Muruganantham Rethinasabapathy

Porous 3D Prussian blue/cellulose aerogel as a decorporation agent for removal of ingested cesium from the gastrointestinal tract

In the present study, we successfully synthesized a porous three-dimensional Prussian blue-cellulose aerogel (PB-CA) composite and used it as a decorporation agent for the selective removal of ingested cesium ions (Cs+) from the gastrointestinal (GI) tract. The safety of the PB-CA composite was evaluated through an in vitro cytotoxicity study using macrophage-like THP-1 cells and Caco-2 intestinal epithelial cells. The results revealed that the PB-CA composite was not cytotoxic. An adsorption study to examine the efficiency of the decorporation agent was conducted using a simulated intestinal fluid (SIF). The adsorption isotherm was fitted to the Langmuir model with a maximum Cs+ adsorption capacity of 13.70 mg/g in SIF that followed pseudo-second-order kinetics. The PB-CA composite showed excellent stability in SIF with a maximum Cs+ removal efficiency of 99.43%. The promising safety toxicology profile, remarkable Cs+ adsorption efficacy, and excellent stability of the composite demonstrated its great potential for use as an orally administered drug for the decorporation of Cs+ from the GI tract.

Visible-light-driven dynamic cancer therapy and imaging using graphitic carbon nitride nanoparticles

Organic graphitic carbon nitride nanoparticles (NP-g-CN), less than 30 nm in size, were synthesized and evaluated for photodynamic therapy (PDT) and cell imaging applications. NP-g-CN particles were prepared through an intercalation process using a rod-like melamine-cyanuric acid adduct (MCA) as the molecular precursor and a eutectic mixture of LiCl-KCl (45:55 wt%) as the reaction medium for polycondensation. The nano-dimensional NP-g-CN penetrated the malignant tumor cells with minimal hindrance and effectively generated reactive oxygen species (ROS) under visible light irradiation, which could ablate cancer cells. When excited by visible light irradiation (λ > 420 nm), NP-g-CN introduced to HeLa and cos-7 cells generated a significant amount of ROS and killed the cancerous cells selectively. The cytotoxicity of NP-g-CN was manipulated by altering the light irradiation and the BP-g-CN caused more damage to the cancer cells than normal cells at low concentrations. As a potential non-toxic organic nanomaterial, the synthesized NP-g-CN are biocompatible with less cytotoxicity than toxic inorganic materials. The combined effects of the high efficacy of ROS generation under visible light irradiation, low toxicity, and bio-compatibility highlight the potential of NP-g-CN for PDT and imaging without further modification.

Cesium-induced inhibition of bacterial growth of Pseudomonas aeruginosa PAO1 and their possible potential applications for bioremediation of wastewater

Radioactive isotopes and fission products have attracted considerable attention because of their long lasting serious damage to the health of humans and other organisms. This study examined the toxicity and accumulation behavior of cesium towards P. aeruginosa PAO1 and its capacity to remove cesium from waste water. Interestingly, the programmed bacterial growth inhibition occurred according to the cesium environment. The influence of cesium was analyzed using several optical methods for quantitative evaluation. Cesium plays vital role in the growth of microorganisms and functions as an anti-microbial agent. The toxicity of Cs to P. aeruginosa PAO1 increases as the concentration of cesium is increased in concentration-dependent manner. P. aeruginosa PAO1 shows excellent Cs removal efficiency of 76.1% from the contaminated water. The toxicity of cesium on the cell wall and in the cytoplasm were studied by transmission electron microscopy and electron dispersive X-ray analysis. Finally, the removal of cesium from wastewater using P. aeruginosa PAO1 as a potential biosorbent and the blocking of competitive interactions of other monovalent cation, such as potassium, were assessed. Overall, P. aeruginosa PAO1 can be used as a high efficient biomaterial in the field of radioactive waste disposal and management.

Versatile poly(diallyl dimethyl ammonium chloride)-layered nanocomposites for removal of cesium in water purification

In this work, we elucidate polymer-layered hollow Prussian blue-coated magnetic nanocomposites as an adsorbent to remove radioactive cesium from environmentally contaminated water. To do this, Fe3O4 nanoparticles prepared using a coprecipitation method were thickly covered with a layer of cationic polymer to attach hollow Prussian blue through a self-assembly process. The as-synthesized adsorbent was confirmed through various analytical techniques. The adsorbent showed a high surface area (166.16 m2/g) with an excellent cesium adsorbent capacity and removal efficiency of 32.8 mg/g and 99.69%, respectively. Moreover, the superparamagnetism allows effective recovery of the adsorbent using an external magnetic field after the adsorption process. Therefore, the magnetic adsorbent with a high adsorption efficiency and convenient recovery is expected to be effectively used for rapid remediation of radioactive contamination.

Hexagonal Co3O4 anchored reduced graphene oxide sheets for high-performance supercapacitors and non-enzymatic glucose sensing

Reduced graphene oxide (RGO) incorporated onto metal–organic framework (MOF)-derived Co3O4 hexagons is prepared via a hydrothermal route for supercapacitor and glucose sensor applications. Various analysis techniques demonstrate that the Co3O4 hexagons were uniformly spread over the thin graphene sheets to assist the electron accessibility of the electrode materials. Under optimized conditions, using 0.1 M KOH electrolyte at a current density of 4 A g−1, a specific capacitance value of 1300 F g−1 is obtained. The fabricated asymmetric supercapacitor cycled reversibly and exhibits high energy and power density values of 65.8 W h kg−1 and 2048 W kg−1, respectively, over the voltage range of −0.1 V to 0.4 V. The asymmetric supercapacitor shows 80.5% capacitance retention even after 5000 cycles at a current density of 4 A g−1, which indicates its high cycling stability in view of the fact that it is binder-free. Furthermore, the RGO–Co3O4 hexagon-modified electrode was optimized to realize the reliable amperometric determination of glucose concentration with a very low detection limit and excellent sensitivity value of 0.4 μM and 1.315 mA mM−1 cm−2, respectively. All of these remarkable performance indicators suggest that RGO–Co3O4 is a promising electrode material for next-generation energy storage devices and electrochemical sensors.

Facile fabrication of paper-based analytical devices for rapid and highly selective colorimetric detection of cesium in environmental samples

Cesium (Cs), a radioactive contaminant of the ecosystem, causes a major risk to human health and environments. Till now, the cesium sensor fabrication methods have been reported with the usage of expensive chemicals that are complex and time-consuming. In this work, we have fabricated a paper-based colorimetric device impregnated with a chrysoidine G (CG) as chemo-indicator which is simple, rapid, low-cost, and portable using a naked-eye quantitative technique for the detection and monitoring of inactive cesium in environmental analysis. This chemo-indicator is designed to exhibit a powerful detection capability featuring high selectivity and sensitivity to inactive Cs, by means of color discrimination from light yellow to red orange. Interestingly, a portable smart phone camera, which determined the relative red/green/blue (RGB) values within 3 s, provided us with further information on environmental pollution. Using our new colorimetric reusable sensor (CRS) platform, the CRS shows excellent detection linearity (R2 = 0.99) of inactive Cs from the contaminated water. Our results will pave the way for portable and versatile sensors and, in turn, for the detection and monitoring of toxic inactive cesium in contaminated water samples.

Electrochemical determination of chloramphenicol using a glassy carbon electrode modified with dendrite-like Fe 3 O 4 nanoparticles

In this study, magnetite (Fe3O4) nanoparticles were electrochemically synthesized in an aqueous electrolyte at a given potential of -1.3 V for 180 s. Scanning electron microscopy revealed that dendrite-like Fe3O4 nanoparticles with a mean size of < 80 nm were electrodeposited on a glassy carbon electrode (GCE). The Fe3O4/GCE was utilized for sensing chloramphenicol (CAP) by cyclic voltammetry and square wave voltammetry. A reduction peak of CAP at the Fe3O4/GCE was observed at 0.62 V, whereas the uncoated GCE exhibited a very small response compared to that of the Fe3O4/GCE. The electrocatalytic ability of Fe3O4 was mainly attributed to the formation of Fe(VI) during the anodic scan, and its reduction to Fe(III) on the cathodic scan facilitated the sensing of CAP. The effects of pH and scan rate were measured to determine the optimum conditions at which the Fe3O4/GCE exhibited the highest sensitivity with a lower detection limit. The reduction current for CAP was proportional to its concentration under optimized conditions in a range of 0.09-47 μM with a correlation coefficient of 0.9919 and a limit of detection of 0.09 μM (S/N=3). Moreover, the fabricated sensor exhibited anti-interference ability towards 4-nitrophenol, thiamphenicol, and 4-nitrobenzamide. The developed electrochemical sensor is a cost effective, reliable, and straightforward approach for the electrochemical determination of CAP in real time applications.