电邮这篇文章 Features of complex formation of native and polymeric β-cyclodextrins with sulfasalazine
- 作者: Agafonov M.A1, Terekhova I.V1
-
隶属关系:
- G.A. Krestov Institute of Chemistry of Solutions of the Russian Academy of Sciences
- 期: 卷 93, 编号 5 (2023)
- 页面: 785-793
- 栏目: Articles
- URL: https://journals.rcsi.science/0044-460X/article/view/145054
- DOI: https://doi.org/10.31857/S0044460X2305013X
- EDN: https://elibrary.ru/DCOKWN
- ID: 145054
如何引用文章
开放存取
##reader.subscriptionAccessGranted##
订阅存取
详细
The work is devoted to the study of the complex formation of sulfasalazine with native and polymeric β-cyclodextrins in buffer solutions with a physiological pH value using isothermal saturation and 1H NMR methods. It was established that sulfasalazine forms two types of complexes when interacting with the cyclodextrins under consideration, but only the process of formation of inclusion complexes determines the observed increase in drug solubility, which is more pronounced in the presence of polymeric β-cyclodextrin. It was determined that complexation with β-cyclodextrin and its polymeric derivative leads to a decrease in the permeability coefficients of sulfasalazine through the model membrane, which is determined by both the stability constant of the complexes and their ability to pass through the membrane.
作者简介
M. Agafonov
G.A. Krestov Institute of Chemistry of Solutions of the Russian Academy of Sciences
I. Terekhova
G.A. Krestov Institute of Chemistry of Solutions of the Russian Academy of Sciences
Email: ivt@isc-ras.ru
参考
- Plosker G.L., Croom K.F. // Drugs. 2005. Vol. 65. N 13. P. 1825. doi: 10.2165/00003495-200565130-00008
- Gassull M.A., Cabre E. In: Crohn's Disease and Ulcerative Colitis / Ed. D.C. Baumgart. Berlin: Springer International Publishing AG, 2017. P. 311.
- Shadid M., Gurau G., Shamshina J.L., Chuang B.-C., Hailu S., Guan E., Chowdhury S.K., Wu J.-T., Rizvi S.A.A., Griffin R.J., Rogers R.D. // Med. Chem. Commun. 2015. Vol. 6. P. 1837. doi: 10.1039/C5MD00290G
- Куранов Д.Ю., Чибунова Е.С., Волкова Т.В., Терехова И.В. // Рос. хим. ж. 2016. Т. 60. № 1. С. 55
- Kuranov D.Yu., Chibunova E.S., Volkova T.V., Terekhova I.V. // Russ. J. Gen. Chem. 2018. Vol. 88. N 6. P. 1325. doi: 10.1134/S1070363218060439
- Shadid M., Gurau G., Shamshina J.L., Chuang B-C., Hailu S., Guan E., Chowdhury S., Wu J-T., Rizvi S.A.A., Griffin R. J., Rogers R. D. // Med. Chem. Commun. 2015. Vol. 6. P. 1837. doi: 10.1039/x0xx00000x
- Wu W-Y, Su C-S // J. Cryst. Growth. 2017. Vol. 460. P. 59. doi: 10.1016/j.jcrysgro.2016.12.017
- Chen X., Li D., Zhang H., Duan Y., Huang Y. // Mol. Pharm. 2022. Vol. 19. N 11. P. 4370. doi: 10.1021/acs.molpharmaceut.2c00785
- Orooji Y., Mortazavi-Derazkola S., Ghoreishi S.M., Amiri M., Salavati-Niasari M. // J. Hazard. Mater. 2020. Vol. 400. Article no. 123140. doi: 10.1016/j.jhazmat.2020.123140
- Jicsinszky L., Martina K. Cravotto G. // J. Drug Deliv. Sci. Technol. 2021. Vol. 64. Article no. 102589. doi: 10.1016/j.jddst.2021.102589
- Braga S.S. // J. Drug Deliv. Sci. Technol. 2022. Vol. 75. Article no. 103650. doi: 10.1016/j.jddst.2022.103650
- Asija R., Asija S., Lamba H.S., Bhandari A., Kataria S. // Res. J. Pharm. Technol. 2012. Vol. 5. N. 1. P. 53.
- Zhou Y.-Q., Huang J., Han P.-F., Lv X.-P. // Asian J. Chem. 2012. Vol. 24. N 5. P. 1991.
- Osman S.K., Soliman G.M., Amin M., Zaky A. // Int. J. Pharm. Pharm. Sci. 2014. Vol. 6. N 7. P. 59.
- Crini G. // Environ. Chem. Lett. 2021. Vol. 19. P. 2383. doi: 10.1007/s10311-021-01204-z
- Simões S.M.N., Rey-Rico A., Concheiro A., Alvarez-Lorenzo C. // Chem. Commun. 2015. Vol. 51. P. 6275. doi: 10.1039/C4CC10388B
- Folch-Cano C., Yazdani-Pedram M., Olea-Azar C. // Molecules. 2014. Vol. 19. N 9. P. 14066. doi: 10.3390/molecules190914066
- Shekhawat P.B., Pokharkar V.B. // Acta Pharm. Sin. (B). 2017. Vol. 7. N 3. P. 260. doi: 10.1016/j.apsb.2016.09.005
- Yang J., Li K., He D., Gu J., Xu J., Xie J., Zhang M., Liu Y., Tan Q. Zhang J. // Drug Metab. Rev. 2020. Vol. 52. P. 19. doi: 10.1080/03602532.2020.1714646
- Loftsson T., Vogensen S.B., Brewster M.E., Konráðsdóttir F. // J. Pharm. Sci. 2007. Vol. 96. N. 10. P. 2532. doi: 10.1002/jps.20992
- Loftsson T., Jarho P., Másson M. Järvinen T. // Expert Opin Drug Deliv. 2005. Vol. 2. N 2. P. 335-351. doi: 10.1517/17425247.2.1.335
- Dahan A., Beig A., Lindley D., Miller J.M. // Adv. Drug Deliv. Rev. 2016. Vol. 101. P. 99. doi: 10.1016/j.addr.2016.04.018
- Păduraru D.N., Niculescu A.-G., Bolocan A., Andronic O., Grumezescu A.M., Birla R. // Pharmaceutics. 2022. Vol. 14. N 8. P. 1748. doi: 10.3390/pharmaceutics14081748
- R. Periasamy // J. Carbohydr. Chem. 2021. Vol. 40. P. 135. doi: 10.1080/07328303.2021.1967970
- Higuchi T., Connons K.A. // Adv. Anal. Chem. Instrum. 1965. Vol. 4. P. 117.
- Jesus M.B, Fraceto L.F., Martini M.F., Pickholz M., Ferreira C.V., Paula E. // J. Pharm. Pharmacol. 2012. Vol. 64. N 6. P. 832. doi: 10.1111/j.2042-7158.2012.01492.x
- Terekhova I.V., Kumeev R.S., Alper G.A. // J. Incl. Phenom. Macrocycl. Chem. 2007. Vol. 59. P. 301. doi: 10.1007/s10847-007-9327-y
- Brandl M., Flaten G.E., Bauer-Brandl A. In: Wiley Encyclopedia of Chemical Biology / Ed. T.P. Begley. Hoboken: John Wiley & Sons, Inc., 2008. Р. 3204.
补充文件
