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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Main Authors: Degong Yang, Xuejun Chen, Ziqing Li, Chunrong Yang
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Pharmaceutics
Subjects:
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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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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AT ziqingli mechanisticstudyofreleasecharacteristicsoftwoactiveingredientsintransdermalpatchcontaininglidocaineflurbiprofenionicliquid
AT chunrongyang mechanisticstudyofreleasecharacteristicsoftwoactiveingredientsintransdermalpatchcontaininglidocaineflurbiprofenionicliquid