- PII
- 10.31857/S0044460X24090073-1
- DOI
- 10.31857/S0044460X24090073
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 94 / Issue number 9
- Pages
- 1000-1010
- Abstract
- A new type of silicone composites in the form of films containing sodium diclofenac were obtained, which can potentially be used as transdermal patches. Glycerol and propylene glycol analogues of tetraethoxysilane, tetrakis(2,3-dihydroxypropoxy)silane and tetrakis(2-hydroxypropoxy)silane, were first used to cure polydimethylsiloxane with terminal hydroxyl groups (PDMS-OH) to obtain silicone composites. It was shown that these cross-linking agents have a number of advantages over tetraethoxysilane.
- Keywords
- трансдермальные пленки сшивающие агенты натриевая соль диклофенака
- Date of publication
- 17.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 9
References
- 1. Haley R.M., von Recum H.A. // Exp. Biol. Med. 2019. Vol. 244. P. 433. doi 10.1177/1535370218787770
- 2. Blanca-Lopez N., Soriano V., Garcia-Martin E., Canto G., Blanca M. // J. Asthma Allergy. 2019. Vol. 12. P. 217. doi 10.2147/JAA.S164806
- 3. McGettigan P., Henry D. // PLoS Medicine. 2013. Vol. 10. N 2. P. 1. e1001388. doi 10.1371/journal.pmed.1001388
- 4. Davis A., Robson J. // British J. Gen. Pract. 2016. Vol. 66. P. 172. doi 10.3399/bjgp16X684433
- 5. Awachat A., Shukla D., Bhola N.D. // Cureus. 2022. Vol. 14. P. e30411. doi 10.7759/cureus.30411
- 6. Kapo S.M., Rakanović-Todić M., Burnazović-Ristić L., Kusturica J., Ćesić A.K., Ademović E., Aganović-Mušinović I. // J. King Saud Univ. Sci. 2023. Vol. 35. N 1. P. 102394. doi 10.1016/j.jksus.2022.102394
- 7. Snorradottir B.S., Gudnason P.I., Scheving R., Thorsteinsson F., Masson M. // Pharmazie. 2009. Vol. 64. P. 19. doi 10.1691/ph.2008.8206
- 8. Ailincai D., Dorobanțu A.M., Dima B., Irimiciuc Ș.A., Lupașcu C., Agop M., Olguta O. // J. Immunol. Res. 2020. P. 1. doi 10.1155/2020/3124304
- 9. Sa’adon S., Ansari M.N.M., Razak S.I.A., Anand J.S., Nayan N.H.M., Ismail A.E., Haider A. // Polymer. 2021. Vol. 15. P. 2459. doi 10.3390/polym13152459
- 10. Stewart S.A., Domínguez-Robles J., Donnelly R.F., Larrañeta E. // Polymer. 2018. Vol. 10. N 12. P. 1379. doi 10.3390/polym10121379
- 11. Soroory H., Mashak A., Rahimi A. // Iran. Polym. J. 2013. Vol. 22. P. 791. doi 10.1007/s13726-013-0178-7
- 12. Mashak A., Rahimi A. // Iran. Polym. J. 2009. Vol. 18. N 4. P. 279.
- 13. Mikolaszek B., Kazlauske J., Larsson A., Sznitowska M. // Polymer. 2020. Vol. 12. N 7. P. 1520. doi 10.3390/polym12071520
- 14. Gafar Ahmed M., AlHammad Z.A., Al-Jandan B. // Cureus. 2023. Vol. 15. N 2. P. e 34524.
- 15. Mojsiewicz-Pieńkowska K. // Handbook of Polymers for Pharmaceutical Technologies, 2015. Vol. 2. P. 363. doi 10.1002/9781119041412
- 16. Aliyar H., Schalau G. 2nd // Therapeutic Deliv. 2015. Vol. 6. N 7. P. 827. doi 10.4155/tde.15.39
- 17. Snorradottir B.S., Gudnason P.I., Scheving R., Thorsteinsson F., Masson M. // Pharmazie. 2009. Vol. 64. P. 19. https://doi.org/10.1691/ph.2008.8206
- 18. Malcolm R., McCullagh S., Woolfson A., Gorman S., Jones D., Cuddy J. // J. Control. Release. 2003. Vol. 97. P. 313. doi 10.1016/j.jconrel.2004.03.029
- 19. Mark J.E., Sullivan J.L. // J. Chem. Phys. 1977. Vol. 66. P. 1006. doi 10.1063/1.434056
- 20. Brook M.A., Holloway A.C., Kenneth K.N., Hrynyk M., Moore C., Ryan L. // Int. J. Pharm. 2008. Vol. 358. P. 121. doi 10.1016/j.ijpharm.2008.02.029
- 21. Soulas D.N., Sanopoulou M., Papadokostaki K.G. // Mater. Sci. Eng. 2013. Vol. C33. P. 2122. doi 10.1016/ j.msec.2013.01.031
- 22. Mark J.E., Jiang C.Y., Tang M.Y. // Macromolecules. 1984. Vol. 17. P. 2613. doi 10.1021/ma00142a026
- 23. Yuan Q.W., Mark J.E. // Macromol. Chem. Phys. 1999. Vol. 200. P. 206. doi 10.1002/(SICI)1521-3935(19990101) 200:1%3C206::AID-MACP206%3E3.0.CO;2-S
- 24. Robinson M.W.C., Swain A.C., Khan N.A. // Polym. Degrad. Stab. 2015. Vol. 116. P. 88. doi 10.1016/ j.polymdegradstab.2013.10.011
- 25. Rajendra V., Chen Y., Brook M.A. // Polym. Chem. 2010. Vol. 1. P. 312. doi 10.1039/B9PY00220K
- 26. Чупахин О.Н., Хонина Т.Г., Ларионов Л.П., Шадрина Е.В., Бойко А.А., Забокрицкий Н.А., Волков А.А. Пат. РФ 2382046 С1; Б. И. 2010. № 5
- 27. Atabekyan M.L., Farmazyan Z.M., Grigoryan S.G., Lavanant L., Topuzyan V.O. Pat. EU 4322906 (2024); Pat. JP2024514128A (2024).
- 28. Mazurek A., Brook M.A., Skov A.L. // Langmuir. 2018. Vol. 34. P. 11559. doi 0.1021/acs.langmuir.8b02039
- 29. Григорян С.Г., Акопян Э.А., Акобян Р.М., Фармазян З.М., Атабекян М.Л., Топузян В.О. // ЖОХ. 2023. Т. 93. № 8. С. 1281. doi 10.31857/S0044460X23080139; Grigoryan S.G., Hakopyan E.H., Hakobyan R.M., Farmazyan Z.M., Atabekyan M.L., Topuzyan V.O. // Russ. J. Gen. Chem. 2023. Vol. 93. N 8. P. 2048. doi 10.1134/S1070363223080133
- 30. Mercier K., Brule Th., Fromentoux L. Quality control of sugar content in beverages using Raman spectroscopy. https://www.horiba.com/