provoking environmental impact in this creek. As, Ni and Pb in all the sampling points and Al, C and Fe in most of those points exceeded the CONAMA 357 standards for water. Most of the elements presented concentration in the water samples at the points upstream from Funil reservoir higher than those downstream, for both rainy and dry seasons. Sediments are impacted by As, Cd, Cr and Pb in almost all the studied points.

Clark, Ian David. « A fluorescence study of the COOH-terminus region of equine platelet tropomyosin ». Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26190.

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The use of fluorescent molecules as probes of protein conformation is recognized as a technique which provides very specific information and has been applied, in recent years, to the study of the role of tropomyosin (TM) in the regulation of contractile processes. The isolation and sequencing of TM from horse blood platelets (P-TM) has shown it to be different from muscle TM, especially near the NH₂-and COOH-termini. These differences have been suggested to weaken end-to-end interaction of P-TM molecules. TM's are two chain coiled coils and P-TM has cysteine residues at the penultimate COOH-terminus position of adjacent chains. These can be labelled with sulfhydryl-specific fluorescent probes that reflect conformational changes in that region of the molecule via changes in their emission characteristics. The results of experiments on both pyrene (Py) (40) and acrylodan (AD) labelled P-TM show that there is a preferred interaction of the COOH-terminus of P-TM with the NH₂-terminus of cardiac TM over that with the NH₂-terminus of P-TM. This indicates that the altered NH₂-terminus of P-TM, with respect to muscle TM, is responsible for the relative loss of polymerizability of P-TM at low salt concentration. Addition of actin to the Py-P-TM (40) and AD-P-TM species showed changes in emission characteristics indicative of binding to the F-actin filaments, suggesting that the presence of the probes had not affected the function of the P-TM adversely. However, the presence of pyrenes at the COOH-terminus seemed to reduce further the ability of P-TM to self-polymerize. Thermal denaturation of AD-P-TM, AD-C-TM and AD-labelled truncated P-TM followed by fluorescence polarization suggested that, contrary to the theory of Skolnick and Holtzer on the stability of two chain coiled coils, the region towards the COOH-terminus is among the last to lose its helical character.
Science, Faculty of
Chemistry, Department of
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Langford, Stephen Richard. « State-to-state molecular photodissociation dynamics ». Thesis, University of Oxford, 1995. http://ora.ox.ac.uk/objects/uuid:771f0638-7d55-4304-b387-7b24de012cc6.

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The water molecule, rotationally state selected in the third and fourth streching overtone (|04>- and |05>-) and stretch-bend combination (|04>|2>-) levels, has been photodissociated at γ ≈ 282 nm via the Ã state. The OH photofragment rotational distributions, determined by OH(A-X) laser-induced fluoresence (LIF), are found to differ from those reported previously by Andresen and coworkers (H₂O|01>- + 193 nm), Grim and coworkers (H₂O|04>- + 239.5 nm) and Rosenwaks and coworkers (H₂O|01>⁺ + 193 nm). These variations become more apparent with increasing angular momentum in the parent water molecule and with an increasing number of OH stretching quanta in the intermediate vibrational overtone. The Franck-Condon model of Balint-Kurti is able to qualitatively reproduce the observed trends, provided that dissociation at lower photolysis photon energies and via higher intermediate overtone states is assumed to occur preferentially from extended R_H-OH configurations. The calculations suggest that the variation in the photofragment rotational distributions lies in a gradual change in the inertial properties of the bound state water molecule as the H-OH bond is stretched. In a second study, the partially deuterated water molecule, rotationally state selected in the third and fourth OH stretching vibrational overtone levels have been photodissociated via the Ã state at γ ≈ 288 nm. A branching ratio betweem the H + OD and D + OH dissociation channels is estimated from OD and OH (A-X) LIF measurements to be φ(OD)/φ(OH) > 20; this compares well with the previous measurements of Grim and coworkers, and the theoretical work of Imre and coworkers. The small shift in the centre of mass in the water molecule arising from the substitution of of a deuterium atom for one of the hydrogen atoms is shown to have a marked effect on the rotational distributions of the OD photofragment. Calculations using a modified Franck-Condon model, which includes an approximate exit-torque, are able to reproduce qualitatively the experimental OD rotational distributions at sensible values of R_R-OD(~ 1.4 Å). In addition to being sensitive to the dynamics of the parent molecule on the ground state potential, the product OD state distributions are shown to be very sensitive to even the smallest exit channel torque on the excited potential surface.

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Livres sur le sujet "Fluorimetry":

D, Eastwood, Cline Love L. J et ASTM Subcommittee E13.06 on Molecular Luminescence., dir. Progress in analytical luminescence. Philadelphia, PA : ASTM, 1988.

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Marra, John. An evaluation of an in situ fluorometer for the estimation of chlorophyll a. Palisades, New York : Lamont-Doherty Earth, 1993.

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1967-, DeEll Jennifer R., et Toivonen, Peter M. A., 1955-, dir. Practical applications of chlorophyll fluorescence in plant biology. Boston : Kluwer Academic Publishers, 2003.

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Ute, Resch-Genger, et Ameloot M, dir. Standardization and quality assurance in fluorescence measurements I : Techniques. New York : Springer, 2008.

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Naohisa, Wada, et Mimuro Mamoru, dir. Recent progress of bio/chemiluminescence and fluorescence analysis in photosynthesis, 2005. Trivandrum, Kerala, India : Research Signpost, 2005.

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International Chlorophyll Fluorescence Symposium (1st 1988 Bad Honnef, Germany). Applications of chlorophyll fluorescence : In photosynthesis research, stress physiology, hydrobiology, and remote sensing. Dordrecht, Netherlands : Kluwer Academic Publishers, 1988.

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Walker, David. The use of the oxygen electrode and fluorescence probes in simple measurements of photosynthesis. Sheffield : Research Institute for Photosynthesis, University of Sheffield, 1987.

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Lars, Munck, dir. Fluorescence analysis in foods. Burnt Mill, Harlow, Essex, England : Longman Scientific & Technical, 1989.

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C, Papageorgiou George, et Govindjee 1933-, dir. Chlorophyll a fluorescence : A signature of photosynthesis. Dordrecht : Kluwer Academic, 2004.

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E, Vidaver W., Canada Forestry Canada, British Columbia. Ministry of Forests., Forest Resource Development Agreement (Canada) et Canada/BC Economic & Regional Development Agreement., dir. A Manual for the use of variable chlorophyll fluorescence in the assessment of the ecophysiology of conifer seedlings. Victoria, B.C : Forestry Canada, 1991.

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Chapitres de livres sur le sujet "Fluorimetry":

Buxbaum, Engelbert. « Fluorimetry ». Dans Biophysical Chemistry of Proteins, 39–55. Boston, MA : Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-7251-4_6.

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Pomeranz, Yeshajahu, et Clifton E. Meloan. « Fluorimetry ». Dans Food Analysis, 99–107. Boston, MA : Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-6998-5_8.

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Kunz, Wolfram S., Kirstin Winkler, Andrey V. Kuznetsov, Hartmut Lins, Elmar Kirches et Claus W. Wallesch. « Detection of mitochondrial defects by laser fluorimetry ». Dans Detection of Mitochondrial Diseases, 97–100. Boston, MA : Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6111-8_15.

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Miller, James N., Marc B. Brown, Nichola J. Seare et Stephen Summerfield. « Analytical Applications of Very Near-IR Fluorimetry ». Dans Fluorescence Spectroscopy, 189–96. Berlin, Heidelberg : Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77372-3_14.

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Fedorov, Oleg, Frank H. Niesen et Stefan Knapp. « Kinase Inhibitor Selectivity Profiling Using Differential Scanning Fluorimetry ». Dans Methods in Molecular Biology, 109–18. Totowa, NJ : Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-337-0_7.

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McGuffin, V. L., et R. N. Zare. « Applications of Laser Fluorimetry to Microcolumn Liquid Chromatography ». Dans ACS Symposium Series, 120–36. Washington, DC : American Chemical Society, 1986. http://dx.doi.org/10.1021/bk-1986-0297.ch008.

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Uniewicz, Katarzyna A., Alessandro Ori, Timothy R. Rudd, Marco Guerrini, Mark C. Wilkinson, David G. Fernig et Edwin A. Yates. « Following Protein–Glycosaminoglycan Polysaccharide Interactions with Differential Scanning Fluorimetry ». Dans Methods in Molecular Biology, 171–82. Totowa, NJ : Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-498-8_12.

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Coremans, J. M. C. C., M. van Aken, H. A. Bruining et G. J. Puppels. « Nadh Fluorimetry to Predict Ischemic Injury in Transplant Kidneys ». Dans Advances in Experimental Medicine and Biology, 335–43. Boston, MA : Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4717-4_40.

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Clarke, Ronald J., et Mohammed A. A. Khalid. « Stopped-Flow Fluorimetry Using Voltage-Sensitive Fluorescent Membrane Probes ». Dans Pumps, Channels, and Transporters, 179–209. Hoboken, NJ : John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119085126.ch7.

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Sorenson, Alanna E., et Patrick M. Schaeffer. « High-Throughput Differential Scanning Fluorimetry of GFP-Tagged Proteins ». Dans Methods in Molecular Biology, 69–85. New York, NY : Springer US, 2019. http://dx.doi.org/10.1007/978-1-0716-0163-1_5.

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Actes de conférences sur le sujet "Fluorimetry":

Banishev, A. A., E. A. Shirshin et V. V. Fadeev. « Non-linear fluorimetry of fluorescent proteins ». Dans International Conference on Lasers, Applications, and Technologies '07, sous la direction de Gennadii Matvienko, Arkadii Ivanov, Petr Nikitin, Eugene Voropay, Mikhail Khodasevich, Vladislav Panchenko et Vladimir Golubev. SPIE, 2007. http://dx.doi.org/10.1117/12.753276.

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Fadeev, V. V., T. A. Dolenko, A. A. Banishev, P. N. Litvinov, D. V. Maslov et E. E. Ostroumov. « Matrix method in laser fluorimetry of organic compounds ». Dans OPTO-Ireland, sous la direction de Hugh J. Byrne, Elfed Lewis, Brian D. MacCraith, Enda McGlynn, James A. McLaughlin, Gerard D. O'Sullivan, Alan G. Ryder et James E. Walsh. SPIE, 2005. http://dx.doi.org/10.1117/12.604954.

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Lundin, Michael A., et Matthew J. Bohn. « Remote sensing phase fluorimetry using mercury vapor lamp ». Dans Defense and Security Symposium, sous la direction de Richard T. Howard et Robert D. Richards. SPIE, 2007. http://dx.doi.org/10.1117/12.718606.

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Kawabata, Yuji, Totaro Imasaka et Nobuhiko Ishibashi. « Fiber Optic pH Sensor Based on Laser Fluorimetry ». Dans Optical Fiber Sensors. Washington, D.C. : OSA, 1986. http://dx.doi.org/10.1364/ofs.1986.65.

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Coremans, J. M. C. C. « NADH fluorimetry and diffuse reflectance spectroscopy on rat heart ». Dans Medical Optical Tomography : Functional Imaging and Monitoring, sous la direction de Gerhard J. Mueller. SPIE, 1993. http://dx.doi.org/10.1117/12.2283781.

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Fadeev, Viktor V., Elena M. Filippova, D. V. Maslov, D. N. Matorin et Pavel S. Venediktov. « Diagnostics of photosynthesizing organisms by linear and nonlinear fluorimetry ». Dans Industrial Lasers and Inspection (EUROPTO Series), sous la direction de Michel R. Carleer, Moira Hilton, Torsten Lamp, Rainer Reuter, George M. Russwurm, Klaus Schaefer, Konradin Weber, Klaus C. H. Weitkamp, Jean-Pierre Wolf et Ljuba Woppowa. SPIE, 1999. http://dx.doi.org/10.1117/12.364186.

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Parigger, Christian, et Lloyd m. Davis. « Photon counting fluorimetry of low repetition rate pulsed plasmas ». Dans OSA Annual Meeting. Washington, D.C. : Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.wy4.

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For the ill-conditioned problem of resolving multiple exponential components from luminescence decay profiles, time correlated photon counting (TCPC) is usually chosen because it yields data over a large dynamic range and with accurately known errors, derived from Poisson photon statistics. However, as no more than one photon is collected after each excitation, TCPC requires a large number of laser pulses to achieve the required dynamic range.

Maslov, D., et E. Ostroumov. « Diagnostics of photosynthesizing organisms by the method of nonlinear fluorimetry ». Dans OPTO-Ireland, sous la direction de Hugh J. Byrne, Elfed Lewis, Brian D. MacCraith, Enda McGlynn, James A. McLaughlin, Gerard D. O'Sullivan, Alan G. Ryder et James E. Walsh. SPIE, 2005. http://dx.doi.org/10.1117/12.604985.

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WEI, X. Y., L. Z. SANG, Y. X. ZHU et Y. ZHANG. « EFFECTS OF LMWOA ON BIODEGRADATION OF PHENANTHRENE STUDIED BY FLUORIMETRY ». Dans Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0101.

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Liu, Yanzhao, Xiuwei Fang, Huiping Xi et Hongtao Xie. « Study on the Determination of Levofloxacin by SDS Enhanced Fluorimetry ». Dans Proceedings of the 2018 7th International Conference on Sustainable Energy and Environment Engineering (ICSEEE 2018). Paris, France : Atlantis Press, 2019. http://dx.doi.org/10.2991/icseee-18.2019.27.

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Rapports d'organisations sur le sujet "Fluorimetry":

Cutlip, L. B. Statistical analysis of fluorimeter operation. Office of Scientific and Technical Information (OSTI), janvier 1991. http://dx.doi.org/10.2172/6256080.

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Klein, R. C., F. T. Horn et R. D. Wilson. Evaluation of an x-ray fluorimeter for measuring lead in paint. Office of Scientific and Technical Information (OSTI), mars 1993. http://dx.doi.org/10.2172/6435571.

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Castro, Alonso. Determination of the Limit of Detection of the Turner Biosystems Modulus Fluorimeter for Comparison with the Attolight SOFIA Detector. Office of Scientific and Technical Information (OSTI), septembre 2014. http://dx.doi.org/10.2172/1154983.

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Parra, Jeremy. Development of an Atmospheric Pressure Laser Induced Fluorimeter (AP-LIF) for NO₂ and Application of AP-LIF for Study of Heterogeneous NO₂ Chemistry. Portland State University Library, janvier 2000. http://dx.doi.org/10.15760/etd.554.

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