Anticancer Activity of New Copper (II) Complexes with 6-Thiguanine Drug

Authors

  • Birjesh Singh Department of Chemistry, MVM College, Bhopal 462008, (M.P), India
  • Jyotsna Mishra Department of Chemistry, Institute of Science and Technology, AISECT University, Bhopal (MP) India
  • K.S. Pitre Department of Chemistry, Dr. H.S. Gour University, Sagar (MP) India
  • Alka Pradhan Department of Chemistry, MVM College, Bhopal 462008, (M.P), India
  • Puspender Soni Department of Pharmacy, Globus Pharmacy college, Bhopal (MP) Indian

DOI:

https://doi.org/10.6000/1927-3037.2013.02.01.6

Keywords:

Cu (II) Complex, Polarography, Amperometry, Biological investigation, anticancer activity

Abstract

A new complex has been synthesized of Cu (II) complex with 6-thioguanine and phyico-chemical characterized by amperometry, polarography elemental analysis and FTIR spectroscopy. After Synthesis of metal complex, it was evaluated it for antibacterial and antifungal activities against various pathogenic microorganisms such as; Streptococcus aureus, Proteus. M., klebsiella pneumonia and Asperginus niger, Nigrosporan S.P. B16-F10 melanoma cell and C-57BL/6 mice has been used for anticancer screening of metal complex for in vitro and in vivo study. The result of pharmacological studies with M: L revealed that the complex is more potent as compared to the pure drug as regards to its anticancer activity.

References

Nelson JA, Carpenter JW, Rose LM, Adamoson DY. Mechanisms of action of 6-thioguanine 6-mercaptopurine and 8 azaguanine. Cancer Res 1975; 32: 2872-78. http://dx.doi.org/10.1590/S0103-50532008000300006

Ensafi AA, Hajian R. Simultaneous determination of captopril and thioguanine in pharmaceutical compounds and blood using cathodic adsorptive stripping voltammetry. J Braz Chem Soc 2008; 19: 405-12. http://dx.doi.org/10.1590/S0103-50532008000300006

Anbu S, Shanmugaraju S, Ravishanker R, Karanda AA, Mukherjee PS. Naphthylhydrazone based selective and sensitive chemosensors for Cu2+ and their application in bioimaging. Dalton Trans 2012; 41: 13330-37. http://dx.doi.org/ 10.1039/C2DT31335A

Belichi-Ferrari M, Bisceglie F, Pelosi G, et al. Synthesis, characterisation, X-ray structure and biological activity of three new 5-formyluracil thiosemicarbazone complexes. J Inorg Biochem 2001; 83: 169-79. http://dx.doi.org/10.1016/S0162-0134(00)00181-1

Belichi-Ferrari M, Biscegliea F, Favaa GG, et al. Synthesis, characterization and biological activity of two new polymeric copper(II) complexes with aketoglutaric acid thiosemicarbazone. J Inorg Biochem 2002; 89: 36-40. http://dx.doi.org/10.1016/S0162-0134(01)00371-3

Arguelles MR, Belichi-Ferrari M, Biscegli F, et al. Synthesis characterization and biological activity of Ni Cu and Zn complexes of isatin hydrazones. J Inorg Biochem 2004; 98: 313-21. http://dx.doi.org/10.1016/j.jinorgbio.2003.10.006

Belichi-Ferrari M, Biscegli F, Buschin A, et al. Synthesis structural characterization and antiproliferative and toxic bio-activities of copper(II) and nickel(II) citronellal N4-

ethylmorpholine thiosemicarbazonates. J Inorg Biochem 2010; 104: 199-206. http://dx.doi.org/10.1016/j.jinorgbio.2009.11.002

Lee PF, Yang CT, Fan D, Vittal JJ, Ranford JD. Synthesis, characterization and physiccochemical properties of copper(II) complexes containing salicylaldehyde semicarbazone, Polyhedron 2003; 22: 2781-86. http://dx.doi.org/10.1016/S0277-5387(03)00402-9

Patole J, Dutta S, Padhey S, Sinn E. Tuning up superoxide dismutase activity of Copper complex of salicylaldehyde semicarbazone by heterocyclic bases pyridine and N- methyl imidazole. Inorg Chim Acta 2001; 318: 207-11. http://dx.doi.org/10.1016/S0020-1693(01)00416-9

Reddy KH, Reddy PS, Babu PR. Synthesis, spectral studies and nuclease activity of mixed ligand copper(II) complexes of heteroaromatic semicarbazones / thiosemicarbazones an pyridine. J Inorg Biochem 1999; 77: 169-76. http://dx.doi.org/10.1016/S0162-0134(99)00188-9

Bassett J, Denny RC, Jeffery GH, Mendam J. Editor Vogels Text Book of quantitative inorganic Analysis. 6th ed. ELBS Longman. Gr. Ltd. London 1996.

Bauer AW, Kirby WMM, Sherris JC, Turck K. Antibiotic Susceptibility testing by standardized single disk method. Am J Clin Pathol 1966; 36: 493-96. http://dx.doi.org/10.4314/ahs.v12i2.9

Smith AL. Principles of microbiology. 7th ed. The L V Mosky company, saint: Louis 1973.

Layek B, Mukherjee B. Tamoxifen Citrate Encapsulated Sustained Release Liposomes: Preparation and Evaluation of Physicochemical Properties. Sci Pharm 2010; 78: 507-15. http://dx.doi.org/10.3797/scipharm.0911-11

Ghosh MN. Fundamentals of experimental pharmacology. Scientific Book Agency, 2nd ed. 1984; 153.

Shrivastava S, Ganesh N. Tumor inhibition and Cytotoxicity assay by aqueous extract of onion (Allium cepa) & Garlic (Allium sativum): an in-vitro analysis. Int J Phytomed 2010; 2: 80-84. http://dx.doi.org:10.5138/ijpm.2010.0975.0185.02013

Hejna M, Raderer M, Zielinsk CC. Inhibition of Metastases by Anticoagulants. J Nat Cancer Inst 1999; 91(1): 22-36. http://dx.doi.org:10.1093/jnci/91.1.22

Rajanaresh RA, Udupa N, Uma DP. Toxicity and antitumor activity of niosomal bleomycin in tumor bearing mice. Indian J Expt Biol 1996; 34: 764-72. http://dx.doi.org/10.1515/BC.2004.081

Lingane JJ. Interpretation of the Polarographic Waves of Complex Metal Ions Chem Rev 1941; 29(1): 1-35. http://dx.doi.org/10.1021/cr60092a001

Casas JS, Castellano EE, Garcia-Tasande MS, et al. Deprotonation reactions of 2- thiouracil with [2-(pyridin-2-yl-) phenyl]mercury(II) acetate. Structural and spectroscopic effects. J Chem Soc Dalton Trans 1996; 9: 1973-78. http://dx.doi.org/10.1039/DT9960001973

Melendez E, Marrero M, Rivera C, Hernandez E, Segal A. Spectroscopic characterization of titanocene complexes with Thionucleobases. Inorganica Chimica Acta 2000; 298: 178-86. http://dx.doi.org/10.1016/S0020-1693(99)00441-7

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Published

2013-03-31

How to Cite

Singh, B., Mishra, J., Pitre, K., Pradhan, A., & Soni, P. (2013). Anticancer Activity of New Copper (II) Complexes with 6-Thiguanine Drug. International Journal of Biotechnology for Wellness Industries, 2(1), 39–44. https://doi.org/10.6000/1927-3037.2013.02.01.6

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