TY - JOUR
T1 - Water-soluble and cytocompatible phospholipid polymers for molecular complexation to enhance biomolecule transportation to cells in vitro
AU - Ishihara, Kazuhiko
AU - Hachiya, Shohei
AU - Inoue, Yuuki
AU - Fukazawa, Kyoko
AU - Konno, Tomohiro
N1 - Funding Information:
Funding: This research was funded by Ministry of Education, Culture, Sports, Science, and Technology of Japan as a Grant-in-Aid for Scientific Research on Innovative Areas “Nanomedicine Molecular Science” (No.2306).
Funding Information:
This research was funded by Ministry of Education, Culture, Sports, Science, and Technology of Japan as a Grant-in-Aid for Scientific Research on Innovative Areas "Nanomedicine Molecular Science" (No.2306). The authors wish to thank Kanjiro Miyata and Kazunori Kataoka, Department of Materials Engineering, The University of Tokyo, for their kind support of this research.
Publisher Copyright:
© 2020 by the authors.
PY - 2020/8
Y1 - 2020/8
N2 - Water-soluble and cytocompatible polymers were investigated to enhance a transporting efficiency of biomolecules into cells in vitro. The polymers composed of a 2-methacryloyloxyethyl phosphorylcholine (MPC) unit, a hydrophobic monomer unit, and a cationic monomer unit bearing an amino group were synthesized for complexation with model biomolecules, siRNA. The cationic MPC polymer was shown to interact with both siRNA and the cell membrane and was successively transported siRNA into cells. When introducing 20-50 mol% hydrophobic units into the cationic MPC polymer, transport of siRNA into cells. The MPC units (10-20 mol%) in the cationic MPC polymer were able to impart cytocompatibility, while maintaining interaction with siRNA and the cell membrane. The level of gene suppression of the siRNA/MPC polymer complex was evaluated in vitro and it was as the same level as that of a conventional siRNA transfection reagent, whereas its cytotoxicity was significantly lower. We concluded that these cytocompatible MPC polymers may be promising complexation reagent for introducing biomolecules into cells, with the potential to contribute to future fields of biotechnology, such as in vitro evaluation of gene functionality, and the production of engineered cells with biological functions.
AB - Water-soluble and cytocompatible polymers were investigated to enhance a transporting efficiency of biomolecules into cells in vitro. The polymers composed of a 2-methacryloyloxyethyl phosphorylcholine (MPC) unit, a hydrophobic monomer unit, and a cationic monomer unit bearing an amino group were synthesized for complexation with model biomolecules, siRNA. The cationic MPC polymer was shown to interact with both siRNA and the cell membrane and was successively transported siRNA into cells. When introducing 20-50 mol% hydrophobic units into the cationic MPC polymer, transport of siRNA into cells. The MPC units (10-20 mol%) in the cationic MPC polymer were able to impart cytocompatibility, while maintaining interaction with siRNA and the cell membrane. The level of gene suppression of the siRNA/MPC polymer complex was evaluated in vitro and it was as the same level as that of a conventional siRNA transfection reagent, whereas its cytotoxicity was significantly lower. We concluded that these cytocompatible MPC polymers may be promising complexation reagent for introducing biomolecules into cells, with the potential to contribute to future fields of biotechnology, such as in vitro evaluation of gene functionality, and the production of engineered cells with biological functions.
KW - 2-methacryloyloxyethyl phosphorylcholine polymer
KW - Amphiphilic nature
KW - Cationic group
KW - Endocytosis
KW - Polymer aggregate
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U2 - 10.3390/polym12081762
DO - 10.3390/polym12081762
M3 - Article
AN - SCOPUS:85090415838
SN - 2073-4360
VL - 12
JO - Polymers
JF - Polymers
IS - 8
M1 - 1762
ER -