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Volumn 188, Issue , 2015, Pages 357-364

Quantification of Nε-(2-Furoylmethyl)-l-lysine (furosine), Nε-(Carboxymethyl)-l-lysine (CML), Nε-(Carboxyethyl)-l-lysine (CEL) and total lysine through stable isotope dilution assay and tandem mass spectrometry

Author keywords

CEL; CML; Furosine; LC MS MS; Lysine; Maillard reaction

Indexed keywords

CHEMICAL MODIFICATION; CHEMICAL REACTIONS; EMITTER COUPLED LOGIC CIRCUITS; GLYCOSYLATION; ISOTOPES; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY;

EID: 84929206913     PISSN: 03088146     EISSN: 18737072     Source Type: Journal    
DOI: 10.1016/j.foodchem.2015.04.137     Document Type: Article
Times cited : (75)

References (40)
  • 1
    • 0022931516 scopus 로고
    • Identification of N-epsilon-carboxymethyllysine as a degradation product of fructoselysine in glycated protein
    • M.U. Ahmed, S.R. Thorpe, and J.W. Baynes Identification of N-epsilon-carboxymethyllysine as a degradation product of fructoselysine in glycated protein Journal of Biological Chemistry 261 11 1986 4889 4894
    • (1986) Journal of Biological Chemistry , vol.261 , Issue.11 , pp. 4889-4894
    • Ahmed, M.U.1    Thorpe, S.R.2    Baynes, J.W.3
  • 2
    • 0028470191 scopus 로고
    • Limit of detection (LOD)/limit of quantitation (LOQ) - Comparison of the empirical and the statistical, methods exemplified with GC-MS assays of abused drugs
    • D.A. Armbruster, M.D. Tillman, and L.M. Hubbs Limit of detection (LOD)/limit of quantitation (LOQ) - Comparison of the empirical and the statistical, methods exemplified with GC-MS assays of abused drugs Clinical Chemistry 40 7 1994 1233 1238
    • (1994) Clinical Chemistry , vol.40 , Issue.7 , pp. 1233-1238
    • Armbruster, D.A.1    Tillman, M.D.2    Hubbs, L.M.3
  • 3
    • 84864918584 scopus 로고    scopus 로고
    • Determination of furosine in food products by capillary zone electrophoresis-tandem mass spectrometry
    • C. Bignardi, A. Cavazza, and C. Corradini Determination of furosine in food products by capillary zone electrophoresis-tandem mass spectrometry Electrophoresis 33 15 2012 2382 2389
    • (2012) Electrophoresis , vol.33 , Issue.15 , pp. 2382-2389
    • Bignardi, C.1    Cavazza, A.2    Corradini, C.3
  • 6
    • 33845910368 scopus 로고    scopus 로고
    • Evaluation of a gas chromatography/mass spectrometry method for the quantification of carboxymethyllysine in food samples
    • A. Charissou, L. Ait-Ameur, and I. Birlouez-Aragon Evaluation of a gas chromatography/mass spectrometry method for the quantification of carboxymethyllysine in food samples Journal of Chromatography A 1140 1-2 2007 189 194
    • (2007) Journal of Chromatography A , vol.1140 , Issue.1-2 , pp. 189-194
    • Charissou, A.1    Ait-Ameur, L.2    Birlouez-Aragon, I.3
  • 8
    • 60649113828 scopus 로고    scopus 로고
    • Analysis of advanced glycation endproducts in dairy products by isotope dilution liquid chromatography-electrospray tandem mass spectrometry. The particular case of carboxymethyllysine
    • T. Delatour, J. Hegele, V. Parisod, J. Richoz, S. Maurer, and M. Steven Analysis of advanced glycation endproducts in dairy products by isotope dilution liquid chromatography-electrospray tandem mass spectrometry. The particular case of carboxymethyllysine Journal of Chromatography A 1216 12 2009 2371 2381
    • (2009) Journal of Chromatography A , vol.1216 , Issue.12 , pp. 2371-2381
    • Delatour, T.1    Hegele, J.2    Parisod, V.3    Richoz, J.4    Maurer, S.5    Steven, M.6
  • 9
    • 34447498699 scopus 로고    scopus 로고
    • Forty years of furosine - Forty years of using Maillard reaction products as indicators of the nutritional quality of foods
    • H.F. Erbersdobler, and V. Somoza Forty years of furosine - Forty years of using Maillard reaction products as indicators of the nutritional quality of foods Molecular Nutrition & Food Research 51 4 2007 423 430
    • (2007) Molecular Nutrition & Food Research , vol.51 , Issue.4 , pp. 423-430
    • Erbersdobler, H.F.1    Somoza, V.2
  • 12
    • 54949084982 scopus 로고    scopus 로고
    • Separation of Amadori peptides from their unmodified analogs by ion-pairing RP-HPLC with heptafluorobutyric acid as ion-pair reagent
    • A. Frolov, and R. Hoffmann Separation of Amadori peptides from their unmodified analogs by ion-pairing RP-HPLC with heptafluorobutyric acid as ion-pair reagent Analytical and Bioanalytical Chemistry 392 6 2008 1209 1214
    • (2008) Analytical and Bioanalytical Chemistry , vol.392 , Issue.6 , pp. 1209-1214
    • Frolov, A.1    Hoffmann, R.2
  • 14
    • 0028361159 scopus 로고
    • Determination of N-epsilon-carboxymethyllysine by a reversed-phase high-performance liquid-chromatography method
    • J. Hartkopf, C. Pahlke, G. Ludemann, and H.F. Erbersdobler Determination of N-epsilon-carboxymethyllysine by a reversed-phase high-performance liquid-chromatography method Journal of Chromatography A 672 1-2 1994 242 246
    • (1994) Journal of Chromatography A , vol.672 , Issue.1-2 , pp. 242-246
    • Hartkopf, J.1    Pahlke, C.2    Ludemann, G.3    Erbersdobler, H.F.4
  • 15
    • 84894334786 scopus 로고    scopus 로고
    • Simultaneous determination of N (epsilon)-(carboxymethyl) lysine and N (epsilon)-(carboxyethyl) lysine in cereal foods by LC-MS/MS
    • J.L. He, M.M. Zeng, Z.P. Zheng, Z.Y. He, and J. Chen Simultaneous determination of N (epsilon)-(carboxymethyl) lysine and N (epsilon)-(carboxyethyl) lysine in cereal foods by LC-MS/MS European Food Research and Technology 238 3 2014 367 374
    • (2014) European Food Research and Technology , vol.238 , Issue.3 , pp. 367-374
    • He, J.L.1    Zeng, M.M.2    Zheng, Z.P.3    He, Z.Y.4    Chen, J.5
  • 19
    • 80054033223 scopus 로고    scopus 로고
    • N-epsilon-(carboxymethyl)lysine content of foods commonly consumed in a Western style diet
    • G.L.J. Hull, J.V. Woodside, J.M. Ames, and G.J. Cuskelly N-epsilon-(carboxymethyl)lysine content of foods commonly consumed in a Western style diet Food Chemistry 131 1 2012 170 174
    • (2012) Food Chemistry , vol.131 , Issue.1 , pp. 170-174
    • Hull, G.L.J.1    Woodside, J.V.2    Ames, J.M.3    Cuskelly, G.J.4
  • 20
    • 1542393391 scopus 로고    scopus 로고
    • Studies on the formation of furosine and pyridosine during acid hydrolysis of different Amadori products of lysine
    • R. Krause, K. Knoll, and T. Henle Studies on the formation of furosine and pyridosine during acid hydrolysis of different Amadori products of lysine European Food Research and Technology 216 4 2003 277 283
    • (2003) European Food Research and Technology , vol.216 , Issue.4 , pp. 277-283
    • Krause, R.1    Knoll, K.2    Henle, T.3
  • 21
    • 0036189946 scopus 로고    scopus 로고
    • Fortification of milk with iron-ascorbate promotes lysine glycation and tryptophan oxidation
    • J. Leclere, I. Birlouez-Aragon, and M. Meli Fortification of milk with iron-ascorbate promotes lysine glycation and tryptophan oxidation Food Chemistry 76 4 2002 491 499
    • (2002) Food Chemistry , vol.76 , Issue.4 , pp. 491-499
    • Leclere, J.1    Birlouez-Aragon, I.2    Meli, M.3
  • 22
    • 47849096112 scopus 로고    scopus 로고
    • Identification and site-specific relative quantification of beta-lactoglobulin modifications in heated milk and dairy products
    • J. Meltretter, C.M. Becker, and M. Pischetsrieder Identification and site-specific relative quantification of beta-lactoglobulin modifications in heated milk and dairy products Journal of Agricultural and Food Chemistry 56 13 2008 5165 5171
    • (2008) Journal of Agricultural and Food Chemistry , vol.56 , Issue.13 , pp. 5165-5171
    • Meltretter, J.1    Becker, C.M.2    Pischetsrieder, M.3
  • 23
    • 38049001563 scopus 로고    scopus 로고
    • N-alpha-(1-deoxy-d-fructos-1-yl)-l-histidine ("d-fructose-l-histidine"): A potent copper chelator from tomato powder
    • V.V. Mossine, and T.P. Mawhinney N-alpha-(1-deoxy-d-fructos-1-yl)-l-histidine ("d-fructose-l-histidine"): A potent copper chelator from tomato powder Journal of Agricultural and Food Chemistry 55 25 2007 10373 10381
    • (2007) Journal of Agricultural and Food Chemistry , vol.55 , Issue.25 , pp. 10373-10381
    • Mossine, V.V.1    Mawhinney, T.P.2
  • 24
    • 84890938996 scopus 로고    scopus 로고
    • N ε-(carboxymethyl)lysine: A review on analytical methods, formation, and occurrence in processed food, and health impact
    • H.T. Nguyen, H.J. van der Fels-Klerx, and M.A.J.S. van Boekel N ε-(carboxymethyl)lysine: A review on analytical methods, formation, and occurrence in processed food, and health impact Food Reviews International 30 1 2013 36 52
    • (2013) Food Reviews International , vol.30 , Issue.1 , pp. 36-52
    • Nguyen, H.T.1    Van Der Fels-Klerx, H.J.2    Van Boekel, M.A.J.S.3
  • 25
    • 78650677924 scopus 로고    scopus 로고
    • Quantification of N-epsilon-carboxymethyl-lysine in selected chocolate-flavoured drink mixes using high-performance liquid chromatography-linear ion trap tandem mass spectrometry
    • C. Niquet-Leridon, and F.J. Tessier Quantification of N-epsilon-carboxymethyl-lysine in selected chocolate-flavoured drink mixes using high-performance liquid chromatography-linear ion trap tandem mass spectrometry Food Chemistry 126 2 2011 655 663
    • (2011) Food Chemistry , vol.126 , Issue.2 , pp. 655-663
    • Niquet-Leridon, C.1    Tessier, F.J.2
  • 26
    • 84867362618 scopus 로고    scopus 로고
    • Okara promoted acrylamide and carboxymethyl-lysine formation in bakery products
    • M. Palermo, A. Fiore, and V. Fogliano Okara promoted acrylamide and carboxymethyl-lysine formation in bakery products Journal of Agriculture and Food Chemistry 60 40 2012 10141 10146
    • (2012) Journal of Agriculture and Food Chemistry , vol.60 , Issue.40 , pp. 10141-10146
    • Palermo, M.1    Fiore, A.2    Fogliano, V.3
  • 27
    • 84862316500 scopus 로고    scopus 로고
    • Glycation products in infant formulas: Chemical, analytical and physiological aspects
    • M. Pischetsrieder, and T. Henle Glycation products in infant formulas: Chemical, analytical and physiological aspects Amino Acids 42 4 2012 1111 1118
    • (2012) Amino Acids , vol.42 , Issue.4 , pp. 1111-1118
    • Pischetsrieder, M.1    Henle, T.2
  • 29
    • 84884611476 scopus 로고    scopus 로고
    • Isotope dilution ESI-LC-MS/MS for quantification of free and total N epsilon-(1-carboxymethyl)-l-lysine and free N epsilon-(1-carboxyethyl)-l-lysine: Comparison of total N epsilon-(1-carboxymethyl)-l-lysine levels measured with new method to ELISA assay in gruel samples
    • E. Tareke, A. Forslund, C.H. Lindh, C. Fahlgren, and E. Ostman Isotope dilution ESI-LC-MS/MS for quantification of free and total N epsilon-(1-carboxymethyl)-l-lysine and free N epsilon-(1-carboxyethyl)-l-lysine: Comparison of total N epsilon-(1-carboxymethyl)-l-lysine levels measured with new method to ELISA assay in gruel samples Food Chemistry 141 4 2013 4253 4259
    • (2013) Food Chemistry , vol.141 , Issue.4 , pp. 4253-4259
    • Tareke, E.1    Forslund, A.2    Lindh, C.H.3    Fahlgren, C.4    Ostman, E.5
  • 30
    • 84929181544 scopus 로고    scopus 로고
    • Technische Universität Dresden. (2014). Age database. Date accessed December 2014
    • Technische Universität Dresden. (2014). Age database. Date accessed December 2014.
  • 31
    • 84862654327 scopus 로고    scopus 로고
    • Health effects of dietary Maillard reaction products: The results of ICARE and other studies
    • F.J. Tessier, and I. Birlouez-Aragon Health effects of dietary Maillard reaction products: The results of ICARE and other studies Amino Acids 42 4 2012 1119 1131
    • (2012) Amino Acids , vol.42 , Issue.4 , pp. 1119-1131
    • Tessier, F.J.1    Birlouez-Aragon, I.2
  • 32
    • 84895906483 scopus 로고    scopus 로고
    • Faox enzymes inhibited Maillard reaction development during storage both in protein glucose model system and low lactose UHT milk
    • A.D. Troise, N.A. Dathan, A. Fiore, G. Roviello, A. Di Fiore, and S. Caira Faox enzymes inhibited Maillard reaction development during storage both in protein glucose model system and low lactose UHT milk Amino Acids 46 2 2014 279 288
    • (2014) Amino Acids , vol.46 , Issue.2 , pp. 279-288
    • Troise, A.D.1    Dathan, N.A.2    Fiore, A.3    Roviello, G.4    Di Fiore, A.5    Caira, S.6
  • 33
    • 84908052855 scopus 로고    scopus 로고
    • Effect of olive mill wastewater phenol compounds on reactive carbonyl species and maillard reaction end-products in ultrahigh-temperature-treated milk
    • A.D. Troise, A. Fiore, A. Colantuono, S. Kokkinidou, D.G. Peterson, and V. Fogliano Effect of olive mill wastewater phenol compounds on reactive carbonyl species and maillard reaction end-products in ultrahigh-temperature-treated milk Journal of Agriculture and Food Chemistry 62 41 2014 10092 10100
    • (2014) Journal of Agriculture and Food Chemistry , vol.62 , Issue.41 , pp. 10092-10100
    • Troise, A.D.1    Fiore, A.2    Colantuono, A.3    Kokkinidou, S.4    Peterson, D.G.5    Fogliano, V.6
  • 34
    • 84908033564 scopus 로고    scopus 로고
    • Simultaneous quantification of amino acids and Amadori products in foods through ion-pairing liquid chromatography-high-resolution mass spectrometry
    • A.D. Troise, A. Fiore, G. Roviello, S.M. Monti, and V. Fogliano Simultaneous quantification of amino acids and Amadori products in foods through ion-pairing liquid chromatography-high-resolution mass spectrometry Amino Acids 2014
    • (2014) Amino Acids
    • Troise, A.D.1    Fiore, A.2    Roviello, G.3    Monti, S.M.4    Fogliano, V.5
  • 38
    • 70449727643 scopus 로고    scopus 로고
    • Beta-glucan-enriched bread reduces energy intake and modifies plasma ghrelin and peptide YY concentrations in the short term
    • P. Vitaglione, R.B. Lumaga, A. Stanzione, L. Scalfi, and V. Fogliano Beta-glucan-enriched bread reduces energy intake and modifies plasma ghrelin and peptide YY concentrations in the short term Appetite 53 3 2009 338 344
    • (2009) Appetite , vol.53 , Issue.3 , pp. 338-344
    • Vitaglione, P.1    Lumaga, R.B.2    Stanzione, A.3    Scalfi, L.4    Fogliano, V.5
  • 39
    • 0029805733 scopus 로고    scopus 로고
    • Ion chemistry of protonated lysine derivatives
    • T. Yalcin, and A.G. Harrison Ion chemistry of protonated lysine derivatives Journal of Mass Spectrometry 31 11 1996 1237 1243
    • (1996) Journal of Mass Spectrometry , vol.31 , Issue.11 , pp. 1237-1243
    • Yalcin, T.1    Harrison, A.G.2
  • 40
    • 0028247972 scopus 로고
    • Chemistry of Amadori rearrangement products - Analysis, synthesis, kinetics, reactions, and spectroscopic properties
    • V.A. Yaylayan, and A. Huyghuesdespointes Chemistry of Amadori rearrangement products - Analysis, synthesis, kinetics, reactions, and spectroscopic properties Critical Reviews in Food Science and Nutrition 34 4 1994 321 369
    • (1994) Critical Reviews in Food Science and Nutrition , vol.34 , Issue.4 , pp. 321-369
    • Yaylayan, V.A.1    Huyghuesdespointes, A.2


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