Badal Kumar Mandal

Biobased green method to synthesise palladium and iron nanoparticles using Terminalia chebula aqueous extract.

There are many methods to synthesise metal and metal oxide nanoparticles (NPs) using different reducing agents which are hazardous in nature. Although some researchers have used biobased materials for synthesis of these NPs, further research is needed in this area. To explore the scope of bio-extract for the synthesis of transition metal NPs, the present paper synthesises metal NPs replacing hazardous traditional reducing agents. This paper reports the synthesis of palladium and iron NPs, using aqueous extract of Terminalia chebula fruit. Reduction potential of aqueous extract of polyphenolic rich T. chebula was 0.63V vs. SCE by cyclic voltammetry study which makes it a good green reducing agent. This helps to reduce palladium and iron salts to palladium and iron NPs respectively. Powder X-ray Diffraction (XRD) and Transmission Electron Microscope (TEM) analyses revealed that amorphous iron NPs were within the size less than 80 nm and cubic palladium NPs were within the size less than 100 nm. The synthesised nanomaterials were remarkably stable for a long period and synthesis of stable metal NPs will need to be explored using biobased materials as reducing agents.

Terminalia chebula mediated green and rapid synthesis of gold nanoparticles

Biologically inspired experimental process in synthesising nanoparticles is of great interest in present scenario. Biosynthesis of nanoparticles is considered to be one of the best green techniques in synthesising metal nanoparticles. Here, an in situ green biogenic synthesis of gold nanoparticles using aqueous extracts of Terminalia chebula as reducing and stabilizing agent is reported. Gold nanoparticles were confirmed by surface plasmon resonance in the range of 535 nm using UV-visible spectrometry. TEM analysis revealed that the morphology of the particles thus formed contains anisotropic gold nanoparticles with size ranging from 6 to 60 nm. Hydrolysable tannins present in the extract of T. chebula are responsible for reductions and stabilization of gold nanoparticles. Antimicrobial activity of gold nanoparticles showed better activity towards gram positive S. aureus compared to gram negative E. coli using standard well diffusion method.

Green synthesis of silver nanoparticles using Terminalia chebula extract at room temperature and their antimicrobial studies

A green rapid biogenic synthesis of silver nanoparticles (Ag NPs) using Terminalia chebula (T. chebula) aqueous extract was demonstrated in this present study. The formation of silver nanoparticles was confirmed by Surface Plasmon Resonance (SPR) at 452 nm using UV-visible spectrophotometer. The reduction of silver ions to silver nanoparticles by T. chebula extract was completed within 20 min which was evidenced potentiometrically. Synthesised nanoparticles were characterised using UV-vis spectroscopy, Fourier transformed infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and atomic force microscopy (AFM). The hydrolysable tannins such as di/tri-galloyl-glucose present in the extract were hydrolyzed to gallic acid and glucose that served as reductant while oxidised polyphenols acted as stabilizers. In addition, it showed good antimicrobial activity towards both Gram-positive bacteria (S. aureus ATCC 25923) and Gram-negative bacteria (E. coli ATCC 25922). Industrially it may be a smart option for the preparation of silver nanoparticles.

Diastase assisted green synthesis of size- controllable gold nanoparticles†

Diastase, a natural enzyme, was used for the one pot aqueous synthesis of gold nanoparticles (AuNPs) of tunable size. During the synthetic process, diastase acts concurrently as both a reducing and stabilizing agent, while no additional chemical reagents or surfactants are added. The formation of AuNPs was confirmed by using a UV-visible spectrophotometer, with a characteristic surface plasmon resonance (SPR) band at 530 nm. The size of the diastase-stabilized AuNPs can be easily controlled by changing the quantity of diastase. The produced AuNPs were characterized by using powder X-ray diffraction (XRD), UV-visible spectroscopy, Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The FTIR spectrum revealed the capping of diastase on the surface of AuNPs. Furthermore, the formed gold nanoparticles are stable for more than three months. In vitro cytotoxicity studies by MTT assay on HCT116 and A549 cancer cells showed that the cytotoxicity of the as-synthesized Au nanocolloids depends on their size and dose.

Cytotoxicity study of Piper nigrum seed mediated synthesized SnO2 nanoparticles towards colorectal (HCT116) and lung cancer (A549) cell lines

Different sized tetragonal tin oxide nanoparticles (SnO2 NPs) were synthesized using Piper nigrum seed extract at three different calcination temperatures (300, 500, 900°C) and these nanoparticles (NPs) were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), dynamic light scattering (DLS) and Fourier transform infrared spectrophotometry (FT-IR). The optical properties were studied using UV-Vis and photoluminescence (PL) spectrophotometers. The generation of reactive oxygen species (ROS) was monitored by using a fluorescence spectrophotometer and fluorescence microscope. The cytotoxicity of the synthesized SnO2 NPs was checked against the colorectal (HCT116) and lung (A549) cancer cell lines and the study results show that SnO2 NPs were toxic against cancer cell lines depending on their size and dose. IC50 values of SnO2 NPs having average particle sizes of 8.85±3.5, 12.76±3.9 and 29.29±10.9nm are 165, 174 and 208μgL-1 against HCT116, while these values are 135, 157 and 187μgL-1 against A549 carcinoma cell lines, respectively. The generated ROS were responsible for the cytotoxicity of SnO2 NPs to the studied cancer cells and smaller size NPs generated more ROS and hence showed higher cytotoxicity over larger size NPs. The results of this study suggest that the synthesized stable nanoparticles could be a potent therapeutic agent towards cancerous cell lines.

Antimicrobial and antioxidant activities of Mimusops elengi seed extract mediated isotropic silver nanoparticles.

The present study reports the use of Mimusops elengi (M. elengi) fruit extract for the synthesis of silver nanoparticles (Ag NPs). The synthesized Ag NPs was initially noticed through visual color change from yellow to reddish brown and further confirmed by surface plasmonic resonance (SPR) band at 429 nm using UV-Visible spectroscopy. Morphology and size of Ag NPs was determined by Transmission Electron Microscopy (TEM) analysis. X-ray Diffraction (XRD) study revealed crystalline nature of Ag NPs. The prolonged stability of Ag NPs was due to capping of oxidized polyphenols which was established by Fourier Transform Infrared Spectroscopy (FTIR) study. The polyphenols present in M. elengi fruit extract was analyzed by High Pressure Liquid Chromatography (HPLC) and the results revealed the presence of ascorbic acid, gallic acid, pyrogallol and resorcinol. In order to study the role of these polyphenols in reducing Ag+ ions to Ag NPs, analyses of extracts before reduction and after reduction were carried out. In addition, the synthesized Ag NPs were tested for antibacterial and antioxidant activities against Staphylococcus aureus (S. Aureus) and Escherichia coli (E. coli). Ag NPs showed good antimicrobial activity against both gram positive (S. aureus) and gram negative (E. coli) bacteria. It also showed good antioxidant activity as compared to ascorbic acid as standard antioxidant.

Green synthesis of nano platinum using naturally occurring polyphenols

We report a simple one step green synthesis of platinum nanoparticles using naturally occurring plant polyphenols obtained from an aqueous extract of Terminalia chebula. No surfactant/stabilizing agent was employed in this method. All the platinum nanoparticles obtained were in the size range of less than 4 nm. The polyphenols responsible for reduction were identified using high performance liquid chromatography. We have demonstrated reduction of Pt+4 to Pt0 and also how the oxidised polyphenols were responsible for stabilizing platinum nanoparticles.

Diastase induced green synthesis of bilayered reduced graphene oxide and its decoration with gold nanoparticles

In this paper, we report an enzyme dependent, green one-pot deoxygenation cum decoration method to synthesize diastase-conjugated reduced graphene oxide (DRG) nanosheets, DRG/gold nanoparticles (DRG/Au) composite. The DRG synthesis was completed in 7h under heating at 90°C on water bath. Selected area electron diffraction (SAED) and Atomic force microscopy (AFM) study has revealed the formation of bilayered reduced graphene oxide sheets. Transmission electron microscopy (TEM) images of DRG/Au composite have shown the uniform decoration of gold nanoparticles (AuNPs) onto the DRG nanosheet surface. Fourier transform infrared spectroscopy (FTIR) and Raman results additionally have shown the functionalization of enzyme molecules onto the DRG nanosheet surface after reduction making it as an effective platform towards the efficient binding of gold nanoparticles. In vitro cytotoxicity studies by MTT assay on A549 and HCT116 cell lines exhibited that the cytotoxicity of the prepared graphene oxide (GO), DRG and DRG/Au is dose dependant. These results have shown that this synthetic method is effective for the production of large scale graphene in a low cost, simple and green method. Since this process avoids the use of hazardous and toxic substances, the produced DRG/Au composites are likely to offer various potential applications in biology and medicine.

Nano-zirconia – Evaluation of its antioxidant and anticancer activity

Bioactivity of nanomaterials largely depends on its size, shape and crystalline nature. In this work, the smaller sized spherical shaped nano-zirconia (ZrO2 NPs) (of ~9 to 11nm) was fabricated and studied its biological activity especially antioxidant and cytotoxicity against human colon carcinoma (HCT-116) and human lung carcinoma (A-549) cell lines. To have its real applications in biological aspects readily available Eucalyptus globulus (E. globulus) leaf extract was used as an effective capping and reducing agent for its synthesis. The prepared ZrO2 NPs was characterized by using different sophisticated instrumentations such as UV-visible spectrophotometer, XRD, FTIR, TEM, SAED, EDX, DLS and fluorescence spectroscopy. Cellular mitochondrial activity i.e. cell viability was measured by MTT assay and anti-oxidant activity was determined by DPPH assay. The smaller sized ZrO2 NPs showed strong antioxidant activity as well as cytotoxicity on human cancer cell lines. Comparative cytotoxic studies were conducted on human cancerous cell lines using different techniques. Results confirmed the efficient anti-cancer activities of the fabricated ZrO2 NPs towards the tested cell lines as well as efficient anti-oxidant activity. This is the first study in which E. globulus leaf extract was used to synthesize smaller spherical shaped ZrO2 NPs for improved bioactivity i.e. antioxidant and cytotoxicity.

Synthesis and characterisation of flower shaped Zinc Oxide nanostructures and its antimicrobial activity

Flower shaped Zinc Oxide nanostructures was synthesized using a simple method without using any structure directing agents. Elemental analysis, crystalline nature, shape and size were examined using Powder X-ray Diffraction (XRD), scanning electron microscopy (SEM), High Resolution Transmission Electron Microscopy (HRTEM) and Energy Dispersive X-ray Spectroscopy (EDAX). XRD revealed the formation of hexagonal ZnO nanostructures. SEM and TEM analyses revealed the formation of crystalline ZnO flowers in which a bunch of ZnO nanorods assembled together to form a leaf like structure followed by flower shaped ZnO nanostructures. Thus synthesised ZnO nanostructures showed good antimicrobial activity towards gram-positive bacteria Staphylococcus aureus as well as gram-negative bacteria Escherichia coli with a MIC/MBC of 25mg/L.