Biodegradable cyclen-based linear and cross-linked polymers as non-viral gene vectors

Bioorg Med Chem. 2012 Feb 15;20(4):1380-7. doi: 10.1016/j.bmc.2012.01.016. Epub 2012 Jan 18.

Abstract

Several 1,4,7,10-tetraazacyclododecane (cyclen)-based linear (3a-c) and cross-linked (8a-d) polymers containing biodegradable ester or disulfide bonds were described. These polymeric compounds were prepared by ring-opening polymerization from various diol glycidyl ethers. The molecular weights of the title polymers were measured by GPC. Agarose gel retardation assays showed that these compounds have good DNA-binding ability and can completely retard plasmid DNA (pDNA) at weight ratio of 20 for linear polymers and 1.2 for cross-linked polymers. The degradation of these polymers was confirmed by GPC. The formed polyplexes have appropriate sizes around 400 nm and zeta-potential values about 15-40 mV. The cytotoxicities of 8 assayed by MTT are much lower than that of 25 KDa PEI. In vitro transfection toward A549 and 293 cells showed that the transfection efficiency (TE) of 8c-DNA polyplex is close to that of 25 kDa PEI at 8c/DNA weight ratio of 4. Structure-activity relationships (SAR) of these linear and cross-linked polymers were discussed in their DNA-binding, cytotoxicity, and transfection studies. In addition, in the presence of serum, the TE of 8/DNA polyplexes could be improved by introducing chloroquine or Ca(2+) to pretreated cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorbable Implants*
  • Cross-Linking Reagents / chemistry*
  • Cyclams
  • Genetic Vectors / chemistry*
  • Heterocyclic Compounds / chemistry*
  • Humans
  • Molecular Weight
  • Polymers / chemistry*
  • Structure-Activity Relationship

Substances

  • Cross-Linking Reagents
  • Cyclams
  • Heterocyclic Compounds
  • Polymers
  • cyclen