Visible and Ultraviolet Absorption and Fluorescence Excitation and Emission Characteristics of Florida Orange Juice and Orange Pulpwash: Detection of Adulteration

1980 ◽  
Vol 63 (6) ◽  
pp. 1317-1331 ◽  
Author(s):  
Donald R Petrus ◽  
John A Attaway

Abstract Visible and ultraviolet absorption and room temperature fluorescence excitation and emission spectra, obtained from alcoholic solutions of Florida orange juice and pulpwash, were investigated to characterize citrus products, and thereby detect adulteration and approximate orange juice content. Absorption shoulders and maxima were observed at 465, 443, and 425 nm of the visible spectrum and at 325, 280, and 245 nm of the ultraviolet spectrum. The spectral curves for orange juice and pulpwash were similar. However, orange pulpwash had weaker visible and stronger ultraviolet absorption than did orange juice. It was determined (416 frozen concentrated orange juice and 206 orange pulpwash samples obtained from Florida commercial processors) that the average sum and standard deviation of absorbance at 443, 325, and 280 nm was 2.410 ± 0.164 for orange juice and 3.781 ± 0.473 for orange pulpwash (based on reconstituted 12.8° Brix products). Average absorbance 443/325 nm ratio was 0.144 ± 0.026 for orange juice and 0.048 ± 0.020 for orange pulpwash. Simple dilutions of orange juice with water and/or sugar solutions resulted in a linear decrease in absorbance sum while the absorbance ratio remained essentially the same. Orange juice and pulpwash systems resulted in a linear increase in absorbance sum and a decrease in absorbance ratio (natural log function). The investigation enabled the derivation of equations, using absorption data, to approximate orange juice and/or pulpwash contents and/or dilution of a sample. The constants used in the equations were based on results obtained from commercially produced Florida citrus products and may vary with other citrus-producing regions. Fluorescence excitation and emission spectra complemented the absorption spectra. Fluorescence excitation for orange juice was maximum at 283 nm with a shoulder at 291 and inflections at 270 and 302 nm with maximum emission at 333 nm. Excitation was also maximum at 291 nm with a shoulder at 283 and inflections at 270 and 302 with maximum emission at 343 nm. Pulpwash excitation was maximum at 270 and 302 nm with a minimum at 283 nm and emission at 353 nm. Peaks or pronounced shoulders at 270 and 302 nm have been indicative of the presence of orange pulpwash.

2022 ◽  
pp. 002215542110649
Author(s):  
Joshua T. Dodge ◽  
Andrew D. Doyle ◽  
Ana C. Costa-da-Silva ◽  
Christopher T. Hogden ◽  
Eva Mezey ◽  
...  

Multiplex immunofluorescence (mIF) is an effective technique for the maximal visualization of multiple target proteins in situ. This powerful tool is mainly limited by the spectral overlap of the currently available synthetic fluorescent dyes. The fluorescence excitation wavelengths ranging between 405 and 488 nm are rarely used in mIF imaging and serve as a logical additional slot for a fluorescent probe. In the present study, we demonstrate that the addition of 2,3,4,5,6-pentafluoroaniline to Atto 465 NHS ester, creating Atto 465-pentafluoroaniline (Atto 465-p), generates a bright nuclear stain in the violet-blue region of the visible spectrum. This allows the 405 nm excitation and emission, classically used for nuclear counterstains, to be used for the detection of another target protein. This increases the flexibility of the mIF panel and, with appropriate staining and microscopy, enables the quantitative analysis of at least six targets in one tissue section. (J Histochem Cytochem XX: XXX–XXX, XXXX)


2021 ◽  
Author(s):  
Joshua T Dodge ◽  
Ana Caroline Costa-da-Silva ◽  
Christopher T Hogden ◽  
Eva Mezey ◽  
Jacqueline W Mays

The architecture of a biologic response is inextricably linked with the tissue architecture of the target site. Multiplex immunofluorescence (mIF) is an effective technique for the maximal visualization of multiple target proteins in situ. This powerful tool is limited by the spectral overlap separation of the currently available synthetic fluorescent dyes. The fluorescence excitation wavelengths ranging between 405nm and 488nm are rarely used in mIF imaging and serve as a logical additional slot for a fluorescent probe. In the present study, we demonstrate that Atto 465-pentafluoroaniline (Atto 465-p), a derivative of the fluorescent dye Atto 465, can serve as a nuclear stain in the violet-blue region of the visible spectrum. This opens the 405nm channel, traditionally used for nuclear stain, for detection of another experimental target. This increases the flexibility of the mIF panel and, with appropriate staining and microscopy, enables the quantitative analysis of at least six targets in one tissue section.


1985 ◽  
Vol 68 (6) ◽  
pp. 1202-1206
Author(s):  
Donald R Petrus ◽  
John A Attaway

Abstract Visible and ultraviolet absorption and room temperature fluorescence excitation and emission spectra, obtained from alcoholic solutions of Florida orange juice (OJ) and orange pulpwash (PW), were used to characterize the collaborative study samples. The absorbance sum at 443, 325, and 280 nm and absorbance 443/325 nm ratio were used to estimate the percent total citrus material (TCM), OJ, PW, and dilution of the samples. Six laboratories participated in the study. Known samples of OJ and PW were given to each laboratory for familiarization and instrumental verification. Ten unknown samples (various combinations of OJ and PW) were analyzed by each laboratory. Three duplicate and 2 "closely matched pair" sample set combinations were reported. The results revealed that the method successfully detected the differences in sample formulations. The UV/vis and fluorescence spectrophotometric method has been adopted official first action for detecting adulteration of Florida orange juice with orange pulpwash.


2012 ◽  
Vol 557-559 ◽  
pp. 1031-1036 ◽  
Author(s):  
Jian Xin Yang ◽  
Xiang Hui Wang

A series of fluorescence compounds, 4-benzofuranyl-1,8-naphthalimides, were prepared through cycloaddition reaction from 4-ethynyl-1,8-naphthalimides and o-iodophenols which catalyzed by a Pd(PPh3)2Cl2 / CuI system under mild conditions. The intermediate material, 4-ethynyl-1,8- naphthalimide, was synthesized from 4-bromo-1,8- naphthalimide and trimethylsilyl- acetylene. The absorption and fluorescence spectra of 4-benzofuranyl-1,8- naphthalimides were studied and the quantum yields were measured. The maximum UV/vis absorption spectra were in the range of 375-400 nm and the maximum emission spectra were in the range of 470-510 nm. The electro- luminescent properties were also mensurated through a doped electroluminescent device which contains 1% 1,8-naphthalimides and 99% CBP (4,4'-N,N'-dicarbazole-biphenyl), It’s shown the maximum brightness reached 3700 cd/ m2 at 22.5V.


1975 ◽  
Vol 53 (1) ◽  
pp. 1-11 ◽  
Author(s):  
D. R. Arnold ◽  
B. M. Clarke Jr.

The ultraviolet absorption and phosphorescence emission spectra of 2-(2-methylbenzoyl) thiophene (1), 2-benzoyl-3-methylthiophene (2), 2-benzoyl-4-methylthiophene (3), and 2-benzoyl-5-methylthiophene (4) are reported and analyzed. Partial energy diagrams are constructed. The lowest triplet is assigned as a π,π* state of the 2-thienoyl chromophore in every case. Photocycloaddition of isobutylene to the carbonyl group was observed with 1 and 2. The oxetanes are thermally unstable; olefins 1-(2-thienyl)-1-(2-methylphenyl)-2-methylpropene (from 1) and 1-phenyl-1-(2-(3-methylthienyl))-2-methylpropene (from 2) were formed and characterized. Irradiation of 1 and 2 in O-deuteromethanol did not lead to incorporation of deuterium; no reaction was observed. These results are discussed in terms of the existing generalizations potentially useful for predicting photochemical reactivity.


1974 ◽  
Vol 57 (6) ◽  
pp. 1392-1396 ◽  
Author(s):  
J A Lansden ◽  
R J Clarkson ◽  
W C Neely ◽  
R J Cole ◽  
J W Kirksey

Abstract The spectral data for a novel fungal metabolite, moniliformin (potassium salt of 1-hydroxycyclobut- 1-ene-3,4-dione), are reported. The corrected ambient temperature fluorescence excitation and emission spectra are given and the quantum efficiency is calculated to be 5.32 × 10舓3. The uncorrected low temperature phosphorescence emission spectrum and lifetime are also reported. Other physical data are given to support spectral evidence that the molecule exists as a dimer in aqueous solutions.


1987 ◽  
Vol 118 (1) ◽  
pp. 91-100 ◽  
Author(s):  
Derek I. Austin ◽  
Robert J. Donovan ◽  
Andrew Hopkirk ◽  
Kenneth P. Lawley ◽  
David Shaw ◽  
...  

1987 ◽  
Vol 87 (10) ◽  
pp. 5664-5669 ◽  
Author(s):  
Giulietta Smulevich ◽  
Paolo Foggi ◽  
Alessandro Feis ◽  
Mario P. Marzocchi

2014 ◽  
Vol 904 ◽  
pp. 99-102
Author(s):  
Hong Qi Li ◽  
Zhen Chen ◽  
Hao Chen ◽  
Jia Wei Zhang ◽  
Yan Tai Chen ◽  
...  

A new coumarin derivative L was synthesized and characterized by1H NMR,13C NMR, IR and mass spectrum. UV-Vis and fluorescence emission spectra of L without or with different anions (NO2, F, Cl, HSO3, HSO4, AcO or NO3) or metal ions were measured, which showed while addition of anions or metal ions Mg2+, Zn2+, Ca2+, Cu2+, Ni2+, Co2+, Fe3+or Al3+led to decrease in intensity of the maximum emission peak at about 480 nm, addition of Hg2+ions caused increase in intensity of the maximum emission peak, suggesting that L may act as a fluorescent probe for detection of Hg2+ions.


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