Defect-Mediated Reactive Oxygen Species Generation in Mg-Substituted ZnO Nanoparticles: Efficient Nanomaterials for Bacterial Inhibition and Cancer Therapy.

Mg-substituted ZnO nanoparticles (MgZnO NPs) were synthesized by a soft chemical approach and were well-characterized by X-ray diffraction, transmission electron microscopy, UV-visible spectroscopy, and photoluminescence spectroscopy. The absorption and photoluminescence spectra show that substitution of Mg ions results in the widening of the band gap and a significant enhancement in the concentration of defects in ZnO NPs. A systemic study of generation of reactive oxygen species (ROS) under dark, daylight, and visible light conditions suggests that the aqueous suspension of MgZnO NPs generates a higher level of ROS because of the surface defects (oxygen vacancies). This capability of MgZnO NPs makes them a more promising candidate for the inhibition of bacterial growth and for killing of cancer cells as compared to pure ZnO NPs, possibly because of the enhanced interaction and accumulation of MgZnO NPs in the cytoplasm or cell membrane in the presence of both Zn2+ and Mg2+ ions. Further, MgZnO NPs exhibit excellent selective killing of nasopharyngeal carcinoma cells (KB) and cervical cancer cells (HeLa) with minimal toxicity to normal fibroblast cells (L929). The results suggest that the generation of ROS and Zn2+ ions are possibly responsible for the higher activity toward the depolarization of cell membrane potential, the lipid peroxidation in bacterial cells, depolarization of the mitochondrial membrane, and cell cycle arrest in the S phase in cancer cells.

Doxorubicin-loaded dendritic-Fe3O4 supramolecular nanoparticles for magnetic drug targeting and tumor regression in spheroid murine melanoma model.

This work evaluates the magnetically-guided delivery of DOX-loaded dendritic-Fe3O4 nanoparticles and their tumor regression efficacy in subcutaneous melanoma in C57BL/6 mice. The hematological, biochemical and histopathological parameters were minimally affected. The nanoparticles localized in lungs, liver and spleen suggesting non-specific uptake. However, in tumor-bearing mice, substantially higher localization in magnetically-targeted tumor was observed when compared to passive localization in non-targeted tumor. The animals of treated group showed significantly high iron levels (161 µg of Fe/mg dry organ weight) in the tumor against the control (<25 µg of Fe/mg dry organ weight). This high localization led to high concentrations of DOX in the tumor which not only induced significant tumor regression but also arrested further growth. Within 14 days, the average tumor volume was reduced to 55±8.3 mm3 (treated) as compared to 4794±844 mm3 (control), i.e. ~88-fold decrease. The tumor disappeared by the end of 20th day post-treatment and ~100% survival rate was observed.

Dual responsive magnetic composite nanogels for thermo-chemotherapy.

With the onset of hyperthermia and their advantage in increasing vascular perfusion and permeability in the cancer milieu, thermo-responsive polymers have become an attractive candidate for designing therapeutic nano-vehicles for targeted on-demand delivery of bioactive agents. For this purpose, we developed a dual (thermo- and pH-) responsive nanotherapeutic composite system rendering a combinational therapy of hyperthermia mediated drug delivery. This composite system comprises of magnetic chitosan-g-PNVCL (MCP) polymeric nanogels loaded with anticancer drug, Doxorubicin (DOX). The size distribution and the stability of the MCP nanogels have been characterized using DLS and Zeta-potential studies. XRD and TG-DTA confirms the presence of magnetic nanoparticles loaded onto MCP nanogel. ICP-AES analysis was done to determine the amount of iron content in the MCP nanogels. The magnetic property of the MCP nanogels was estimated to be ∼37 emu/g using Vibrating Sample Magnetometer (VSM). The heating ability of MCP nanogels was calculated to be ∼204W/g for the concentration of 2mg/mL using time-dependent Specific Absorption Rate (SAR) method. Magnetic field induced thermo-responsive and pH responsive drug release studies were carried out and it was found that MCP nanogels have a good on-demand drug release properties. The DOX-MCP nanogels were evaluated for its in vitro killing efficacy of breast cancer cells MCF 7 and MDAMB 231 cells with synergistic effects of both hyperthermia and chemotherapy in presence of magnetic field at the concentration of 2mg/mL. Thus, MCP nanogels can be a potential dual modal on-demand hyperthermia mediated drug delivery platform for the breast cancer treatment.

Visible light driven mesoporous Ag-embedded ZnO nanocomposites: reactive oxygen species enhanced photocatalysis, bacterial inhibition and photodynamic therapy.

We present here the multitasking capabilities of Ag-embedded ZnO nanocomposites (Ag-ZnO NCs), which include the photocatalytic degradation of organic dyes, bacterial inhibition, and cancer therapeutics. Ag-embedded ZnO nanocomposites (Ag-ZnO NCs) of mesoporous spherical morphology (size ∼ 150 ± 50 nm) are successfully synthesized by a facile and single step soft-chemical approach. To understand the effect of Ag loading on multitasking properties, Ag-ZnO NCs are synthesized with different wt% of Ag. It was found that Ag5-ZnO NCs (5 wt% of Ag) showed excellent solar light-induced photocatalytic degradation properties against both cationic as well as anionic dyes. In addition, the presence of Ag in these NCs makes them strongly antibacterial, and kills 100% Escherichia coli (E. coli) cells within 2 hours (under dark), and within 30 min (under solar light). The enhanced photocatalytic and antibacterial activity of Ag-ZnO NCs is due to the anchoring of Ag NPs onto ZnO as well as minor substitution of Ag ions in the lattice of ZnO. This produces abundant charge carriers and generates significantly enhanced reactive oxygen species (ROS), which seem responsible for the multitasking properties. Furthermore, the cytotoxic study shows that Ag5-ZnO NCs kill oral carcinoma (KB) cells under visible light irradiation, and work as photosensitizers towards the photodynamic therapy of cancer due to the excellent photocatalytic activity. The high ROS concentration depolarizes the mitochondrial membrane potential, which in turn initiates apoptosis in oral carcinoma (KB) cells inducing cell death. Therefore, the as-prepared mesoporous Ag-ZnO NCs show great promise in waste water treatment, and cancer therapeutics.

Cation/Anion Substitution in Cu2ZnSnS4 for Improved Photovoltaic Performance.

Cations and anions are replaced with Fe, Mn, and Se in CZTS in order to control the formations of the secondary phase, the band gap, and the micro structure of Cu2ZnSnS4. We demonstrate a simplified synthesis strategy for a range of quaternary chalcogenide nanoparticles such as Cu2ZnSnS4 (CZTS), Cu2FeSnS4 (CFTS), Cu2MnSnS4 (CMTS), Cu2ZnSnSe4 (CZTSe), and Cu2ZnSn(S0.5Se0.5)4 (CZTSSe) by thermolysis of metal chloride precursors using long chain amine molecules. It is observed that the crystal structure, band gap and micro structure of the CZTS thin films are affected by the substitution of anion/cations. Moreover, secondary phases are not observed and grain sizes are enhanced significantly with selenium doping (grain size ~1 µm). The earth-abundant Cu2MSnS4/Se4 (M = Zn, Mn and Fe) nanoparticles have band gaps in the range of 1.04-1.51 eV with high optical-absorption coefficients (~104 cm-1) in the visible region. The power conversion efficiency of a CZTS solar cell is enhanced significantly, from 0.4% to 7.4% with selenium doping, within an active area of 1.1 ± 0.1 cm2. The observed changes in the device performance parameters might be ascribed to the variation of optical band gap and microstructure of the thin films. The performance of the device is at par with sputtered fabricated films, at similar scales.

Thermoresponsive polymeric gel as an on-demand transdermal drug delivery system for pain management.

The main aim of this work is to design a heat triggered transdermal drug delivery system (TDDS) using a thermoresponsive polymer, poly (N-vinyl caprolactam) [PNVCL] based gel, where in patients can themselves administer a pulse of drug on mere application of heat pad over the TDDS, whenever pain is experienced. The phase transition temperature of PNVCL was tuned to 35 °C by grafting it onto a pH sensitive biopolymer, Chitosan, to synthesize Chitosan-g-PNVCL (CP) co-polymer which render the gel both thermo- and pH-responsive property. The application of triggered delivery was explored by loading acetamidophenol (a model hydrophilic drug) and etoricoxib (a model hydrophobic drug). In vitro drug release experiments were performed at three different temperatures (25, 32 and 39 °C) at two different pH (5.5 and 7) to study its drug release with response to temperature and pH. Drug release profiles obtained were found to have enhanced release for both the drugs respectively at 39 °C (above LCST) and pH5.5 when compared to other release conditions. In vitro skin permeation of both the drugs performed in rat abdominal skin using Franz diffusion cell showed enhanced drug release when the skin was subjected to higher temperature (39 °C). Moreover, it was also found that skin permeation for hydrophobic drug was better than that of hydrophilic drug. The in vivo biocompatibility studies of the CP gel in rat skin proved that the gel is biocompatible. The results obtained demonstrated the potential use of the thermoresponsive CP gel as an on-demand localized drug delivery system.

A pH-responsive folate conjugated magnetic nanoparticle for targeted chemo-thermal therapy and MRI diagnosis.

Polyacrylic acid functionalized Fe3O4 nanoparticles (PAA-MNPs) of average size of 10 nm are prepared by a simple soft chemical approach. These PAA-MNPs are conjugated with folic acid through peptide bonding between the carboxylic group on the surface of PAA-MNPs and the amine group of folic acid. The good colloidal stability of FA conjugated MNPs makes it a promising candidate for targeted drug delivery, hyperthermia and as a MRI contrast agent with a transverse relaxivity R2 value of 105 mM(-1) s(-1). Folic acid conjugated magnetic nanoparticles (FA-MNPs) achieved ∼ 95% loading efficiency of doxorubicin (DOX) which could be due to strong electrostatic interaction of highly negatively charged FA-MNPs and the positively charged DOX. The drug release study shows a pH-dependent behavior and is higher in acidic pH (4.3 and 5.6) as compared to the physiological pH (7.3). Flow cytometry and confocal microscopic image analysis reveal that around 75-80% of HeLa cells undergo apoptosis due to DNA disintegration upon incubation with DOX-MNPs for 24 h. DOX-MNPs exhibit the synergistic effect due to the combination of DOX induced apoptosis and magnetic hyperthermia treatment (MHT) which enhance the cell death ∼ 95.0%. Thus, this system may serve as a potential pH sensitive nanocarrier for synergistic chemo-thermal therapy as well as a possible MRI contrast agent.

Ice-templated synthesis of multifunctional three dimensional graphene/noble metal nanocomposites and their mechanical, electrical, catalytic, and electromagnetic shielding properties.

In-situ homogeneous dispersion of noble metals in three-dimensional graphene sheets is a key tactic for producing macroscopic architecture, which is desirable for practical applications, such as electromagnetic interference shielding and catalyst. We report a one-step greener approach for developing porous architecture of 3D-graphene/noble metal (Pt and Ag) nanocomposite monoliths. The resulting graphene/noble metal nanocomposites exhibit a combination of ultralow density, excellent elasticity, and good electrical conductivity. Moreover, in order to illuminate the advantages of the 3D-graphene/noble metal nanocomposites, their electromagnetic interference (EMI) shielding and electrocatalytic performance are further investigated. The as-synthesized 3D-graphene/noble metal nanocomposites exhibit excellent EMI shielding effectiveness when compared to bare graphene; the effectiveness has an average of 28 dB in the 8.2-12.4 GHz X-band range. In the electro-oxidation of methanol, the 3D-graphene/Pt nanocomposite also exhibits significantly enhanced electrocatalytic performance and stability than compared to reduced graphene oxide/Pt and commercial Pt/C.

Enhanced cell apoptosis triggered by a multi modal mesoporous amphiphilic drug delivery system.

Mesoporous magnetic nanoparticles (MMNPs) have been synthesized through a facile soft chemical route and are conjugated with multiple therapeutic agents. These MMNPs have the ability to contain and deliver both hydrophilic and hydrophobic drugs simultaneously with the mediation of an AC magnetic field (ACMF). Furthermore, the synthesis and characterization of doxorubicin hydrochloride:paclitaxel (DOX:TXL) and doxorubicin hydrochloride:cisplatin (DOX:Cis-Pt) conjugates are demonstrated. MMNPs show an excellent loading efficiency of ~96:83% (DOX:TXL) and ~93:83% (DOX:Cis-Pt) along with a loading capacity of ~0.002:0.002 mg mg(-1) (DOX:TXL) and ~0.002:0.002 mg mg(-1) (DOX:Cis-Pt), respectively. Over a period of 180 h, a sustained release of drugs is observed and shows a better efficiency at pH 4.3 (~85:63%-DOX:TXL and ~86:73%-DOX:Cis-Pt) compared to that under physiological pH conditions (~28:22%-DOX:TXL and ~26:22%-DOX:Cis-Pt). The MMNPs can release ~37:22% (DOX:TXL) and ~34:25% (DOX:Cis-Pt) within 30 min when triggered by an ACMF (at ~43 °C). The in vitro cytotoxic effect, the ROS generation level and cell cycle distribution analysis of DOX:TXL-MMNPs and DOX:Cis-Pt-MMNPs treated MDA-MB231, MCF-7 and PC3 cancer cells are demonstrated. Enhanced cell apoptosis is observed by thermo-chemotherapy which includes application of an ACMF for 15 min. Specifically, DOX:TXL-MMNPs are more effective than DOX:Cis-Pt-MMNPs towards the PC3 cell line. The internalization of multiple drug loaded MMNPs by cells and their morphological changes due to thermo-chemotherapy are confirmed through confocal microscopy. From the present results, it is observed that the DOX:TXL and DOX:Cis-Pt conjugated MMNPs, under an ACMF, can readily minimize drug resistance. This has significantly enhanced the cell apoptosis of target cancer cells.

Magneto-thermally responsive hydrogels for bladder cancer treatment: Therapeutic efficacy and in vivo biodistribution.

Bladder cancer is one of the deadliest forms of cancer in modern medicine which despite recent progress has remained incurable and challenging for researchers. There is unmet need to address this endemic as the number of patients are growing by about 10,000 every year world-wide. Here, we report a minimally invasive magnetic chemotherapy method to address this problem where polyethylene glycol (PEG) functionalized Fe3O4 magnetic nanostructures (MNS) are homogeneously embedded in thermally responsive poly(N-isopropylacrylamide, NIPAAm) hydrogels (HG). The system (HG-MNS) loaded with anti-cancer drug doxorubicin (DOX) incubated with cancer cell lines subjected to external radiofrequency (RF) field can remotely stimulate the release of drug smartly at the site. The in vitro efficacy investigated on bladder cancer (T-24) cell lines showed the potential of the system in dealing with the disease successfully. Further, the materials preferential accumulation via systemic delivery was studied using swiss mice model. Vital tissue organs like liver, lung and heart were analysed by magnetic resonance imaging (MRI). A detail accounts of the materials optimization, cytotoxicity and anti-proliferation activity tests with apoptosis analysis by flow cytometry after RF exposure (250 kHz) to the cells and in vivo biodistribution data are discussed in the paper.

Catalytic and antibacterial activity of Ag decorated magnetic core shell nanosphere.

We report a facile approach for the preparation of Ag nanoparticles decorated magnetic Fe3O4@SiO2 core shell nanosphere (Ag-MCN) and investigated its potential application for the catalytic reduction of organic pollutants and inhibition of bacterial pathogens. The successful formation of Ag-MCN was confirmed by X-ray diffraction (XRD), transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS). The average size of this nanosphere was found to be 85nm and it exhibits superparamagnetic behavior at room temperature. These nanospheres even at low concentration and short incubation period showed good catalytic performance for the reduction of Rhodamine B (RhB) and 4-nitrophenol (4-NP). Further, these magnetic nanosphere possess good antibacterial activity for Gram negative, Escherichia coli (E. coli). Ag-MCN are found to be efficient for complete inhibition of E. coli at a concentration of 50mgL(-1) after incubation for a period of 3h. Furthermore, the generation of reactive oxygen species (ROS) by nanosphere and its effect in the antibacterial activity has been investigated. These nanospheres exhibit good colloidal stability, recycling capability, and could be easily separated from solution via external magnet.

Iron oxide nanorods as high-performance magnetic resonance imaging contrast agents.

An efficient magnetic resonance imaging (MRI) contrast agent with a high R2 relaxivity value is achieved by controlling the shape of iron oxide to rod like morphology with a length of 30-70 nm and diameter of 4-12 nm. Fe3O4 nanorods of 70 nm length, encapsulated with polyethyleneimine show a very high R2 relaxivity value of 608 mM(-1) s(-1). The enhanced MRI contrast of nanorods is attributed to their higher surface area and anisotropic morphology. The higher surface area induces a stronger magnetic field perturbation over a larger volume more effectively for the outer sphere protons. The shape anisotropy contribution is understood by calculating the local magnetic field of nanorods and spherical nanoparticles under an applied magnetic field (3 Tesla). As compared to spherical geometry, the induced magnetic field of a rod is stronger and hence the stronger magnetic field over a large volume leads to a higher R2 relaxivity of nanorods.

Fluorescent ZnO for imaging and induction of DNA fragmentation and ROS-mediated apoptosis in cancer cells.

Fluorescein isothiocyanate (FITC)-encapsulated ZnO nanocomposite has been synthesized using the soft chemical approach. X-ray diffraction reveals the formation of highly crystalline single-phase hexagonal wurtzite nanostructure. TEM and SEM micrographs indicate the formation of spherical porous nanoassembly of ZnO of size ∼ 100-400 nm. On the other hand, FITC-ZnO nanocomposite is spherical and porous but with a uniform size of ∼150 nm. The size of single particles is ∼20 nm for the ZnO nanoassembly and ∼15 nm for FITC-ZnO nanocomposite. The UV-visible, fluorescence, FTIR and XPS spectra confirm the formation of FITC-ZnO nanocomposite. The FITC-ZnO nanocomposite demonstrates excellent selectivity in preferential killing of cervical (HeLa) and breast (MCF-7) cancer cells with minimal toxicity to normal fibroblast cells (L929). Apoptotic cells are observed and analyzed by confocal microscopy and flow cytometry. Our results show that cytotoxicity of FITC-ZnO nanocomposite towards cancer cells is due to the generation of reactive oxygen species (ROS) and preferential dissolution of Zn2+ ions in an acidic cancer microenvironment. Furthermore, generated ROS and dissolved Zn+2 ions induce cellular apoptosis, DNA fragmentation, and depolarization of mitochondrial membrane and cell cycle arrest in S phase. The FITC encapsulated multifunctional ZnO nanocomposite can be used as smart nanostructures for cell imaging and cancer therapy.

Chemically derived defects in zinc oxide nanocrystals and their enhanced photo-electrocatalytic activities.

This paper reports the influence of surface defects on the photocatalytic degradation of methylene blue (MB) for zinc oxide (ZnO) nanocrystals (NCs) synthesized in different organic solvents. A simple chemical approach has been adopted for the promotion of oxygen vacancies in pristine ZnO using solvents namely dimethylformamide (DMF), N-methyl-2-pyrrolidone (NMP) and dimethylsulfoxide (DMSO). This alters the growth of NCs through the promotion of oxygen vacancies depending on the fact that the solvent with minimum viscosity supports faster nucleation and growth exhibiting maximum surface defects. DMF with minimum viscosity results in largest particle size and superior photocatalytic activity. Further, X-ray diffraction, UV-visible reflectance spectroscopy and transmission electron microscopy confirm that the DMF supports the faster growth of NCs as compared to NMP and DMSO. Electron paramagnetic resonance, Raman, X-ray photoelectron, and photoluminescence spectroscopies confirm different states of oxygen vacancies in the NCs and their dependence on the nature of solvents. The photocatalytic activities of these NCs were investigated against the degradation of MB as a model dye. The results show that the oxygen defects at the surface of NCs are more responsible for higher photocatalytic activity than the specific surface area of NCs. The electrochemical investigations of MB degradation suggest that these defects upon interaction with MB influence the storage capacity and charge-discharge profiles of NCs. During degradation, MB passivates these defects, which has been explained in terms of increased charge-discharge time and storage capacity.

pH- and thermosensitive thin lipid layer coated mesoporous magnetic nanoassemblies as a dual drug delivery system towards thermochemotherapy of cancer.

A new pH-sensitive and thermosensitive dual drug delivery system consisting of thin lipid layer encapsulated mesoporous magnetite nanoassemblies (MMNA) has been developed which can deliver two anticancer drugs simultaneously. The formulation of lipid layer used is 5:2:2:2 w/w, DPPC:cholesterol:DSPE-PEG2000:MMNA. The structure, morphology and magnetic properties of MMNA and lipid coated MMNA (LMMNA) were thoroughly characterized. This hybrid system was investigated for its ability to carry two anticancer drugs as well as its ability to provide heat under an alternating current magnetic field (ACMF). A very high loading efficiency of up to ∼81% of doxorubicin hydrochloride (DOX) with an ∼0.02 mg mg(-1) loading capacity and ∼60% of paclitaxel (TXL) with an ∼0.03 mg mg(-1) loading capacity are obtained with LMMNA. A sustained release of drug is observed over a period of 172 h, with better release, of ∼88:53% (DOX:TXL), at pH 4.3 compared to the ∼28:26% (DOX:TXL) in physiological conditions (pH 7.4). An enhanced release of ∼72 and ∼68% is recorded for DOX and TXL, respectively, during the first hour with the application of an ACMF (∼43°C). A greater in vitro cytotoxic effect is observed with the two drugs compared to them individually in HeLa, MCF-7 and HepG2 cancer cells. With the application of an ACMF for 10 min, the cell killing efficiency is improved substantially due to simultaneous thermo- and chemotherapy. Confocal microscopy confirms the internalization of drug loaded MMNA and LMMNA by cells and their morphological changes during thermochemotherapy.

Role of different platinum precursors on the formation and reaction mechanism of FePt nanoparticles and their electrocatalytic performance towards methanol oxidation.

We report the formation mechanism of FePt nanoparticles (NPs) by a high temperature polyol method using an equimolar ratio of Fe and Pt-precursor with different Pt-precursors. Pt(acac)2, PtCl2, PtCl4 and H2PtCl6·H2O were used as Pt-precursors and Fe(acac)3 as the only Fe-precursor. Different stoichiometric compositions along with variation in size were obtained by using different precursors of Pt. Nearly, equiatomic FePt having a size ~2 nm was formed with Pt(acac)2. However, Pt rich phases were formed using all other precursors with a size ranging between 3.6 to 6.4 nm. It was found that the atomic percentage (at%) of Fe in the FePt NPs depends on the reaction parameters. The decomposition behaviour of Fe and Pt-precursors were examined by vibrating sample magnetometer and thermogravimetric measurements. A possible reaction mechanism for Fe depleted FePt formation is proposed which suggests that the reduction potential and decomposition behaviour of the organic and inorganic salts of Pt significantly modify the nucleation behaviour. The electrocatalytic properties of all the four nanomaterials towards methanol oxidation have been investigated by cyclic voltammetry. It is found that Fe19Pt81 with an average size of 6.2 nm shows the highest catalytic response.

Carboxyl decorated Fe3O4 nanoparticles for MRI diagnosis and localized hyperthermia.

We report the development of carboxyl decorated iron oxide nanoparticles (CIONs) by a facile soft-chemical approach for magnetic resonance imaging (MRI) and hyperthermia applications. These superparamagnetic CIONs (~10 nm) are resistant to protein adsorption under physiological medium and exhibit good colloidal stability, magnetization and cytocompatibility with cell lines. Analysis of the T2-weighted MRI scans of CIONs in water yields a transverse relaxivity (r2) value of 215 mM(-1) s(-1). The good colloidal stability and high r2 value make these CIONs as promising candidates for high-efficiency T2 contrast agent in MRI. Further, these biocompatible nanoparticles show excellent self-heating efficacy under external AC magnetic field (AMF). The infrared thermal imaging confirmed the localized heating of CIONs under AMF. Thus, these carboxyl decorated Fe3O4 nanoparticles can be used as a contrast agent in MRI as well as localized heat activated killing of cancer cells. Furthermore, the active functional groups (COOH) present on the surface of Fe3O4 nanoparticles can be accessible for routine conjugation of biomolecules/drugs through well-developed bioconjugation chemistry.

The role of ionic electrolytes on capacitive performance of ZnO-reduced graphene oxide nanohybrids with thermally tunable morphologies.

In the present work, the role of the reaction temperatures on the morphologies of zinc oxide-reduced graphene oxide (ZnO-RGO) nanohybrids and their supercapacitive performance in two different aqueous electrolytes (1.0 M KCl and Na2SO4) were investigated. The ZnO-RGO nanohybrids were synthesized at two different temperatures (ca. 95 and 145 °C) by solvothermal method and labeled as ZnO-RGO-1 and ZnO-RGO-2, respectively. The structure and composition of ZnO-RGO nanohybrids were confirmed by means of X-ray diffraction, electron microscopes (scanning and transmission), X-ray photoelectron, photoluminescence, and Raman spectroscopy. These results show that the temperature allows a good control on loading and morphology of ZnO nanoassemblies in ZnO-RGO nanohybrids and at elevated temperature of 145 °C, ZnO nanoassemblies break and get completely embedded into RGO matrices. The electrochemical performance of ZnO-RGO nanohybrids was examined by cyclic voltammograms (CVs), galvanostatic charge-discharge (chronopotentiometry) and electrochemical impedance spectroscopy (EIS) in 1.0 M KCl and Na2SO4 aqueous electrolytes respectively. Combining the EIS and zeta potential behavior, a direct link between the charge transfer resistance and electrical double layers is established which is responsible for excellent capacitive performance of ZnO-RGO-2. The ZnO-RGO-2 displays high specific capacitance (107.9 F/g, scan rate = 50 mVs(-1)) in 1.0 M KCl and exhibits merely 4.2% decay in specific capacitance values over 200 cycles.

Biocompatibility, biodistribution and efficacy of magnetic nanohydrogels in inhibiting growth of tumors in experimental mice models.

We report in vivo evaluation of a thermo-responsive poly(N-isopropylacrylamide)-chitosan based magnetic nanohydrogel (MNHG) incorporated with Fe3O4 nanoparticles (NPs) in mice models with expandible scope for use in localized delivery of chemotherapeutics. Biocompatibility and biodistribution of the MNHG are studied in normal Swiss mice while efficacy in tumor growth inhibition is studied in a subcutaneous fibrosarcoma tumor. The ex vivo time-dependent pattern of accumulated MNHG into vital organs; lung, liver, spleen, kidney and brain collected at 1 h, 48 h, 7 d and 14 d post intravenous administration are investigated using both a vibrating sample magnetometer (VSM) and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) method. The doses of MNHG (dose I ∼ 650 and dose II ∼ 325 µg g-1 body wt) used in the study are determined based on induced thermal activation of MNHG under an AC magnetic field (AMF). Fibrosarcoma tumor bearing mice are subjected to hyperthermia with a field of 325 Oe and 265 kHz for 30 min following intratumoral administration of dose I. Tumor size measured at an interval of 72 h for a period of 2 weeks reveals that the NPs mediated therapy decelerated the growth of the transplanted tumor by about three-fold (size, 1545 ± 720 mm3) as compared to the exponential growth of the tumor (size, 4510 ± 735 mm3) in control mice. These results suggest the feasibility of using poly(NIPAAm)-chitosan hydrogels loaded with NPs for combined thermo-chemotherapy where the efficacy may further be improved by temperature dependent release of the drugs from the magneto hydrogels.

Visible light-driven novel nanocomposite (BiVO4/CuCr2O4) for efficient degradation of organic dye.

In the present study, BiVO4/CuCr2O4 nanocomposites synthesized via a chemical route are applied as a photocatalyst for the degradation of methylene blue (MB) dye. The photocatalytic activity results indicated a substantial degradation of MB dye by ~90% over the surface of nanocomposite catalyst under visible light illumination. The nanocomposite showed a photocatalytic activity for MB dye degradation which is three times higher compared to that of BiVO4. This has been attributed to photogenerated electron-hole pair charge separation. The prepared photocatalysts were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-Vis absorption and photoluminescence spectroscopy. Furthermore, an oxidizing reagent such as H2O2 was added to the photocatalytic system, which may act as an alternative electron scavenger and resulting in a notably enhanced rate of pollutant destruction. In addition, the effect of polyaniline has also been studied by synthesizing an organic/inorganic hybrid material (BiVO4/CuCr2O4/PANI). It has been observed that 95% photodegradation of organic dye takes place on the nanocomposite surface with visible light. A possible mechanism explaining the origin of enhanced performance of nanocomposite and nanohybrid is proposed.