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Updated: May 12, 2026

Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery
Published on: September 26, 2025
Matrix type transdermal therapeutic system containing captopril: formulation optimization, in vitro and ex vivo
Oya Kerimoğlu1, Ebru Keskin, Betül Dortunç
1Faculty of Pharmacy, Department of Pharmaceutical Technology, Marmara University, 34668 Haydarpaşa, Istanbul, Turkey. osipahigil@marmara.edu.tr
New transdermal therapeutic systems (TTS) for captopril delivery were developed using Eudragit polymers. Two formulations (F15, F16) showed promising controlled release and diffusion profiles, indicating suitability for transdermal captopril administration.
Area of Science:
- Pharmaceutical Sciences
- Drug Delivery Systems
- Materials Science
Background:
- Transdermal drug delivery offers a non-invasive route for systemic medication.
- Captopril, an angiotensin-converting enzyme inhibitor, requires effective delivery systems for chronic conditions.
- Developing stable and efficient transdermal therapeutic systems (TTS) for captopril is crucial for patient compliance and therapeutic outcomes.
Purpose of the Study:
- To develop and characterize novel transdermal therapeutic systems (TTS) for captopril delivery.
- To evaluate the in vitro release kinetics and ex vivo diffusion profiles of captopril from the developed TTS.
- To identify optimal formulations suitable for transdermal captopril administration.
Main Methods:
- Synthesis and characterization of transdermal therapeutic systems (TTS) using Eudragit RL 100 and RS 100 polymers.
- Assessment of formulation properties including appearance, thickness, and captopril content.
- In vitro drug release studies and ex vivo diffusion studies using Franz diffusion cells across synthetic membranes and human skin.
Main Results:
- Successfully developed transdermal therapeutic systems (TTS) containing captopril with controlled release characteristics.
- Diffusion profiles were influenced by membrane properties (thickness, pore size, hydrophilicity/hydrophobicity) and formulation composition.
- Formulations F15 and F16 demonstrated favorable release and diffusion behavior.
Conclusions:
- Transdermal therapeutic systems (TTS) containing captopril were successfully prepared using pH-independent Eudragit polymers.
- The study identified specific formulations (F15 and F16) as highly suitable for transdermal captopril delivery.
- This research contributes to the advancement of non-invasive drug delivery methods for antihypertensive agents.
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