| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2083578 | European Journal of Pharmaceutics and Biopharmaceutics | 2014 | 7 Pages |
•Transdermal delivery of ACE inhibitors.•Five ACE inhibitors extensively studied.•Potential irritancy, physicochemical properties, potency, stability are key issues.
The Angiotensin Converting Enzyme (ACE) inhibitor class of drugs has been in clinical use since the 1970s for the management of all grades of heart failure, hypertension, diabetic nephropathy and prophylaxis of cardiovascular events. Because of the advantages associated with transdermal delivery compared with oral delivery many researchers have investigated the skin as a portal for administration of ACE inhibitors. This review summarises the various studies reported in the literature describing the development and evaluation of transdermal formulations of ACE inhibitors. Captopril, enalapril maleate, lisinopril dihydrate, perindopril erbumine and trandolapril are the most studied in connection with transdermal preparations. The methodologies reported are considered critically and the limitations of the various skin models used are also highlighted. Finally, opportunities for novel transdermal preparations of ACE inhibitor drugs are discussed with an emphasis on rational formulation design.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (72 K)Download as PowerPoint slide
