Cationic lipid-coated magnetic nanoparticles (MPs) associated with transferrin were evaluated as gene transfer vectors in the presence of a static magnetic field. MPs were prepared by chemical precipitation and were surface-coated with cationic lipids, composed of DDAB/soy PC (60:40mole/mole). These cationic MPs were then combined with polyethylenimine (PEI) condensed plasmid DNA, followed by transferrin. The resulting magnetic electrostatic complexes retained relatively compact particle size and showed complete DNA condensation. Their transfection activity in the presence of a static magnetic field was evaluated by luciferase and green fluorescent protein (GFP) reporter genes. The magnetic complexes exhibited up to 300-fold higher transfec...
New approaches to increase the efficiency of non-viral gene delivery are still required. Here we rep...
Abstract: The discovery in the early 2000’s that magnetic nanoparticles (MNPs) complexed to nonviral...
Gene delivery technologies to introduce foreign genes into highly differentiated mammalian cells hav...
Magnetofection; represents nucleic acid delivery by using magnetic nanoparticles (MNPs) under the in...
Newapproaches to increase theefficiencyofnon-viral gene delivery are still required. Here we report ...
Objective: To evaluate the feasibility of using magnetic nanoparticles (MNPs) as gene vector and the...
Human diseases due to genetic mutations, such as cancer, have become the leading cause of death worl...
n recent years, nanotechnology has deployed a new set of theragnostic tools, including magnetic reso...
WOS: 000379969900003Magnetic nanoparticles are effective delivery systems to target therapeutic gene...
Superparamagnetic nanoparticles are promising candidates for gene delivery into mammalian somatic ce...
The safe, targeted and effective delivery of gene therapeutics remains a significant barrier to thei...
This paper describes core-shell-type magnetic nanoparticles (MNPs) and magnetic lipoplexes, comprisi...
Magnetic nanoparticles are effective delivery systems to target therapeutic genes by the attractive ...
Gene therapy is a developing method for the treatment of various diseases. For this purpose, the sea...
Several physical methods have been developed to introduce nucleic acid expression vectors into mamma...
New approaches to increase the efficiency of non-viral gene delivery are still required. Here we rep...
Abstract: The discovery in the early 2000’s that magnetic nanoparticles (MNPs) complexed to nonviral...
Gene delivery technologies to introduce foreign genes into highly differentiated mammalian cells hav...
Magnetofection; represents nucleic acid delivery by using magnetic nanoparticles (MNPs) under the in...
Newapproaches to increase theefficiencyofnon-viral gene delivery are still required. Here we report ...
Objective: To evaluate the feasibility of using magnetic nanoparticles (MNPs) as gene vector and the...
Human diseases due to genetic mutations, such as cancer, have become the leading cause of death worl...
n recent years, nanotechnology has deployed a new set of theragnostic tools, including magnetic reso...
WOS: 000379969900003Magnetic nanoparticles are effective delivery systems to target therapeutic gene...
Superparamagnetic nanoparticles are promising candidates for gene delivery into mammalian somatic ce...
The safe, targeted and effective delivery of gene therapeutics remains a significant barrier to thei...
This paper describes core-shell-type magnetic nanoparticles (MNPs) and magnetic lipoplexes, comprisi...
Magnetic nanoparticles are effective delivery systems to target therapeutic genes by the attractive ...
Gene therapy is a developing method for the treatment of various diseases. For this purpose, the sea...
Several physical methods have been developed to introduce nucleic acid expression vectors into mamma...
New approaches to increase the efficiency of non-viral gene delivery are still required. Here we rep...
Abstract: The discovery in the early 2000’s that magnetic nanoparticles (MNPs) complexed to nonviral...
Gene delivery technologies to introduce foreign genes into highly differentiated mammalian cells hav...