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Enhanced cellular uptake of lactosomes using cell-penetrating peptides
Polymeric micelles that are composed of synthetic polymers are generally size controllable and can be easily modified for various applications. Lactosomes (A(3)B-type) are biodegradable polymeric micelles composed of an amphipathic polymer, including three poly(sarcosine) blocks and a poly(l-lactic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101896/ https://www.ncbi.nlm.nih.gov/pubmed/27877876 http://dx.doi.org/10.1080/14686996.2016.1178056 |
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author | Akahoshi, Akiya Matsuura, Eiji Ozeki, Eiichi Matsui, Hayato Watanabe, Kazunori Ohtsuki, Takashi |
author_facet | Akahoshi, Akiya Matsuura, Eiji Ozeki, Eiichi Matsui, Hayato Watanabe, Kazunori Ohtsuki, Takashi |
author_sort | Akahoshi, Akiya |
collection | PubMed |
description | Polymeric micelles that are composed of synthetic polymers are generally size controllable and can be easily modified for various applications. Lactosomes (A(3)B-type) are biodegradable polymeric micelles composed of an amphipathic polymer, including three poly(sarcosine) blocks and a poly(l-lactic acid) block. Lactosomes accumulate in tumors in vivo through the enhanced permeability and retention (EPR) effect, even on frequently administering them. However, lactosomes cannot be efficiently internalized by cells. To improve cellular uptake of lactosomes, cell-penetrating peptide (CPP)-modified lactosomes were prepared. Seven CPPs (including EB1 and Pep1) were used, and most of them improved the cellular uptake efficiency of lactosomes. In particular, EB1- and Pep1-modified lactosomes were efficiently internalized by cells. In addition, by using CPP-modified and photosensitizer-loaded lactosomes, we demonstrated the photoinduced killing of mammalian cells, including human cancer cells. Accumulation of the EB1-modified lactosomes in NCI-N87 tumors was shown by in vivo imaging. Thus, this study demonstrated that the CPP-modified lactosome is a promising drug carrier. |
format | Online Article Text |
id | pubmed-5101896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-51018962016-11-22 Enhanced cellular uptake of lactosomes using cell-penetrating peptides Akahoshi, Akiya Matsuura, Eiji Ozeki, Eiichi Matsui, Hayato Watanabe, Kazunori Ohtsuki, Takashi Sci Technol Adv Mater Focus issue on Nanomedicine molecular science Polymeric micelles that are composed of synthetic polymers are generally size controllable and can be easily modified for various applications. Lactosomes (A(3)B-type) are biodegradable polymeric micelles composed of an amphipathic polymer, including three poly(sarcosine) blocks and a poly(l-lactic acid) block. Lactosomes accumulate in tumors in vivo through the enhanced permeability and retention (EPR) effect, even on frequently administering them. However, lactosomes cannot be efficiently internalized by cells. To improve cellular uptake of lactosomes, cell-penetrating peptide (CPP)-modified lactosomes were prepared. Seven CPPs (including EB1 and Pep1) were used, and most of them improved the cellular uptake efficiency of lactosomes. In particular, EB1- and Pep1-modified lactosomes were efficiently internalized by cells. In addition, by using CPP-modified and photosensitizer-loaded lactosomes, we demonstrated the photoinduced killing of mammalian cells, including human cancer cells. Accumulation of the EB1-modified lactosomes in NCI-N87 tumors was shown by in vivo imaging. Thus, this study demonstrated that the CPP-modified lactosome is a promising drug carrier. Taylor & Francis 2016-06-08 /pmc/articles/PMC5101896/ /pubmed/27877876 http://dx.doi.org/10.1080/14686996.2016.1178056 Text en © 2016 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License CC-BYhttp://creativecommons.org/licenses/by/4.0/which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Focus issue on Nanomedicine molecular science Akahoshi, Akiya Matsuura, Eiji Ozeki, Eiichi Matsui, Hayato Watanabe, Kazunori Ohtsuki, Takashi Enhanced cellular uptake of lactosomes using cell-penetrating peptides |
title | Enhanced cellular uptake of lactosomes using cell-penetrating peptides |
title_full | Enhanced cellular uptake of lactosomes using cell-penetrating peptides |
title_fullStr | Enhanced cellular uptake of lactosomes using cell-penetrating peptides |
title_full_unstemmed | Enhanced cellular uptake of lactosomes using cell-penetrating peptides |
title_short | Enhanced cellular uptake of lactosomes using cell-penetrating peptides |
title_sort | enhanced cellular uptake of lactosomes using cell-penetrating peptides |
topic | Focus issue on Nanomedicine molecular science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101896/ https://www.ncbi.nlm.nih.gov/pubmed/27877876 http://dx.doi.org/10.1080/14686996.2016.1178056 |
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