TY - JOUR
T1 - Temperature-responsive polymeric carriers incorporating hydrophobic monomers for effective transfection in small doses
AU - Takeda, Naoya
AU - Nakamura, Emiko
AU - Yokoyama, Masayuki
AU - Okano, Teruo
N1 - Funding Information:
This work was partially supported by a grant for ‘Research for the Future’ Program from the Japan Society for the Promotion of Science (JSPS-RFTF96I00201) and Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports Science, and Technology, Japan (nos. 11650913 and 14780651). Dr. J.L. Whitton (Scripps Research Institute) is acknowledged for his kind gift of pCMV-LacZ. Prof. D.W. Grainger (Colorado State University) is also appreciated for both his technical and grammatical comments.
PY - 2004/3/5
Y1 - 2004/3/5
N2 - A series of thermoresponsive ternary random copolymers, poly[N-isopropylacrylamide (PIPAAm)-co-(dimethylamino)ethylmethacrylate (DMAEMA)-co-butylmethacrylate (BMA)], was synthesized and their in vitro gene transfection efficiency in cell culture was evaluated. A control copolymer containing 20 mol% DMAEMA units, IP-20D (mole ratio of IPAAm/DMAEMA/BMA=80/20/0 in feed, no BMA units) was inert in transfection. In contrast, copolymer IP-20D-10B (IPAAm/DMAEMA/BMA=70/20/10 in feed) effectively transfected plasmid DNA into COS-1 cell cultures even under small dosing conditions of 0.1 μg of plasmid DNA per well in a 96-well plate, suggesting that incorporation of the appropriate amount of hydrophobic unit is crucial to transfection efficiency. Gene expression was much more significant when transfected by the IP-20D-10B carrier in comparison with control homopolymer poly-DMAEMA, and almost equal to that of the highly competent lipid carrier, LipofectAMINE PLUS™. Furthermore, the transfection efficiency of IP-20D-10B is altered in a thermally responsive manner. By temporarily lowering the cell culture incubation temperature to 20°C in the posttransfection period, gene expression doubled over that for incubation temperature at 37°C. The DNA EtBr intercalation assay suggested that DNA affinity for IP-20D-10B is decreased by lowering incubation temperature, implying that the thermally regulated gene expression could provide more efficient DNA release from the polymeric carrier.
AB - A series of thermoresponsive ternary random copolymers, poly[N-isopropylacrylamide (PIPAAm)-co-(dimethylamino)ethylmethacrylate (DMAEMA)-co-butylmethacrylate (BMA)], was synthesized and their in vitro gene transfection efficiency in cell culture was evaluated. A control copolymer containing 20 mol% DMAEMA units, IP-20D (mole ratio of IPAAm/DMAEMA/BMA=80/20/0 in feed, no BMA units) was inert in transfection. In contrast, copolymer IP-20D-10B (IPAAm/DMAEMA/BMA=70/20/10 in feed) effectively transfected plasmid DNA into COS-1 cell cultures even under small dosing conditions of 0.1 μg of plasmid DNA per well in a 96-well plate, suggesting that incorporation of the appropriate amount of hydrophobic unit is crucial to transfection efficiency. Gene expression was much more significant when transfected by the IP-20D-10B carrier in comparison with control homopolymer poly-DMAEMA, and almost equal to that of the highly competent lipid carrier, LipofectAMINE PLUS™. Furthermore, the transfection efficiency of IP-20D-10B is altered in a thermally responsive manner. By temporarily lowering the cell culture incubation temperature to 20°C in the posttransfection period, gene expression doubled over that for incubation temperature at 37°C. The DNA EtBr intercalation assay suggested that DNA affinity for IP-20D-10B is decreased by lowering incubation temperature, implying that the thermally regulated gene expression could provide more efficient DNA release from the polymeric carrier.
KW - Gene delivery
KW - Poly(N-isopropylacrylamide)
KW - Polymer carrier
KW - Thermoresponsive
KW - Transfection
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U2 - 10.1016/j.jconrel.2003.12.001
DO - 10.1016/j.jconrel.2003.12.001
M3 - Article
C2 - 14980782
AN - SCOPUS:1242338833
SN - 0168-3659
VL - 95
SP - 343
EP - 355
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 2
ER -