Journals / Marmara Pharmaceutical Journal / 2017 / Cilt: 21 - Sayı: 2

Potentiometric and Chromatographic Study of Cu(II) and Al(III) Complexes of Quercetin

Pages
330–337
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Mobile phase was 0.01 M HClO 4 / 8.33 x 10 -5 M quercetin in Methanol (40/60), column was XTerra RP18, 5 μm, 4.6 x 150 mm , detector was Diode Array Detector at λ = 373 ve 421 nm (band width 4nm).

📌 3 Key Takeaways

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Objective & Hypothesis:In this study, the stability constants of the copper(II) and aluminium(III) complexes of quercetin were determined potentiometrically by using Calvin-Bjerrum and Irwing Rossotti methods.
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Key Findings & Data:The protonation constants of quercetin were found: logK 1 = 11.15±0.118, logK 2 = 10.42±0.144, logK 3 = 9.44±0.162, logK 4 = 8.28±0.151.
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Conclusion & Impact:Mobile phase was 0.01 M HClO 4 / 8.33 x 10 -5 M quercetin in Methanol (40/60), column was XTerra RP18, 5 μm, 4.6 x 150 mm , detector was Diode Array Detector at λ = 373 ve 421 nm (band width 4nm).
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

In this study, the stability constants of the copper(II) and aluminium(III) complexes of quercetin were determined potentiometrically by using Calvin-Bjerrum and Irwing Rossotti methods. The protonation constants of quercetin were found: logK 1 = 11.15±0.118, logK 2 = 10.42±0.144, logK 3 = 9.44±0.162, logK 4 = 8.28±0.151. For copper complex formation constant was found by Irwing-Rossotti method: logK 1 = 19.92±0.367 and for aluminium complex complex: logK 1 = 23.02±0.459. From the results, the components of quercetin / metal complexes are given as 1/1 both copper(II) and aluminium(III). A reversed phase high pressure liquid chromatographic method was developed for the metal complexes which were prepared according to potentiometric results with the ratio quercetin / metal =1/1. Mobile phase was 0.01 M HClO 4 / 8.33 x 10 -5 M quercetin in Methanol (40/60), column was XTerra RP18, 5 μm, 4.6 x 150 mm , detector was Diode Array Detector at λ = 373 ve 421 nm (band width 4nm).

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Cite This Article

YILMAZ, D. Ç., PEKİN, M. (2017). Potentiometric and Chromatographic Study of Cu(II) and Al(III) Complexes of Quercetin. Marmara Pharmaceutical Journal, Cilt: 21 - Sayı: 2, 330–337. https://ajindex.com/articles/283746

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References (14)

  1. Amic D, Davidovic-Amic D, Beslo D, Rastija V, Lucic B, Trinajstic N. SAR and QSAR of the antioxidant activity of flavonoids. Curr Med Chem 2007;14: 827-45
  2. George VC, Dellaire G, Rupasinghe HPV. Plant flavonoids in cancer chemoprevention: Role in genome stability. J Nutr Biochem 2017;45: 1-14.
  3. Corradini E, Foglia P, Giansanti P, Gubbiotti R, Samperi R, Lagana A. Flavonoids: Chemical properties and analytical methodologies of identification and quantitation in foods and plants. Nat Prod Res 2011;25: 469-95.
  4. Ravishankar D, Rajora AK, Greco F, Osborn HMI. Flavonoids as prospective compounds for anti-cancer therapy. Int J Biochem Cell Biol 2013;45: 2821-31.
  5. Spoerlein C, Mahal K, Schmidt H, Schobert R. Effects of chrysin, apigenin, genistein and their homoleptic copper(II) complexes on the growth and metastatic potential of cancer cells. J Inorg Biochem 2013;127: 107-15.
  6. Frezza M, Hindo S, Chen D, Davenport A, Schmitt S, Tomco D, Dou QP. Novel metals and metal complexes as platforms for cancer therapy. Curr Pharm Des 2010;16: 1813-25.
  7. Kostova I, Balkansky S. Metal complexes of biologically active ligands as potential antioxidants. Curr Med Chem 2013;20: 4508-39.
  8. Mladenka P, Macakova K, Filipsky T, Zatloukalova L, Jahodar L, Bovicelli P, Silvestri IP, Hrdina R, Saso L. In vitro analysis of iron chelating activity of flavonoids. J Inorg Biochem 2011;105: 693-701.
  9. Samsonowicz M, Regulska E. Spectroscopic study of molecular structure, antioxidant activity and biological effects of metal hydroxyflavonol complexes. Spectrochim Acta A Mol Biomol Spectrosc 2017;173: 757-71.
  10. Amic D, Davidovic-Amic D, Beslo D, Rastija V, Lucic B, Trinajstic N. SAR and QSAR of the antioxidant activity of flavonoids. Curr Med Chem 2007;14: 827-45
  11. Jabeen E, Janjua NK, Ahmed S, Murtaza I, Ali T, Hameed S. Radical scavenging propensity of Cu 2+, Fe 3+ complexes of flavonoids and in-vivo radical scavenging by Fe 3+ -primuletin.Spectrochim Acta A Mol Biomol Spectrosc 2017;171: 432-8. de Souza RFV, De Giovani WF. Antioxidant properties of complexes of flavonoids with metal ions. Redox Rep 2004;9: 97-104.
  12. Cornard JP, Merlin JC. Spectroscopic and structural study of complexes of quercetin with Al(III). J Inorg Biochem 2002;92: 19-27.
  13. Fernandez MT, Mira ML, Florencio MH, Jennings KR. Iron and copper chelation by flavonoids: An electrospray mass spectrometry study. J Inorg Biochem 2002;92:105-11.
  14. Ikeda NEA, Novak EM, Maria DA, Velosa AS, Pereira RMS. Synthesis, characterization and biological evalua