Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Brief Communication
  • Published:

Prolonged organ retention and safety of plasmid DNA administered in polyethylenimine complexes

Abstract

Polyethylenimine (PEI) has been studied as an efficient nonviral gene transfer vector. Here, we report the biodistribution fates and safety of plasmid DNA intravenously administered in PEI complexes. Using pCMVβ as a model gene, the biodistribution of plasmid DNA was measured by quantitative polymerase chain reaction. A deletion mutant of pCMVβ was used as an internal standard. After intravenous administration of PEI/DNA complexes, the serum levels of DNA rapidly declined for up to 15 min. However, after this point, the serum levels of DNA diminished slowly. At 15 min after dose, PEI/DNA complexes showed 33-fold higher distribution of DNA in the lung than did naked DNA. At 24 h, all the organs tested showed much higher levels of plasmid DNA in PEI/DNA complexes, with distribution in the liver and lung being three orders of magnitude higher than naked DNA. The mRNA expression of DNA was observed in various organs of PEI/DNA-treated mice at 12 days after dose. Once a week dosing of PEI/DNA complexes over 3 consecutive weeks did not alter the histology of the organs. However, twice a week dosing over 3 weeks induced a sign of inflammation in the liver. These results indicate that PEI enhances the delivery and retention of plasmid DNA in the organs, especially the liver, but that safe delivery requires proper dosing intervals.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7

Similar content being viewed by others

References

  1. Boussif O et al. A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine Proc Natl Acad Sci USA 1995 92: 7297–7301

    Article  CAS  Google Scholar 

  2. Ringenbach L et al. Polyethylenimine-mediated transfection of human monocytes with the IFN-γ gene: an approach for cancer adoptive immunotherapy Gene Therapy 1998 5: 1508–1516

    Article  CAS  Google Scholar 

  3. Diebold SS et al. Efficient gene delivery into human dendritic cells by adenovirus polyethylenimine and mannose polyethylenimine transfection Hum Gene Ther 1999 10: 775–786

    Article  CAS  Google Scholar 

  4. Dodds E, Piper TA, Murphy SJ, Dickson G . Cationinc lipids and polymers are able to enhance adenoviral infection of culture mouse myotubes J Neurochem 1999 72: 2105–2112

    Article  CAS  Google Scholar 

  5. Bandyopadhyay P et al. Nucleotide exchange in genomic DNA of rat hepatocytes using RNA/DNA oligonucleotides: targeted delivery of liposomes and polyethylenimine to the asialoglycoprotein receptor J Biol Chem 1999 274: 10163–10172

    Article  CAS  Google Scholar 

  6. Boletta A et al. Nonviral gene delivery to the rat kidney with polyethylenimine Hum Gene Ther 1997 8: 1243–1251

    Article  CAS  Google Scholar 

  7. Chemin I et al. Liver-directed gene transfer: a linear polyethyleneimine derivative mediates highly efficient DNA delivery to primary hepatocytes in vitro and in vivo J Viral Hepatitis 1998 5: 369–375

    Article  CAS  Google Scholar 

  8. Ferrari S et al. ExGen 500 is an efficient vector for gene delivery to lung epithelial cells in vitro and in vivo Gene Therapy 1997 4: 1100–1106

    Article  CAS  Google Scholar 

  9. Abdallah B et al. A powerful nonviral vector for in vivo gene transfer into the adult mammalian brain: polyethylenimine Hum Gene Ther 1996 7: 1947–1954

    Article  CAS  Google Scholar 

  10. Oh YK et al. Nasal absorption and biodistribution of plasmid DNA: an alternative route of DNA vaccine delivery Vaccine 2001 19: 4519–4525

    Article  CAS  Google Scholar 

  11. Lew D et al. Cancer gene therapy using plasmid DNA: pharmacokinetic study of DNA following injection in mice Hum Gene Ther 1995 6: 553–564

    Article  CAS  Google Scholar 

  12. Godbey WT et al. Poly(ethylenimine)-mediated transfection: a new papradigm for gene delivery J Biomed Mater Res 2000 51: 321–328

    Article  CAS  Google Scholar 

  13. Osaka G et al. Pharmacokinetics, tissue distribution, and expression efficiency of plasmid [33P]DNA following intravenous administration of DNA/cationic lipid complexes in mice: use of a novel radionuclide approach J Pharm Sci 1996 85: 612–618

    Article  CAS  Google Scholar 

  14. Kawabata K, Takakura Y, Hashida M . The fate of plasmid DNA after intravenous injection in mice: involvement of scavenger receptors in its hepatic uptake Pharm Res 1995 12: 825–830

    Article  CAS  Google Scholar 

  15. Goula D et al. Rapid crossing of the pulmonary endothelial barrier by polyethylenimine/DNA complexes Gene Therapy 2000 7: 499–504

    Article  CAS  Google Scholar 

  16. Klemm AR, Young D, Lloyd JB . Effects of polyethylenimine on endocytosis and lysosome stability Biochem Pharmacol 1998 56: 41–46

    Article  CAS  Google Scholar 

  17. Plank C, Mechtler K, Szoka F, Wagner E . Activation of the complement system by synthetic DNA complexes Hum Gene Ther 1996 7: 1437–1446

    Article  CAS  Google Scholar 

  18. Oral HB et al. Ex vivo adenovirus-mediated gene transfer and immunomodulatory protein production in human cornea Gene Therapy 1997 4: 639–647

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by a grant of the Korea Health 98 R&D Project, Ministry of Health & Welfare, Republic of Korea (HMP-98-D-5–0048).

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Oh, YK., Kim, JP., Yoon, H. et al. Prolonged organ retention and safety of plasmid DNA administered in polyethylenimine complexes. Gene Ther 8, 1587–1592 (2001). https://doi.org/10.1038/sj.gt.3301516

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.gt.3301516

Keywords

This article is cited by

Search

Quick links