Nano Ag@bioactive microspheres from marine sponge Clathria frondifera: Fabrication, fortification, characterization, anticancer and antibacterial potential evaluation.

Bioresources are attaining much importance in the discovery of drugs and delivering agents. In particular, marine sponges are of great interest due to their metabolites production for the survival in risky environment. The incorporation of silver nanoparticles with marine sponge derived metabolites was reported for the first time. In this work, a facile material has been generated of great efficacy in solving environmental and health issues, as a recipe of silver and marine sponge Clathria frondifera, named as Ag Fortified Sponge spheres (AFS). AFS spheres were successfully synthesized after method optimization, using the various extracts of marine sponge Clathria frondifera as effective reducing agent in Ag (I) to Ag (0) reduction. Bioactive material from marine sponge and AgNP from the reduction of AgNO3 solution stablishing one another and thus AFS spheres were attaining long lifetime along with enhanced antimicrobial activity. The characterization of synthesized AFS and other AgNPs (1-4) has done using FT-IR, PXRD, FESEM, TEM, and UV-vis data. The presence of functional groups such as, Ag-O, and Ag-C stretching bonds in the AFS compounds indicated that it is composed of silver oxides and organo-silver, respectively. The synthesized Ag NPs were found to be spherical like structure with an average size of ∼20 nm. The cytotoxic response of AFS was assessed by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) and morphological changes. AFS are exact spherical, micro sized and effective in inhibiting the growth of both gram positive and gram-negative bacteria. Anticancer studies were also carried out and ensued with excellent activity in the HELA cells with potential application in the medical industry.

Reduction of hexavalent chromium and degradation of tetracycline using a novel indium-doped Mn2O3 nanorod photocatalyst.

This study investigates the photocatalytic reduction of hexavalent chromium (Cr(VI)) and degradation of tetracycline (TC) via visible-light-active In-doped Mn2O3 photocatalysis. Mn2O3 photocatalysts loaded with different In doses are prepared using a simple hydrothermal method, and the results indicate the formation of Mn2O3 nanorod-like structures with good crystallinity. The most significant photocatalytic parameters, namely the catalyst and substrate concentrations, pH, and co-existing ions for the Cr(VI) reduction and TC degradation reactions are systematically examined. Result demonstrates that the Cr(VI) reduction and TC mineralization efficiencies of 52% and 40%, respectively are achieved at the optimum pH of 7, undoped Mn2O3 (10 mg/L), and Cr(VI) or TC concentration of 50 mg/L. However, these efficiencies are remarkably increased to 95% and 93%, respectively, when 10 mg/L of 5% In-doped Mn2O3 is used as the photocatalyst under the same reaction conditions. Moreover, the co-existing HCO3- anions and Ca2+ and Mg2+ divalent cations considerably deteriorate the performance of the In-doped photocatalysts compared with the SO42- and Cl- anions and Na+ and K+ monovalent cations. Liquid chromatography-mass spectrometry analysis reveals that the photodegradation of TC is mainly driven by the elimination of the -CH3 group followed by the subsequent cleavage of the primary -NHCH3 group.

Ultrasonication and hydrothermal assisted synthesis of cloud-like zinc molybdate nanospheres for enhanced detection of flutamide.

Ultrasonication is one of the emerging probes for nanoparticles synthesis as well as promoting the material property by treasuring the precious time during a chemical reaction. In this present work, we successfully designed a cloud-like α-ZnMoO4 nanospheres (ZMNS) using ultrasound assistance (bath sonication with the power of 60 W and frequency of 37/80 kHz) hydrothermal method for catalyzing the effective electrochemical determination of anti-androgen drug candidate flutamide (FLT). The crystallinity and phase purity were investigated using powder X-ray diffractometric analysis. The FTIR and Raman spectra information were compared to detect the possible bonding in ZMNS. The texture and surface morphology were studied using Field emission scanning electron microscope and High-resolution Transmission electron microscope images. The presence of the elements (Zn, Mo and O) and the absence of any other impurities were monitored and confirmed using EDAX analysis. The fabrication of ZMNS modified GCE was performed carefully. Additionally, the ZMNS modified glassy carbon electrode (GCE) exhibits superior electrocatalytic activity by means of higher cathodic peak current towards the detection of FLT. The fashioned electrode attained two wide linear response ranges (0.1 to 73 µM; 111 to 1026 µM) with a lower detection limit of about 33 nM correspondingly. Furthermore, the fabricated sensor displayed excellent sensitivity of 1.095 µA µM-1 cm-2 and good selectivity for FLT sensing even in the existence of similar interfering compounds and biomolecules. Along with that, the designed sensor executed noticeable reproducibility, repeatability, and enduring stability.

In Situ Synthesis, Characterization, and Catalytic Performance of Polypyrrole Polymer-Incorporated Ag2MoO4 Nanocomposite for Detection and Degradation of Environmental Pollutants and Pharmaceutical Drugs.

Material combinations of semiconductor with conducting polymer are gaining growing interest due to their enhanced activities in photocatalysis as well as electrochemical sensing. In this present work, we report a facile in situ synthesis of polypyrrole (PPy) polymer-incorporated silver molybdate (Ag2MoO4) nanocomposite that is utilized as a photocatalyst and electrocatalyst for the degradation of pollutant heavy metals, namely, methylene blue (MB) and heavy metal (Cr(VI)), and ciprofloxacin (CIP) and for detection of the drug, azomycin. The synthesized nanocomposite was characterized by various theoretical, spectral, and microscopic studies. Matching of the powder X-ray diffraction pattern with JCPDS no. 76-1747 confirmed the formation of α-Ag2MoO4/PPy. The surface topography and spherical morphology of the nanocomposite were studied using field emission-scanning electron microscopy and transmission electron microscopy. Fourier transform infrared spectral detail expounds the smooth incorporation of PPy to Ag2MoO4. The as-synthesized nanocomposite performs as an efficient photocatalyst in the degradation of MB (99.9%), Cr(VI) (99%), and CIP drug (99.8%) within 10 min. In addition to this, the Ag2MoO4/PPy-modified glassy carbon electrode (GCE) demonstrated excellent electrocatalytic activity in terms of a higher cathodic peak current and lower peak potential when compared with other modified and unmodified GCEs for the detection of azomycin. The Ag2MoO4/PPy/GCE displayed a broader linear response range and lower detection limit of 0.5-499 µM and 65 nM, respectively. Moreover, other potentially co-interfering compounds, such as a similar functional group-containing biological substances and inorganic species, have no interference effect toward azomycin sensing.

Synthesis, characterization and catalytic performance of nanostructured dysprosium molybdate catalyst for selective biomolecule detection in biological and pharmaceutical samples.

The current study reports a new, simple and fast method using a flake-like dysprosium molybdate (Dy2MoO6; FL-DyM) nanostructured material to detect the antibiotic drug metronidazole (METZ). This nanocomposite material was employed on the surface of a glassy carbon electrode (GCE) to develop the electrode (FL-DyM/GCE). Further, the synthesized FL-DyM was systematically characterized by powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray diffraction (EDS), elemental mapping, X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) analyses. Cyclic (CV) and differential pulse voltammetry (DPV) techniques were used to study the electrochemical properties. The FL-DyM/GCE-based sensor demonstrated excellent selectivity and sensitivity for the detection of the drug METZ, which could be attributed to the strong affinity of FL-DyM towards the -NO2 group in METZ, and the good electrocatalytic activity and conductivity of FL-DyM. The fabrication and optimization of the working electrode were accomplished with CV and DPV obtained by scan rate and pH studies. Compared to the bare GCE and other rare-earth metal molybdates, the FL-DyM/GCE sensor displayed a superior electrocatalytic activity response for METZ detection. The sensor demonstrated a good linear relationship over the concentration range of 0.01-2363 µM. The quantification and detection limits were found to be 0.010 µM and 0.0030 µM, respectively. The FL-DyM/GCE sensor displayed excellent selectivity, repeatability, reproducibility, and stability for the detection of METZ in human urine and commercial METZ tablet samples, which validates the new technique for efficient drug sensing in practical applications.