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On the stability of the bioactive flavonoids quercetin and luteolin under oxygen-free conditions

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Abstract

The natural flavonoid compounds quercetin (3,3′,4′,5,7-pentahydroxyflavone) and luteolin (3′,4′,5,7-tetrahydroxyflavone) are important bioactive compounds with antioxidative, anti-allergic, and anti-inflammatory properties. However, both are unstable when exposed to atmospheric oxygen, which causes degradation and complicates their analytical determinations. The oxidative change of these flavonoids was observed and followed by UV–visible spectrophotometry, both in aqueous and ethanolic solutions. The distribution of the degradation products in aqueous media was monitored by LC–MS and LC–DAD analysis. The amounts of oxidative reaction products increase with the exposure time. The oxidative degradation reduces the pharmacological efficiency of these antioxidants and renders analytical determination inaccurate. The oxidative changes in flavonoid test solutions can explain the inconsistent dissociation constants reported in the literature. Dissociation constants of quercetin and luteolin were determined both by alkalimetric titration and by UV–visible spectrophotometry under deaerated conditions. The values pK 1 = 5.87 ± 0.14 and pK 2 = 8.48 ± 0.09 for quercetin, and pK 1 = 5.99 ± 0.32 and pK 2 = 8.40 ± 0.42 for luteolin were found.

The change of absorption spectra of quercetin during the exposure to the air oxygen

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References

  1. Hollman P, Arts IJ (2000) Flavonols, flavones and flavanols - nature, occurrence and dietary burden. Sci Food Agric 80(7):1081–1093

    Article  CAS  Google Scholar 

  2. Matsuda H, Morikawa T, Ando S, Togucida I, Yoshikawa M (2003) Structural requirements of flavonoids for nitric oxide production inhibitory activity and mechanism of action. Bioorg Med Chem 11(9):1995–2000

    Article  CAS  Google Scholar 

  3. Kandaswami C, Perkins E, Soloniuk DS, Drzewiecki G, JrE M (1991) Antiproliferative effects of citrus flavonoids on a human squamous-cell carcinoma invitro. Cancer Lett 56(2):147–152

    Article  CAS  Google Scholar 

  4. Dadáková E, Procházková E, Křížek M (2001) Application of micellar electrokinetic capillary chromatography for quantitative analysis of quercetin in plant materials. Electrophoresis 22(8):1573–1578

    Article  Google Scholar 

  5. Kobayashi T, Nakata T, Kuzumaki T (2002) Effect of flavonoids on cell cycle progression in prostate cancer cells. Cancer Lett 176(1):17–23

    Article  CAS  Google Scholar 

  6. Hofenk de Graaf J (2004) The Colourful Past, Origins, Chemistry and Identification of Natural Dyestuffs. Abegg-Stiftung and Archetype Publications Ltd

  7. Wouters J, Rosario-Chirinos N (1992) Dye analysis of pre-columbian peruvian textiles with high-performace liquid chromatography and diode-array detection. J Am Inst Conservation 31:237–255

    Article  Google Scholar 

  8. Schweppe H (1992) Handbuch der Naturfarbstoffe; Vorkommen, Verlagsgesellschaft. Lech, Landeberg

    Google Scholar 

  9. Ferreira ESB, Quye A, McNab H, Hulme AN (2002) Photo-oxidation products of quercetin and Morin as markers for the characterisation of natural flavonoid yellow dyes in ancient textiles. Dyes in history and archaeology 18:63–72

    CAS  Google Scholar 

  10. Papouchado L, Petrie G, Adams RN (1972) Anodic-oxidation pathways of phenolic compounds 1.anodic hydroxylation reactions. J Electroanal Chem 38(2):389–395

    Article  CAS  Google Scholar 

  11. Ryan D, Yueh A, Chen W-Y (1980) The electrochemical oxidation of substituted catechols. J Electrochem Soc 127(7):1489–1495

    Article  CAS  Google Scholar 

  12. Bailey SI, Ritchie IM, Hewgill FR (1983) The construction and use of potential-pH diagrams in organic oxidation-reduction reactions. J Chem Soc Perkin Trans II 5:645–652

    Article  Google Scholar 

  13. Laviron E (1984) Electrochemical reactions with protonations at equilibrium 10. The kinetics of the para-benzoquinone hydroquinone couple on a platinum-electrode. J Electroanal Chem 164(2):213–227

    Article  CAS  Google Scholar 

  14. Sokolová R, Degano I, Hromadová M, Bulíčková J, Gál M, Valášek M (2010) Oxidation pathways of natural dye hematoxylin in aqueous solution. Collect Czech Chem Commun 75(11):1097–1114

    Article  Google Scholar 

  15. Costentin C, Louault C, Robert M, Savéant J-M (2008) Evidence for concerted proton-electron transfer in the electrochemical oxidation of phenols with water as proton acceptor. Tri-tert-butylphenol J Am Chem Soc 130(47):15817–15819

    CAS  Google Scholar 

  16. Musialik M, Kuzmicz R, Pawlowski TS, Litwinienko G (2009) Acidity of hydroxyl groups: an overlooked influence on antiradical properties of flavonoids. J Org Chem 74(7):2699–2709

    Article  CAS  Google Scholar 

  17. Jacq J (1971) Squares scheme – establishment and discussion of general equation for intensity – potential curve in stationary flow and convective diffusion. J Electroanal Chem Interfacial Electrochem 29(1):149–180

    CAS  Google Scholar 

  18. Lalor GC (1962) Studies on haematoxylin and haematein, the colouring principles of logwood III fading of haematein in aqueous acidic solutions. J Soc Dyers Colour 78(11):549–551

    Article  CAS  Google Scholar 

  19. Bettinger Ch, Zimmermann HW (1991) New investigations on hematoxylin, hematein and hematein-aluminum complexes I. spectroscopic and physicochemical properties of hematoxylin and hematein. Histochemistry 95(3):279–288

    Article  CAS  Google Scholar 

  20. Lalor GC, Martin SL (1959) Studies on haematoxylin and haematein the colouring principles of logwood 2. behaviour in aqueous solutions at varying pH, and the pK values. J Soc Dyers Colour 75(11):517–521

    Article  CAS  Google Scholar 

  21. Zheng Y, Haworth IS, Zuo Z, Chow MSS, Chow AHL (2005) Physicochemical and structural characterization of quercetin-beta-cyclodextrin complexes. J Pharm Sci 94(5):1079–1089

    Article  CAS  Google Scholar 

  22. Jovanovic SV, Steenken S, Tosic M, Marjanovic B, Simic MG (1994) Flavonoids as antioxidants. J Am Chem Soc 116(11):4846–4851

    Article  CAS  Google Scholar 

  23. Escandar GM, Sala LF (1991) Complexing behavior or rutin and quercetin. Can J Chem 69(12):1994–2001

    Article  CAS  Google Scholar 

  24. Dangles O, Dufour C, Bret S (1999) Flavonol-serum albumin complexation. Two-electron oxidation of flavonols and their complexes with serum albumin. J Chem Soc Perkin Trans 2(4):737–744

    Google Scholar 

  25. Zenkevich IG, Guschina SV (2010) Determination of dissociation constants of species oxidizable in aqueous solution by Air oxygen on an example of quercetin. J Anal Chem 65(4):371–375

    Article  CAS  Google Scholar 

  26. Brett AMO, Ghica M-E (2003) Electrochemical oxidation of quercetin. Electroanalysis 15(22):1745–1750

    Article  CAS  Google Scholar 

  27. Makris DP, Rossiter JT (2002) Hydroxyl free radical-mediated oxidative degradation of quercetin and Morin: a preliminary investigation. J Food Composition Anal 15(1):103–113

    Article  CAS  Google Scholar 

  28. Tournaire C, Hocquaux M, Beck I, Oliveros E, Maurette M-T (1994) Antioxidant activity of flavonoids – reactivity with potassium superoxide in the heterogeneous phase. Tetrahedron 50(31):9303–9314

    Article  CAS  Google Scholar 

  29. Jungbluth G, Ruhling I, Ternes W (2000) Oxidation of flavonols with Cu(II), Fe(II) and Fe(III) in aqueous media. Chem Soc Perkin Trans 2(9):1946–1952

    Article  Google Scholar 

  30. Jorgensen LV, Cornett C, Justesen U, Skibsted LH, Dragsted LO (1998) Two-electron electrochemical oxidation of quercetin and kaempferol changes only the flavonoid C-ring. Free Rad Res 29(4):339–350

    Article  CAS  Google Scholar 

  31. Timbola AK, De Souza CD, Giacomelli C, Spinelli A, Braz J (2006) Electrochemical oxidation of quercetin in hydro-alcoholic solution. Chem Soc 17(1):139–148

    CAS  Google Scholar 

  32. Sokolová R, Degano I, Ramešová Š, Bulíčková J, Hromadová M, Gál M, Fiedler J, Valášek M (2011) The oxidation mechanism of the antioxidant quercetin in nonaqueous media. Electrochim Acta 56(21):7421–7427

    Article  Google Scholar 

  33. Hendrickson HP, Kaufman AD, Lunte CE (1994) Electrochemistry of catechol-containing flavonoids. J Pharm Biomed Anal 12(3):325–334

    Article  CAS  Google Scholar 

  34. Zenkevich IG, Eshchenko AY, Makarova SV, Vitenberg AG, Dobryakov YG, Utsal VA (2007) Identification of the products of oxidation of quercetin by Air oxygen at ambient temperature. Molecules 12(3):654–672

    Article  CAS  Google Scholar 

  35. Zhou A, Kikandi S, Sadik OA (2007) Electrochemical degradation of quercetin: Isolation and structural elucidation of the degradation products. Electrochem Commun 9(9):2246–2255

    Article  CAS  Google Scholar 

  36. Lei R, Xu X, Yu F, Li N, Liu HW, Li K (2008) A method to determine quercetin by enhanced luminol electrogenerated chemiluminescence (ECL) and quercetin autoxidation. Talanta 75(4):1068–1074

    Article  CAS  Google Scholar 

  37. Surowiec I, Szostek B, Trojanowicz M (2007) HPLC–MS of anthraquinoids, flavonoids, and their degradation products in analysis of natural dyes in archeological objects. J Sep Sci 30(13):2070–2079

    Article  CAS  Google Scholar 

  38. Dangles O, Fargeix G, Dufour C (1999) One-electron oxidation of quercetin and quercetin derivatives in protic and non protic media. J Chem Soc Perkin Trans 2(7):1387–1395

    Google Scholar 

  39. Bettinger C, Zimmermann HW (1991) New investigations on hematoxylin, hematein and hematein–aluminium complexes. Histochemistry 95(3):279–288

    Article  CAS  Google Scholar 

  40. Pérez R, Galvín RM, Mellado JMR (2002) Ultraviolet absorption spectra and dissociation constants of diamino-1,3,5-triazines. Collect Czech Chem Commun 67(4):429–438

    Article  Google Scholar 

  41. Daffy LM, Prasanna de Silva A, Gunaratne HQN, Huber Ch, Lynch PLM, Werner T, Wolfbeis OS (1998) Arenedicarboximide building blocks for fluorescent photoinduced electron transfer pH sensors applicable with different media and communication wavelengths. Chem Eur J 4(9):1810–1815

    Article  CAS  Google Scholar 

  42. http://chemlab.truman.edu/CHEM222manual/pdf/pka1.pdf

  43. Shao Y, Molnar LF, Jung Y, Kussmann J, Ochsenfeld C, Brown ST, Gilbert ATB, Slipchenko LV, Levchenko SV, O'Neill DP, DiStasio RA, Lochan RC, Wang T, Beran GJO, Besley NA, Herbert JM, Lin CY, Van Voorhis T, Chien SH, Sodt A, Steele RP, Rassolov VA, Maslen PE, Korambath PP, Adamson RD, Austin B, Baker J, Byrd EFC, Dachsel H, Doerksen RJ, Dreuw A, Dunietz BD, Dutoi AD, Furlani TR, Gwaltney SR, Heyden A, Hirata S, Hsu CP, Kedziora G, Khalliulin RZ, Klunzinger P, Lee AM, Lee MS, Liang W, Lotan I, Nair N, Peters B, Proynov EI, Pieniazek PA, Rhee YM, Ritchie J, Rosta E, Sherrill CD, Simmonett AC, Subotnik JE, Woodcock HL, Zhang W, Bell AT, Chakraborty AK, Chipman DM, Keil FJ, Warshel A, Hehre WJ, Schaefer HF, Kong J, Krylov AI, Gill PMW, Head-Gordon M (2006) Advances in methods and algorithms in a modern quantum chemistry program package. Phys Chem Chem Phys 8:3172–3191

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by the Grant Agency of the Czech Republic (203/09/1607) and by the MONDI project (Fondo per le Aree Sottoutilizzate Delibera CIPE 166/2007, granted by the Regione Toscana, Italy).

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Correspondence to Romana Sokolová.

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Ramešová, Š., Sokolová, R., Degano, I. et al. On the stability of the bioactive flavonoids quercetin and luteolin under oxygen-free conditions. Anal Bioanal Chem 402, 975–982 (2012). https://doi.org/10.1007/s00216-011-5504-3

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