CITRUS PECTIN COMPLEXES WITH NIFEDIPINE: PREPARATION AND PHYSICOCHEMICAL PROPERTIES

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Abstract

The formation of stable complexes of pectin polysaccharides with the hypotensive drug “Nifedipine” was confirmed by IR and UV spectroscopy, their stoichiometry was determined and the conditions of their production were optimized. Peculiarities of thermal decomposition of pectin and synthesized complexes with nifedipine were studied by TGA/DSC method. The results obtained are a scientific basis for the creation of a new water-soluble non-toxic dosage form of nifedipine, which will significantly expand the use of the drug in medicine.

About the authors

S. T. Minzanova

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Author for correspondence.
Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

E. V. Chekunkov

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

A. V. Khabibullina

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

D. M. Arkhipova

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

L. G. Mironova

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

A. R. Hamatgalimov

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

V. A. Milyukov

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

V. F. Mironov

Arbuzov Institute of Organic and Physical Chemistry, “Kazan Scientific Center of Russian Academy of Sciences”

Email: minzanova@iopc.ru
Russian Federation, 420111, Kazan

References

  1. Лекарственные средства. Машковский М.Д. (ред.). М.: Новая Волна, 2012. 1216 с.
  2. Квачахия Л.Л., Шорманов В.К. // Вест. нов. мед. техн. 2018. Т. 25. № 1. С. 71–78. https://doi.org/10.24411/1609-2163-2018-15943
  3. Кукес В.Г., Сычев Д.А. // Рацион. Фарм. Кардиол. 2006. № 1. С. 49–54. https://doi.org/10.20996/1819-6446-2006-2-1-49-54
  4. De R., Mahata M.K., Kim K.-T. // Adv. Sci. 2022. V. 9. Art. 2105373. https://doi.org/10.1002/advs.202105373
  5. Weerapol Y., Limmatvapirat S., Nunthanid J., Konthong S., Suttiruengwong S., Sriamornsak P. // Asian J. Pharm. Sci. 2017. V. 12. P. 335–343. https://doi.org/10.1016/j.ajps.2017.01.002
  6. Yang Y.Q., Lin W.J., Zhao B., Wen X.F., Guo X.D., Zhang L.J. // Langmuir. 2012. V. 28. P. 8251–8259. https://doi.org/10.1021/la301099q
  7. Li D.-Q., Li J., Dong H.-L., Li X., Zhang J.-Q., Ramaswamy S., Xu F. // Int. J. Biol. Macromol. 2021. № 185. P. 49–65. https://doi.org/10.1016/j.ijbiomac.2021.06.088
  8. Taokaew S., Ofuchi M., Kobayashi T. // Sustain. Chem. Pharm. 2020. V. 17. Art. 100284. https://doi.org/10.1016/j. scp.2020.100284
  9. Chekunkov Y.V., Minzanova S.T., Khabibullina A.V., Arkhipova D.M., Mironova L.G., Nemtarev A.V., Khamatgalimov A.R., Gubaidullin A.T., Milyukov V.A. // Russ. Chem. Bull. 2020. V. 69. № 3. P. 572–580. https://doi.org/10.1007/s11172-020-2801-z
  10. Kim H., Fassihi R. // J. Pharm. Sci. 1997. V. 86. № 3. P. 323–328. https://doi.org/10.1021/js960307p
  11. Bektaş A., Cevher E., Güngör S., Özsoy Y. // Chem. Pharm. Bull. 2014. V. 62. № 2. P. 144–152. https://doi.org/10.1248/cpb.c13-00579
  12. Bashir S., Asad M., Qamar S., Hassnain F., Karim S., Nazir I. // Trop. J. Pharm. Res. 2014. V. 13. № 4. P. 505–510. https://doi.org/10.4314/tjpr.v13i4.3
  13. Ajaz N., Khalid I., Minhas M.U., Barkat K., Khan I.U., Syed H.K., Asghar S., Munir R., Aslam F. // Polymer Bull. 2020. V. 77. P. 6063–6083. https://doi.org/10.1007/s00289-019-03065-7
  14. Horvat G., Pantić M., Knez Ž., Novak Z. // J. Non-Crystal. Solids. 2018. V. 481. P. 486–493. https://doi.org/10.1016/j.jnoncrysol.2017.11.037
  15. Khvostov M.V., Chernonosov A.A., Borisov S.A., Boriso-va M.S., Meteleva E.S., Evseenko V.I., Polyakov N.E, Dushkin A.V., Tolstikova T.G. // Therapeutic Delivery. 2021. V. 12. № 2. P. 119–131. https://doi.org/10.4155/tde-2020-0115
  16. Гурьянова Е.Н., Гольдштейн И.П., Ромм И.П. Донорно-акцепторная связь. М.: Химия, 1973. 400 с.

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Copyright (c) 2023 С.Т. Минзанова, Е.В. Чекунков, А.В. Хабибуллина, Д.М. Архипова, Л.Г. Миронова, А.Р. Хаматгалимов, В.А. Милюков, В.Ф. Миронов