Lipid nanocapsules for dermal application: A comparative study of lipid-based versus polymer-based nanocarriers
Lipid nanocarriers are efficient transdermal drug delivery systems while polymeric nanoparticles are better suited for local effects on the skin. Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse ad...
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| Published in: | European journal of pharmaceutics and biopharmaceutics Vol. 79; no. 1; pp. 36 - 42 |
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| Main Authors: | , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Netherlands
Elsevier B.V
01.09.2011
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| Subjects: | |
| ISSN: | 0939-6411, 1873-3441, 1873-3441 |
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| Abstract | Lipid nanocarriers are efficient transdermal drug delivery systems while polymeric nanoparticles are better suited for local effects on the skin.
Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse administration routes. However, they have not been explored before for transdermal application. Here, we study the behavior of LNC as a transdermal drug delivery system using ibuprofen as a model drug. A comparison to other lipid nanocarriers such as solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) and polymeric nanocarriers has been made. It was found that LNC could increase the flux rate of ibuprofen 21.9
±
0.5 compared to 5.8
±
0.4
μg/cm
2
h in case of drug solution. Similar flux rates were obtained for SLN and NLC with average values of 22.9
±
0.5 and 22.5
±
2.0
μg/cm
2
h, respectively. On the other side, comparison to polymeric nanoparticles showed that the polymer-based carriers of the same particle size had lower permeation-enhancing effect with a flux rate of 10.62
±
1.84
μg/cm
2
h. Polymeric carriers had fourfold higher accumulation in the skin compared to that of the LNC and twice the accumulation of SLN and NLC. These results would suggest that the LNC can be considered as efficient as SLN and NLC for the transdermal drug delivery while polymeric nanoparticles are more suitable for localized drug delivery to the skin. |
|---|---|
| AbstractList | Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse administration routes. However, they have not been explored before for transdermal application. Here, we study the behavior of LNC as a transdermal drug delivery system using ibuprofen as a model drug. A comparison to other lipid nanocarriers such as solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) and polymeric nanocarriers has been made. It was found that LNC could increase the flux rate of ibuprofen 21.9±0.5 compared to 5.8±0.4 μg/cm(2)h in case of drug solution. Similar flux rates were obtained for SLN and NLC with average values of 22.9±0.5 and 22.5±2.0 μg/cm(2)h, respectively. On the other side, comparison to polymeric nanoparticles showed that the polymer-based carriers of the same particle size had lower permeation-enhancing effect with a flux rate of 10.62±1.84 μg/cm(2)h. Polymeric carriers had fourfold higher accumulation in the skin compared to that of the LNC and twice the accumulation of SLN and NLC. These results would suggest that the LNC can be considered as efficient as SLN and NLC for the transdermal drug delivery while polymeric nanoparticles are more suitable for localized drug delivery to the skin. Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse administration routes. However, they have not been explored before for transdermal application. Here, we study the behavior of LNC as a transdermal drug delivery system using ibuprofen as a model drug. A comparison to other lipid nanocarriers such as solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) and polymeric nanocarriers has been made. It was found that LNC could increase the flux rate of ibuprofen 21.9±0.5 compared to 5.8±0.4 μg/cm(2)h in case of drug solution. Similar flux rates were obtained for SLN and NLC with average values of 22.9±0.5 and 22.5±2.0 μg/cm(2)h, respectively. On the other side, comparison to polymeric nanoparticles showed that the polymer-based carriers of the same particle size had lower permeation-enhancing effect with a flux rate of 10.62±1.84 μg/cm(2)h. Polymeric carriers had fourfold higher accumulation in the skin compared to that of the LNC and twice the accumulation of SLN and NLC. These results would suggest that the LNC can be considered as efficient as SLN and NLC for the transdermal drug delivery while polymeric nanoparticles are more suitable for localized drug delivery to the skin.Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse administration routes. However, they have not been explored before for transdermal application. Here, we study the behavior of LNC as a transdermal drug delivery system using ibuprofen as a model drug. A comparison to other lipid nanocarriers such as solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) and polymeric nanocarriers has been made. It was found that LNC could increase the flux rate of ibuprofen 21.9±0.5 compared to 5.8±0.4 μg/cm(2)h in case of drug solution. Similar flux rates were obtained for SLN and NLC with average values of 22.9±0.5 and 22.5±2.0 μg/cm(2)h, respectively. On the other side, comparison to polymeric nanoparticles showed that the polymer-based carriers of the same particle size had lower permeation-enhancing effect with a flux rate of 10.62±1.84 μg/cm(2)h. Polymeric carriers had fourfold higher accumulation in the skin compared to that of the LNC and twice the accumulation of SLN and NLC. These results would suggest that the LNC can be considered as efficient as SLN and NLC for the transdermal drug delivery while polymeric nanoparticles are more suitable for localized drug delivery to the skin. Lipid nanocarriers are efficient transdermal drug delivery systems while polymeric nanoparticles are better suited for local effects on the skin. Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse administration routes. However, they have not been explored before for transdermal application. Here, we study the behavior of LNC as a transdermal drug delivery system using ibuprofen as a model drug. A comparison to other lipid nanocarriers such as solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) and polymeric nanocarriers has been made. It was found that LNC could increase the flux rate of ibuprofen 21.9 ± 0.5 compared to 5.8 ± 0.4 μg/cm 2 h in case of drug solution. Similar flux rates were obtained for SLN and NLC with average values of 22.9 ± 0.5 and 22.5 ± 2.0 μg/cm 2 h, respectively. On the other side, comparison to polymeric nanoparticles showed that the polymer-based carriers of the same particle size had lower permeation-enhancing effect with a flux rate of 10.62 ± 1.84 μg/cm 2 h. Polymeric carriers had fourfold higher accumulation in the skin compared to that of the LNC and twice the accumulation of SLN and NLC. These results would suggest that the LNC can be considered as efficient as SLN and NLC for the transdermal drug delivery while polymeric nanoparticles are more suitable for localized drug delivery to the skin. |
| Author | Abdel-Mottaleb, Mona M.A. Neumann, Dirk Lamprecht, Alf |
| Author_xml | – sequence: 1 givenname: Mona M.A. surname: Abdel-Mottaleb fullname: Abdel-Mottaleb, Mona M.A. email: mona_abdelmottaleb@yahoo.com, alf.lamprecht@uni-bonn.de organization: Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Bonn, Germany – sequence: 2 givenname: Dirk surname: Neumann fullname: Neumann, Dirk organization: Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Bonn, Germany – sequence: 3 givenname: Alf surname: Lamprecht fullname: Lamprecht, Alf organization: Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Bonn, Germany |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21558002$$D View this record in MEDLINE/PubMed |
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| Copyright | 2011 Elsevier B.V. Copyright © 2011 Elsevier B.V. All rights reserved. |
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| Keywords | Polymer nanoparticles Skin Transdermal Lipid nanocapsules Nanocarriers |
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| Snippet | Lipid nanocarriers are efficient transdermal drug delivery systems while polymeric nanoparticles are better suited for local effects on the skin.
Lipid... Lipid nanocapsules (LNC) are colloidal carriers providing controlled release profiles and improved bioavailability for many drug substances and diverse... |
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| SubjectTerms | Administration, Cutaneous Animals Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - analysis Anti-Inflammatory Agents, Non-Steroidal - chemistry Anti-Inflammatory Agents, Non-Steroidal - pharmacology Cellulose - analogs & derivatives Cellulose - chemistry Delayed-Action Preparations Drug Carriers - chemistry Drug Compounding Drug Delivery Systems Drug Evaluation, Preclinical Ear - physiology Ibuprofen - administration & dosage Ibuprofen - analysis Ibuprofen - chemistry Ibuprofen - pharmacology Lipid nanocapsules Lipids - chemistry Nanocapsules - chemistry Nanocarriers Nanoparticles - chemistry Nanostructures - chemistry Particle Size Permeability Polyethylene Glycols - chemistry Polymer nanoparticles Polymers - chemistry Skin Skin - metabolism Stearic Acids - chemistry Surface-Active Agents - chemistry Swine Transdermal |
| Title | Lipid nanocapsules for dermal application: A comparative study of lipid-based versus polymer-based nanocarriers |
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