TY - JOUR
T1 - Robust Polyion Complex Vesicles (PICsomes) under Physiological Conditions Reinforced by Multiple Hydrogen Bond Formation Derived by Guanidinium Groups
AU - Hori, Mao
AU - Cabral, Horacio
AU - Toh, Kazuko
AU - Kishimura, Akihiro
AU - Kataoka, Kazunori
N1 - Funding Information:
This work was financially supported in part by a Grant-in-Aid for Specially Promoted Research (No. 25000006 to K.K.) of Japan Society for the Promotion of Science (JSPS) and the Center of Innovation (COI) Program, Japan Science and Technology Agency (JST), Japan. M.H. thanks the Research Fellowships of JSPS and Graduate Program for Leaders in Life Innovation (GPLLI), The University of Tokyo. TEM measurements were conducted at Research Hub for Advanced Nano Characterization at the University of Tokyo, with valuable help from Mr. H. Hoshi. We thank Mr. A. Kobayashi and Dr. M. Naito for their helpful technical assistance and advice.
Publisher Copyright:
Copyright © 2018 American Chemical Society.
PY - 2018/10/8
Y1 - 2018/10/8
N2 - Polyion complex vesicles (PICsomes) formed from a self-assembly of an oppositely charged pair of block- and homo-polyelectrolytes have shown exceptional features for functional loading of bioactive agents. Nevertheless, the stability of PICsomes is often jeopardized in a physiological environment, and only PICsomes having chemically cross-linked membranes have endured in harsh in vivo conditions, such as in the bloodstream. Herein, we developed versatile PICsomes aimed to last in in vivo settings by stabilizing their membrane through a combination of ionic and hydrogen bonding, which is widely found in natural proteins as a salt bridge, by controlled introduction of guanidinium groups in the polycation fraction toward concurrent polyion complexation and hydrogen bonding. The guanidinylated PICsomes were successfully assembled under physiological salt conditions, with precise control of their morphology by tuning the guanidinium content, and the ratio of anionic and cationic components. Guanidinylated PICsomes with 100 nm diameter, which are relevant to nanocarrier development, were stable in high urea concentration, at physiological temperature, and under serum incubation, persisting in blood circulation in vivo.
AB - Polyion complex vesicles (PICsomes) formed from a self-assembly of an oppositely charged pair of block- and homo-polyelectrolytes have shown exceptional features for functional loading of bioactive agents. Nevertheless, the stability of PICsomes is often jeopardized in a physiological environment, and only PICsomes having chemically cross-linked membranes have endured in harsh in vivo conditions, such as in the bloodstream. Herein, we developed versatile PICsomes aimed to last in in vivo settings by stabilizing their membrane through a combination of ionic and hydrogen bonding, which is widely found in natural proteins as a salt bridge, by controlled introduction of guanidinium groups in the polycation fraction toward concurrent polyion complexation and hydrogen bonding. The guanidinylated PICsomes were successfully assembled under physiological salt conditions, with precise control of their morphology by tuning the guanidinium content, and the ratio of anionic and cationic components. Guanidinylated PICsomes with 100 nm diameter, which are relevant to nanocarrier development, were stable in high urea concentration, at physiological temperature, and under serum incubation, persisting in blood circulation in vivo.
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U2 - 10.1021/acs.biomac.8b01097
DO - 10.1021/acs.biomac.8b01097
M3 - Article
C2 - 30157369
AN - SCOPUS:85053678039
SN - 1525-7797
VL - 19
SP - 4113
EP - 4121
JO - Biomacromolecules
JF - Biomacromolecules
IS - 10
ER -