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Updated: Feb 27, 2026

Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery
Published on: September 26, 2025
Dermal and transdermal delivery of pharmaceutically relevant macromolecules
S Münch1, J Wohlrab2, R H H Neubert3
1Institute of Applied Dermatopharmacy (IADP), Martin Luther University Halle-Wittenberg, Halle/Saale, Germany.
Transdermal drug delivery faces challenges with large molecules. This review explores physical, chemical, and biological methods to enhance macromolecule penetration through the skin's stratum corneum for effective therapeutic administration.
Area of Science:
- Dermal and transdermal drug delivery
- Biomedical engineering
- Pharmaceutical sciences
Background:
- The skin's stratum corneum presents a significant barrier to drug delivery, particularly for macromolecules.
- Conventional transdermal delivery is limited to small molecules (≤1kDa) with specific lipophilicity and polarity.
- Macromolecules typically do not penetrate human skin without assistance, limiting therapeutic options.
Purpose of the Study:
- To review and evaluate various methods for enhancing dermal and transdermal delivery of macromolecules.
- To discuss physical, chemical, and biological approaches to overcome the skin barrier.
- To assess the potential of these methods for effective therapeutic administration of large molecules.
Main Methods:
- Physical methods: microneedles, microjets, lasers, electroporation, sonophoresis, iontophoresis.
- Chemical methods: penetration enhancers.
- Biological methods: peptides.
Main Results:
- Microneedles create skin micropores for macromolecule delivery.
- Other physical methods like electroporation and sonophoresis show promise.
- Penetration enhancers and biological peptides offer alternative strategies for macromolecule transport.
Conclusions:
- Multiple advanced techniques exist to facilitate macromolecule transdermal delivery.
- These methods hold potential for improving therapeutic efficacy by enabling the delivery of larger drug molecules.
- Further evaluation is needed to optimize and implement these strategies for clinical use.
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