2007
DOI: 10.1016/j.biomaterials.2007.07.023
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A comparative evaluation of poly-l-lysine-palmitic acid and Lipofectamine ™ 2000 for plasmid delivery to bone marrow stromal cells

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Cited by 88 publications
(72 citation statements)
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“…MSCs were infected with the 50 multiplicity of infection (MOI; particle forming units per cell) of adenovirus for 48 hours. We choose the AdGFP as control virus and had consistent results with Clements et al in transfection efficiency and long-term assessment for hBMSCs [27].…”
Section: Adenoviral Transfectionsmentioning
confidence: 84%
“…MSCs were infected with the 50 multiplicity of infection (MOI; particle forming units per cell) of adenovirus for 48 hours. We choose the AdGFP as control virus and had consistent results with Clements et al in transfection efficiency and long-term assessment for hBMSCs [27].…”
Section: Adenoviral Transfectionsmentioning
confidence: 84%
“…In the context of alginate, we did not observe a clear additive effect from the use of liposomal transfection agent, even though literature describes this as an even more successful transfection method than the use of calcium phosphate precipitation 186 . Normally the positively charged liposome complexes make it easier for DNA liposome complexes to access the negatively charged cell membrane 135 . The sugarchains of alginate however, might neutralize the effect of liposome complexation on the cell membrane.…”
Section: Discussionmentioning
confidence: 99%
“…The DNA uptake and thus transfection efficiencies were enhanced by 10-fold, up to 22 %, making it comparable to liposome-based transfection efficiencies, which were used as a control 134 . The combination of both increased transfection efficiencies even more 135 . Other examples of synthetic polymer-based delivery agents are the biodegradable polylactic acid (PLA), poly(lactide-co-glycolide) (PLG) and poly(lactic-co-glycolic acid) (PLGA) 122 136 .…”
Section: Synthetic Polymer-based Transfectionsmentioning
confidence: 96%
“…Generally, viral (e.g., adenoviruses, lentiviruses and retroviruses) and nonviral vectors (e.g., lipids and polymers) can be used for cellular transfection and/or nucleofection, thus offering durable gene expression within stem cells [93][94][95][96]. Nonviral carriers have a number of advantages over viral vectors, since they exhibit low-risk immunogenicity and insertional mutagenesis, controllable toxicity, and excellent gene-carrying capacity [95].…”
Section: A U T H O R P R O O Fmentioning
confidence: 99%
“…Many efforts for the improvement of nonviral vectors are focused on cationic polymers that interact with negatively charged DNA or RNAi. Polymers, including poly(l-lysine)-palmitic acid, poly(l-lysine) and polyethylenimine, condense the genetic material into particles of 200-300 nm in diameter, protect them from enzymes and facilitate cellular entrance [94,97]. These complexes of polymers and genetic material (called 'polyplexes') have a transfection efficiency that is equivalent to adenoviral vectors [97].…”
Section: A U T H O R P R O O Fmentioning
confidence: 99%