Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery
Owing to its hydrophilicity, negative charge, small size, and labile degradation by endogenous nucleases, small interfering RNA (siRNA) delivery must be achieved by a carrier system. In this study, cationic copolymers composed of low-molecular-weight polyethylenimine and polythiophenes were synthesi...
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Online Access: | http://dx.doi.org/10.1155/2015/406389 |
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doaj-850d553c00954e1297e7e68794dc6c192020-11-24T23:19:36ZengHindawi LimitedBioMed Research International2314-61332314-61412015-01-01201510.1155/2015/406389406389Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA DeliveryPan He0Kyoji Hagiwara1Hui Chong2Hsiao-hua Yu3Yoshihiro Ito4Nano Medical Engineering Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, JapanNano Medical Engineering Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, JapanResponsive Organic Materials Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, JapanResponsive Organic Materials Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, JapanNano Medical Engineering Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, JapanOwing to its hydrophilicity, negative charge, small size, and labile degradation by endogenous nucleases, small interfering RNA (siRNA) delivery must be achieved by a carrier system. In this study, cationic copolymers composed of low-molecular-weight polyethylenimine and polythiophenes were synthesized and evaluated as novel self-tracking siRNA delivery vectors. The concept underlying the design of these copolymers is that hydrophobicity and rigidity of polythiophenes should enhance the transport of siRNA across the cell membrane and endosomal membrane. A gel retardation assay showed that the nanosized complexes formed between the copolymers and siRNA were stable even at a molar ratio of 1 : 2. The high cellular uptake (>80%) and localization of the copolymer vectors inside the cells were easily analyzed by tracking the fluorescence of polythiophene using fluorescent microscopy and cytometry. An in vitro luciferase knockdown (KD) assay in A549-luc cells demonstrated that the siRNA complexes with more hydrophobic copolymers achieved a higher KD efficiency of 52.8% without notable cytotoxicity, indicating protein-specific KD activity rather than solely the cytotoxicity of the materials. Our polythiophene copolymers should serve as novel, efficient, low cell toxicity, and label-free siRNA delivery systems.http://dx.doi.org/10.1155/2015/406389 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Pan He Kyoji Hagiwara Hui Chong Hsiao-hua Yu Yoshihiro Ito |
spellingShingle |
Pan He Kyoji Hagiwara Hui Chong Hsiao-hua Yu Yoshihiro Ito Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery BioMed Research International |
author_facet |
Pan He Kyoji Hagiwara Hui Chong Hsiao-hua Yu Yoshihiro Ito |
author_sort |
Pan He |
title |
Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery |
title_short |
Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery |
title_full |
Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery |
title_fullStr |
Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery |
title_full_unstemmed |
Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery |
title_sort |
low-molecular-weight polyethyleneimine grafted polythiophene for efficient sirna delivery |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2015-01-01 |
description |
Owing to its hydrophilicity, negative charge, small size, and labile degradation by endogenous nucleases, small interfering RNA (siRNA) delivery must be achieved by a carrier system. In this study, cationic copolymers composed of low-molecular-weight polyethylenimine and polythiophenes were synthesized and evaluated as novel self-tracking siRNA delivery vectors. The concept underlying the design of these copolymers is that hydrophobicity and rigidity of polythiophenes should enhance the transport of siRNA across the cell membrane and endosomal membrane. A gel retardation assay showed that the nanosized complexes formed between the copolymers and siRNA were stable even at a molar ratio of 1 : 2. The high cellular uptake (>80%) and localization of the copolymer vectors inside the cells were easily analyzed by tracking the fluorescence of polythiophene using fluorescent microscopy and cytometry. An in vitro luciferase knockdown (KD) assay in A549-luc cells demonstrated that the siRNA complexes with more hydrophobic copolymers achieved a higher KD efficiency of 52.8% without notable cytotoxicity, indicating protein-specific KD activity rather than solely the cytotoxicity of the materials. Our polythiophene copolymers should serve as novel, efficient, low cell toxicity, and label-free siRNA delivery systems. |
url |
http://dx.doi.org/10.1155/2015/406389 |
work_keys_str_mv |
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