Issue 49, 2020

Dual-targeting RNA nanoparticles for efficient delivery of polymeric siRNA to cancer cells

Abstract

A new dual-targeting polymeric siRNA nanoparticle (Dual-PSNP) was developed via multiple processes: rolling circle transcription, condensation, electrostatic deposition, and click chemistry. The Dual-PSNP showed significantly improved cancer-specific intracellular delivery, gene knockdown efficacy, and apoptosis-mediated cytotoxicity through additive receptor-mediated interactions of the two ligands.

Graphical abstract: Dual-targeting RNA nanoparticles for efficient delivery of polymeric siRNA to cancer cells

Supplementary files

Article information

Article type
Communication
Submitted
10 Mar 2020
Accepted
24 Apr 2020
First published
25 Apr 2020

Chem. Commun., 2020,56, 6624-6627

Dual-targeting RNA nanoparticles for efficient delivery of polymeric siRNA to cancer cells

T. Kim, H. N. Hyun, R. Heo, K. Nam, K. Yang, Y. M. Kim, Y. S. Lee, J. Y. An, J. H. Park, K. Y. Choi and Y. H. Roh, Chem. Commun., 2020, 56, 6624 DOI: 10.1039/D0CC01848A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements