Europium-(7-carboxymethoxy-4-methyl coumarin)2 Complex based Electrochemical Probe for DNA based on the Interaction between Them

Europium-(7-carboxymethoxy-4-methyl coumarin)2 Complex based Electrochemical Probe for DNA based on the Interaction between Them

Belal Hussein* Moustafa Gouda Walid Fathall Sherin Arabi

Department of Chemistry, Faculty of Science and Arts, Al Ula, Taibah University, Madina Monawarh, KSA

Department of Chemistry, Faculty of Science, Suez Canal University, Ismailia, Egypt

Department of Chemistry, Faculty of Science, El-Mansoura University, El-Mansoura-35516, Egypt

Department of Mathematical and Physical Sciences, Faculty of Engineering, Port-Said University, Port-Said, Egypt

Department of Mathematical and Physical Sciences, Faculty of Engineering, Suez Canal University, Ismailia, Egypt

Corresponding Author Email: 
belalhussein102@yahoo.com
Page: 
189-195
|
DOI: 
https://doi.org/10.14447/jnmes.v20i4.445
Received: 
02 August 2017
| |
Accepted: 
25 August 2017
| | Citation
Abstract: 

The interaction of Eu(III) ion with 7-carboxymethoxy-4-methylcoumarin (CMMC) has been investigated using the potentiometric method in the ethanol-water mixture solvent (0.15 volume fraction). The formation of the different binary, ternary complexes is confirmed by the corresponding pH-potentiometric curves. SUPERQUAD computer program has been used for the refinement of all the calculated constants in our present study. Electroanalytical techniques have been used to confirm the formation of different binary and ternary complexes under investigation. The binding constant of the ternary complex Eu(III)-CMMC-DNA calculated by cyclic voltammetry (CV) and differential pulse (DP) was found to be 1.8 and 2.5x 105 M-1 in Tris-HCl, respectively. The changes in the current intensity have been used for the quantitative determination of DNA over a linear concentration range with LOD of 1.0-1.3 µg/ ml in 0.1 M Tris-HCl buffer.

Keywords: 

potentiometry, Eu(III) -7- carboxymethoxy - 4- methyl coumarin (CMMC), voltammetry, DNA binding

1. Introduction
2. Experimental
3. Results and Discussion
4. Conclusion
5. Acknowledgments
  References

[1] H. A. Azab, B. H.M. Hussein, M. F. El-Azab, M. Gomaa, A. I. El-Falouji, Bioorgan. Med. Chem., 1, 223 (2013).

[2] D. B. Hall, R. E Holmlin, J. K Barton, Nature, 382, 731 (1996).

[3] L. N. Ji, X. H. Zou, J. G. Liu, Coord. Chem. Rev., 513, 216 (2001).

[4] J. K Barton, , J. M. Goldberg, , C. V. Kumar, N. J. Turro, J. Am. Chem. Soc., 108, 2081 (1968).

[5] B. Ambert J. B, LePecq, DNA-Ligand Interactions, from Drugs to Proteins; Guschibaver, W., Saenger, W., Eds.; Plenum: New York, 141, 1968.

[6] M.R. Robinson, M.B. O’Regnan, G.C, Bazan, Chem. Com-mun., 1645 (2000).

[7] L. Rutao, Y. Jinghe, W. Xia, J. Lumin., 96, 201 (2001).

[8] H. K. Kim, S. Roh, G.; K.-S. Hong, J.-W. Ka, N. S. Baek, J.B. Oh, M.-K. Nah, Y. H. Cha, Macromol. Res., 11, 133 (2003).

[9] F. J. Steemers, W. Verboom, D. N. Reinhoudt, , E. B. van der Tol, J. W. Verhoeven, J. Am. Chem. Soc., 117, 9408 (1995).

[10]S. Mohammad, M. MustafaM. A., El-Abadelah, G. Randa, Molecules, 16, 4305 (2011).

[11]G. Kokotos, V. Theodorou, C. Tzougraki, D. Deforce, E. Van den Eeckhout. Bioorg. Med. Chem. Lett., 7(17), 2165 (1997).

[12]A. Karaliota, O. Kretsi, and C. Tzougraki, J. Inorg. Biochem, 84(1-2), 33 (2001).

[13]I. Kostova, I. Manolov, I. Nicolova, S. Konstantinov, and M. Karaivanova, Eur. J. Med. Chem., 36(4), 339 (2001).

[14]H. B. Singh, Acta cienc. Indica.[ser.] chem., 6, 88 (1980).

[15]H. A. Azab, Z. M. Anwar, R. G. Ahmed, J. Chem. Eng. Data, 55(1), 459 (2010).

[16]E. Niyama, H.F. Brito, M. Cremona, E.E.S. Teotonio, R. G.E.S. Birto, M.C.F.C. Felinto, Spectrochim. Acta PartA, 61, 2643 (2005).

[17]S. Sato, W. Wada, Bull. Chem. Soc. Japan., 43, 1955 (1970).

[18]B.H. M. Hussein, H.A. Azab, M.F. El-Azab, A. I. El-Falouji, Eur. J. Med. Chem., 51, 99 (2012).

[19]H. A. Azab, B. H. M. Hussein, A. I. El-Falouji, J. Fluoresc., 22, 639 (2012).

[20]B.H.M. Hussein, G.M. Khairy, R.M. Kamel, Spectrochimica Acta Part A, 158, 34 (2016).

[21]Z. M. Anwar, H. A. Azab, J. Chem. Eng. Data, 46, 34 (2001).

[22]Z. M. Anwar, H. A. Azab, J. Chem. Eng. Data 46, 613 (2001).

[23]H. A. Azab, I. I. Abd El-Gwad, R. M. Kamel, J. Chem. Eng. Data, 54(11), 3078 (2009).

[24]H. A. Azab, Z. M. Anwar, R. G. Ahmed, J. Chem. Eng. Data, 55(1), 459 (2010).

[25]C. Stefano, B. Marco, and C. Barbara, Tetrahedron, 58, 4851 (2002).

[26]B.H.M. Hussein, H. A. Azab, W. Fathalla, S. A.M. Ali, J. Lu-min., 134, 441 (2013).

[27]F. J. Welcher, The Analytical Uses of Ethylene diaminetet-raacetic acid. D. Von. Nostrand Co., Inc., Princeton, 1965.

[28]H.A Azab, S.A El-Korashy, Z.M Anwar, B. H. M. Hussein, and G. M. Khairy, J. Chem. Eng. Data, 55, 3130 (2010).

[29]A. J. Bard and L. R. Faulkner, Electrochemical Methods: Fun-damentals and Applications, Second Edition, John Wiley and Sons Publishers, 2001.

[30]R. S. Nicholson, Anal. Chem., 37, 1351 (1965).

[31]M.T. Carter, M. Rodoriguez, A.J., Bard, J. Am. Chem. Soc., 111, 8901 (1989).

[32]Z.X Wang,. D.J. Liu, S.J. Dong, J. Chem. Chin., 19, 662 (2001).

[33]S. S. Kalanur, and J. Seetharamappa. Anal. Lett., 43, 618 (2010).

[34]Y. Q. Li, Y. J. Guo, X. F. Li, & J. H. Pan, Talanta, 71(1), 123 (2007).