Photophysical deactivation behaviour of Rhodamine B using different graphite materials.

In the present work, an attempt has been made to elucidate the structural features of synthesized graphite materials, i.e., expanded graphite (EG) and an expanded graphite/silver nanoparticles (EG/AgNPs) nanocomposite. In order to obtain knowledge about the functional groups present, the interlayer spacing between the carbon layers, topographical features, and the characterization of the materials were carried out using Fourier-transformer infrared spectroscopy, X-ray diffraction, Raman spectroscopy, field emission scanning electron microscopy-energy dispersive X-ray spectroscopy and atomic force microscope. Furthermore, the quenching efficiency of the synthesized graphite materials was also compared using Rhodamine B (Rhd B) as a fluorescent probe. The non-linear behaviour of the Stern-Volmer plots suggested that the complex quenching mechanism (a combination of static and dynamic quenching) was responsible for the decrease in photoluminescence intensity. At a lower concentration of the quencher, the static quenching mechanism was dominant whereas at a higher concentration dynamic processes seemed to be more likely. The binding strength of the complexation between the fluorophore and the quencher at lower concentrations was studied in detail for both of the synthesized materials. The analysis showed that the EG/AgNPs exhibited better quenching efficiency and possessed a strong binding strength in comparison to EG. The thermodynamic parameters of this association suggested that the interaction process was spontaneous and exothermic in nature. Thus, this work offers helpful insights into the fluorescence quenching mechanisms of the Rhd B/EG and its composite system.

Exploring drying pattern of a sessile droplet of genomic DNA in the presence of hematite nanoparticles.

For the first time, drying pattern of a sessile droplet of genomic DNA, in the presence of hematite nanoparticles was sighted by polarizing optical microscopy (POM) in this research article. POM results indicated that only at an appreciably high concentration of hematite nanoparticles dried pattern of deoxyribonucleic acid from calf thymus (CT-DNA) was altered. Iron hybridized cetylpyridinium chloride was utilized for the preparation of iron oxide nanoparticles through hydrothermal method. Fourier transforms infrared spectroscopy (FTIR) and powder x-ray diffraction (PXRD) studies confirmed the formation of highly crystalline hematite i.e. α-Fe2O3 nanoparticles. Morphology of the synthesized nanoparticle was visualized by transmission electron microscope (TEM) and field emission scanning electron microscope (FESEM), which revealed that nanoparticles were rhombohedral in shape with a size of 45 ± 10 nm. Based upon all the findings, hydrothermal growth mechanism was also proposed having bilayer protection of surfactant around the nanoparticles. UV-Vis spectroscopy and fluorescence spectroscopy were explored to study the affinity of thus prepared nanoparticles towards calf thymus deoxyribonucleic acid (CT-DNA). The low value of binding constant calculated from the spectroscopy data confirmed the weak interaction between nanoparticles and the CT-DNA.

Experimental validation of DNA interactions with nanoparticles derived from metal coupled amphiphiles.

In the present report, a facile strategy for the synthesis of copper nanoparticles utilizing copper@cetylpyridinium chloride as the metal precursor in combination with vitamin C, was been developed. Synthesized nanoparticles (NPs) were well characterized through UV-Vis spectroscopy, dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, energy dispersive X-ray (EDX) spectroscopy, and powder X-ray diffraction (XRD). The as-obtained NPs were used for binding with deoxyribonucleic acid from calf thymus (CT-DNA). Binding potential of synthesized NPs towards DNA was checked by calculating apparent binding constant and various thermodynamic parameters, like ΔG, ΔH, ΔS and number of binding sites from UV-Vis, circular dichroism, and fluorescence spectroscopy. NPs lead to the change in conformation and mobility of the genomic DNA as notify by the circular dichroism and DNA gel electrophoresis. Synergistic effect of synthesized nanoparticles on DNA was also visualized by the tapping mode atomic force microscopy. Research findings of the present work are expected to have an impact on genomic activities.