Advanced SearchSearch Tips
Study on the Interaction between Curcumin and Ethylamines by Absorption and Fluorescence Spectroscopic Techniques
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
  • Journal title : Textile Coloration and Finishing
  • Volume 27, Issue 4,  2015, pp.340-344
  • Publisher : The Korean Society of Dyers and Finishers
  • DOI : 10.5764/TCF.2015.27.4.340
 Title & Authors
Study on the Interaction between Curcumin and Ethylamines by Absorption and Fluorescence Spectroscopic Techniques
Kim, Sung Hoon; Gwon, Seon Yeong; Lee, Eun-Mi; Bae, Jin-Seok;
  PDF(new window)
The interaction between curcumin(1,7-bis[4-hydroxy-3-methoxyphenyl]-1,6-heptadiene-3,5-dione) and ethylamines was studied in DMSO:(5:1, v/v) using absorption and fluorescence measurements. The association constant, , and the Stern-Volmer constants were calculated by the Benesi-Hildebrand and Stern-Volmer equation, respectively. Curcumin displayed marked UV-Vis absorption changes and highly responsive fluorescence quenching in the presence of ethylamine and the quenching ability was enhanced almost linearly with the concentration of ethylamines. The apparent Stern-Volmer constant measured for the ethylamine-curcumin system was about 1000-fold greater than that of the triethylamine-curcumin system, indicating considerably greater quenching efficiency of ethylamines.
 Cited by
A. J. Ruby, G. Kuttan, K. D. Babu, K. N. Rajasekharan, and R. Kuttan, Anti-tumour and Antioxidant Activity of Natural Curcuminoids, Cancer Lett., 94, 79(1995). crossref(new window)

A. Duvoix, R. Blasius, S. Delhalle, M. Schnekenburger, F. Morceau, E. Henry, M. Dicato, and M. Diederich, Chemopreventive and Therapeutic Effects of Curcumin, Cancer Lett., 223(2), 181(2005). crossref(new window)

T. Masuda, K. Hidaka, A. Shinohara, T. Maekawa, Y. Takeda, and H. Yamaguchi, Chemical Studies on Antioxidant Mechanism of Curcuminoid: Analysis of Radical Reaction Products from Curcumin, J. Agric. Food Chem., 47(1), 71(1999). crossref(new window)

C. X. Zhou, X. Y. Zhang, X. W. Dong, Q. F. Tao, H. Dou, R. P. Zhang, K. X. Huang, X. K. Li, C. X. Chen, S. Zeng, and Y. Z. Chin, Three New Diarylheptanoids and their Antioxidant Property, Chem. Lett., 18, 1243(2007).

A. Mazumder, N. Neamati, S. Sunder, J. Schulz, H. Pertz, E. Eich, and Y. Pommier, Curcumin Analogs with Altered Potencies against HIV-1 Integrase as Probes for Biochemical Mechanisms of Drug Action, J. Med. Chem., 40(19), 3057(1997). crossref(new window)

A. Khar, A. M. Ali, B. V. V. Pardhasaradhi, Z. Begum, and R. Anjum, Antitumor Activity of Curcumin is Mediated through the Induction of Apoptosis in AK-5 Tumor Cells, FEBS Lett., 445(1), 165(1999). crossref(new window)

N. Sreejayan and M. N. Rao, Free Radical Scavenging Activity of Curcuminoids, Arzneim Forsch., 46(2), 169(1996).

J. T. Mague, W. L. Alworth, and F. L. Payton, Curcumin and Derivatives, Acta. Cryst. C., 60, 608 (2004). crossref(new window)

T. M. Kolev, E. A. Velcheva, B. A. Stamboliyska, and M. Spiteller, DFT and Experimental Studies of the Structure and Vibrational Spectra of Curcumin, Int. J. Quant. Chem., 102, 1069(2005). crossref(new window)

S. Subrahmanyam, S. A. Piletsky, E. V. Piletska, B. Chen, R. Day, and A. P. F. Turner, "Bite-and- Switch" Approach to Creatine Recognition by Use of Molecularly Imprinted Polymers, Adv. Mater., 12, 722(2000). crossref(new window)

Z. Q. Li, L. G. Qiu, W. Wang, T. Xu, Y. Wu, and X. Jiang, Fabrication of Nanosheets of a Fluorescent Metal-organic Framework [Zn(BDC)($H_2O$)]n (BDC=1,4-benzenedicarboxylate): Ultrasonic Synthesis and Sensing of Ethylamine, Inorg. Chem. Commun., 11, 1375(2008).

S. Y. Gwon, J. S. Bae, Y. A. Son, S. Wang, and S. H. Kim, Colorimetric Signaling of Mono-, Di-, and Triethylamine Based on Intermolecular n-${\pi}$ Charge Transfer Interaction, Fibers. Polym., 10(6), 855(2009). crossref(new window)

E. M. Lee, S. Y. Gwon, Y. A. Son, and S. H. Kim, Fast Ethylamine Gas Sensing based on Intermolecular Charge-transfer Complexation, Chin. Chem. Lett., 23(4), 484(2012). crossref(new window)

S. H. Kim, S. Y. Gwon, S. M. Burkinshaw, and Y. A. Son, The Photo- and Electrophysical Properties of Curcumin in Aqueous Solution, Spectrochimica Acta Part A., 76, 384(2010). crossref(new window)

H. J. Kim, J. E. Park, M. G. Choi, S. Ahn, and S. K. Chang, Selective Chromogenic and Fluorogenic Signalling of $Hg^{2+}$ Ions using a Fluorescein -coumarin Conjugate, Dyes and Pigments, 84(1), 54(2010). crossref(new window)

J. R. Jadhav, C. H. Bae, and H. S. Kim, Fluorescence Sensing of $H_2PO_4$ by a Imidazolium-based Cholestane Receptor, Tetra. Lett., 52, 1623(2011). crossref(new window)

J. S. Bae and S. H. Kim, Spectral Properties of a pH Responsive Water Soluble Spironaphthoxazine and Its Multi-Switching Property, Textile Coloration and Finishing, 25(1), 18(2013). crossref(new window)

J. S. Bae, S. Y. Gwon, and S. H. Kim, Anthraquinone-carbamodithiolate Assembly as Selective Chromogenic Chemosensor for $Fe^{3+}$, Textile Coloration and Finishing, 25(1), 13(2013). crossref(new window)

F. Zsila, Z. Bikadi, and M. Simonyi, Unique, pH-dependent Biphasic Band Shape of the Visible Circular Dichroism of Curcumin-serum Albumin Complex, Biochem. Biophys. Res. Commun., 301(3), 7762(2003).

F. Zsila, Z. Bikadi, and M. Simonyi, Circular Dichroism Spectroscopic Studies Reveal pH Dependent Binding of Curcumin in the Minor Groove of Natural and Synthetic Nucleic Acids, Org. Biomol. Chem., 2, 2902(2004). crossref(new window)