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Magnetically enhanced nucleic acid delivery. Ten years of magnetofection—Progress and prospects
- Source :
- Advanced Drug Delivery Reviews
- Publication Year :
- 2011
- Publisher :
- Elsevier BV, 2011.
-
Abstract
- Nucleic acids carry the building plans of living systems. As such, they can be exploited to make cells produce a desired protein, or to shut down the expression of endogenous genes or even to repair defective genes. Hence, nucleic acids are unique substances for research and therapy. To exploit their potential, they need to be delivered into cells which can be a challenging task in many respects. During the last decade, nanomagnetic methods for delivering and targeting nucleic acids have been developed, methods which are often referred to as magnetofection. In this review we summarize the progress and achievements in this field of research. We discuss magnetic formulations of vectors for nucleic acid delivery and their characterization, mechanisms of magnetofection, and the application of magnetofection in viral and nonviral nucleic acid delivery in cell culture and in animal models. We summarize results that have been obtained with using magnetofection in basic research and in preclinical animal models. Finally, we describe some of our recent work and end with some conclusions and perspectives.<br />Graphical abstract
- Subjects :
- Surface Properties
Genetic enhancement
Genetic Vectors
Static Electricity
Pharmaceutical Science
Computational biology
Gene delivery
Biology
Transfection
Article
Adenoviridae
Magnetics
Magnetic targeting
Gene therapy
Pharmaceutical technology
Magnetofection
Basic research
Nucleic Acids
Nucleic acid delivery
Animals
Humans
Magnetite Nanoparticles
Drug Carriers
Magnetic drug targeting
Lentivirus
Genetic transfer
Biochemistry
Magnetic nanoparticles
Nucleic acid
Shut down
Nucleic acid therapy
Subjects
Details
- ISSN :
- 0169409X
- Volume :
- 63
- Database :
- OpenAIRE
- Journal :
- Advanced Drug Delivery Reviews
- Accession number :
- edsair.doi.dedup.....9b46bf963f3414600d3e33e7695e3a94
- Full Text :
- https://doi.org/10.1016/j.addr.2011.08.002