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Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8
Skin, being the largest organ of the body, is an important site for drug administration. However, most of the drugs have poor permeability and thus drug delivery through the skin is very challenging. In this study, we examined the transdermal delivery capability of IMT-P8, a novel cell-penetrating p...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870705/ https://www.ncbi.nlm.nih.gov/pubmed/27189051 http://dx.doi.org/10.1038/srep26278 |
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author | Gautam, Ankur Nanda, Jagpreet Singh Samuel, Jesse S. Kumari, Manisha Priyanka, Priyanka Bedi, Gursimran Nath, Samir K. Mittal, Garima Khatri, Neeraj Raghava, Gajendra Pal Singh |
author_facet | Gautam, Ankur Nanda, Jagpreet Singh Samuel, Jesse S. Kumari, Manisha Priyanka, Priyanka Bedi, Gursimran Nath, Samir K. Mittal, Garima Khatri, Neeraj Raghava, Gajendra Pal Singh |
author_sort | Gautam, Ankur |
collection | PubMed |
description | Skin, being the largest organ of the body, is an important site for drug administration. However, most of the drugs have poor permeability and thus drug delivery through the skin is very challenging. In this study, we examined the transdermal delivery capability of IMT-P8, a novel cell-penetrating peptide. We generated IMT-P8-GFP and IMT-P8-KLA fusion constructs and evaluated their internalization into mouse skin after topical application. Our results demonstrate that IMT-P8 is capable of transporting green fluorescent protein (GFP) and proapoptotic peptide, KLA into the skin and also in different cell lines. Interestingly, uptake of IMT-P8-GFP was considerably higher than TAT-GFP in HeLa cells. After internalization, IMT-P8-KLA got localized to the mitochondria and caused significant cell death in HeLa cells signifying an intact biological activity. Further in vivo skin penetration experiments revealed that after topical application, IMT-P8 penetrated the stratum corneum, entered into the viable epidermis and accumulated inside the hair follicles. In addition, both IMT-P8-KLA and IMT-P8-GFP internalized into the hair follicles and dermal tissue of the skin following topical application. These results suggested that IMT-P8 could be a potential candidate to be used as a topical delivery vehicle for various cosmetic and skin disease applications. |
format | Online Article Text |
id | pubmed-4870705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48707052016-06-01 Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 Gautam, Ankur Nanda, Jagpreet Singh Samuel, Jesse S. Kumari, Manisha Priyanka, Priyanka Bedi, Gursimran Nath, Samir K. Mittal, Garima Khatri, Neeraj Raghava, Gajendra Pal Singh Sci Rep Article Skin, being the largest organ of the body, is an important site for drug administration. However, most of the drugs have poor permeability and thus drug delivery through the skin is very challenging. In this study, we examined the transdermal delivery capability of IMT-P8, a novel cell-penetrating peptide. We generated IMT-P8-GFP and IMT-P8-KLA fusion constructs and evaluated their internalization into mouse skin after topical application. Our results demonstrate that IMT-P8 is capable of transporting green fluorescent protein (GFP) and proapoptotic peptide, KLA into the skin and also in different cell lines. Interestingly, uptake of IMT-P8-GFP was considerably higher than TAT-GFP in HeLa cells. After internalization, IMT-P8-KLA got localized to the mitochondria and caused significant cell death in HeLa cells signifying an intact biological activity. Further in vivo skin penetration experiments revealed that after topical application, IMT-P8 penetrated the stratum corneum, entered into the viable epidermis and accumulated inside the hair follicles. In addition, both IMT-P8-KLA and IMT-P8-GFP internalized into the hair follicles and dermal tissue of the skin following topical application. These results suggested that IMT-P8 could be a potential candidate to be used as a topical delivery vehicle for various cosmetic and skin disease applications. Nature Publishing Group 2016-05-18 /pmc/articles/PMC4870705/ /pubmed/27189051 http://dx.doi.org/10.1038/srep26278 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gautam, Ankur Nanda, Jagpreet Singh Samuel, Jesse S. Kumari, Manisha Priyanka, Priyanka Bedi, Gursimran Nath, Samir K. Mittal, Garima Khatri, Neeraj Raghava, Gajendra Pal Singh Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 |
title | Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 |
title_full | Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 |
title_fullStr | Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 |
title_full_unstemmed | Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 |
title_short | Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8 |
title_sort | topical delivery of protein and peptide using novel cell penetrating peptide imt-p8 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870705/ https://www.ncbi.nlm.nih.gov/pubmed/27189051 http://dx.doi.org/10.1038/srep26278 |
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