オオサワ シゲヒト
Oosawa Shigehito
大澤 重仁 所属 医学研究科 医学研究科 (医学部医学科をご参照ください) 職種 非常勤講師 |
|
論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Installation of a thermoswitchable hydrophobic domain into a unimer polyion complex for enhanced cellular uptake of siRNA |
掲載誌名 | 正式名:Bioconjugate chemistry 略 称:Bioconjug Chem ISSNコード:10431802/15204812 |
掲載区分 | 国外 |
巻・号・頁 | 31(5),pp.1320-1326 |
総ページ数 | 7 |
著者・共著者 | Beob Soo Kim, Shigehito Osawa, Jongmin Yum, Mitsuru Naito, Kanjiro Miyata |
担当区分 | 2nd著者 |
発行年月 | 2020/04/30 |
概要 | Whereas small siRNA nanocarriers with a size of 10–20 nm exert high tissue-permeability, they encounter the challenge of inefficient adsorption on the cell surface, resulting in poor cellular uptake of siRNA. To solve this dilemma, this study aims to control the hydrophobicity of a small siRNA nanocarrier, unimer polyion complex (uPIC), with a size of ∼10 nm. The uPICs are fabricated to consist of a single pair between siRNA and a smart triblock copolymer comprising hydrophilic poly(2-ethyl-2-oxazoline) (PEtOx), thermoswitchable poly(2-n-propyl-2-oxazoline) (PnPrOx), and cationic poly(l-lysine) (PLL). The PnPrOx segment is dehydrated at 37 °C (>lower critical solution temperature) to enhance the hydrophobicity of uPICs. The uPICs with a hydrophobic domain facilitates cellular uptake of the siRNA payload through stronger binding to the cell surface, compared with control uPICs without a PnPrOx segment, leading to a significantly enhanced gene silencing effect in cultured cancer cells. |
DOI | 10.1021/acs.bioconjchem.0c00238 |