The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Overcoming the Stratum Corneum: The Modulation of Skin Penetration
Abstract
It is preferred that topically administered drugs act either dermally or transdermally. For that reason they have to penetrate into the deeper skin layers or permeate the skin. The outermost layer of the human skin, the stratum corneum, is responsible for its barrier function. Most topically administered drugs do not have the ability to penetrate the stratum corneum. In these cases modulations of the skin penetration profiles of these drugs and skin barrier manipulations are necessary. A skin penetration enhancement can be achieved either chemically, physically or by use of appropriate formulations. Numerous chemical compounds have been evaluated for penetration-enhancing activity, and different modes of action have been identified for skin penetration enhancement. In addition to chemical methods, skin penetration of drugs can be improved by physical options such as iontophoresis and phonophoresis, as well as by combinations of both chemical and physical methods or by combinations of several physical methods. There are cases where skin penetration of the drug used in the formulation is not the aim of the topical administration. Penetration reducers can be used to prevent chemicals entering the systemic circulation. This article concentrates on the progress made mainly over the last decade by use of chemical penetration enhancers. The different action modes of these substances are explained, including the basic principles of the physical skin penetration enhancement techniques and examples for their application.
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Citations
Cites
Current status and future potential of transdermal drug delivery
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Healing sound: the use of ultrasound in drug delivery and other therapeutic applications
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Passive skin penetration enhancement and its quantification in vitro
Moser, K. (2001) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/s0939-6411(01)00166-7 · Cited by 553
Mitragotri, S., & Kost, J. (2004) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2003.10.024 · Cited by 401
Design principles of chemical penetration enhancers for transdermal drug delivery
Karande, P., Jain, A., Ergun, K., Kispersky, V., & Mitragotri, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501176102 · Cited by 399
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Wertz, P. W. (2000) · Acta Dermato-Venereologica · doi:10.1080/000155500750042790 · Cited by 292
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Karande, P., Jain, A., & Mitragotri, S. (2004) · Nature Biotechnology · doi:10.1038/nbt928 · Cited by 280
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Cited by
Nanostructured lipid carriers: Promising drug delivery systems for future clinics
Beloqui, A., Solinís, M. Á., Rodríguez-Gascón, A., Almeida, A. J., & Préat, V. (2016) · Nanomedicine: Nanotechnology, Biology and Medicine · doi:10.1016/j.nano.2015.09.004 · Cited by 769
Nanotechnology and the transdermal routeA state of the art review and critical appraisal
Cevc, G., & Vierl, U. (2010) · Journal of Controlled Release · doi:10.1016/j.jconrel.2009.10.016 · Cited by 560
Garcês, A., Amaral, M. H., Sousa Lobo, J. M., & Silva, A. C. (2018) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2017.11.023 · Cited by 396
Elmowafy, M., & Al-Sanea, M. M. (2021) · Saudi Pharmaceutical Journal · doi:10.1016/j.jsps.2021.07.015 · Cited by 382
Strat-M® synthetic membrane: Permeability comparison to human cadaver skin
Haq, A., Goodyear, B., Ameen, D., Joshi, V., & Michniak-Kohn, B. (2018) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2018.06.012 · Cited by 231
Metadata
- Authors
- Trommer, H., & Neubert, R. H. H.
- Venue
- Skin Pharmacology and Physiology
- Publisher
- S. Karger AG
- Published
- 2006
- Volume
- 19
- Issue
- 2
- Pages
- 106-121
- ISSN
- 1422-2868 (ISSN-L)
- 1660-5527
- 1660-5535
- OpenAlex
- W2002218627
- Cited by
- 572
- References
- 47
- FWCI
- 7.18
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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