Asami Yutaro, Yoshioka Kotaro, Nishina Kazutaka, Nagata Tetsuya, Yokota Takanori
Department of Neurology and Neurological Science, Graduate School, Tokyo Medical and Dental University.
Drug Discov Ther. 2016;10(5):256-262. doi: 10.5582/ddt.2016.01065.
Therapeutic oligonucleotides are promising technologies. Nevertheless, improvement of their efficacy is an important issue. Introducing this drug delivery system (DDS) makes for a great enhancement for delivery of oligonucleotides to targeted tissue or cells. The strategy of DDS for therapeutic oligonucleotides is divided into four categories, A) single piece of oligonucleotide, B) oligonucleotide-ligand conjugate, C) oligonucleotide-polymer conjugate, and D) nanoparticle. In this review we will describe those basic concepts, especially for the technology of conjugating ligand. In addition, we developed a new technology, heteroduplex oligonucleotide (HDO), binding ligand-molecule to antisense oligonucleotide indirectly. We also outline α-tocopherol (a natural isomer of vitamin E) conjugated HDO.
治疗性寡核苷酸是很有前景的技术。然而,提高其疗效是一个重要问题。引入这种药物递送系统(DDS)可极大增强寡核苷酸向靶向组织或细胞的递送。治疗性寡核苷酸的DDS策略分为四类,A)单链寡核苷酸,B)寡核苷酸 - 配体缀合物,C)寡核苷酸 - 聚合物缀合物,以及D)纳米颗粒。在本综述中,我们将描述这些基本概念,特别是关于配体缀合技术。此外,我们开发了一种新技术,异源双链寡核苷酸(HDO),它将配体分子间接结合到反义寡核苷酸上。我们还概述了α - 生育酚(维生素E的天然异构体)缀合的HDO。