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Bioactive silicon-iron-containing glycerohydrogel synthesized by the sol—gel method in the presence of chitosan

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Abstract

A novel biologically active nanocomposite glycerohydrogel based on two biocompatible precursors, silicon and iron glycerolates, was synthesized by the sol—gel method in the presence of chitosan (Ch). The composition and structural features of the gel were characterized by advanced analytical methods including transmission electron microscopy, X-ray diffraction, and atomic emission spectroscopy. It was shown that iron(iii) monoglycerolate undergoes partial hydrolysis under the gelation conditions and exists as a separate nanoscale phase along with the hydrolysis products in cells of the 3D Si-containing polymeric gel network. This network is formed as a result of incomplete hydrolysis of silicon glycerolates in excess glycerol followed by homo- and heterofunctional condensation of silanol groups with the formation of Si-O-Si units containing residual glyceroxy groups at the silicon atom. Chitosan forms numerous intermolecular bonds with the 3D gel network, accelerates the process of gelation, makes the gel morphostructure more ordered, and increases the stability of the gel. The Si-Fe-Ch-containing glycerohydrogel is nontoxic and possesses hemostatic and wound-healing activity, being a promising topical medication for medical and veterinary practice.

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Authors and Affiliations

  1. I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 ul. S. Kovalevskoy, 620990, Ekaterinburg, Russian Federation

    T. G. Khonina, D. S. Tishin, E. V. Shadrina, E. Yu. Nikitina & O. N. Chupakhin

  2. Ural State Agrarian University, 42 ul. K. Libknekhta, 620075, Ekaterinburg, Russian Federation

    T. G. Khonina

  3. Ural State Medical University of the Ministry of Health of the Russian Federation, 3 ul. Repina, 620219, Ekaterinburg, Russian Federation

    L. P. Larionov, M. N. Dobrinskaya, I. P. Antropova, N. V. Izmozherova & A. V. Osipenko

  4. Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 91 ul. Pervomayskaya, 620990, Ekaterinburg, Russian Federation

    E. A. Bogdanova

  5. Institute of Chemical Engineering, Ural Federal University named after the first President of Russia B. N. Yeltsin, 19 ul. Mira, 620002, Ekaterinburg, Russian Federation

    M. S. Karabanalov & O. N. Chupakhin

  6. Ural Research Institute for Dermatology, Venereology, and Immunopathology, 8 ul. Shcherbakova, 620076, Ekaterinburg, Russian Federation

    N. P. Evstigneeva & M. M. Kokhan

Authors
  1. T. G. Khonina
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  2. D. S. Tishin
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  7. A. V. Osipenko
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  8. E. V. Shadrina
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  9. E. Yu. Nikitina
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  10. E. A. Bogdanova
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  11. M. S. Karabanalov
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  14. O. N. Chupakhin
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Corresponding author

Correspondence to T. G. Khonina.

Additional information

This work was carried out under the financial support from the Russian Science Foundation (Project No. 22-23-20032) and from the Government of the Sverdlovsk Region using the equipment of the “Modern Nanotechnologies” Center for Joint Use at the Ural Federal University and the “Spectroscopy and Analysis of Organic Compounds” Center for Joint Use at the I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences. Powder X-ray diffraction and electron microscopy studies were carried out within the framework of the State Programs of the Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences and the Ural Federal University, respectively.

No human or animal subjects were used in this research.

The authors declare no competing interests.

Based on the materials of the V Russian Conference on Medicinal Chemistry with international participation “MedChem-Russia 2021” (May 16–19, 2022, Volgograd, Russia).

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2342–2351, November, 2022.

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Khonina, T.G., Tishin, D.S., Larionov, L.P. et al. Bioactive silicon-iron-containing glycerohydrogel synthesized by the sol—gel method in the presence of chitosan. Russ Chem Bull 71, 2342–2351 (2022). https://doi.org/10.1007/s11172-022-3661-5

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  • DOI: https://doi.org/10.1007/s11172-022-3661-5

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