Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid
Ionic liquids (ILs) have been proven to be an efficient technology for enhancing drug skin permeability. However, the question of whether the two components of ILs are released synchronously in transdermal preparations has remained unclear. Thus, this study aimed to investigate the release character...
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MDPI AG
2022-10-01
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Online Access: | https://www.mdpi.com/1999-4923/14/10/2158 |
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author | Degong Yang Xuejun Chen Ziqing Li Chunrong Yang |
author_facet | Degong Yang Xuejun Chen Ziqing Li Chunrong Yang |
author_sort | Degong Yang |
collection | DOAJ |
description | Ionic liquids (ILs) have been proven to be an efficient technology for enhancing drug skin permeability. However, the question of whether the two components of ILs are released synchronously in transdermal preparations has remained unclear. Thus, this study aimed to investigate the release characteristics of two components of ILs and their underlying molecular mechanism. The ILs containing flurbiprofen (FLU) and lidocaine (LID) were synthesized and characterized. The four typical acrylates pressure sensitive adhesives (PSAs) with different functional groups were synthesized and characterized. The effects of PSAs on the release characteristics of two components of ILs were investigated by drug release tests and verified by skin permeation experiments. The action mechanisms were revealed by FTIR, Raman, dielectric spectrum, and molecular docking. The results showed that the average release amount of FLU (0.29 μmol/cm<sup>2</sup>) and LID (0.11 μmol/cm<sup>2</sup>) of ILs in the four PSAs was significantly different (<i>p</i> < 0.05), which illustrated that the two components did not release synchronously. The PSA−none and PSA−OH with low permittivity (7.37, 9.82) interacted with drugs mainly by dipole-dipole interactions and hydrogen bonds. The PSA−COOH and PSA−CONH<sub>2</sub> with high permittivity (11.19, 15.32) interacted with drugs mainly by ionic bonds and ionic hydrogen bonds. Thus, this study provides scientific guidance for the application of ILs in transdermal preparations. |
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issn | 1999-4923 |
language | English |
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spelling | doaj.art-c0d645006e5f47e0aa14694026df6c412023-11-24T01:57:13ZengMDPI AGPharmaceutics1999-49232022-10-011410215810.3390/pharmaceutics14102158Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic LiquidDegong Yang0Xuejun Chen1Ziqing Li2Chunrong Yang3Department of Pharmacy, Shantou University Medical College, No. 22 Xinling Road, Shantou 515041, ChinaDepartment of Pharmacy, Shantou University Medical College, No. 22 Xinling Road, Shantou 515041, ChinaDepartment of Pharmacy, Shantou University Medical College, No. 22 Xinling Road, Shantou 515041, ChinaDepartment of Pharmacy, Shantou University Medical College, No. 22 Xinling Road, Shantou 515041, ChinaIonic liquids (ILs) have been proven to be an efficient technology for enhancing drug skin permeability. However, the question of whether the two components of ILs are released synchronously in transdermal preparations has remained unclear. Thus, this study aimed to investigate the release characteristics of two components of ILs and their underlying molecular mechanism. The ILs containing flurbiprofen (FLU) and lidocaine (LID) were synthesized and characterized. The four typical acrylates pressure sensitive adhesives (PSAs) with different functional groups were synthesized and characterized. The effects of PSAs on the release characteristics of two components of ILs were investigated by drug release tests and verified by skin permeation experiments. The action mechanisms were revealed by FTIR, Raman, dielectric spectrum, and molecular docking. The results showed that the average release amount of FLU (0.29 μmol/cm<sup>2</sup>) and LID (0.11 μmol/cm<sup>2</sup>) of ILs in the four PSAs was significantly different (<i>p</i> < 0.05), which illustrated that the two components did not release synchronously. The PSA−none and PSA−OH with low permittivity (7.37, 9.82) interacted with drugs mainly by dipole-dipole interactions and hydrogen bonds. The PSA−COOH and PSA−CONH<sub>2</sub> with high permittivity (11.19, 15.32) interacted with drugs mainly by ionic bonds and ionic hydrogen bonds. Thus, this study provides scientific guidance for the application of ILs in transdermal preparations.https://www.mdpi.com/1999-4923/14/10/2158transdermal patchionic liquidsrelease characteristicshydrogen bondionic hydrogen bond |
spellingShingle | Degong Yang Xuejun Chen Ziqing Li Chunrong Yang Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid Pharmaceutics transdermal patch ionic liquids release characteristics hydrogen bond ionic hydrogen bond |
title | Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid |
title_full | Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid |
title_fullStr | Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid |
title_full_unstemmed | Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid |
title_short | Mechanistic Study of Release Characteristics of Two Active Ingredients in Transdermal Patch Containing Lidocaine−Flurbiprofen Ionic Liquid |
title_sort | mechanistic study of release characteristics of two active ingredients in transdermal patch containing lidocaine flurbiprofen ionic liquid |
topic | transdermal patch ionic liquids release characteristics hydrogen bond ionic hydrogen bond |
url | https://www.mdpi.com/1999-4923/14/10/2158 |
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