The potential and advances in RNAi therapy: chemical and structural modifications of siRNA molecules and use of biocompatible nanocarriers

J Control Release. 2014 Nov 10:193:113-21. doi: 10.1016/j.jconrel.2014.05.030. Epub 2014 May 24.

Abstract

Small interfering RNA (siRNA) has attracted great attention as a potential new drug due to its highly sequence-specific gene silencing ability and generality in therapeutic target. However, the medical applications of siRNA have been severely hindered by the lack of an optimal systemic delivery methodology. This poor delivery performance of siRNA is mainly caused by its inherent physicochemical properties including short and stiff structure, low charge density and vulnerability to nuclease cleavage. Thus, the successful development of efficient systemic delivery platform for siRNA is a fundamental requirement necessary to bring siRNA-based drugs to the market. Herein, we describe some siRNA delivery methods based on the chemical and structural modifications of delivery materials and siRNA itself to carry siRNA therapeutics safely to the targeted place without adverse effects. This review particularly explains the latest progress of chemically and structurally modified siRNA polymer (poly-siRNA)-based delivery systems. The stable and compact siRNA polyplexes, which are formed by poly-siRNA and different types of biocompatible materials, can enhance serum stability and target delivery efficiency in vitro and in vivo. In addition, this review provides specific information on poly-siRNA delivery systems from basics to therapeutic applications in different animal disease models.

Keywords: Chemical and structural modifications; Gene delivery; Polymerized siRNA; RNA interference.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biocompatible Materials / chemistry*
  • Cell Line, Tumor
  • Drug Carriers / chemistry*
  • Drug Design
  • Drug Stability
  • Genetic Therapy
  • Humans
  • Microscopy, Fluorescence
  • Molecular Structure
  • Nanoparticles / chemistry*
  • Neoplasms / therapy
  • RNA Interference*
  • RNA, Small Interfering / administration & dosage*
  • RNA, Small Interfering / blood
  • RNA, Small Interfering / genetics
  • Surface Properties
  • Xenograft Model Antitumor Assays

Substances

  • Biocompatible Materials
  • Drug Carriers
  • RNA, Small Interfering