Multifunctional characteristics of biosynthesized CoFe2O4@Ag nanocomposite by photocatalytic, antibacterial and cytotoxic applications.

Carissa carandas, a traditional medicinal herb with a high concentration of antioxidant phytochemicals, has been used for thousands of years in the Ayurveda, Unani, and homoeopathic schools of medicine. By employing Carissa carandas bark extract as a reducing and capping agent in green biosynthesis, we extend this conventional application to produce CoFe2O4 and CoFe2O4@Ag nanocomposite. A variety of techniques have been used to characterize the synthesised nanocomposite, including UV-Vis, FTIR, XRD, FESEM, EDX, and BET. The CoFe2O4 and CoFe2O4@Ag nanocomposite demonstrated promising antibacterial action against human bacterial pathogens like B. subtilis and S. aureus as gram positive and P. aeruginosa and E. coli as gram negative with inhibition zones of 24.3 ± 0.57, 17.4 ± 0.75 and 20.5 ± 0.5, 19.8 ± 1.6 mm respectively, and the obtained results were superior to the nanocomposite without silver. Moreover, in-vitro cytotoxicity effects of biosynthesized CoFe2O4 and CoFe2O4@Ag were performed on the human breast cancer cell MCF-7. It was found that the MCF-7 cells' 50% inhibitory concentration (IC50) was 60 µg/mL. Additionally, biosynthesized CoFe2O4 and CoFe2O4@Ag nanocomposite was used to demonstrate the photocatalytic eradication of Rhodamine Blue (RhB). Due to the addition of Ag, which increases surface area, conductivity, and increased charge carrier separation, the CoFe2O4@Ag nanocomposite exhibits a high percentage of photocatalytic degradation of ⁓ 98% within 35 min under UV light irradiation. The photocatalytic performance of as-synthesised nanocomposite was evaluated using dye degradation-adsorption in both natural light and dark condition. Under dark conditions, it was found that 2 mg mL-1 CoFe2O4@Ag in RhB aqueous solution (5 ppm) causes dye adsorption in 30 min with an effectiveness of 72%. Consequently, it is anticipated that the CoFe2O4@Ag nanocomposite will be a promising photocatalyst and possibly a noble material for environmental remediation applications.

An ultra-sensitive laccase/polyaziridine-bismuth selenide nanoplates modified GCE for detection of atenolol in pharmaceuticals and urine samples.

The analysis of ß-blockers in pharmaceutical, biological and environmental samples has gained much interest due to their wide applications. The aim of this study was to develop an enzyme-based biosensor using hexagonal-shaped low-dimensional Bi2Se3 NPs decorated with laccase through polyaziridine (PAZ) modified glassy carbon electrode (Lac/PAZ-Bi2Se3 NPs/GCE). Surface properties were examined using SEM, TEM, EDX, XRD, XPS, FTIR, UV-Visible, and zeta potential. Electrochemical studies were performed with cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The enzymatic biosensor exhibited excellent catalytic activity towards the oxidation of ATN at +1.05 V (vs Ag/AgCl). Under the optimum experimental conditions, Ip (µA) was linearly related to the concentrations of ATN in the range of 3 to 130 µM (R2 = 0.9972) with an LOD of 0.15 µM and 0.21 µM with and without Lac enzyme. Additionally, the validation of the biosensor was tested to determine ATN on within a day and between-day basis. The biosensor was applied successfully to detect ATN in real samples. The obtained recoveries range from 98.5 % to 99.2 % with an RSD (n = 5) of 0.95 (±0.02). The findings of this study have potential biomedical applications in drug detection employing a promising nano electrode sensor of Lac/PAZ-Bi2Se3 NPs/GCE.

Modeling of neotame and fructose thermochemistry: Comparison with mono and divalent metal ions by Computational and experimental approach.

The metal complexes can demonstrate various interesting biological activities in the human body. However, the role of certain metal ions for specific cell activities is still subject to debate. This study is aimed at comparing the thermochemical properties of neotame (artificial sweetener) and α, ß-fructose in gas phase and water medium. The interaction of α and ß-fructose, neotame with monovalent and divalent metal ions was studied and comprehended by density functional theory (DFT) using B3LYP functional, 6-311 + G (d, p) and D3 basis set. Metal ion affinities (MIA) values depicted that ionic radius of metal ions played an important role in the interaction of α, ß-fructose and neotame. The ∆G parameter was calculated to predict and understand the interaction of metal ions with α and ß-fructose, neotame. The results suggested that the presence of hydroxyl groups and oxygen atoms in sugar molecules acted as preferred sites for the binding and interaction of mono and divalent ions. For the first time computational study has been introduced in the present study to review the progress in the application of metal binding with sugar molecules especially with neotame. Moreover, voltammetric behaviour of neotame-Zn2+ was studied using cyclic and differential pulse voltammetry. The obtained results suggest that the peak at -1.13 V is due to the reduction of Zn2+ in 0.1 M phosphate buffer medium at pH 5.5. Whereas, addition of 6-fold higher concentration of neotame to the ZnCl2.2H2O resulted in a new irreversible cathodic peak at -0.83, due to the reduction of neotame-Zn2+ complex. The Fourier transform infrared spectroscopy (FTIR) results indicates that the ß-amino group (-NH) and carboxyl carbonyl (-C = O) groups of neotame is participating in the chelation process, which is further supported by DFT studies. The findings of this study identify the efficient chelation factors as major contributors into metal ion affinities, with promising possibilities to determine important biological processes in cell wall and glucose transmembrane transport.

Near infrared light activatable PEI-wrapped bismuth selenide nanocomposites for photothermal/photodynamic therapy induced bacterial inactivation and dye degradation.

The inactivation of bacteria and the degradation of organic pollutants by engineered nanomaterials (NMs) are very effective approaches for producing safe and clean drinking water. The development of new NMs which can act as NIR light mediated antimicrobial agents as well as photocatalytic agents is highly desired. In this study, a novel Bi2Se3 nanoplates (NPs) NM was prepared by a high-temperature reaction (colloidal synthesis) followed by wrapping of the surface with polyethyleneimine (PEI) through electrostatic interactions. The developed Bi2Se3 NPs/PEI exhibited excellent NIR light activated antimicrobial properties for bacterial eradication and efficient photocatalytic properties for organic dye degradation. The results showed that upon 808 nm laser irradiation the engineered Bi2Se3 NPs/PEI eradicated ∼99% of S. aureus and ∼97% of E. coli bacteria within 10 minutes of irradiation through combined dual-modal photothermal therapy (PTT) and photodynamic therapy (PDT) via the generation of heat and reactive oxygen species, respectively. The contributions of PTT and PDT were found to be in a ratio of nearly 4 : 1 in the killing of both species of bacteria. In addition, Bi2Se3 NPs/PEI also acted as an excellent photocatalyst under illumination by a halogen lamp equipped with a 700-1100 nm band pass filter to achieve degradation efficiencies of ∼95% for methylene blue and ∼93% for Rhodamine B within 3 and 4 h, respectively. To the best of our knowledge, this is the first demonstration of these NIR light activated antimicrobial properties, photodynamic properties and photocatalytic properties mediated by Bi2Se3 NPs.

An ultrasensitive performance enhanced novel cytochrome c biosensor for the detection of rebaudioside A.

In this study a novel cyctochrome c modified nanocomposite electrochemical biosensor was developed for the electrochemical determination of rebaudioside A in different food samples. The electrode surface was fabricated with graphene oxide assimilated with gold nanoparticles decorated on multiwalled carbon nanotubes/cytochrome c. The developed biosensor exhibited a 10-fold enhancement in the differential pulse voltammetry signal carried out at pH 11.0 in a 0.1M borate buffer. Under the optimized conditions, Ip (µA) was proportional to the rebaudioside A concentration in the range of 0.001-0.05 mM (R(2)=0.8308) and 0.075-1.25 mM (R(2)=0.9920) with a detection limit (S/N=3) of 0.264 µM. Results of this study revealed that cyctochrome c was adsorbed tightly onto the surface of the modified electrode and showed an enzymatic catalytic activity towards the quasi-reversible reduction of rebaudioside A at -0.1 V (vs Ag/AgCl). The direct electron transfer by cytochrome c was further supported by HOMO-LUMO calculations performed at the density functional theory level. Additionally, the molecular docking simulations predicted a stronger binding affinity of rebaudioside A towards cytochrome c, thus supporting their host-guest relationship. The use of novel electrode materials in this study demonstrates the application of the electrochemical biosensor in the food industry.

Fabrication of copper nanoparticles decorated multiwalled carbon nanotubes as a high performance electrochemical sensor for the detection of neotame.

A highly sensitive and novel electrochemical sensor for the detection of neotame using differential pulse voltammetry with a modified glassy carbon electrode is presented. The method was further customized by the fabrication of the electrode surface with copper nanoparticles-ammonium piperidine dithiocarbamate-mutiwalled carbon nanotubes assimilated with ß-cyclodextrin. The multiwalled carbon nanotubes assimilated with ß-cyclodextrin/glassy carbon electrode exhibited catalytic activity towards the oxidation of neotame at a potential of 1.3 V at pH 3.0. The transmission electron microscopy, thermogravimetric analysis, frontier transform infrared spectroscopy and cyclic voltammetry were employed to characterize the electrochemical sensor. The sensitivity and detection limits of the electrode increased two-fold in contrast to the ß-CD-MWCNTs/GCE sensor. The developed method was successfully applied for the determination of neotame in food samples, with results similar to those achieved by our modified capillary electrophoresis method with a 96% confidence level.