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Synthesis, Characterization of Ceftibuten-Copper(II) Complex and Prediction of Its Biological Activity

https://doi.org/10.14233/ajchem.2021.22982
Shuchismita Dey
Department of Chemistry, University of Dhaka, Dhaka-1000, Bangladesh
Md. Zakir Sultan
Centre for Advanced Research in Sciences (CARS), University of Dhaka, Dhaka-1000, Bangladesh
Md. Abdus Salam
Department of Chemistry, University of Dhaka, Dhaka-1000, Bangladesh

Corresponding Author(s) : Md. Abdus Salam

masalam@du.ac.bd

Asian Journal of Chemistry, Vol. 33 No. 1 (2021): Vol 33 Issue 1

Abstract

Ceftibuten dihydrate, one of the third-generation cephalosporin antibiotic is effectively used in curing several infectious diseases. The complexation of drug with metal may enhance the antibacterial activity. In this work, a new complex of ceftibuten dihydrate with Cu(II) was synthesized, characterized and antibacterial activity is reported. The in vitro test showed that the antibacterial activity of complex of ceftibuten was greatly enhanced against Staphylococcus aureus and Salmonella typhi.

Keywords

Ceftibuten Copper(II) complex Biological activity
Dey, S., Zakir Sultan, M., & Abdus Salam, M. (2020). Synthesis, Characterization of Ceftibuten-Copper(II) Complex and Prediction of Its Biological Activity. Asian Journal of Chemistry, 33(1), 190–194. https://doi.org/10.14233/ajchem.2021.22982
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References
  1. B.T. Hathiram, D.S. Grewal, P. Tankwal, N. Shah and R. Agarwal, Indian J. Otolaryngol. HNS, 51, 104 (1999);https://doi.org/10.1007/BF02998005
  2. R. Vijayalakshmi, P. Bhargavi, P.S. Kumari, P. Sruthi and M.D. Dhanaraju, E-J. Chem., 7, 551 (2010);https://doi.org/10.1155/2010/120417
  3. A. Bauernfeind, Diagn. Microbiol. Infect. Dis., 14, 89 (1991); https://doi.org/10.1016/0732-8893(91)90095-W
  4. R. Shawar, M. Larocco and T.G. Cleary, Antimicrob. Agents Chemother.,33, 781 (1989); https://doi.org/10.1128/AAC.33.5.781
  5. M. Shahid, F. Sobia, A. Singh, A. Malik, H.M. Khan, D. Jonas and P.M. Hawkey, Crtic. Rev. Microbiol., 35, 81 (2009); https://doi.org/10.1080/10408410902733979
  6. X. Zeng and J. Lin, Front. Microbiol., 4, 128 (2013); https://doi.org/10.3389/fmicb.2013.00128
  7. M. Selevaganapathy and N. Raman, J. Chem. Biol. Therap., 1, 108 (2016); https://doi.org/10.4172/2572-0406.1000108
  8. S, Ramotowska, M, Wysocka, J. Brzeski, A. Chylewska and M. Malowski, TrAC-Trends Analyt. Chem., 123, 115771 (2020); https://doi.org/10.1016/j.trac.2019.115771
  9. Z.H. Chohan, C.T. Supuran and A. Scozzafava, J. Enzyme Inhib. Med.Chem., 20, 303 (2005);https://doi.org/10.1080/14756360310001624948
  10. A.N. Mustapha, N.P. Ndahi, B.B. Paul and M.B. Fugu, J. Chem. Pharm.Res., 6, 588 (2014).
  11. J.R. Anacona and G.D. Silva, J. Chil. Chem. Soc., 50, 447 (2005).
  12. S.H. Auda, Y. Mrestani, M.I. Fetouh and R.H.H. Neubert, Pharmazie,63, 555 (2008).
  13. D.C. Ware, P.J. Brothers, G.R. Clark, W.A. Denny, B.D. Palmer and W.R. Wilson, J. Chem. Soc., Dalton Trans., 925 (2000); https://doi.org/10.1039/a909447d
  14. M.S. Islam, K.Y. Sikdar, A.M. Hossain and A. Faroque, Dhaka Univ. J.Pharm. Sci., 18, 135 (2019); https://doi.org/10.3329/dujps.v18i2.43255
  15. D.R. Williams, The Metals of Life: the Solution Chemistry of Metal Ions in Biological Systems, Van Nostrand Reinhold: London (1971).
  16. H.H.A. Dollwet and J.R.J. Sorenson, Trace Elem. Med., 2, 80 (1985).
  17. I. Neda, T. Kaukorat, R. Schmutzler, U. Niemeyer, B. Kutscher and J.Pohl, Phosphorus Sulfur Silicon Rel. Elem., 162, 81 (2000); https://doi.org/10.1080/10426500008045221
  18. S.-A. Filimon, C.G. Hrib, S. Randoll, I. Neda, P.G. Jones and M. Tamm,Z. Anorg. Allg. Chem., 636, 691 (2010);https://doi.org/10.1002/zaac.200900485
  19. S. Rafique, M. Idrees, A. Nasim, H. Akbar and A. Athar, Biotechnol.Mol. Biol. Rev., 5, 38 (2010).
  20. M.S. Arayne, N. Sultana, S. Shamim and A. Naz, Modern Chem. Appl., 2, 133 (2014); https://doi.org/10.4172/2329-6798.1000127
  21. A.W. Bauer, W.M.M. Kirby, J.C. Sherris and M. Turck, Am. J. Clin.Pathol., 45(4_ts), 493 (1966); https://doi.org/10.1093/ajcp/45.4_ts.493
  22. A.U. Rahman, M.I. Choudhary and W.J. Thomson, Bioassay Techniques for Drug Development, Harwood Academic Publishers: Netherland (2001).
  23. M. Balouiri, M. Sadiki and S.K. Ibnsouda, J. Pharm. Anal., 6, 71 (2016); https://doi.org/10.1016/j.jpha.2015.11.005
  24. M.H.U. Biswas, A.H.M.Z. Shaheed and A. Farooque, Bangladesh Pharm. J., 12, 43 (2002).
  25. K. Seku, A.K. Yamala, M. Kancherla, K. Kumar and V. Badathala, J.Anal. Sci. Technol., 9, 14 (2018); https://doi.org/10.1186/s40543-018-0147-z
  26. B. Vimala, S.R. Jayapradha and A. Selvan, Asian J. Chem., 32, 488 (2020);https://doi.org/10.14233/ajchem.2020.22362
  27. F. Aktar, M.Z. Sultan and M.A. Rashid, Dhaka Univ. J. Pharm. Sci.,18, 271 (2019); https://doi.org/10.3329/dujps.v18i2.44467
  28. G.B. Deacon and R.J. Philips, Coord. Chem. Rev., 33, 227 (1980); https://doi.org/10.1016/S0010-8545(00)80455-5
  29. N. Sultana, M.S. Arayne and M. Afzal, Pak. J. Pharm. Sci., 16, 59 (2003).
  30. N. Sultana, M.S. Arayne and M. Afzal, Pak. J. Pharm. Sci., 18, 36 (2005).
  31. S.F. Tan, K.P. Ang and H.L. Jayachandran, Transition Met. Chem., 9,390 (1984); https://doi.org/10.1007/BF00637026
  32. J.R. Anacona and C. Toledo, Transition Met. Chem., 26, 228 (2001); https://doi.org/10.1023/A:1007154817081
  33. J.R. Anacona and J. Serrano, J. Coord. Chem., 56, 313 (2003); https://doi.org/10.1080/0095897031000069085
  34. J.R. Anacona, J. Coord. Chem., 54, 355 (2001); https://doi.org/10.1080/00958970108022648
  35. M. Tümer, H. Köksal, M.K. Sener and S. Serin, Transition Met. Chem.,24, 414 (1999); https://doi.org/10.1023/A:1006973823926
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