4.3 Article

Fluorescent Magnetic Mesoporous Nanoprobes for Biotechnological Enhancement Procedures in Gene Therapy

Journal

MAGNETOCHEMISTRY
Volume 9, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/magnetochemistry9030067

Keywords

superparamagnetic iron oxide nanoparticles; mesoporous silica nanoparticles; transfection; magnetofection

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In recent years, nanotechnology has made significant advancements in cancer therapy through the use of magnetic resonance contrast agents, nano-delivery systems, and magnetic hyperthermia treatments. By exploiting the small size and properties of nanoparticles, such as superparamagnetism, these theragnostic tools offer new possibilities for not only theragnosis, but also biotech procedures. One particular application is the use of bioconjugated magnetic nanoparticles in genetic engineering processes, which have shown enhanced efficiency, specificity, and speed in gene transfer systems compared to conventional methods.
In recent years, nanotechnology has deployed a new set of theragnostic tools, including magnetic resonance contrast agents, nano-delivery systems and magnetic hyperthermia treatments in cancer therapy, exploiting not only the small size of nanoparticles, but also relevant nanoscale properties such as superparamagnetism. Specifically, magnetic nanostructures can be remotely manipulated by external magnetic fields, incrementing their possibilities not only for theragnosis, but also for biotech procedures. Genetic engineering processes involve a set of steps like extracting cells from complex environments, their selection and subsequent cultivation or modification by transfection and can benefit from the use of bioconjugated magnetic nanoparticles. Magnetofection of cells with genes or biological material uploaded on superparamagnetic nanoparticles attracted by a magnetic field greatly increases the efficiency, specificity and speed of the biotechnological procedure in gene transfer systems. This article presents a preliminary investigation into the enhanced transfection efficiency of fluorescent magnetic mesoporous silica nanostructures functionalized with mCherry plasmid, which were used to transfect HeLa cells in just 15 min via magnetic transfection. This method was compared to passive transfection (4 h) and conventional gene transfer using the commercial K2 Transfection System (16 h). The results demonstrated that the fluorescent magnetic mesoporous silica nanostructures were similarly effective to the commercial kit, without the need for reagents that increase costs in clinical therapy. Furthermore, viability assays conducted with HeLa cells showed negligible toxicity at concentrations of up to 50 mu g/mL.

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