Synthesis and evaluation of poly(ethylene glycol)-polylysine block copolymers as carriers for gene delivery

S. Vanderkerken, T. Vanheede, V. Toncheva, E. Schacht, M.A. Wolfert, L. Seymour, A. Urtti

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Different types of poly(ethylene glycol)-poly(L-lysine) PEG-PLL block copolymers were examined for their ability to form polyelectrolyte complexes with DNA, their toxicity toward red blood cells and their in vitro transfection efficiency. The complexation of the polymers with DNA was studied using the ethidium bromide fluorescence technique. All polymers complexed DNA to form particles with sizes ranging from 80 nm to 150 nm. In most cases, smaller particles were also observed, and sometimes populations of even larger particles could be detected. In vitro toxicity toward red blood cells was low. Agglutination of red blood cells with some of the noncomplexed block copolymers was observed, but the aggregates were less dense than with polylysine. Transfection efficiency of 293 cells in vitro in the presence of chloroquine was dependent upon the charge ratio of polymer/DNA. Efficient transfection was achieved for the PEG-PLL block copolymers with linear PLL blocks. On the other hand, very low transfection efficiency was obtained from the PEG-PLL with a dendritic PLL block.
Original languageEnglish
Pages (from-to)115-138
Number of pages24
JournalJournal of Bioactive and Compatible Polymers
Volume15
Issue number2
DOIs
Publication statusPublished - 16 Mar 2000
Externally publishedYes

Keywords

  • chloroquine
  • copolymer
  • macrogol
  • polylysine
  • animal cell
  • article
  • concentration response
  • controlled study
  • DNA transfection
  • drug DNA binding
  • drug synthesis
  • gene targeting
  • gene therapy
  • hemagglutination
  • hemolysis
  • human
  • human cell
  • nonhuman
  • particle size

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