Sibnath Kayal

Insights into the mechanism of magnetic particle assisted gene delivery

In magnetic particle assisted gene delivery DNA is complexed with polymer-coated aggregated magnetic nanoparticles (AMNPs) to effect transfection. In vitro studies based on COS-7 cells were carried out using pEGFP-N1 and pMIR-REPORT-complexed, polyethylenimine (PEI)-coated iron oxide magnetic nanoparticles (MNPs). PEI-coated AMNPs (PEI-AMNPs) with average individual particle diameters of 8, 16 and 30 nm were synthesized. Normal, reverse and retention magnetic transfection experiments and cell wounding assays were performed. Our results show that the optimum magnetic field yields maximum transfection efficiency with good viability. The results of the normal, reverse and retention magnetic transfection experiments show that the highest transfection efficiency was achieved in normal magnetic transfection mode due to clustering of the PEI-AMNPs on the cells. Cell wounding assay results suggest that the mechanism of magnetic transfection is endocytosis rather than cell wounding.

The flow of magnetic nanoparticles in magnetic drug targeting

Magnetic drug targeting has been explored by an in vitro study of the deposition of polyvinyl alcohol (PVA) coated magnetic carrier nanoparticles (MCNPs) in a tube under the influence of an externally applied magnetic field. Experiments and simulations show a steady decrease in the retention of MCNPs with increasing flow rate and weaker magnetic field strength. The retention of MCNPs has been significantly influenced by the fluid flow behaviour resulting from the position and shape of the magnet, magnetic properties and size of the MCNPs, and the magnetic field strength. Under strong magnetic fields, the MCNPs tend to creep along the wall of the tube and undergo high shear before reaching the targeted region. These results highlight the importance of choosing the region of MCNP injection, magnetic field strength and, the magnetic properties and size of the MCNPs to minimize the loss of the drug.

Impact of Alkali-Metal Impregnation on MIL-101 (Cr) Metal-Organic Frameworks for CH4 and CO2 Adsorption Studies

In this article, an assessment of the impact of alkali-metal-ion impregnation on metal-organic frameworks (MOF) is presented employing CH4 and CO2 adsorption isotherm data. At first, the parent MOF, MIL-101(Cr), is prepared by a fluorine-free hydrothermal reaction procedure and impregnated with Li, Na, and K alkali cations. These synthesised MOFs are characterized by N2 adsorption/desorption isotherm analysis, X-ray diffraction (XRD) measurement and scanning electron microscopy (SEM). The amount of CH4 and CO2 adsorption uptakes onto parent and alkali ions impregnated MIL-101(Cr) are conducted for wide ranges of pressures and temperatures. For understanding the effects of MOF synthesis process and alkali cations impregnation, CH4 /CO2 uptakes on perfect crystalline MIL-101(Cr) MOF are also calculated by Grand Canonical Monte Carlo (GCMC) simulation and the results are compared with experimental isotherm data of synthesised parent and alkali ions impregnated MIL-101(Cr) MOFs. It is found that the limiting uptakes and the isosteric heats are mainly influenced by the modified adsorbent structures due to alkali ions impregnation and the polarity of adsorbate molecules. Employing Dubinin-Astakhov (DA) equation, the energy distribution of synthesised parent and alkali doped MIL-101 (Cr) MOFs are also presented to identify the alkali cation effects and the surface heterogeneity.