Polymer/Nanoceria Hybrid Polyplexes for Gene and Antioxidant Delivery.
Landon MottMatthew L HancockEric A GrulkeDaniel W PackPublished in: ACS applied bio materials (2023)
Various diseases, including cancers and inflammatory diseases, are characterized by a disruption of redox homeostasis, suggesting the need for synergistic treatments involving co-delivery of gene therapies and free radical scavengers. In this report, polyethylenimine (PEI), nanoceria (NC), and DNA were complexed to form nanoparticles providing simultaneous delivery of a gene and an antioxidant. NC was coated in citric acid to provide stable, 4 nm particles that electrostatically bound PEI/DNA polyplexes. The resulting ternary particles transfected HeLa cells with similar efficiency to that of ternary polyplexes comprising 15 kDa poly-l-α-glutamic acid/PEI/DNA while providing smaller particle sizes by more than 100 nm. NC/PEI/DNA polyplexes exhibited enhanced radical-scavenging activity compared to free NC, and oxidative stress from the superoxide-generating agent, menadione, could be completely reversed by the delivery of NC/PEI/DNA polyplexes. Transfection by NC/PEI/DNA polyplexes was demonstrated to occur efficiently through caveolin-mediated endocytosis and macropinocytosis. Co-delivery of genes encoding reactive oxygen species-scavenging proteins, transcription factors, growth factors, tumor suppressors, or anti-inflammatory genes with NC, therefore, may be a promising strategy in synergistic therapeutics.
Keyphrases
- circulating tumor
- oxidative stress
- cell free
- single molecule
- anti inflammatory
- genome wide
- genome wide identification
- reactive oxygen species
- induced apoptosis
- copy number
- nucleic acid
- small molecule
- photodynamic therapy
- dna damage
- signaling pathway
- gene expression
- circulating tumor cells
- cell proliferation
- cell cycle arrest
- cell death
- heat shock protein
- ischemia reperfusion injury
- young adults
- dna binding
- visible light