1979
DOI: 10.1016/0003-2697(79)90783-8
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Front-face fluorometry of liquid samples

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Cited by 117 publications
(49 citation statements)
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“…high concentrations of the fluorescent species. To avoid these problems, the method of front-face fluorescence spectroscopy (Figure 1) can be used for bulk liquid samples and solid samples (Parker 1968;Hirschfeld 1978;Eisinger & Flores 1979;Blumberg et al 1980;Hirsch & Nagel 1989;Genot et al 1992a, b;Sóti et al 1993;Herbert et al 2000;Patra & Mishra 2002). The incidence angle of the excitation radiation is usually set at 56° (Table 1).…”
Section: Fluorescence Spectroscopy and Chemometrics In The Food Classmentioning
confidence: 99%
“…high concentrations of the fluorescent species. To avoid these problems, the method of front-face fluorescence spectroscopy (Figure 1) can be used for bulk liquid samples and solid samples (Parker 1968;Hirschfeld 1978;Eisinger & Flores 1979;Blumberg et al 1980;Hirsch & Nagel 1989;Genot et al 1992a, b;Sóti et al 1993;Herbert et al 2000;Patra & Mishra 2002). The incidence angle of the excitation radiation is usually set at 56° (Table 1).…”
Section: Fluorescence Spectroscopy and Chemometrics In The Food Classmentioning
confidence: 99%
“…In front face illumination, the fluorescence intensities become independent of concentration at high optical densities and all the incident light is absorbed near the surface of the cuvette. Moreover, in front-face geometry the exciting and emitted light enter and leave the same cell face 50 . The excitation light penetrates a very short distance of the sample.…”
Section: Preparation Of Asphaltene -Prodan Solutionsmentioning
confidence: 99%
“…These were indistinguishable from the comparable absorption spectra of Hb A. The fluorescence excitation and emission maxima and intensity of Hb Evanston were also the same as those of Hb A when they were determined by a front surface method (27) or with short path length cuvettes.…”
Section: Resultsmentioning
confidence: 63%
“…Fluorometric studies of the purified hemoglobins were performed with short path-length cuvettes and by a front surface technique (27). For these determinations the hemoglobins were prepared in Tris-glycine buffer, pH 7.0, at a concentration of 90 uM.…”
Section: Methodsmentioning
confidence: 99%