Home Physical Sciences Probing Inclusion Complexes of Pentoxifylline and Pralidoxim inside Cyclic Oligosaccharides by Physicochemical Methodologies
Article
Licensed
Unlicensed Requires Authentication

Probing Inclusion Complexes of Pentoxifylline and Pralidoxim inside Cyclic Oligosaccharides by Physicochemical Methodologies

  • Biraj Kumar Barman , Kanak Roy and Mahendra Nath Roy EMAIL logo
Published/Copyright: December 7, 2018

Abstract

Structurally different Molecules namely Pentoxifylline and Pralidoxim were chosen along with α-cyclodextrin and β-cyclodextrin to study host-guest inclusion phenomena. The formations of host guest inclusion complexes were confirmed by studying 1H-NMR spectra, FT-IR spectra, apparent molar volume and viscosity co-efficient. The stabilities of inclusion complexes were compared calculating the binding constant from UV-VIS spectroscopic study. The 1:1 stoichiometry of the inclusion complexes were also determined by analysing the Jobs plot and surface tension data. The values for Gibbs’ free energy were found negative for both the processes. Based on all the above experiments the inclusion processes were found feasible for both the compounds. These types of inclusion complexes are of high interest in the field of research and industry as these are used as drug delivery systems.

Acknowledgement

Authors are grateful to University Grants Commission, New Delhi, India (No. 540/27/DRS/2007, SAP-DSR) and UGC-RGNF India (No. F117.1/201617/RGNF201517SCWES1846 and F.1/2012-13/RGNF-2012-13-SC-WES-17229) for financial and instrumental support to perform this research work. Prof. M. N. Roy is grateful to the UGC, New Delhi, Govt. of India, for being awarded one-time grant under the Basic Scientific Research by the Grant-in-Aid no. F4-10/2010 (BSR) regarding his active service for expanding research facilities to help further research work.

References

1. D. Stepanovs, M. Jure, L. N. Kuleshova, D. W. M. Hofmann, A. Mishnev, Cryst. Growth Des. 15 (2015) 3652.10.1021/acs.cgd.5b00185Search in Google Scholar

2. M. K. Mone, K. B. Chandrasekhar, J. Pharm. Biomed. Anal. 53 (2010) 335.10.1016/j.jpba.2010.04.006Search in Google Scholar PubMed

3. M. Riyad Yasser, C. Laube, S. Naumov, R. Hermann, B. Abel, Z. Phys. Chem. 229 (2015) 1831.10.1515/zpch-2015-0639Search in Google Scholar

4. T. Namba, C. T. Nolte, J. Jackrel, D. Grob, Am. J. Med. 50 (1971) 475.10.1016/0002-9343(71)90337-8Search in Google Scholar PubMed

5. J. Milan, P. Milica, Curr. Med. Chem. 16 (2009) 2177.10.2174/092986709788612729Search in Google Scholar PubMed

6. Y. Sueishi, S. Itami, Z. Phys. Chem. 217 (2003) 677.10.1524/zpch.217.6.677.20440Search in Google Scholar

7. J.-Z. Yang, J. Wang, Y. Yue, K. Zhuo, Z. Phys. Chem. 216 (2002) 1085.10.1524/zpch.2002.216.9.1085Search in Google Scholar

8. M. N. Roy, A. Roy, S. Saha, Carbohydr. Polym. 151 (2016) 458.10.1016/j.carbpol.2016.05.100Search in Google Scholar PubMed

9. C.-W. Lee, S.-J. Kim, Y.-S. Youn, E. Widjojokusumo, Y.-H. Lee, J. Kim, Y.-W. Lee, R. R. Tjandrawinata, J. Supercrit. Fluids 55 (2010) 348.10.1016/j.supflu.2010.05.028Search in Google Scholar

10. J. Szejtli, Chem. Rev. 98 (1998) 1743.10.1021/cr970022cSearch in Google Scholar PubMed

11. S. Amajjahe, S. Choi, M. Munteanu, H. Ritter, Angew. Chem. Int. Ed. 47 (2008) 3435.10.1002/anie.200704995Search in Google Scholar PubMed

12. B. Rajbanshi, S. Saha, K. Das, B. K. Barman, S. Sengupta, A. Bhattacharjee, M. N. Roy, Sci. Rep. 8 (2018) 13031.10.1038/s41598-018-31373-xSearch in Google Scholar PubMed PubMed Central

13. S. Saha, A. Roy, K. Roy, M. N. Roy, Sci. Rep. 6 (2016) 35764.10.1038/srep35764Search in Google Scholar PubMed PubMed Central

14. S. Saha, T. Ray, S. Basak, M. N. Roy, New J. Chem. 40 (2016) 651.10.1039/C5NJ02179KSearch in Google Scholar

15. N. Roy Mahendra, S. Barman, S. Saha, Z. Phys. Chem. 231 (2017) 1111.10.1515/zpch-2016-0804Search in Google Scholar

16. M. N. Roy, M. C. Roy, K. Roy, RSC Adv. 5 (2015) 56717.10.1039/C5RA09823HSearch in Google Scholar

17. H. Y. Wang, J. Han, X. G. Feng, Spectrochim. Acta. A Mol. Biomol. Spectrosc. 66 (2007) 578.10.1016/j.saa.2006.03.035Search in Google Scholar PubMed

18. M. N. Roy, S. Saha, M. Kundu, B. C. Saha, S. Barman, Chem. Phys. Lett. 655 (2016) 43.10.1016/j.cplett.2016.05.031Search in Google Scholar

19. P. Zhao, C. Xiong, H. Wang, Q. Cao, Z. Yang, Z. Phys. Chem. 228 (2014) 939.10.1515/zpch-2014-0552Search in Google Scholar

20. C. N. Sanramé, R. H. de Rossi, G. A. Argüello, J. Phys. Chem. 100 (1996) 8151.10.1021/jp953369xSearch in Google Scholar

21. F. Cramer, W. Saenger, H. C. Spatz, J. Am. Chem. Soc. 89 (1967) 14.10.1021/ja00977a003Search in Google Scholar

22. H. A. Benesi, J. H. Hildebrand, J. Am. Chem. Soc. 71 (1949) 2703.10.1021/ja01176a030Search in Google Scholar

23. Y. Honda, S. Fujitani, S. Tamaki, N. Inazumi, T. Hanaya, Y. Sueishi, Z. Phys. Chem. 230 (2016) 1153.10.1515/zpch-2015-0611Search in Google Scholar

24. P. K. Sambasevam, S. Mohamad, M. N. Sarih, A. N. Ismail, Int. J. Mol. Sci. 14 (2013) 3571.10.3390/ijms14023671Search in Google Scholar

25. J. Rak, D. Ondo, M. Tkadlecova, V. Dohnal, Z. Phys. Chem. 224 (2010) 893.10.1524/zpch.2010.5526Search in Google Scholar

26. Y. Sueishi, M. Ishikawa, M. Hori, N. Inazumi, Z. Phys. Chem. 227 (2013) 49.10.1524/zpch.2012.0233Search in Google Scholar

27. T. Bojinova, Y. Coppel, N. Lauth-de Viguerie, A. Milius, I. Rico-Lattes, A. Lattes, Langmuir 19 (2003) 5233.10.1021/la030030qSearch in Google Scholar

28. J. S. Negi, S. Singh, Carbohydr. Polym. 92 (2013) 1835.10.1016/j.carbpol.2012.11.082Search in Google Scholar PubMed

29. S. Milovanovic, D. Markovic, K. Aksentijevic, D. B. Stojanovic, J. Ivanovic, I. Zizovic, Carbohyd. Polym. 147 (2016) 344.10.1016/j.carbpol.2016.03.093Search in Google Scholar PubMed

30. R. Le Provost, T. Wille, L. Louise, N. Masurier, S. Muller, G. Reiter, P.-Y. Renard, O. Lafont, F. Worek, F. Estour, Org. Biomol. Chem. 9 (2011) 3026.10.1039/c0ob00931hSearch in Google Scholar PubMed

31. I. M. Abdulagatov, N. D. Azizov, Fluid Phase Equilib. 240 (2006) 204.10.1016/j.fluid.2005.12.036Search in Google Scholar

32. F. J. Millero, Chem. Rev. 71 (1971) 147.10.1021/cr60270a001Search in Google Scholar

33. D. Ekka, M. N. Roy, Amino Acids 45 (2013) 755.10.1007/s00726-013-1519-8Search in Google Scholar PubMed

34. M. N. Roy, K. Roy, K. Das, B. K. Barman, J. Mol. Liq. 216 (2016) 132.10.1016/j.molliq.2015.12.097Search in Google Scholar

35. M. N. Roy, D. Ekka, S. Saha, M. Chandra Roy, RSC Adv. 4 (2014) 42383.10.1039/C4RA07877BSearch in Google Scholar

36. S. Fang, D.-H. Ren, J. Chem. Eng. Data 58 (2013) 845.10.1021/je300953uSearch in Google Scholar


Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/zpch-2017-1020).


Received: 2018-08-09
Accepted: 2018-11-16
Published Online: 2018-12-07
Published in Print: 2019-08-27

©2019 Walter de Gruyter GmbH, Berlin/Boston

Downloaded on 16.3.2026 from https://www.degruyterbrill.com/document/doi/10.1515/zpch-2017-1020/html
Scroll to top button