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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Main Authors: Pan He, Kyoji Hagiwara, Hui Chong, Hsiao-hua Yu, Yoshihiro Ito
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2015/406389
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spelling 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
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