Abstract
Cationic and highly branched poly (trimethylphosphonium ethylacrylate- co-poly (ethylene glycol) acrylate) (p (TMPEA- co-PEGA)), and its ammonium equivalent, have been synthesised from post-polymerisation modification of a poly (bromo ethylacrylate- co-poly (ethylene glycol) acrylate) (p (BEA- co-PEGA)) precursor polymer produced using reversible addition fragmentation chain transfer (RAFT) polymerisation. The cationic polymers were evaluated for their ability to complex nucleic acids, their i n vitro cytotoxicity and their GFP pDNA transfection efficiency. The results show RAFT copolymerisation of BEA and PEGA is a simple route to polyphosphoniums showing reduced cytotoxicities and higher transfection efficiencies than their polyammonium alternatives.
| Original language | English |
|---|---|
| Pages (from-to) | 164-174 |
| Number of pages | 11 |
| Journal | Journal of Interdisciplinary Nanomedicine |
| Volume | 3 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1 Dec 2018 |
| Externally published | Yes |
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