Department of Food Science
Faculty of Life Sciences
University of Copenhagen
FOODFLUOR - FOOD FLUORESCENCE LIBARY
A food fluorescence library by Jakob Christensen, 2005
Background
The present site contains a food fluorescence library (FOODFLUOR) in the form of steady-state fluorescence landscapes from a variety of intact food samples, plus a list of some food relevant fluorophores in pure solutions. The listed fluorescence measurements are intended to serve as a work of reference, a library, which can hopefully inspire and help scientists that are interested in or want to start exploring the intrinsic fluorescence of food and food systems.
Fluorescence database
Fluorescence landscapes of eleven fluorophores and a broad variety of intact food samples is included in this database. Measurements of the fluorophores were performed on two different instruments, yielding three separate lists:
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Fluorophores measured on Perkin Elmer LS50 B spectrofluorometer
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Fluorophores measured on Varian Cary Eclipse spectrofluorometer
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Intact food samples measured on Perkin Elmer LS50 B spectrofluorometer
The fluorescence properties of the selected samples can be viewed at this site or the data from the experiments can be downloaded in MS-Excel format. Please note that the presented fluorescence landscapes are not corrected.
Reference
If you want to use the data or refer to the results, please refer to:
Food Fluorescence Library
Quality and Technology, Department of Food Science
The Royal Veterinary and Agricultural University, Denmark
www.models.life.ku.dk
LS50 FLUOROPHORE RESULTS OVERVIEW
Pure solutions of fluorophores are measured. Appropriate concentration levels were chosen for each fluorophore in order to avoid concentration quenching. Fluorescence landscapes were measured on PerkinElmer LS50B spectrofluorometer in a cuvette with the traditional right-angle sampling geometry. Water was used as solvent, iso-octan when the fluorophore is not soluble in water. The landscapes were measured in different spectral ranges, using an obey-file in the FLDM instrument controlling software. Common measurement parameters:
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Slit width: 5 nm for both excitation and emission light
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Step size: 2 nm for excitation
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Step size: 1 nm for emission
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Fluorescence emission was only recorded between the 1st and 2nd order Rayleigh scatter. No emission above 700 nm was recorded.
If any minor Rayleigh scatter appeared in the recorded fluorescence data, it was removed in the preliminary signal processing, before further data analysis.
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Overview two: Excitation and emission profiles of all fluorophores
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Overview three: Comparison between Perkin Elmer LS50B and Varian Cary Eclipse spectrofluorometer.
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Download the data as MS-Excel file (each sheet is one fluorophore, 5.3MB); also available in Matlab format
List of measured compounds Fluorophore Conc. (M) EX λmax (nm) EM λmax (nm) Imax * Measuring range
(EX, nm)Solvent Phenyl alanine 10-3 M 258 284 32 250-320 Water Tyrosine 10-5 M 276
302 28 250-320 Water Tryptophan 10-5 M 280 357 100 250-320 Water Vitamin A
(Retinol)10-5 M 346 480 16 250-380 Iso-octane Vitamin B2
(Riboflavin)10-5 M 270
(382,448)518 167 250-510 Water Vitamin B6
(Pyridoxin)10-5 M 328 393 51 250-360 Water Vitamin E
(α-Tocopherol)10-4 M 298 326 167 250-320 Iso-octane NADH 10-4 M 344 465 16 260-470 Water ATP 10-3 M 292 388 33 260-320 Water Chlorophyll A 10-6 M 428 663 56 340-650 Iso-octane Hematoporphyrin 10-5 M 396 614 27 300-550 Iso-octane *normalized according to tryptophan (= 100)
VARIAN CARY ECLIPSE FLUOROPHORE OVERVIEW
Pure solutions of fluorophores are measured. Appropriate concentration levels were chosen for each fluorophore in order to avoid concentration quenching. Fluorescence landscapes were measured on Cary Varian Eclipse spectrofluorometer in a cuvette with the traditional right-angle sampling geometry. Water was used as solvent, iso-octan when the fluorophore is not soluble in water. The landscapes were measured in different spectral ranges, using a measuring routine programmed in ADL in the instrument controlling software. Common measurement parameters:
- Slit width: 5 nm for both excitation and emission light
- Step size: 2 nm for excitation
- Step size: 1 nm for emission
- Fluorescence emission was by maximum recorded between 1st and 2nd order Rayleigh scatter.
- Picture of the instrument
Rayleigh scatter appearing in the recorded fluorescence data was removed in the preliminary signal processing, before further data analysis.
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Overview two: Excitation and emission profiles of all fluorophores
-
Overview three: Comparison between Perkin Elmer LS50B and Varian Cary Eclipse spectrofluorometer.
-
Download the data as MS-Excel file (each sheet is one fluorophore, 4.6MB); also available in Matlab format
List of measured compounds Fluorophore Conc. (M) EX λmax (nm) EM λmax (nm) Imax * Measuring range
(EX, nm)Solvent Phenyl alanine 10-3 M 262 281 38 230-310/ 230-450 Water Tyrosine 10-5 M 278 302 96 230-310/ 230-450 Water Tryptophan 10-5 M (230) 276 355 100 230-310/ 230-450 Water Vitamin A
(Retinol)10-5 M 328 484 8 260-380/ 400-620 Iso-octane Vitamin B2
(Riboflavin)10-5 M 268
(372+444)528 58 250-500/ 480-590 Water Vitamin B6
(Pyridoxin)10-5 M 326 396 18 220-360/ 350-470 Water Vitamin E
(α-Tocopherol)10-4 M 298 323 70 220-320/ 290-380 Iso-octane NADH 10-4 M 338 465 16 260-460/ 380-590 Water ATP 10-3 M 292 392 20 260-320/ 320-500 Water Chlorophyll A 10-6 M 428 663 16 350-650/ 640-690 Iso-octane Hematoporphyrin 10-5 M 394 613 12 300-550/ 590-690 Iso-octane *normalized according to tryptophan (= 100)
LS50 FOOD SAMPLES OVERVIEW
Fluorescence landscapes of a variety of intact food samples liquid as well as solid - were measured on Perkin Elmer LS50B spectrofluorometer using a front-face solid sample accessory with 60o sampling geometry. Liquid samples were measured in quartz cuvettes and solid samples in sample cups. The landscapes were recorded using an obey-file in the FLDM instrument controlling software with following measurement parameters:
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Slit width, excitation: 5 nm
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Slit width, emission: 10 nm
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Step size: 5 nm for excitation
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Step size: 1 nm for emission
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Excitation range: 250-650 nm
All fluorescence emission was only recorded between the 1st and 2nd order Rayleigh scatter. No emission above 700 nm was recorded. An emission 1% attenuation filter was used for samples yielding too high fluorescence intensity. If any minor Rayleigh scatter appeared in the recorded fluorescence data, it was removed in the preliminary signal processing, before further data analysis.
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Download the data as MS-Excel file (each sheet is one food sample, 8.3MB); also available in Matlab format
List of measured food samples Sample pH Filter EX λmax (nm) EM λmax (nm) Imax Milk (1.5 % fat) 6.69 √ 285 340 6900* Yoghurt, plain (3.5 %) 3.98 √ 285 341 6200* Rape seed oil 360 444 812 Olive oil 610 681 643 Orange juice 3.62 510 530 53 Apple juice 4.02 390 461 57 Soy sauce 4.66 640 685 8 Beer, Carlsberg 4.32 390 465 242 Beer, Elephant 4.29 400 489 221 White wine 3.21 385 456 199 Rice 410 488 584 Wheat flour 285 338 185 Cane sugar 345 462 56 Oatmeal 285 338 18 Emmenthaler √ 295 354 4500* Gorgonzola √ 290 346 4300* Butter 325 407 923 Beef 285 326 135 Pork 296 334 888 Olive, green 420 677 170 Marzipan 460 517 488 Chocolate 285 338 20 Carrot 285 360 101 Potato 290 377 218 Pear 290 371 100 Tomato 635 655 46 Apple 510 530 60 *calculated value; recorded with 1% attenuation, so Ix100 is listed.
Matlab users
All the Fluorescence landscapes (both fluorophores for both instruments and intact food samples in one big file) are available in Matlab, version 5/6 compatible.
Also available: the DOMFluor database (Dissolved Organic Matter)