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Study of the Structure of Chitosan Succinate Bombyx mori

Received: 5 October 2017    Accepted: 9 November 2017    Published: 1 December 2017
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Abstract

The first time water solubility derivates of chitosan Bombyx mori was obtain. By FTIR method it was established the fact of formation of chitosan succinate. Influence of synthesis condition to structure of chitosan succinate was shown. It is revealed that, gel formation of chitosan succinate depend on the formation of both polyelectrolytic complex and covalent bonds.

Published in American Journal of Applied Chemistry (Volume 5, Issue 6)
DOI 10.11648/j.ajac.20170506.12
Page(s) 96-100
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Chitosan Bombyx mori, Succinate Chitosan, Sodium-Succinate, Succinate Anhydride

References
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[2] Hatim S. Al Khatib, Khaled M. Aiedeh, Yasser Bustanji, Saja Hamed, M. K. Mohammad, Bashar AlKhalidi, Samer Najjar. Modulation of buspirone HCl release from hypromellose matrices using chitosan succinate: Implications for pH-independent release. European Journal of Pharmaceutics and Biopharmaceutics 70 (2008) 804–812.
[3] Mamasoliev U. M., Vokhidova N. R., Rashidova S. Sh. Study of the interaction of chitosan Bombyx mori succinate with anhydride in aqueous solutions. Republican Scientific and Practical Conference, Urgench, 2017. P. 9-10.
[4] К. Noerati, Cynthia L. Radiman, Sadijah Achmad, I. Made Arcana Synthesis chitosan succinate as environmentally anti bacterial and crease resistant agent on cotton // Proceeding of The International Seminar on Chemistry 2008 (pp. 703-708) Jatinangor, 30-31 October 2008.
[5] Chengyun Yan, et. al Preparation of N-Succinyl-chitosan and Their Physical-Chemical Properties as a Novel excipient // YAKUGAKU ZASSHI 126(9) 789-793 (2006) The Pharmaceutical Society of Japan.
[6] Hatim S. Al Khatib, Khaled M. Aiedeh, Yasser Bustanji, Saja Hamed, M. K. Mohammada, Bashar AlKhalidi, Samer Najjar Modulation of buspirone HCl release from hypromellose matrices using chitosan succinate: Implications for pH-independent release // European Journal of Pharmaceutics and Biopharmaceutics 70 (2008) 804—812 pp.
[7] Sui, W., Wang, Y., Dong, S, et al. (2008) Preparation and Properties of an Amphiphilic Derivative of Succinyl- Chitosan. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 316,171-175. http://dx.doi.org/10.1016/j.colsurfa.2007.09.016
[8] Zhu, A.P., Chen, T., Yuan, L. H., Wu, H. and Lu, P. (2006) Synthesis and Characterization of N-Succinyl-Chitosan and Its Self-Assembly of Nanospheres. Carbohydrate Polymers, 66, 274-279. http://dx.doi.org/10.1016/j.carbpol.2006.03.014
[9] Kato, Y., Onishi, H. and Machida, Y. (2001) Biological Characteristics of Lactosaminated N- Succinyl-Chitosan as a Liver-Specific Drug Carrier in Mice. Journal of Controlled Release, 70, 295-307. http://dx.doi.org/10.1016/S0168-3659(00)00356-4.
[10] Kato, Y., Onishi, H. and Machida, Y. (2001) Lactosaminated and Intact N-Succinyl-Chitosans as Drug Carriers in Liver Metastasis. International Journal of Pharmaceutics, 226, 93-106. http://dx.doi.org/10.1016/S0378-5173(01)00777-3.
[11] K. M. Aiedeh, M. O. Taha, H. Al-Khatib, Evaluation of chitosan succinate and chitosan phthalate as enteric coating polymers for diclofenac sodium tablets, J. Drug Deliv. Sci. Tec. 15 (3) (2005) 207–211.
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[13] Khaled Aiedeh, Mutasem O. Taha, Synthesis of chitosan succinate and chitosan phthalate and their evaluation as suggested matrixes in orally administered colon-specific drug delivery systems, Arch. Pharm. 332 (3) (1999) 103–107.
[14] Udhumansha Ubaidulla, Roop Kishan Khar, Fahan Jalees Ahmad, Yasmin Sultana, Amulya Kumar Panda, Development and characterization of chitosan succinate microspheres for the improved oral bioavailability of insulin, J. Pharm. Sci. 96 (11) (2007) 3010–3023.
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[16] Noerati К., Cynthia L. Radiman, Sadijah Achmad, I. Made Arcana Synthesis chitosan succinate as environmentally anti bacterial and crease resistant agent on cotton // Proceeding of The International Seminar on Chemistry 2008 Jatinangor, 30-31 October 2008. pp. 703-708.
[17] Chengyun Yan, et. al Preparation of N-Succinyl-chitosan and Their Physical-Chemical Properties as a Novel excipient // Yakugaku Z AS Shi 126(9) 789-793 (2006) The Pharmaceutical Society of Japan.
[18] Hatim S. Al Khatib, Khaled M. Aiedeh, Yasser Bustanji, Saja Earned, M. K. Mohammada, Bashar AlKhalidi, Samer Najjar Modulation of buspirone HCl release from hypromellose matrices using chitosan succinate: Implications for pH-independent release //European Journal of Pharmaceutics and Biopharmaceutics. (2008) 804-812.
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  • APA Style

    N. R. Vokhidova, U. M. Mamasoliev, S. M. Yugay, S. Sh. Rashidova. (2017). Study of the Structure of Chitosan Succinate Bombyx mori. American Journal of Applied Chemistry, 5(6), 96-100. https://doi.org/10.11648/j.ajac.20170506.12

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    ACS Style

    N. R. Vokhidova; U. M. Mamasoliev; S. M. Yugay; S. Sh. Rashidova. Study of the Structure of Chitosan Succinate Bombyx mori. Am. J. Appl. Chem. 2017, 5(6), 96-100. doi: 10.11648/j.ajac.20170506.12

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    AMA Style

    N. R. Vokhidova, U. M. Mamasoliev, S. M. Yugay, S. Sh. Rashidova. Study of the Structure of Chitosan Succinate Bombyx mori. Am J Appl Chem. 2017;5(6):96-100. doi: 10.11648/j.ajac.20170506.12

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  • @article{10.11648/j.ajac.20170506.12,
      author = {N. R. Vokhidova and U. M. Mamasoliev and S. M. Yugay and S. Sh. Rashidova},
      title = {Study of the Structure of Chitosan Succinate Bombyx mori},
      journal = {American Journal of Applied Chemistry},
      volume = {5},
      number = {6},
      pages = {96-100},
      doi = {10.11648/j.ajac.20170506.12},
      url = {https://doi.org/10.11648/j.ajac.20170506.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajac.20170506.12},
      abstract = {The first time water solubility derivates of chitosan Bombyx mori was obtain. By FTIR method it was established the fact of formation of chitosan succinate. Influence of synthesis condition to structure of chitosan succinate was shown. It is revealed that, gel formation of chitosan succinate depend on the formation of both polyelectrolytic complex and covalent bonds.},
     year = {2017}
    }
    

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    T1  - Study of the Structure of Chitosan Succinate Bombyx mori
    AU  - N. R. Vokhidova
    AU  - U. M. Mamasoliev
    AU  - S. M. Yugay
    AU  - S. Sh. Rashidova
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    N1  - https://doi.org/10.11648/j.ajac.20170506.12
    DO  - 10.11648/j.ajac.20170506.12
    T2  - American Journal of Applied Chemistry
    JF  - American Journal of Applied Chemistry
    JO  - American Journal of Applied Chemistry
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    PB  - Science Publishing Group
    SN  - 2330-8745
    UR  - https://doi.org/10.11648/j.ajac.20170506.12
    AB  - The first time water solubility derivates of chitosan Bombyx mori was obtain. By FTIR method it was established the fact of formation of chitosan succinate. Influence of synthesis condition to structure of chitosan succinate was shown. It is revealed that, gel formation of chitosan succinate depend on the formation of both polyelectrolytic complex and covalent bonds.
    VL  - 5
    IS  - 6
    ER  - 

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Author Information
  • Institute of Polymer Chemistry and Physics Uzbekistan, Academy of Sciences, Tashkent, Uzbekistan

  • Institute of Polymer Chemistry and Physics Uzbekistan, Academy of Sciences, Tashkent, Uzbekistan

  • Institute of Polymer Chemistry and Physics Uzbekistan, Academy of Sciences, Tashkent, Uzbekistan

  • Institute of Polymer Chemistry and Physics Uzbekistan, Academy of Sciences, Tashkent, Uzbekistan

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