An in vivo evaluation of amphiphilic, biodegradable peptide copolymers as siRNA delivery agents

Int J Pharm. 2014 May 15;466(1-2):58-67. doi: 10.1016/j.ijpharm.2014.03.011. Epub 2014 Mar 5.

Abstract

A series of amphiphilic, biodegradable polypeptide copolymers were prepared for the delivery of siRNA (short interfering ribonucleic acid). The molecular weight (or polymer chain length) of the linear polymer was controlled by reaction stoichiometry for the 11.5, 17.2, and 24.6 kDa polypeptides, and the highest molecular weight polypeptide was prepared using a sequential addition method to obtain a polypeptide having a molecular weight of 38.6 kDa. These polymers were used to prepare polymer conjugate systems designed to target and deliver an apolipoprotein B (ApoB) siRNA to hepatocyte cells and to help delineate the effect of polymer molecular weight or polymer chain length on siRNA delivery in vivo. A clear trend in increasing potency was found with increasing molecular weight of the polymers examined (at a constant polymer:siRNA (w/w) ratio), with minimal toxicity found. Furthermore, the biodegradability of these polymer conjugates was examined and demonstrates the potential of these systems as siRNA delivery vectors.

Keywords: Poly(peptides); Polymer conjugates; RNA delivery; siRNA.

MeSH terms

  • Animals
  • Apolipoproteins B / genetics*
  • Female
  • Liver / metabolism
  • Molecular Weight
  • Ornithine / chemistry*
  • Peptides / administration & dosage*
  • Peptides / chemistry
  • Phenylalanine / chemistry*
  • Polymers / administration & dosage*
  • Polymers / chemistry
  • RNA, Messenger / genetics
  • RNA, Small Interfering / administration & dosage*
  • RNA, Small Interfering / chemistry
  • Rats, Sprague-Dawley

Substances

  • Apolipoproteins B
  • Peptides
  • Polymers
  • RNA, Messenger
  • RNA, Small Interfering
  • Phenylalanine
  • Ornithine