Skip to main content
Log in

Determination of Thermodynamics Constant of Interaction among of Atenolol and Metoprolol with Human Serum Albumin: Spectroscopic and Molecular Modeling Approaches

  • BIOPHYSICAL CHEMISTRY
  • Published:
Russian Journal of Physical Chemistry A Aims and scope Submit manuscript

Abstract

Interaction of atenolol (Atn) and metoprolol (Met) beta-blocker drugs with human serum albumin (HSA) at pH 7.4 was investigated by UV–Vis spectroscopy and molecular modeling methods. In addition, the binding interaction information of Atn and Met with HSA practicaly of binding constant (Kb) were determined by the UV–Vis absorption titration at body actual temperature (310.15 K), and were found to be 9.5 × 103, 1.4 × 104, and 2.3 × 104 M–1 for Atn, Met, and Atn + Met, respectively. The results indicated that addition of Atn in many concentrations causes decrease, while addition of Met and Met + Atn leads to an increase in absorption upon complexation with HSA. The binding mechanisms of two target drugs are different from each other, as indicated by spectroscopic analysis. The results show that interactions in all systems are exothermic with negative entropy, which lead to more spontaneous reaction at lower temperatures. Molecular dynamics simulation calculations show that the number of interactive residues between Met and protein is less than the number of interactive residues between Atn and protein.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5.
Fig. 6.
Fig. 7.
Fig. 8.
Fig. 9.

Similar content being viewed by others

REFERENCES

  1. H. R. Costantino, L. Illum, G. Brandt, P. H. Johnson, and S. C. Quay, Int. J. Pharm. 337, 1 (2007).

    Article  CAS  PubMed  Google Scholar 

  2. G. M. Currie, J. M. Wheat, and H. Kiat, Open Cardiovasc. Med. J. 5, 130 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. T.-Y. Jiang, K.-L. Zhou, Y.-Y. Lou, D.-Q. Pan, and J.‑H. Shi, J. Biomol. Struct. Dyn. 36, 1095 (2018).

    Article  CAS  PubMed  Google Scholar 

  4. B. X. Huang, H. Y. Kim, and Ch. Dass, J. Am. Soc. Mass Spectrom. 15, 1237 (2004).

    Article  CAS  PubMed  Google Scholar 

  5. P. Keen, in Concepts in Biochemical Pharmacology (Springer, Berlin, Heidelberg, 1971), p. 213.

    Google Scholar 

  6. B. B. Brodie and C. A. M. Hogben, J. Pharm. Pharmacol. 9, 345 (1957).

    Article  CAS  PubMed  Google Scholar 

  7. Sh. Zhou, J. W. Paxton, Ph. Kestell, M. D. Tingle, and Ph. Kestell, J. Pharm. Pharmacol. 53, 463 (2001).

    Article  CAS  PubMed  Google Scholar 

  8. K. E. D. Coan and B. K. Shoichet, Mol. Biosyst. 3, 208 (2007).

    Article  CAS  PubMed  Google Scholar 

  9. M. George and T. E. Abraham, J. Control. Release 114, 1 (2006).

    Article  CAS  PubMed  Google Scholar 

  10. W. J. Jusko and M. Gretch, Drug Metab. Rev. 5, 43 (1976).

    Article  CAS  PubMed  Google Scholar 

  11. B. E. P. Murphy, J. Clin. Endocrinol. Metab. 27, 973 (1967).

    Article  CAS  PubMed  Google Scholar 

  12. M. Maciążek-Jurczyk, A. Sułkowska, B. Bojko, J. Równicka, and W. W. Sułkowski, J. Mol. Struct. 924, 378 (2009).

    Article  CAS  Google Scholar 

  13. M. M. Browne, G. V. Lubarsky, M. R. Davidson, and R. H. Bradley, Surf. Sci. 553, 155 (2004).

    Article  CAS  Google Scholar 

  14. P. B. Desai and A. K. Srivastava, Sens. Actuators, B 176, 632 (2013).

    Article  CAS  Google Scholar 

  15. L. Kranitz and P. Lehrer, Cardiol. Rev. 12, 177 (2004).

    Article  PubMed  Google Scholar 

  16. D. E. Donald, D. A. Ferguson, and S. E. Milburn, Circul. Res. 22, 127 (1968).

    Article  CAS  Google Scholar 

  17. A. Najafi, V. Sequeira, D. W. D. Kuster, and J. van der Velden, Eur. J. Clin. Invest. 46, 362 (2016).

    Article  CAS  PubMed  Google Scholar 

  18. C. J. Homcy, S. F. Vatner, and D. E. Vatner, Ann. Rev. Physiol. 53, 137 (1991).

    Article  CAS  Google Scholar 

  19. D. A. Sica, T. W. B. Gehr, and S. Ghosh, Pharmacokinetics 44, 797 (2005).

    Article  CAS  Google Scholar 

  20. M. R. Housaindokht, Z. R. Zaeri, and M. Bahrololoom, Spectrochim. Acta, Part A 85, 79 (2012).

    Article  CAS  Google Scholar 

  21. Y. Landry and J.-P. Gies, Fundam. Clin. Pharmacol. 22, 1 (2008).

    Article  CAS  PubMed  Google Scholar 

  22. X. Li, X. Xu, J. Wang, H. Yu, X. Wang, H. Yang, H. Xu, et al., PloS One 7 (9), e43918 (2012).

  23. P. Ascenzi, G. Fanali, M. Fasano, V. Pallottini, and V. Trezza, J. Mol. Struct. 1077, 4 (2014).

    Article  CAS  Google Scholar 

  24. M. Bern, K. M. K. Sand, J. Nilsen, I. Sandlie, and J. T. Andersen, J. Control. Release 211, 144 (2015).

    Article  CAS  PubMed  Google Scholar 

  25. B. P. Espósito and R. Najjar, Coord. Chem. Rev. 232, 137 (2002).

    Article  Google Scholar 

  26. F. A. de Wolf and G. M. Brett, Pharmacol. Rev. 52, 207 (2000).

    CAS  PubMed  Google Scholar 

  27. Md Tabish Rehman and A. U. Khan, Curr. Pharm. Des. 21, 1785 (2015).

    Article  CAS  PubMed  Google Scholar 

  28. X. M. He and D. C. Carter, Nature (London, U.K.) 358 (6383), 209 (1992).

    Article  CAS  Google Scholar 

  29. U. Kragh-Hansen, F. Hellec, B. de Foresta, M. le Maire, and J. V. Møller, Biophys. J. 80, 2898 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. J. Costa Pessoa and I. Tomaz, Curr. Med. Chem. 17, 3701 (2010).

    Article  PubMed  Google Scholar 

  31. M. S. Benedetti, R. Whomsley, I. Poggesi, W. Cawello, F.-X. Mathy, M.-L. Delporte, P. Papeleu, and J.‑B. Watelet, Drug Metab. Rev. 41, 344 (2009).

    Article  CAS  PubMed  Google Scholar 

  32. K. Yamasaki, V. T. Giam Chuang, T. Maruyama, and M. Otagiri, Biochim. Biophys. Acta 1830, 5435 (2013).

    Article  CAS  PubMed  Google Scholar 

  33. F. Poureshghi, P. Ghandforoushan, A. Safarnejad, and S. Soltani, J. Photochem. Photobiol. B 166, 187 (2017).

    Article  CAS  PubMed  Google Scholar 

  34. X.-X. Cheng, Y. Lui, B. Zhou, X.-H. Xiao, and Y. Liu, Spectrochim. Acta, Part A 72, 922 (2009).

    Article  CAS  Google Scholar 

  35. B. Sandhya, A. H. Hegde, Sh. S. Kalanur, U. Katrahalli, and J. Seetharamappa, J. Pharm. Biomed. Anal. 54, 1180 (2011).

    Article  CAS  PubMed  Google Scholar 

  36. H. Xu, N. Yao, H. Xu, T. Wang, G. Li, and Zh. Li, Int. J. Mol. Sci. 14, 14185 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  37. S. Gao and R. Liu, New J. Chem. 42, 9065 (2018).

    Article  CAS  Google Scholar 

  38. T. S. Banipal, A. Kaur, and P. K. Banipal, Spectrochim. Acta, Part A 170, 214 (2017).

    Article  CAS  Google Scholar 

  39. X.-L. Han, F.-F. Tian, Y.-Sh. Ge, F. L. Jiang, L. Lai, D.-W. Li, Q.-L. Yu, J. Wang, Ch. Lin, and Y. Liu, J. Photochem. Photobiol. B 109, 1 (2012).

    Article  CAS  PubMed  Google Scholar 

  40. B. Knapp, S. Frantal, M. Cibena, W. Schreiner, and P. Bauer, J. Comput. Biol. 18, 997 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. O. Carugo and S. Pongor, Protein Sci. 10, 1470 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. H. Lei, Ch. Wu, H. Liu, and Y. Duan, Proc. Natl. Acad. Sci. U. S. A. 104, 4925 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. M. R. Housaindokht, M. R. Bozorgmehr, and H. Monhemi, J. Supercrit. Fluids 63, 180 (2012).

    Article  CAS  Google Scholar 

  44. Farideh Mirzaee, Leila Hosseinzadeh, Mohammad Reza Ashrafi-Kooshk, Sajjad Esmaeili, Sirous Ghobadi, Mohammad Hosein Farzaei, Mahmoud Reza Zad-Bari, and Reza Khodarahmi, Protein and Peptide Lettes 26 (2), 132 (2019). https://doi.org/10.2174/0929866525666181114152242

Download references

ACKNOWLEDGMENTS

The authors wish to acknowledge the support of this work by Sadri Ebrahimnia and Radvin Raoufi.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mahmoud Ebrahimi.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Raoufi, A., Ebrahimi, M. & Bozorgmehr, M.R. Determination of Thermodynamics Constant of Interaction among of Atenolol and Metoprolol with Human Serum Albumin: Spectroscopic and Molecular Modeling Approaches. Russ. J. Phys. Chem. 95, 1269–1276 (2021). https://doi.org/10.1134/S0036024421140181

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0036024421140181

Keywords:

Navigation