Publication | Open Access
Breaking up the correlation between efficacy and toxicity for nonviral gene delivery
441
Citations
29
References
2007
Year
Tissue EngineeringEngineeringIn Vivo Gene TherapyImmunologyGene DeliveryBiomedical EngineeringNanomedicineIdeal Delivery SystemNew Transfection MaterialsNonviral Gene DeliveryGene TransferVirologyHivMolecular EngineeringPharmacologyCell EngineeringCommercial Transfection ReagentsGene TherapiesPolymer-drug ConjugateNano-drug DeliveryGene VectorMedicine
Nonviral nucleic acid delivery to cells and tissues is considered a standard tool in life science research. However, although an ideal delivery system should have high efficacy and minimal toxicity, existing materials fall short, most of them being either too toxic or little effective. We hypothesized that disulfide cross-linked low-molecular-weight (MW) linear poly(ethylene imine) (MW<4.6 kDa) would overcome this limitation. Investigations with these materials revealed that the extracellular high MW provided outstandingly high transfection efficacies (up to 69.62+/-4.18% in HEK cells). We confirmed that the intracellular reductive degradation produced mainly nontoxic fragments (cell survival 98.69+/-4.79%). When we compared the polymers in >1,400 individual experiments to seven commercial transfection reagents in seven different cell lines, we found highly superior transfection efficacies and substantially lower toxicities. This renders reductive degradation a highly promising tool for the design of new transfection materials.
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