DNA delivery systems based on complexes of DNA with synthetic polycations and their copolymers

D. Oupický, Č Koňák, K. Ulbrich, M. A. Wolfert, L. W. Seymour

Research output: Contribution to journalArticle

126 Citations (Scopus)

Abstract

Block and graft copolymers of N-(2-hydroxypropyl)methacrylamide (HPMA) with 2-(trimethylammonio)ethyl methacrylate were synthesised and used for preparation of polyelectrolyte complexes with calf thymus DNA intended for targeted delivery of genes in vivo. In this study the effects of the speed of component mixing, total concentration of polymers, ionic strength of solvents, copolymer structure and content of HPMA in the copolymers on parameters of the polyelectrolyte complexes was investigated. Static and dynamic light scattering methods were used as a main tool for characterising these complexes. The presence of HPMA units in the polycation had no significant effect on its ability to form complexes with DNA, but did affect molecular parameters and aggregation (precipitation) of the complexes. The size of the complexes increases whereas their molecular weight decreases with increasing content of HPMA units. The density of the complexes decreases with increasing HPMA content independently of the copolymer structure. In order to prepare stable DNA complexes containing single DNA molecule, the following rules should be observed: (1) copolymers should have a content of HPMA units higher than 40%; (2) the DNA concentrations in solutions should be kept below 4·10-5 g/ml and (3) both components should be mixed together in deionised water. The stability of the complexes against precipitation in 0.15 M NaCl and the resistance of the complexed DNA to the action of nucleases was also studied. Whereas DNA complexes of all copolymers showed very good nuclease stability, the presence of a sufficiently high content of HPMA is necessary for their good stability in 0.15 M NaCl. The investigation of the stability and the interaction of DNA complexes in aqueous solutions of serum albumin and dilute human blood serum revealed adsorption of biomacromolecules on DNA complexes accompanied by significant changes in the ζ-potential which finally resulted in formation of a 'protein layer' and in undesirable precipitation of DNA complexes. In in vitro transfection experiments, the transfection efficiency of DNA complexes with copolymers was always higher than that of the cationic homopolymer slightly increasing with increasing content of HPMA in the copolymers but being about 10-100-times lower than the complexes DNA-poly(L-lysine. In the cytoplasmic injections, it was observed that DNA complexes produced greater gene expression than a direct microinjection of free DNA. The block copolymer complexes were also found to be more efficient than the corresponding simple polycation complexes. In the nuclear microinjection, precisely the opposite behaviour was observed. (C) 2000 Elsevier Science B.V.

Original languageEnglish (US)
Pages (from-to)149-171
Number of pages23
JournalJournal of Controlled Release
Volume65
Issue number1-2
DOIs
StatePublished - Mar 1 2000

Fingerprint

DNA
Microinjections
polycations
Transfection
N-(2-hydroxypropyl)methacrylamide
Serum Albumin
Osmolar Concentration
Adsorption
Lysine
Polymers
Molecular Weight
Transplants
Gene Expression
Injections
Water
Serum
Genes
Proteins

Keywords

  • Calf thymus DNA
  • Diblock and graft copolymers
  • Interpolyelectrolyte complexes
  • Light scattering methods
  • Polycations
  • Self- assembly
  • Stability of complexes
  • Transfection efficiency

ASJC Scopus subject areas

  • Pharmaceutical Science

Cite this

DNA delivery systems based on complexes of DNA with synthetic polycations and their copolymers. / Oupický, D.; Koňák, Č; Ulbrich, K.; Wolfert, M. A.; Seymour, L. W.

In: Journal of Controlled Release, Vol. 65, No. 1-2, 01.03.2000, p. 149-171.

Research output: Contribution to journalArticle

Oupický, D. ; Koňák, Č ; Ulbrich, K. ; Wolfert, M. A. ; Seymour, L. W. / DNA delivery systems based on complexes of DNA with synthetic polycations and their copolymers. In: Journal of Controlled Release. 2000 ; Vol. 65, No. 1-2. pp. 149-171.
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