Inclusion Complex of Gd(III) with β-Cyclodextrin and L-Tryptophan

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

An inclusion complex of gadolinium(III) with L-tryptophan (Trp) and β-cyclodextrin (β-CD) with the composition Gd(Trp)3Cl3∙3β-CD∙nH2O was synthesized. It was established that the complex is formed due to the entry of the aromatic part of the L-Trp molecule into the β-CD cavity, and the Gd3+ ions are located in the outer sphere.

Full Text

Restricted Access

About the authors

S. S. Khasaeva

Kuban State University

Author for correspondence.
Email: justchemist@mail.ru
ORCID iD: 0000-0002-8462-8801
Russian Federation, Krasnodar, 350040

N. N. Bukov

Kuban State University

Email: justchemist@mail.ru
ORCID iD: 0000-0001-8559-110X
Russian Federation, Krasnodar, 350040

S. N. Ivanin

Kuban State University

Email: justchemist@mail.ru
ORCID iD: 0000-0001-9352-5970
Russian Federation, Krasnodar, 350040

S. L. Kuznetsova

Kuban State University

Email: justchemist@mail.ru
ORCID iD: 0009-0000-8868-0730
Russian Federation, Krasnodar, 350040

E. L. Isaeva

Chechen State University named after A. A. Kadyrov

Email: justchemist@mail.ru
ORCID iD: 0000-0001-8403-5240
Russian Federation, Grozny, 364024

References

  1. Ahmad K., Khan M.Q., Khan R.A., Kim H. // Mater. Chem. Phys. 2022. Vol. 287. P. 126297. doi 10.1016/ j.matchemphys.2022.126297
  2. Garrido M., Rodríguez A.B., Terrón M.P. // Aging: Oxidative Stress and Dietary Antioxidants. 2014. P. 129. doi: 10.1016/B978-0-12-405933-7.00013-5
  3. Болотин С.Н., Буков Н.Н., Волынкин В.А., Панюшкин В.Т. Координационная химия природных аминокислот. M.: LKI, 2008. С. 240.
  4. Kowalska-Baron A. // Comput. Theor. Chem. 2015. Vol. 1057. P. 7. doi: 10.1016/j.comptc.2015.01.010
  5. Löbmann K., Grohganz H., Laitinen R., Strachan C., Rades T. // Eur. J. Pharm. Biopharm. 2013. Vol. 85. P. 873. doi: 10.1016/j.ejpb.2013.03.014
  6. Ляшенко Д.Ю. // Поверхность. 2018. Т. 25. Вып. 10. С. 153. doi: 10.15407/Surface.2018.10.154
  7. Zarzycki P.K., Fenert B., Głód B.K. // Encapsulations. 2016. Vol. 2. P. 717. doi: 10.1016/B978-0-12-804307-3.00017-X
  8. Roy M.N., Roy A., Saha S. // Carbohydr. Polym. 2016. Vol. 151. P. 458. doi: 10.1016/j.carbpol.2016.05.100
  9. Nishijo J., Tsuchitani M. // J Pharm Sci. 2001. Vol. 90. P. 134. doi: 10.1002/1520-6017(200102)90:2<134::AID-JPS4>3.0.CO;2-T
  10. Shanmugama M., Ramesh D., Nagalakshmi V., Kavitha R., Rajamohan R., Stalin T. // Spectrochim. Acta (A). 2008. Vol. 71. P. 125. doi: 10.1016/j.saa.2007.10.054
  11. Caso J.V., Russo L., Palmieri M., Malgieri G., Galdiero S., Falanga A.,Isernia C., Iacovino R. // Amino Acids. 2015. Vol. 47. P. 2215. doi: 10.1007/s00726-015-2003-4
  12. Song L.X., Teng C.F., Yang Y. // J. Incl. Phenom. Macrocycl. Chem. 2006. Vol. 54. P. 221. doi: 10.1007/s10847-005-7970-8
  13. Xie G., Tian W., Wen L., Xiao K., Zhang Z., Liu Q., Hou G., Li P., Tiana Y., Jiang L. // ChemCommun. 2015. Vol. 51. P. 3135. doi: 10.1039/C4CC09577D
  14. Esmaeilpour D., Shityakov S., Tamaddon A.M., Bordbar A.K. // Carbohydr. Polym. 2021. Vol. 262. P. 117868. doi: 10.1016/j.carbpol.2021.117868
  15. Akita T., Matsui Y., Yamamoto T. // J. Mol. Struct.2014. Vol. 1060. P. 138. doi: 10.1016/j.molstruc.2013.12.020
  16. Liu Y., Han B.-H., Li B., Zhang Y.-M., Zhao P., Chen Y.-T., Wada T., Inoue Y. // J. Org. Chem. 1998. Vol. 63. P. 1444. doi: 10.1021/jo971466b
  17. Norkus E. // J. Incl. Phenom. Macrocycl. Chem. 2009. Vol. 65.P. 237. doi: 10.1007/s10847-009-9586-x
  18. Braga S.S., Ferreira R.A., Goncalves I.S., Pillinger M., Rocha J., Teixeira-Dias J.J.C., Carlos L.D. // J. Phys. Chem. (B). 2002. Vol. 106. P. 11430. doi: 10.1021/jp0204004
  19. Ribeiro A.O., Serra O.A. // J. Braz. Chem. Soc. 2007. Vol. 18. P. 273. doi: 10.1590/S0103-50532007000200005
  20. Brown S.E., Coates J.H., Easton Ch.J., Eyk S.J., Lincoln S.F., May B.L., Stile M.A., Whalland C.B., Williams M.L. // J. Chem. Soc. Chem. Commun. 1994. P. 47. doi: 10.1039/C39940000047
  21. Shojaei M., Pirouzmanda M., Khatamiana M., Azizi S., Soleymani J. // J. Mol. Struct. 2023. Vol. 1275. P. 134659. doi: 10.1016/j.molstruc.2022.134659
  22. Gao Z.-W., Zhao X.-P. // J. Colloid Interface Sci. 2005. Vol. 289. P. 56. doi: 10.1016/j.jcis.2005.03.027
  23. Phan T.N.T., Bacquet M., Laureyns J., Morcellet M. // Phys. Chem. Chem. Phys. 1999. Vol. 1. P. 5189. doi: 10.1039/A905713G
  24. Cao X., Fischer G. // J. Phys. Chem. (A). 1999. Vol. 103. P. 9995. doi: 10.1021/jp992421c
  25. Тен Г.Н., Глухова О.Е., Слепченков М.М., Щербакова Н.Е., Баранов В.И. // Изв. Сарат. унив. Нов. сер. Сер. Физика. 2017. Т. 17. Вып. 1. С. 20. doi: 10.18500/1817-3020-2017-17-1-20-32
  26. Mohandoss S., Ahmad N., Khan M.R., Lee Y.R. // J. Mol. Liq. 2023. Vol. 385. P. 122411. doi: 10.1016/j.molliq.2023.12241127
  27. Mazur M., Poprac P., Valko M., Rhodes C.J. // J. Sol-Gel Sci. Technol. 2016. Vol. 79. P. 220. doi: 10.1007/s10971-016-4014-3
  28. Rada S., Chelcea R., Culea M., Culea E. // J. Mater. Sci. 2011. Vol. 46. P. 1289. doi: 10.1007/s10853-010-4913-6
  29. Iwamoto W., Vargas J.M., Holanda Jr. L.M., Alves E., Moreno M.S., Oseroff S.B., Paglius P.G., Rettori C. // J. Nanosci. Nanotechnol. 2010. Vol. 10. P. 1. doi: 10.1166/jnn.2010.2438

Supplementary files

Supplementary Files
Action
1. JATS XML
Download
2. Fig. 1. Thermogram of the β-cyclodextrin inclusion complex with gadolinium(III) and L-tryptophan.

Download (185KB)
Indexing metadata
3. Fig. 2. IR spectra of GdTrp, β-CD, inclusion complex (GdTrp/β-CD).

Download (188KB)
Indexing metadata
4. Fig. 3. Schematic representation of a fragment of the proposed inclusion complex.

Download (58KB)
Indexing metadata
5. Fig. 4. Diffractogram of the inclusion complex (GdTrp/β-CD), β-CD, Trp, GdCl3×6H2O.

Download (226KB)
Indexing metadata
6. Fig. 5. EPR spectrum of the Gd(Trp)3Cl3*3β-CD*nH2O inclusion complex.

Download (76KB)
Indexing metadata

Copyright (c) 2024 Russian Academy of Sciences

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies