2009
DOI: 10.2478/s11532-009-0045-8
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Polycationic graft copolymers of poly(N-vinylpyrrolidone) as non-viral vectors for gene transfection

Abstract: Novel graft copolymers of 2-(dimethylamino)ethyl methacrylate (DMAEMA) with N-vinylpyrrolidone (NVP) were designed and synthesized by the free radical copolymerization of DMAEMA with precursor polymers of vinyl-functionalized poly(N-vinylpyrrolidone) (PVP). The ability of the PVP-grafted copolymers to bind and condense DNA was confirmed by ethidium bromide displacement assay, agarose gel electrophoresis and transmission electron microscopy. The presence of PVP in the copolymers had a favorable effect on the bi… Show more

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Cited by 4 publications
(2 citation statements)
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“…We investigated a synthetic polymer because of its great versatility in terms of chemical structures while providing safe and cost‐effective alternative. In particular, we used the cationic polymer PVP‐co‐DMAEMA, a biocompatible and not toxic polymer that was previously tested in human cells in vitro as a potential gene delivery system in gene therapies . In addition, poly(1‐vinylpyrrolidone) (PVP) is widely used as binder in tablet formulations, as particle surface stabilizer in nanoparticle synthesis and as cryo‐protectant for adipose tissue‐derived stem cells (hADSC) .…”
Section: Resultsmentioning
confidence: 99%
“…We investigated a synthetic polymer because of its great versatility in terms of chemical structures while providing safe and cost‐effective alternative. In particular, we used the cationic polymer PVP‐co‐DMAEMA, a biocompatible and not toxic polymer that was previously tested in human cells in vitro as a potential gene delivery system in gene therapies . In addition, poly(1‐vinylpyrrolidone) (PVP) is widely used as binder in tablet formulations, as particle surface stabilizer in nanoparticle synthesis and as cryo‐protectant for adipose tissue‐derived stem cells (hADSC) .…”
Section: Resultsmentioning
confidence: 99%
“…They act as neuromuscular relaxants [26], as selective inhibitors of Aβ fibril formation [27], or as antagonists to neuronal nicotinic acetylcholine receptors mediating dopamine release [28,29]. Recently QUATs and polycationic compounds have been intensively investigated as possible non-viral vectors for gene transfection [30][31][32][33].…”
Section: Introductionmentioning
confidence: 99%