Oligonucleotides as a tool for intracellular DDS

Research output: Contribution to journalArticle

Abstract

Oligonucleotides attaching a reactive molecule may cause irreversible change to the target sequence at the reactive site. Inhibition of transcription, site-directed mutagenesis (or site-directed manipulation of genes) at the specific site has been proposed as a new tool of biotechnology with the use of a triplex-forming oligonucleotide. Thus, the oligonucleotides are regarded as a tool for intracellular DOS of useful reactive molecules. This review deals with development of a new alkylating group with high selectivity toward cytosine as well as new non-natural base analogs for the formation of stable non-natural triplexes.

Original languageEnglish
Pages (from-to)478-485
Number of pages8
JournalDrug Delivery System
Volume17
Issue number6
DOIs
Publication statusPublished - Jan 1 2002

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Oligonucleotides
Cytosine
Biotechnology
Site-Directed Mutagenesis
Catalytic Domain
Genes

All Science Journal Classification (ASJC) codes

  • Pharmaceutical Science

Cite this

Oligonucleotides as a tool for intracellular DDS. / Sasaki, Shigeki.

In: Drug Delivery System, Vol. 17, No. 6, 01.01.2002, p. 478-485.

Research output: Contribution to journalArticle

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