TY - JOUR
T1 - Enhanced cellular uptake of lactosomes using cell-penetrating peptides
AU - Akahoshi, Akiya
AU - Matsuura, Eiji
AU - Ozeki, Eiichi
AU - Matsui, Hayato
AU - Watanabe, Kazunori
AU - Ohtsuki, Takashi
N1 - Publisher Copyright:
© 2016 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Polymeric micelles that are composed of synthetic polymers are generally size controllable and can be easily modified for various applications. Lactosomes (A3B-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.
AB - Polymeric micelles that are composed of synthetic polymers are generally size controllable and can be easily modified for various applications. Lactosomes (A3B-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.
KW - Cell penetrating peptide
KW - drug delivery
KW - lactosome
KW - photosensitizer
KW - polymeric micelle
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U2 - 10.1080/14686996.2016.1178056
DO - 10.1080/14686996.2016.1178056
M3 - Article
AN - SCOPUS:85019066251
SN - 1468-6996
VL - 17
SP - 245
EP - 252
JO - Science and Technology of Advanced Materials
JF - Science and Technology of Advanced Materials
IS - 1
ER -